CAGE-defined promoter regions of the genes implicated in Rett Syndrome. - Test2 - elhamkhani - TriplyDB

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

http://www.wikidata.org/entity/Q35533684

about

Characterisation of CDKL5 Transcript Isoforms in Human and Mouse Novel biomarkers that assist in accurate discrimination of squamous cell carcinoma from adenocarcinoma of the lung.Gene therapy for Rett syndrome: prospects and challenges

P2860

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P2860

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

http://www.wikidata.org/entity/Q35533684

description

2014 nî lūn-bûn

@nan

2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

@ast

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

@en

type

label

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

@ast

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

@en

prefLabel

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

@ast

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

@en

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1471-2164-15-1177

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CAGE-defined promoter regions of the genes implicated in Rett Syndrome

@en

P2093

Alka Saxena

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Annarita Patrizi

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FANTOM Consortium

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Leonard Lipovich

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

Michela Fagiolini

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

Peter Zhang

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

Thomas Ha

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

P2860

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation

The winged-helix protein brain factor 1 interacts with groucho and hes proteins to repress transcription

Rett syndrome: revised diagnostic criteria and nomenclature

Histone H3K27ac separates active from poised enhancers and predicts developmental state

Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA

FOXG1 is responsible for the congenital variant of Rett syndrome

P304

1177

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scholarly article

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10.1186/1471-2164-15-1177

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P407

P478

15

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Robin Andersson

Daniel Goldowitz

Alistair Forrest

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2014-12-24T00:00:00Z

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270003127

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25539566

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4522966

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