Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder. - Test2 - elhamkhani - TriplyDB

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

http://www.wikidata.org/entity/Q33943718

about

Relationships between gene expression and brain wiring in the adult rodent brain The neuropathology of autism: where do we stand?Neurobiological Correlates of Autism: A Review of Recent Research The genetics of autistic disorders and its clinical relevance: a review of the literature Genetics of autism spectrum disorder Advances in autism genetics: on the threshold of a new neurobiology Genetics of austim: complex aetiology for a heterogeneous disorder On the epigenetic regulation of the human reelin promoter Reelin expression and glycosylation patterns are altered in Alzheimer's disease Methodological factors influencing measurement and processing of plasma reelin in humans Linkage and candidate gene studies of autism spectrum disorders in European populations Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia Genetics of autistic disorders: review and clinical implications The involvement of Reelin in neurodevelopmental disorders.Constitutional downregulation of SEMA5A expression in autism Current developments in the genetics of autism: from phenome to genome The Reelin signaling pathway promotes dendritic spine development in hippocampal neurons A genetic variant that disrupts MET transcription is associated with autism Canonical and Non-canonical Reelin Signaling RELN Mutations in Autism Spectrum Disorder In Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric Disorders Consensus paper: pathological role of the cerebellum in autism DISC1: a key lead in studying cortical development and associated brain disorders Cytokine dysregulation in autism spectrum disorders (ASD): possible role of the environment Mice with Dab1 or Vldlr insufficiency exhibit abnormal neonatal vocalization patterns Mice that lack the C-terminal region of Reelin exhibit behavioral abnormalities related to neuropsychiatric disorders.Genetic aspects of autism spectrum disorders: insights from animal models Reelin and Neuropsychiatric Disorders.Reelin and disabled-1 expression in developing and mature human cortical neurons No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network Autism: the quest for the genes Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism A heterogeneity-based genome search meta-analysis for autism-spectrum disorders Analysis of the RELN gene as a genetic risk factor for autism Tipping the balance of autism risk: potential mechanisms linking pesticides and autism An evo-devo approach to thyroid hormones in cerebral and cerebellar cortical development: etiological implications for autism A brain region-specific predictive gene map for autism derived by profiling a reference gene set Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains Differential monocyte responses to TLR ligands in children with autism spectrum disorders.Advanced microscopic imaging methods to investigate cortical development and the etiology of mental retardation.

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P2860

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

http://www.wikidata.org/entity/Q33943718

description

2001 nî lūn-bûn

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2001 թուականի Մարտին հրատարակուած գիտական յօդուած

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2001 թվականի մարտին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年论文

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name

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

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Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

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type

label

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

@ast

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

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prefLabel

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

@ast

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

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Molecular Psychiatry

P1476

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

@en

P2093

A M Persico

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

A Totaro

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

C Bravaccio

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

C C Quattrocchi

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

C Schneider

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

Collaborative Linkage Study of Autism

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

F Montecchi

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L D'Agruma

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L Zelante

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M Conciatori

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P2860

A genomic screen of autism: evidence for a multilocus etiology.

A decrease of reelin expression as a putative vulnerability factor in schizophrenia

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

Genetic studies of autistic disorder and chromosome 7

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

Embryological origin for autism: developmental anomalies of the cranial nerve motor nuclei

A protein related to extracellular matrix proteins deleted in the mouse mutant reeler

Defective corticogenesis and reduction in Reelin immunoreactivity in cortex and hippocampus of prenatally infected neonatal mice.

Autism: recent molecular genetic advances.

Genetic studies of autism: from the 1970s into the millennium.

P2888

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150-159

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10.1038/SJ.MP.4000850

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2

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6

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Tiziana Pascucci

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2001-03-01T00:00:00Z

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11317216

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