Species Translation, Human Data, and Disease Models

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Species Translation, Human Data, and Disease Models

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Source: https://github.com/AllenNeuralDynamics/ComputationalReviewPV/blob/df9fc7e8d455b084152c9d713558dae0013cef21/content/11_species_disease.md

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  • 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer’s disease (AD), but the strength...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer’s disease (AD), but the strength...

  • 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer’s disease (AD), but the strength...

  • 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer’s disease (AD), but the strength...

  • 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer’s disease (AD), but the strength...

  • 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer’s disease (AD), but the strength...

  • 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...

  • 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...

  • 8Citationpaper:paper-0e592639bc4bAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...

  • 9Citationpaper:paper-ad3f81ab4798Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference0 Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference1 Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference2 Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference3 Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference4 Cross-study evidence for GAD67 mRNA reduction in PV+ neurons in schizophrenia. Studies span multiple cortical regions and quantification methods (ISH, qPCR, microarray). All findings have been independently replicated. Note: heterogeneous metrics preclude direct effect-size comparison across studies; the table format reflects this limitation. Sources: [Hashimoto2003gene,Lewis2012cortical,GonzalezBurgos2010alteration...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference5 Cross-study evidence for GAD67 mRNA reduction in PV+ neurons in schizophrenia. Studies span multiple cortical regions and quantification methods (ISH, qPCR, microarray). All findings have been independently replicated. Note: heterogeneous metrics preclude direct effect-size comparison across studies; the table format reflects this limitation. Sources: [Hashimoto2003gene,Lewis2012cortical,GonzalezBurgos2010alteration...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference6 Cross-study evidence for GAD67 mRNA reduction in PV+ neurons in schizophrenia. Studies span multiple cortical regions and quantification methods (ISH, qPCR, microarray). All findings have been independently replicated. Note: heterogeneous metrics preclude direct effect-size comparison across studies; the table format reflects this limitation. Sources: [Hashimoto2003gene,Lewis2012cortical,GonzalezBurgos2010alteration...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference7 Cross-study evidence for GAD67 mRNA reduction in PV+ neurons in schizophrenia. Studies span multiple cortical regions and quantification methods (ISH, qPCR, microarray). All findings have been independently replicated. Note: heterogeneous metrics preclude direct effect-size comparison across studies; the table format reflects this limitation. Sources: [Hashimoto2003gene,Lewis2012cortical,GonzalezBurgos2010alteration...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference8 Cross-study evidence for GAD67 mRNA reduction in PV+ neurons in schizophrenia. Studies span multiple cortical regions and quantification methods (ISH, qPCR, microarray). All findings have been independently replicated. Note: heterogeneous metrics preclude direct effect-size comparison across studies; the table format reflects this limitation. Sources: [Hashimoto2003gene,Lewis2012cortical,GonzalezBurgos2010alteration...

  • 2Citationpaper:paper-fd04a507b4b6The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference9 Beyond GAD67, meta-analytic evidence directly addresses PV cell density. A systematic review of PV interneuron alterations in stress-related mood disorders found that stress-induced changes in PV cells are reported in only a minority of studies, with effects that are region-, age-, sex-, and stress recency-dependent 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference0. These modest effect sizes challenge the “PV deficit hypothesis” as original...

  • 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference1 Beyond GAD67, meta-analytic evidence directly addresses PV cell density. A systematic review of PV interneuron alterations in stress-related mood disorders found that stress-induced changes in PV cells are reported in only a minority of studies, with effects that are region-, age-, sex-, and stress recency-dependent 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference2. These modest effect sizes challenge the “PV deficit hypothesis” as original...

  • 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference3 Beyond GAD67, meta-analytic evidence directly addresses PV cell density. A systematic review of PV interneuron alterations in stress-related mood disorders found that stress-induced changes in PV cells are reported in only a minority of studies, with effects that are region-, age-, sex-, and stress recency-dependent 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference4. These modest effect sizes challenge the “PV deficit hypothesis” as original...

  • 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference5 Beyond GAD67, meta-analytic evidence directly addresses PV cell density. A systematic review of PV interneuron alterations in stress-related mood disorders found that stress-induced changes in PV cells are reported in only a minority of studies, with effects that are region-, age-, sex-, and stress recency-dependent 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference6. These modest effect sizes challenge the “PV deficit hypothesis” as original...

