New Insights Into Intellectual Disability Caused by Mutations in a Chromatin Regulator.

about

Identification and Function of Enhancers in the Human Genome.

P2860

Q38893481-0D526266-6A04-4293-9296-A151D1E69644

P2860

New Insights Into Intellectual Disability Caused by Mutations in a Chromatin Regulator.

Item

http://www.wikidata.org/entity/Q41003302

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

New Insights Into Intellectual Disability Caused by Mutations in a Chromatin Regulator.

@en

type

Item

label

New Insights Into Intellectual Disability Caused by Mutations in a Chromatin Regulator.

@en

prefLabel

New Insights Into Intellectual Disability Caused by Mutations in a Chromatin Regulator.

@en

P1476

New Insights Into Intellectual Disability Caused by Mutations in a Chromatin Regulator.

@en

P2093

Emily Brookes

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

P2860

The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases

Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation.

A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C.

H3K4me3 demethylation by the histone demethylase KDM5C/JARID1C promotes DNA replication origin firing

Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.

A Mouse Model of X-linked Intellectual Disability Associated with Impaired Removal of Histone Methylation

The dendritic tree and brain disorders.

The Histone Demethylase KDM5 Activates Gene Expression by Recognizing Chromatin Context through Its PHD Reader Motif.

NSD1 mutations generate a genome-wide DNA methylation signature.

Balancing of Histone H3K4 Methylation States by the Kdm5c/SMCX Histone Demethylase Modulates Promoter and Enhancer Function

P304

2-3

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

P31

scholarly article

P356

10.1016/J.EBIOM.2016.04.001

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

P478

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

P50

Emily Brookes

P577

2016-04-04T00:00:00Z

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

P5875

301236497

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

P698

27211531

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

P921

disability

P932

4856783

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

New Insights Into Intellectual Disability Caused by Mutations in a Chromatin Regulator.

about

P2860

P2860

New Insights Into Intellectual Disability Caused by Mutations in a Chromatin Regulator.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P5875

P698

P921

P932