Version history

{
  "scope": "mouse; V1, visual cortex; Nature",
  "claim_text": "Combined physiological imaging and large-scale electron microscopy to study an excitatory network in V1.",
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    "doi": "10.1038/nature17192",
    "claim": "Combined physiological imaging and large-scale electron microscopy to study an excitatory network in V1.",
    "cite_key": "Lee2016",
    "evidence": "Circuits in the cerebral cortex consist of thousands of neurons connected by millions of synapses. A precise understanding of these local networks requires relating circuit activity with the underlying network structure. For pyramidal cells in superficial mouse visual cortex (V1), a consensus is emerging that neurons with similar visual response properties excite each other, but the anatomical basis of this recurrent synaptic network is unknown. Here we combined physiological imaging and large-s...",
    "effect_size": "Local 40° Gabor-like circular patches (sigmoidal 10%–90% falloff in 10°) containing either square-wave (for mapping retinotopy with widefield intrinsic autofluorescence and targeting GCaMP3 injections) or sine-wave (for mapping position of receptive fields with two-photon imaging) drifting gratings (80% contrast) were alternated with periods of uniform mean luminance (59 cd/m).",
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    "effect_size_source_sentence": "Local 40° Gabor-like circular patches (sigmoidal 10%–90% falloff in 10°) containing either square-wave (for mapping retinotopy with widefield intrinsic autofluorescence and targeting GCaMP3 injections) or sine-wave (for mapping position of receptive fields with two-photon imaging) drifting gratings (80% contrast) were alternated with periods of uniform mean luminance (59 cd/m)."
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  "effect_size": "Local 40° Gabor-like circular patches (sigmoidal 10%–90% falloff in 10°) containing either square-wave (for mapping retinotopy with widefield intrinsic autofluorescence and targeting GCaMP3 injections) or sine-wave (for mapping position of receptive fields with two-photon imaging) drifting gratings (80% contrast) were alternated with periods of uniform mean luminance (59 cd/m).",
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  "study_system": "mouse; V1, visual cortex; Nature",
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  "section_title": "9. Physiological signature I — recurrent amplification of weak inputs in mouse cortex; balanced-amplification regimes; ISN operation",
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  "evidence_summary": "Circuits in the cerebral cortex consist of thousands of neurons connected by millions of synapses. A precise understanding of these local networks requires relating circuit activity with the underlying network structure. For pyramidal cells in superficial mouse visual cortex (V1), a consensus is emerging that neurons with similar visual response properties excite each other, but the anatomical basis of this recurrent synaptic network is unknown. Here we combined physiological imaging and large-s...",
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