  • 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference7 Beyond GAD67, meta-analytic evidence directly addresses PV cell density. A systematic review of PV interneuron alterations in stress-related mood disorders found that stress-induced changes in PV cells are reported in only a minority of studies, with effects that are region-, age-, sex-, and stress recency-dependent 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference8. These modest effect sizes challenge the “PV deficit hypothesis” as original...

  • 3Citationpaper:paper-fd8f15e7c2e1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference9 Beyond PV cell density, chandelier cell-specific alterations present a more complex picture. Axon cartridge density — the morphological hallmark of chandelier cell output at pyramidal neuron axon initial segments — shows bidirectional changes across brain regions and pathological contexts (Conflict C12). In the dentate gyrus, GABA bouton subpopulations associated with chandelier-like axonal structures are differenti...

  • 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference0 Beyond PV cell density, chandelier cell-specific alterations present a more complex picture. Axon cartridge density — the morphological hallmark of chandelier cell output at pyramidal neuron axon initial segments — shows bidirectional changes across brain regions and pathological contexts (Conflict C12). In the dentate gyrus, GABA bouton subpopulations associated with chandelier-like axonal structures are differenti...

  • 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference1 A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference2. A critical review...

  • 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference3 A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference4. A critical review...

  • 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference5 A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference6. A critical review...

  • 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference7 A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference8. A critical review...

  • 4Citationpaper:paper-4cb1cf98f0c1The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference9 A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference0. A critical review...

  • 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference1 A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference2. A critical review...

  • 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference3 A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference4. A critical review...

  • 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference5 A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference6. A critical review...

  • 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference7 A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference8. A critical review...

  • 5Citationpaper:paper-faa24c65b3ddThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference9 Whether NMDAR hypofunction in schizophrenia is primarily localized to PV interneurons (C41) and whether PV dysfunction is a primary deficit or secondary to upstream excitatory drive reduction (C42) remain unresolved. Pharmacological blockade affects multiple cell types 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference0, while genetic models show PV-specific vulnerability 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference1. Resolution likely requires cell-type-specific...

  • 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference2 Whether NMDAR hypofunction in schizophrenia is primarily localized to PV interneurons (C41) and whether PV dysfunction is a primary deficit or secondary to upstream excitatory drive reduction (C42) remain unresolved. Pharmacological blockade affects multiple cell types 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference3, while genetic models show PV-specific vulnerability 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference4. Resolution likely requires cell-type-specific...

  • 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference5 The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference6. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...

  • 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference7 The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference8. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...

  • 6Citationpaper:paper-5404be9f8464The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference9 The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference0. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...

  • 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference1 The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference2. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...

  • 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference3 The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference4. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...

  • 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference5 The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference6. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...

  • 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference7 The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference8. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...

  • 7Citationpaper:paper-9febfa10db1aAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference9 The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference0. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...

  • 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference1 The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference2. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...

  • 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference3 Evidence hierarchy for PV interneuron dysfunction in schizophrenia, from molecular/genetic evidence (broadest, most replicated) through cellular/histological and functional/circuit levels to causal/therapeutic evidence (narrowest, greatest translation gap). Meta-analytic effect sizes from 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference4. The dashed arrow highlights Conflict C48: cellular-level PV reduction does not straightforwardly predic...

  • 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference5 Oxidative stress provides a mechanistic bridge between molecular vulnerability and cellular dysfunction. PV interneurons are particularly susceptible to oxidative damage owing to their high metabolic demands, and redox dysregulation during critical developmental periods can permanently compromise PV cell maturation 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference6. Perineuronal nets (PNNs), which no...

  • 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference7 Oxidative stress provides a mechanistic bridge between molecular vulnerability and cellular dysfunction. PV interneurons are particularly susceptible to oxidative damage owing to their high metabolic demands, and redox dysregulation during critical developmental periods can permanently compromise PV cell maturation 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference8. Perineuronal nets (PNNs), which no...

  • 1Citationpaper:paper-6d36973b50abThe oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}sec-oscillations-network, {ref}sec-synaptic-physiology, and {ref}sec-circuit-motifs acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...content/11_species_disease.md:line 4Open reference9 Oxidative stress provides a mechanistic bridge between molecular vulnerability and cellular dysfunction. PV interneurons are particularly susceptible to oxidative damage owing to their high metabolic demands, and redox dysregulation during critical developmental periods can permanently compromise PV cell maturation 8Citationpaper:paper-0e592639bc4bAmong psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...content/11_species_disease.md:line 8Open reference0. Perineuronal nets (PNNs), which no...

