An investigation of ribosomal protein L10 gene in autism spectrum disorders. - Wikidata - awgldk - TriplyDB

An investigation of ribosomal protein L10 gene in autism spectrum disorders.

An investigation of ribosomal protein L10 gene in autism spectrum disorders.

http://www.wikidata.org/entity/Q33402638

about

Genetics of autistic disorders: review and clinical implications A novel ribosomopathy caused by dysfunction of RPL10 disrupts neurodevelopment and causes X-linked microcephaly in humans.Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implications Comorbid Analysis of Genes Associated with Autism Spectrum Disorders Reveals Differential Evolutionary Constraints High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.Protein signatures of oxidative stress response in a patient specific cell line model for autism.RPL10mutation segregating in a family with X-linked syndromic Intellectual Disability Mutation and expression analyses of the ribosomal protein gene RPL10 in an extended German sample of patients with autism spectrum disorder Genome-wide mRNA expression analysis of peripheral blood from patients with obsessive-compulsive disorder

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P2860

An investigation of ribosomal protein L10 gene in autism spectrum disorders.

http://www.wikidata.org/entity/Q33402638

description

2009 nî lūn-bûn

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2009 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2009 թվականի հունվարին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

An investigation of ribosomal protein L10 gene in autism spectrum disorders.

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An investigation of ribosomal protein L10 gene in autism spectrum disorders.

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type

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An investigation of ribosomal protein L10 gene in autism spectrum disorders.

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An investigation of ribosomal protein L10 gene in autism spectrum disorders.

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An investigation of ribosomal protein L10 gene in autism spectrum disorders.

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An investigation of ribosomal protein L10 gene in autism spectrum disorders.

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BMC Medical Genetics

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An investigation of ribosomal protein L10 gene in autism spectrum disorders.

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Christelle M Durand

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Fabien Fauchereau

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Gudrun Nygren

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Hany Goubran-Botros

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I Carina Gillberg

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Pauline Chaste

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Svenny Kopp

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Xiaohong Gong

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P2860

X-inactivation profile reveals extensive variability in X-linked gene expression in females

Assembly of the QM protein onto the 60S ribosomal subunit occurs in the cytoplasm

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

Association between microdeletion and microduplication at 16p11.2 and autism

Autism as a strongly genetic disorder: evidence from a British twin study

The systematic functional characterisation of Xq28 genes prioritises candidate disease genes.

Analysis of X chromosome inactivation in autism spectrum disorders.

Genetics of autism: overview and new directions.

Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism.

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10.1186/1471-2350-10-7

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10

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Christopher Gillberg

Thomas Bourgeron

Catalina Betancur

Henrik Anckarsäter

Marie-Christine Mouren-Simeoni

Richard Delorme

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2009-01-23T00:00:00Z

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Autism spectrum

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