Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study - Wikidata - wikimedia - TriplyDB

Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study

Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study

http://www.wikidata.org/entity/Q35041438

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The Interaction between the Immune System and Epigenetics in the Etiology of Autism Spectrum Disorders Molecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disorders TLR3 downregulates expression of schizophrenia gene Disc1 via MYD88 to control neuronal morphology Language Impairments in ASD Resulting from a Failed Domestication of the Human Brain Altered functional brain network connectivity and glutamate system function in transgenic mice expressing truncated Disrupted-in-Schizophrenia 1 Do Apparent Overlaps between Schizophrenia and Autistic Spectrum Disorders Reflect Superficial Similarities or Etiological Commonalities?Imaging-genetics in autism spectrum disorder: advances, translational impact, and future directions.Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.Association analysis of DISC1 gene polymorphisms with Attention-Deficit Hyperactivity Disorder in Iranian population DISC1 genetics, biology and psychiatric illness Disorders and borders: psychiatric genetics and nosology.The Number of Parvalbumin-Expressing Interneurons Is Decreased in the Medial Prefrontal Cortex in Autism.Expression of mutant DISC1 in Purkinje cells increases their spontaneous activity and impairs cognitive and social behaviors in mice.Genetic and Developmental Perspective of Language Abnormality in Autism and Schizophrenia: One Disease Occurring at Different Ages in Humans?Autism spectrum disorder: prospects for treatment using gene therapy.

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P2860

Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study

http://www.wikidata.org/entity/Q35041438

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2011 nî lūn-bûn

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2011 թուականի Մայիսին հրատարակուած գիտական յօդուած

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Dai Zhang

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Fanfan Zheng

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Jing Liu

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Jun Li

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Lifang Wang

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Meixiang Jia

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Tianlan Lu

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Weihua Yue

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Yan Ruan

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P2860

Genetics of austim: complex aetiology for a heterogeneous disorder

DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation

DISC1-NDEL1/NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1

Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia

Disc1 regulates granule cell migration in the developing hippocampus

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

Circuit-based framework for understanding neurotransmitter and risk gene interactions in schizophrenia

Neuroimaging of the functional and structural networks underlying visuospatial vs. linguistic reasoning in high-functioning autism

Haploview: analysis and visualization of LD and haplotype maps

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