  • ... 111 additional anchors in refs_json

References

  1. [Lewis2012cortical] paper:paper-6d36973b50ab “The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}`sec-oscillations-network`, {ref}`sec-synaptic-physiology`, and {ref}`sec-circuit-motifs` acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...”
  2. [GonzalezBurgos2015alterations] paper:paper-fd04a507b4b6 “The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}`sec-oscillations-network`, {ref}`sec-synaptic-physiology`, and {ref}`sec-circuit-motifs` acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...”
  3. [Ogiwara2007nav] paper:paper-fd8f15e7c2e1 “The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}`sec-oscillations-network`, {ref}`sec-synaptic-physiology`, and {ref}`sec-circuit-motifs` acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...”
  4. [Verret2012inhibitory] paper:paper-4cb1cf98f0c1 “The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}`sec-oscillations-network`, {ref}`sec-synaptic-physiology`, and {ref}`sec-circuit-motifs` acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...”
  5. [Nakazawa2012gabaergic] paper:paper-faa24c65b3dd “The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}`sec-oscillations-network`, {ref}`sec-synaptic-physiology`, and {ref}`sec-circuit-motifs` acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...”
  6. [Selten2018inhibitory] paper:paper-5404be9f8464 “The oscillation deficits, synaptic disruptions, and circuit-level phenotypes described in {ref}`sec-oscillations-network`, {ref}`sec-synaptic-physiology`, and {ref}`sec-circuit-motifs` acquire clinical urgency when mapped onto human neurological and psychiatric disease. PV interneuron dysfunction is implicated in schizophrenia, epilepsy, autism spectrum disorder (ASD), and Alzheimer's disease (AD), but the strength...”
  7. [Hashimoto2003gene] paper:paper-9febfa10db1a “Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...”
  8. [GonzalezBurgos2010alterations] paper:paper-0e592639bc4b “Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...”
  9. [Hashimoto2005relationship] paper:paper-ad3f81ab4798 “Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...”
  10. [Dienel2019alterations] paper:paper-9d05b8b1560a “Among psychiatric disorders, schizophrenia has the longest history of implicating PV interneuron dysfunction. The postmortem literature consistently reports reduced GAD67 (glutamic acid decarboxylase 67 kDa) mRNA in PV+ neurons of the dorsolateral prefrontal cortex (DLPFC), a finding independently replicated across multiple laboratories using in situ hybridization, quantitative PCR, and microarray methods [Hashimoto...”
  11. [Perlman2021parvalbumin] paper:paper-f309f67acd4e “Beyond GAD67, meta-analytic evidence directly addresses PV cell density. A systematic review of PV interneuron alterations in stress-related mood disorders found that stress-induced changes in PV cells are reported in only a minority of studies, with effects that are region-, age-, sex-, and stress recency-dependent [Perlman2021parvalbumin]. These modest effect sizes challenge the "PV deficit hypothesis" as original...”
  12. [Kalanithi2005altered] paper:paper-1ed6118d28b1 “Beyond GAD67, meta-analytic evidence directly addresses PV cell density. A systematic review of PV interneuron alterations in stress-related mood disorders found that stress-induced changes in PV cells are reported in only a minority of studies, with effects that are region-, age-, sex-, and stress recency-dependent [Perlman2021parvalbumin]. These modest effect sizes challenge the "PV deficit hypothesis" as original...”
  13. [Schobel2013imaging] paper:paper-336819c0d57f “Beyond GAD67, meta-analytic evidence directly addresses PV cell density. A systematic review of PV interneuron alterations in stress-related mood disorders found that stress-induced changes in PV cells are reported in only a minority of studies, with effects that are region-, age-, sex-, and stress recency-dependent [Perlman2021parvalbumin]. These modest effect sizes challenge the "PV deficit hypothesis" as original...”
  14. [Alhourani2020gaba] paper:paper-026e39c932f7 “Beyond PV cell density, chandelier cell-specific alterations present a more complex picture. Axon cartridge density — the morphological hallmark of chandelier cell output at pyramidal neuron axon initial segments — shows bidirectional changes across brain regions and pathological contexts (Conflict C12). In the dentate gyrus, GABA bouton subpopulations associated with chandelier-like axonal structures are differenti...”
  15. [Rocco2017alterations] paper:paper-088fa528776a “Beyond PV cell density, chandelier cell-specific alterations present a more complex picture. Axon cartridge density — the morphological hallmark of chandelier cell output at pyramidal neuron axon initial segments — shows bidirectional changes across brain regions and pathological contexts (Conflict C12). In the dentate gyrus, GABA bouton subpopulations associated with chandelier-like axonal structures are differenti...”
