The Cortico-Striatal Interface: Topography, Cell Types, and Input Convergence

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^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...
^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...
^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference} Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}0 partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}1 showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}2 Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}3 partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}4 showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}5 Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}6 partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}7 showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}8 The numbers, however, are not directly comparable. Hintiryan’s 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt’s three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster’s striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}9 The numbers, however, are not directly comparable. Hintiryan’s 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt’s three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster’s striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}0 The numbers, however, are not directly comparable. Hintiryan’s 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt’s three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster’s striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}1 The numbers, however, are not directly comparable. Hintiryan’s 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt’s three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster’s striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}2 The numbers, however, are not directly comparable. Hintiryan’s 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt’s three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster’s striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}3 The numbers, however, are not directly comparable. Hintiryan’s 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt’s three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster’s striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}4 Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}5. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}6 Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}7. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}8 Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}9. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}0 Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}1. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}2 Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}3. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}4 Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}5. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}6 Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}7. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}8 Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}9. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}0 Whether IT and PT inputs function equivalently on striatal projection neurons is contested. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}1 used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display identical spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}2 Whether IT and PT inputs function equivalently on striatal projection neurons is contested. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}3 used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display identical spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}4 Whether IT and PT inputs function equivalently on striatal projection neurons is contested. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}5 used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display identical spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}6 Whether IT and PT inputs function equivalently on striatal projection neurons is contested. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}7 used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display identical spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}8 Whether IT and PT inputs function equivalently on striatal projection neurons is contested. ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}9 used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display identical spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}0 Whether IT and PT inputs function equivalently on striatal projection neurons is contested. ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}1 used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display identical spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}2 This reconciliation also exposes how convergent versus segregated the channels are. Anterograde tracing across mouse motor and frontal cortices shows substantial regional convergence onto a single striatal domain ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}3, while paired in-vivo recordings show that even within a small striatal volume single SPNs receive coordinated drive from multiple cortical areas ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}4. PT a...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}5 This reconciliation also exposes how convergent versus segregated the channels are. Anterograde tracing across mouse motor and frontal cortices shows substantial regional convergence onto a single striatal domain ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}6, while paired in-vivo recordings show that even within a small striatal volume single SPNs receive coordinated drive from multiple cortical areas ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}7. PT a...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}8 This reconciliation also exposes how convergent versus segregated the channels are. Anterograde tracing across mouse motor and frontal cortices shows substantial regional convergence onto a single striatal domain ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}9, while paired in-vivo recordings show that even within a small striatal volume single SPNs receive coordinated drive from multiple cortical areas ^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}0. PT a...
^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}1 This reconciliation also exposes how convergent versus segregated the channels are. Anterograde tracing across mouse motor and frontal cortices shows substantial regional convergence onto a single striatal domain ^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}2, while paired in-vivo recordings show that even within a small striatal volume single SPNs receive coordinated drive from multiple cortical areas ^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}3. PT a...
^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}4 This reconciliation also exposes how convergent versus segregated the channels are. Anterograde tracing across mouse motor and frontal cortices shows substantial regional convergence onto a single striatal domain ^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}5, while paired in-vivo recordings show that even within a small striatal volume single SPNs receive coordinated drive from multiple cortical areas ^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}6. PT a...
^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}7 This reconciliation also exposes how convergent versus segregated the channels are. Anterograde tracing across mouse motor and frontal cortices shows substantial regional convergence onto a single striatal domain ^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}8, while paired in-vivo recordings show that even within a small striatal volume single SPNs receive coordinated drive from multiple cortical areas ^{3Citationpaper:paper-054c1c11810aWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}9. PT a...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}0 The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}1 was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}2, cell-type-specific input mapping showe...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}3 The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}4 was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}5, cell-type-specific input mapping showe...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}6 The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}7 was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}8, cell-type-specific input mapping showe...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}9 The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}0 was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}1, cell-type-specific input mapping showe...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}2 The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}3 was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}4, cell-type-specific input mapping showe...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}5 The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}6 was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}7, cell-type-specific input mapping showe...
^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}8 The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers ^{2Citationpaper:paper-79995db40fc1Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}9 was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In ^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}0, cell-type-specific input mapping showe...
^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}1 The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers ^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}2 was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In ^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}3, cell-type-specific input mapping showe...
^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}4 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}5, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}6. Single-cell and translatome studie...
^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}7 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}8, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{4Citationpaper:paper-2ff9ceab970eWhole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}9. Single-cell and translatome studie...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}00 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}01, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}02. Single-cell and translatome studie...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}03 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}04, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}05. Single-cell and translatome studie...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}06 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}07, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}08. Single-cell and translatome studie...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}09 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}10, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}11. Single-cell and translatome studie...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}12 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}13, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}14. Single-cell and translatome studie...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}15 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}16, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}17. Single-cell and translatome studie...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}18 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}19, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}20. Single-cell and translatome studie...
^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}21 Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}22, while matrix SPNs are organised into matrisomes that align with cortical body-map representations ^{1Citationpaper:paper-8d85b2b35d13Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...content/sec_03_corticostriatal_interface.md:line 9Open reference}23. Single-cell and translatome studie...
