Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
about
The neuropathology of autism: where do we stand?The genetics of autistic disorders and its clinical relevance: a review of the literatureGenetics of autism spectrum disorderGenetics of autistic disorders: review and clinical implicationsThe involvement of Reelin in neurodevelopmental disorders.Wnt signaling in neuropsychiatric disorders: ties with adult hippocampal neurogenesis and behaviorReelin and Neuropsychiatric Disorders.Autism: the quest for the genesA heterogeneity-based genome search meta-analysis for autism-spectrum disordersThe ups and downs of Wnt signaling in prevalent neurological disordersAnalysis of the RELN gene as a genetic risk factor for autismNeuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum DisordersAn evo-devo approach to thyroid hormones in cerebral and cerebellar cortical development: etiological implications for autismNeurodevelopment in schizophrenia: the role of the wnt pathways.No association between polymorphisms of WNT2 and schizophrenia in a Korean populationParaoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.Altered posterior cingulate cortical cyctoarchitecture, but normal density of neurons and interneurons in the posterior cingulate cortex and fusiform gyrus in autism.Synaptic Wnt signaling-a contributor to major psychiatric disorders?Molecular genetics of autism spectrum disorder.Reelin glycoprotein: structure, biology and roles in health and disease.Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.Early pharmacological treatment of autism: a rationale for developmental treatment.Advances in behavioral genetics: mouse models of autism.A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.A review of the evidence for the canonical Wnt pathway in autism spectrum disorders.Epigenetic factors and autism spectrum disorders.Association between the g.296596G > A genetic variant of RELN gene and susceptibility to autism in a Chinese Han population.Pentapeptide sharing between Corynebacterium diphtheria toxin and the human neural protein network.Differential activation of the calcium/protein kinase C and the canonical beta-catenin pathway by Wnt1 and Wnt7a produces opposite effects on cell proliferation in PC12 cells.Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene.Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.
P2860
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P2860
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
description
2004 nî lūn-bûn
@nan
2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@ast
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@en
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@nl
type
label
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@ast
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@en
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@nl
prefLabel
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@ast
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@en
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@nl
P2093
P2860
P3181
P356
P1476
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
@en
P2093
Christopher Gleason
Donna Spiker
Linda Lotspeich
Loan Nguyen
Neil Risch
Richard M Myers
P2860
P3181
P356
10.1002/AJMG.B.20122
P407
P577
2004-04-01T00:00:00Z