  16. [Belforte2010postnatal] paper:paper-31c511f98d76 “A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities [Belforte2010postnatal,Nakazawa2012gabaergic]. A critical review...”
  17. [Bygrave2019methyl] paper:paper-6e52adc0c72b “A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities [Belforte2010postnatal,Nakazawa2012gabaergic]. A critical review...”
  18. [GonzalezBurgos2012nmda] paper:paper-e5b6d90799d6 “A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities [Belforte2010postnatal,Nakazawa2012gabaergic]. A critical review...”
  19. [Nakazawa2020origin] paper:paper-f895edf20e89 “A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities [Belforte2010postnatal,Nakazawa2012gabaergic]. A critical review...”
  20. [Xiao2021biomarker] paper:paper-4c1bef659eb8 “A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities [Belforte2010postnatal,Nakazawa2012gabaergic]. A critical review...”
  21. [Lisman2008circuit] paper:paper-2e307cde19ef “A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities [Belforte2010postnatal,Nakazawa2012gabaergic]. A critical review...”
  22. [Ferguson2018interneurons] paper:paper-0b942dc09a15 “A parallel line of evidence implicates NMDA receptor (NMDAR) hypofunction as an upstream mechanism driving PV interneuron dysfunction. Postnatal ablation of NMDARs in 40–50% of cortical and hippocampal interneurons produces schizophrenia-like phenotypes in mice, including reduced PV expression, impaired gamma oscillations, and behavioral abnormalities [Belforte2010postnatal,Nakazawa2012gabaergic]. A critical review...”
  23. [GonzalezBurgos2008gaba] paper:paper-7d1f48246bb8 “The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits [GonzalezBurgos2015alterations,GonzalezBurgos2008gaba]. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...”
  24. [Lodge2009loss] paper:paper-6b9d5ae87be7 “The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits [GonzalezBurgos2015alterations,GonzalezBurgos2008gaba]. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...”
  25. [Kaar2019pre] paper:paper-8a23937e9dab “The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits [GonzalezBurgos2015alterations,GonzalezBurgos2008gaba]. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...”
  26. [DePieri2025resting] paper:paper-1aa62508f29b “The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits [GonzalezBurgos2015alterations,GonzalezBurgos2008gaba]. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...”
  27. [Gandal2012gamma] paper:paper-4527ec33c155 “The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits [GonzalezBurgos2015alterations,GonzalezBurgos2008gaba]. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...”
  28. [Tsunada2020dissociation] paper:paper-dea6d53f4cca “The functional consequences of PV alterations in schizophrenia center on gamma oscillation deficits. Frontal cortex gamma oscillation induction during cognitive tasks is attenuated in patients, a finding linked to PV interneuron-mediated perisomatic inhibition deficits [GonzalezBurgos2015alterations,GonzalezBurgos2008gaba]. Reduced PV interneuron density in medial prefrontal cortex and ventral hippocampus correlates...”
  29. [Steullet2017oxidative] paper:paper-11e919e39fbf “Oxidative stress provides a mechanistic bridge between molecular vulnerability and cellular dysfunction. PV interneurons are particularly susceptible to oxidative damage owing to their high metabolic demands, and redox dysregulation during critical developmental periods can permanently compromise PV cell maturation [Steullet2017oxidative,Cabungcal2013perineuronal,Cuenod2022caught]. Perineuronal nets (PNNs), which no...”
  30. [Cabungcal2013perineuronal] paper:paper-9db5fbcbb76a “Oxidative stress provides a mechanistic bridge between molecular vulnerability and cellular dysfunction. PV interneurons are particularly susceptible to oxidative damage owing to their high metabolic demands, and redox dysregulation during critical developmental periods can permanently compromise PV cell maturation [Steullet2017oxidative,Cabungcal2013perineuronal,Cuenod2022caught]. Perineuronal nets (PNNs), which no...”
  31. [Cuenod2022caught] paper:paper-8c11fd67cfe2 “Oxidative stress provides a mechanistic bridge between molecular vulnerability and cellular dysfunction. PV interneurons are particularly susceptible to oxidative damage owing to their high metabolic demands, and redox dysregulation during critical developmental periods can permanently compromise PV cell maturation [Steullet2017oxidative,Cabungcal2013perineuronal,Cuenod2022caught]. Perineuronal nets (PNNs), which no...”

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