Genome-wide methylation analysis in Silver-Russell syndrome patients - Wikidata - awgldk - TriplyDB

Genome-wide methylation analysis in Silver-Russell syndrome patients

Genome-wide methylation analysis in Silver-Russell syndrome patients

http://www.wikidata.org/entity/Q36056485

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Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects.Genomic insights into growth and its disorders: an update.A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes New developments in Silver-Russell syndrome and implications for clinical practice Diagnosis and management of Silver-Russell syndrome: first international consensus statement.An Update on Molecular Diagnostic Testing of Human Imprinting Disorders.Genome-wide analysis of differential DNA methylation in Silver-Russell syndrome.Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children.Epigenetics and Metabolism in Health and Disease BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin-Siris and Nicolaides-Baraitser syndromes

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Genome-wide methylation analysis in Silver-Russell syndrome patients

http://www.wikidata.org/entity/Q36056485

description

2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Genome-wide methylation analysis in Silver-Russell syndrome patients

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Genome-wide methylation analysis in Silver-Russell syndrome patients

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type

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Genome-wide methylation analysis in Silver-Russell syndrome patients

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Genome-wide methylation analysis in Silver-Russell syndrome patients

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Genome-wide methylation analysis in Silver-Russell syndrome patients

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Genome-wide methylation analysis in Silver-Russell syndrome patients

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Genome-wide methylation analysis in Silver-Russell syndrome patients

@en

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A R Prickett

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

G E Moore

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

J M Frost

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

M Ishida

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S Abu-Amero

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S Böhm

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W Puszyk

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P2860

Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia

SWAN: Subset-quantile within array normalization for illumina infinium HumanMethylation450 BeadChips

The role of imprinted genes in humans

The retinoblastoma protein and cell cycle control

Genomic imprinting in mammalian development: a parental tug-of-war

CpG islands and the regulation of transcription

Functions of DNA methylation: islands, start sites, gene bodies and beyond

Galaxy: a platform for interactive large-scale genome analysis.

Using GOstats to test gene lists for GO term association

Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse.

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317-332

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3

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134

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Rebecca J. Oakey

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2015-01-07T00:00:00Z

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270516546

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