Population-based and family-based association study of 5'UTR polymorphism of the reelin gene and schizophrenia.
about
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in womenReplication of association between working memory and Reelin, a potential modifier gene in schizophreniaThe involvement of Reelin in neurodevelopmental disorders.The Reelin signaling pathway promotes dendritic spine development in hippocampal neuronsStructural Insights into Reelin Function: Present and FutureMice that lack the C-terminal region of Reelin exhibit behavioral abnormalities related to neuropsychiatric disorders.The myelin-pathogenesis puzzle in schizophrenia: a literature review.No effect of a common allelic variant in the reelin gene on intermediate phenotype measures of brain structure, brain function, and gene expressionFamily- and population-based designs identify different rare causal variants.The benzamide MS-275 is a potent, long-lasting brain region-selective inhibitor of histone deacetylases.Is treatment-resistant schizophrenia categorically distinct from treatment-responsive schizophrenia? a systematic review.Synaptic dysfunction and oxidative stress in Alzheimer's disease: emerging mechanisms.Opportunities and challenges of psychiatric drug discovery: roles for scientists in academic, industry, and government settings.Adult neurogenesis and neurodegenerative diseases: A systems biology perspective.Statistical epistasis and progressive brain change in schizophrenia: an approach for examining the relationships between multiple genes.Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study.Association of Disrupted in Schizophrenia 1 (DISC1) missense variants with ultra-resistant schizophrenia.Analysis of common genetic variants identifies RELN as a risk gene for schizophrenia in Chinese population.Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia.Dorsal Forebrain-Specific Deficiency of Reelin-Dab1 Signal Causes Behavioral Abnormalities Related to Psychiatric Disorders.
P2860
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P2860
Population-based and family-based association study of 5'UTR polymorphism of the reelin gene and schizophrenia.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Population-based and family-ba ...... reelin gene and schizophrenia.
@en
Population-based and family-ba ...... reelin gene and schizophrenia.
@nl
type
label
Population-based and family-ba ...... reelin gene and schizophrenia.
@en
Population-based and family-ba ...... reelin gene and schizophrenia.
@nl
prefLabel
Population-based and family-ba ...... reelin gene and schizophrenia.
@en
Population-based and family-ba ...... reelin gene and schizophrenia.
@nl
P2093
P2860
P50
P356
P1476
Population-based and family-ba ...... reelin gene and schizophrenia.
@en
P2093
Céline Goldberger
David Gourion
Marie-Chantal Bourdel
Sophie Leroy
P2860
P356
10.1002/AJMG.B.30191
P577
2005-08-01T00:00:00Z