... 70 additional anchors in refs_json

References

[Hintiryan2016] paper:paper-8d85b2b35d13 “Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...”
[Foster2021] paper:paper-79995db40fc1 “Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...”
[Hunnicutt2016] paper:paper-054c1c11810a “Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...”
[Peters2021] paper:paper-2ff9ceab970e “Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...”
[Hooks2018] paper:paper-470beb0644b3 “Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...”
[Amroune2025] paper:paper-f092a34fa3c2 “Whole-brain anterograde projectomes have replaced single-tracer studies as the reference description of cortical input topography. [Hintiryan2016] partitioned the mouse dorsal striatum into 29 functional domains using community-detection on cortical input vectors, and the partner reconstruction in [Foster2021] showed that those 29 striatal domains feed forward into 14 substantia nigra pars reticulata domains, 36 glo...”
[Selemon1985] paper:paper-3a2a266bc9c8 “The numbers, however, are not directly comparable. Hintiryan's 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt's three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster's striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...”
[Yeterian1991] paper:paper-7cf1f0b64120 “The numbers, however, are not directly comparable. Hintiryan's 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt's three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster's striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...”
[SaintCyr1990] paper:paper-d4af3e8c4a09 “The numbers, however, are not directly comparable. Hintiryan's 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt's three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster's striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...”
[Flaherty1991] paper:paper-a8be9dded567 “The numbers, however, are not directly comparable. Hintiryan's 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt's three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster's striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...”
[Cowan1994] paper:paper-de00a3f7e39a “The numbers, however, are not directly comparable. Hintiryan's 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt's three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster's striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...”
[Selemon1988] paper:paper-b0cefaddc46d “The numbers, however, are not directly comparable. Hintiryan's 29 domains are derived from community detection on a high-dimensional cortical input matrix; Hunnicutt's three-plus-one parcellation is a coarser anatomical subdivision verified by slice-physiology contrasts; Foster's striatal domain count inherits the Hintiryan partition and reuses it as a node set for whole-brain loop reconstruction. In primates, tradi...”
[Economo2016] paper:b99d7c4a-9270-42c0-b083-2109f9c1eabf “Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures [Economo2016,Tantirigama2015,Gerfen2016,Anderson2020]. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...”
[Tantirigama2015] paper:paper-89006181f9d5 “Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures [Economo2016,Tantirigama2015,Gerfen2016,Anderson2020]. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...”
[Gerfen2016] paper:paper-b0b284f0f8b1 “Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures [Economo2016,Tantirigama2015,Gerfen2016,Anderson2020]. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...”
[Anderson2020] paper:2fb0d69a-a5e5-4629-9856-1d98636e335e “Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures [Economo2016,Tantirigama2015,Gerfen2016,Anderson2020]. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...”
[Winnubst2019] paper:041efce6-fc13-4416-8aca-e196f82f3d70 “Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures [Economo2016,Tantirigama2015,Gerfen2016,Anderson2020]. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...”
[Coude2018] paper:paper-77a2dd07b413 “Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures [Economo2016,Tantirigama2015,Gerfen2016,Anderson2020]. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...”
[Park2022] paper:paper-6bb281c30a56 “Cortical pyramidal neurons that project to striatum fall broadly into intratelencephalic (IT, callosal-projecting) and pyramidal-tract (PT, brainstem-projecting) classes, with distinct molecular profiles, laminar positions, and biophysical signatures [Economo2016,Tantirigama2015,Gerfen2016,Anderson2020]. Single-neuron reconstructions in the Mouse Light atlas show that >85% of cortical neurons projecting through the...”
[Ballion2008] paper:paper-c38c21fbb36c “Whether IT and PT inputs *function* equivalently on striatal projection neurons is contested. [Ballion2008] used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display *identical* spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...”
[Morgenstern2022] paper:paper-10_1126_sciadv_abh4315 “Whether IT and PT inputs *function* equivalently on striatal projection neurons is contested. [Ballion2008] used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display *identical* spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...”
[Tepper2008] paper:paper-1ff7ae8aacac “Whether IT and PT inputs *function* equivalently on striatal projection neurons is contested. [Ballion2008] used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display *identical* spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...”
[Znamenskiy2013] paper:paper-f9391808aa5b “Whether IT and PT inputs *function* equivalently on striatal projection neurons is contested. [Ballion2008] used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display *identical* spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...”
[Stuber2011] paper:paper-1c4705b237f1 “Whether IT and PT inputs *function* equivalently on striatal projection neurons is contested. [Ballion2008] used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display *identical* spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...”
[Britt2012] paper:paper-5600a2aa4075 “Whether IT and PT inputs *function* equivalently on striatal projection neurons is contested. [Ballion2008] used antidromic identification in rat to show that, despite a 4.6-fold faster PT conduction velocity, striatonigral and striatopallidal neurons display *identical* spike-response latencies to cortical stimulation; the inference was that IT supplies the dominant excitation and PT a weaker, slower input that nev...”
