Chromodomain proteins in development: lessons from CHARGE syndrome. - Wikidata - awgldk - TriplyDB

Chromodomain proteins in development: lessons from CHARGE syndrome.

Chromodomain proteins in development: lessons from CHARGE syndrome.

http://www.wikidata.org/entity/Q34990736

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Chromodomain helicase DNA-binding proteins in stem cells and human developmental diseases Connecting teratogen-induced congenital heart defects to neural crest cells and their effect on cardiac function The neural crest in cardiac congenital anomalies Mutation update on the CHD7 gene involved in CHARGE syndrome Epigenetic regulation in the inner ear and its potential roles in development, protection, and regeneration.Kismet/CHD7 regulates axon morphology, memory and locomotion in a Drosophila model of CHARGE syndrome.Architects of the genome: CHD dysfunction in cancer, developmental disorders and neurological syndromes Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE Syndrome.Different CHD chromatin remodelers are required for expression of distinct gene sets and specific stages during development of Dictyostelium discoideum.Chd7 is indispensable for mammalian brain development through activation of a neuronal differentiation programme.The Chromodomain Helicase DNA-Binding Chromatin Remodelers: Family Traits that Protect from and Promote Cancer.Cerebellar vermis hypoplasia in CHARGE syndrome: clinical and molecular characterization of 18 unrelated Korean patients.Radiologic and Audiologic Findings in the Temporal Bone of Patients with CHARGE Syndrome.Epigenetic reprogramming converts human Wharton's jelly mesenchymal stem cells into functional cardiomyocytes by differential regulation of Wnt mediators.Structural pituitary abnormalities associated with CHARGE syndrome.Versatile Roles of the Chromatin Remodeler CHD7 during Brain Development and Disease.CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.Guilty as CHARGED: p53's expanding role in disease.Phenotype in 18 Danish subjects with genetically verified CHARGE syndrome.Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome.Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7.Evidence for replicative mechanism in a CHD7 rearrangement in a patient with CHARGE syndrome.

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Chromodomain proteins in development: lessons from CHARGE syndrome.

http://www.wikidata.org/entity/Q34990736

description

2010 nî lūn-bûn

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2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Chromodomain proteins in development: lessons from CHARGE syndrome.

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Chromodomain proteins in development: lessons from CHARGE syndrome.

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Chromodomain proteins in development: lessons from CHARGE syndrome.

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Chromodomain proteins in development: lessons from CHARGE syndrome.

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Chromodomain proteins in development: lessons from CHARGE syndrome.

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Chromodomain proteins in development: lessons from CHARGE syndrome.

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Chromodomain proteins in development: lessons from CHARGE syndrome.

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Chromodomain proteins in development: lessons from CHARGE syndrome.

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Chromodomain proteins in development: lessons from CHARGE syndrome.

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J.1399-0004.2010.01446.X

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Clinical Genetics

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Chromodomain proteins in development: lessons from CHARGE syndrome

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E A Hurd

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W S Layman

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P2860

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

CHARGE syndrome: an update

Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

Immunological abnormalities in CHARGE syndrome

Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.

CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome

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11-20

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Donna M. Martin

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