Lack of evidence for an association between WNT2 and RELN polymorphisms and autism - Test2 - elhamkhani - TriplyDB

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

http://www.wikidata.org/entity/Q28253103

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The neuropathology of autism: where do we stand?The genetics of autistic disorders and its clinical relevance: a review of the literature Genetics of autism spectrum disorder Genetics of autistic disorders: review and clinical implications The involvement of Reelin in neurodevelopmental disorders.Wnt signaling in neuropsychiatric disorders: ties with adult hippocampal neurogenesis and behavior Reelin and Neuropsychiatric Disorders.Autism: the quest for the genes A heterogeneity-based genome search meta-analysis for autism-spectrum disorders The ups and downs of Wnt signaling in prevalent neurological disorders Analysis of the RELN gene as a genetic risk factor for autism Neuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum Disorders An evo-devo approach to thyroid hormones in cerebral and cerebellar cortical development: etiological implications for autism Neurodevelopment in schizophrenia: the role of the wnt pathways.No association between polymorphisms of WNT2 and schizophrenia in a Korean population Paraoxonase 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.

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P2860

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

http://www.wikidata.org/entity/Q28253103

description

2004 nî lūn-bûn

@nan

2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի ապրիլին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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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

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

@en

P2093

Christopher Gleason

http://www.w3.org/2001/XMLSchema#string

Donna Spiker

http://www.w3.org/2001/XMLSchema#string

Jun Li

http://www.w3.org/2001/XMLSchema#string

Linda Lotspeich

http://www.w3.org/2001/XMLSchema#string

Loan Nguyen

http://www.w3.org/2001/XMLSchema#string

Neil Risch

http://www.w3.org/2001/XMLSchema#string

Richard M Myers

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P2860

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

Consed: a graphical tool for sequence finishing

Autism and genetics. A decade of research.

Statistical refinement of primer design parameters

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51-7

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scholarly article

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2926045

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10.1002/AJMG.B.20122

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15048648

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