[Pawlak2008] paper:paper-35c9f2a65167 “This reconciliation also exposes how convergent versus segregated the channels are. Anterograde tracing across mouse motor and frontal cortices shows substantial regional convergence onto a single striatal domain [Hintiryan2016,Hunnicutt2016], while paired in-vivo recordings show that even within a small striatal volume single SPNs receive coordinated drive from multiple cortical areas [Pawlak2008,Aronoff2010]. PT a...”
[Aronoff2010] paper:paper-3890a436fee7 “This reconciliation also exposes how convergent versus segregated the channels are. Anterograde tracing across mouse motor and frontal cortices shows substantial regional convergence onto a single striatal domain [Hintiryan2016,Hunnicutt2016], while paired in-vivo recordings show that even within a small striatal volume single SPNs receive coordinated drive from multiple cortical areas [Pawlak2008,Aronoff2010]. PT a...”
[Gerfen1984] paper:paper-2012e75bd4bd “The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers [Gerfen1984,Hersch1995,Berendse1992a] was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In [Smith2016], cell-type-specific input mapping showe...”
[Hersch1995] paper:paper-6a6238e2e03c “The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers [Gerfen1984,Hersch1995,Berendse1992a] was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In [Smith2016], cell-type-specific input mapping showe...”
[Berendse1992a] paper:paper-f83c2c8584ae “The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers [Gerfen1984,Hersch1995,Berendse1992a] was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In [Smith2016], cell-type-specific input mapping showe...”
[Smith2016] paper:paper-13ae59d0e41f “The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers [Gerfen1984,Hersch1995,Berendse1992a] was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In [Smith2016], cell-type-specific input mapping showe...”
[Miyamoto2018] paper:paper-af27099c1079 “The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers [Gerfen1984,Hersch1995,Berendse1992a] was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In [Smith2016], cell-type-specific input mapping showe...”
[Crittenden2022] paper:paper-2961aa317bd5 “The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers [Gerfen1984,Hersch1995,Berendse1992a] was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In [Smith2016], cell-type-specific input mapping showe...”
[Friedman2015] paper:paper-36af14df61c5 “The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers [Gerfen1984,Hersch1995,Berendse1992a] was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In [Smith2016], cell-type-specific input mapping showe...”
[Banghart2015] paper:paper-d7668c3dad2f “The striosome/matrix architecture identified by acetylcholinesterase, opioid-receptor, and dopaminergic markers [Gerfen1984,Hersch1995,Berendse1992a] was originally interpreted as a strict input dichotomy: matrix receives sensorimotor cortex, striosomes receive limbic and orbitofrontal cortex. Modern viral tracing has eroded the strict version of that dichotomy. In [Smith2016], cell-type-specific input mapping showe...”
[Fujiyama2019] paper:paper-3231f2ad956e “Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons [Fujiyama2019,McGregor2019a,Prager2020,Prager2019], while matrix SPNs are organised into matrisomes that align with cortical body-map representations [Pommer2021,Crittenden2022]. Single-cell and translatome studie...”
[McGregor2019a] paper:paper-e57e2bfec43e “Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons [Fujiyama2019,McGregor2019a,Prager2020,Prager2019], while matrix SPNs are organised into matrisomes that align with cortical body-map representations [Pommer2021,Crittenden2022]. Single-cell and translatome studie...”
[Prager2020] paper:paper-c30dbaabf25a “Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons [Fujiyama2019,McGregor2019a,Prager2020,Prager2019], while matrix SPNs are organised into matrisomes that align with cortical body-map representations [Pommer2021,Crittenden2022]. Single-cell and translatome studie...”
[Prager2019] paper:paper-e04473484b83 “Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons [Fujiyama2019,McGregor2019a,Prager2020,Prager2019], while matrix SPNs are organised into matrisomes that align with cortical body-map representations [Pommer2021,Crittenden2022]. Single-cell and translatome studie...”
[Pommer2021] paper:paper-4c962950370f “Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons [Fujiyama2019,McGregor2019a,Prager2020,Prager2019], while matrix SPNs are organised into matrisomes that align with cortical body-map representations [Pommer2021,Crittenden2022]. Single-cell and translatome studie...”
[Munoz2018] paper:paper-191813f01755 “Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons [Fujiyama2019,McGregor2019a,Prager2020,Prager2019], while matrix SPNs are organised into matrisomes that align with cortical body-map representations [Pommer2021,Crittenden2022]. Single-cell and translatome studie...”
[BengtssonGonzales2020] paper:paper-2b7f5cfcae25 “Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons [Fujiyama2019,McGregor2019a,Prager2020,Prager2019], while matrix SPNs are organised into matrisomes that align with cortical body-map representations [Pommer2021,Crittenden2022]. Single-cell and translatome studie...”
[Ryan2024] paper:paper-a472c44d6e47 “Compartmental identity also extends inside the dopaminergic and SPN populations: striosomal SPNs are enriched for direct-pathway markers and provide privileged feedback to substantia-nigra dopamine neurons [Fujiyama2019,McGregor2019a,Prager2020,Prager2019], while matrix SPNs are organised into matrisomes that align with cortical body-map representations [Pommer2021,Crittenden2022]. Single-cell and translatome studie...”

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