Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes (Q28594392)

31 January 2017

title

Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes (English)

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Chromodomain helicase DNA binding protein 4

31 January 2017

main subject

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Chromodomain helicase DNA binding protein 7

GOA release 2020-03-11

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GOA release 2020-03-11

Christel Kockx

8

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Shoumo Bhattacharya

Shoumo Bhattacharya

13

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Jeroen Demmers

Jeroen Demmers

11

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Boris Lenhard

Boris Lenhard

18

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Wilfred F J van IJcken

Wilfred van Ijcken

9

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Frank Grosveld

16

Frank G. Grosveld

1 reference

31 January 2017

1

Erik Engelen

1 reference

31 January 2017

3

Jan Christian Bryne

1 reference

31 January 2017

6

Maaike Moen

1 reference

31 January 2017

10

Dick H. W. Dekkers

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31 January 2017

14

Sjaak Philipsen

1 reference

31 January 2017

19

Raymond A. Poot

1 reference

31 January 2017

Umut Akinci

2

1 reference

31 January 2017

Jun Hou

4

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31 January 2017

Cristina Gontan

5

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31 January 2017

Dorota Szumska

7

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31 January 2017

Erik-Jan Rijkers

12

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31 January 2017

Larysa H. Pevny

15

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31 January 2017

Robbert J. Rottier

17

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31 January 2017

language of work or name

English

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publication date

1 June 2011

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31 January 2017

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31 January 2017

volume

43

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31 January 2017

issue

6

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31 January 2017

page(s)

607–611

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Having it both ways: Sox protein function between conservation and innovation

31 January 2017

cites work

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

21 April 2017

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Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome

21 April 2017

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An Oct4-centered protein interaction network in embryonic stem cells

21 April 2017

1 reference

GenePaint.org: an atlas of gene expression patterns in the mouse embryo

21 April 2017

1 reference

Role of Sox2 in the development of the mouse neocortex

21 April 2017

1 reference

SOX2 is a dose-dependent regulator of retinal neural progenitor competence

21 April 2017

1 reference

Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome

21 April 2017

1 reference

CHD7 cooperates with PBAF to control multipotent neural crest formation

21 April 2017

1 reference

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

21 April 2017

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Multipotent cell lineages in early mouse development depend on SOX2 function

21 April 2017

1 reference

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

21 April 2017

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Notch ligands with contrasting functions: Jagged1 and Delta1 in the mouse inner ear

21 April 2017

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Sox2 is required for sensory organ development in the mammalian inner ear

21 April 2017

1 reference

Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology

21 April 2017

1 reference

Niche-independent symmetrical self-renewal of a mammalian tissue stem cell

21 April 2017

1 reference

Dissecting self-renewal in stem cells with RNA interference

21 April 2017

1 reference

Gene expression-based classification of non-small cell lung carcinomas and survival prediction

21 April 2017

1 reference

Sox2 roles in neural stem cells

21 April 2017

1 reference

Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome

21 January 2018

1 reference

Mutations in SOX2 cause anophthalmia

21 January 2018

1 reference

MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.

21 January 2018

1 reference

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

21 January 2018

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Exportin 4 mediates a novel nuclear import pathway for Sox family transcription factors

21 January 2018

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Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues.

21 January 2018

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The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects

21 January 2018

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Memory in Induced Pluripotent Stem Cells: Reprogrammed Human Retinal-Pigmented Epithelial Cells Show Tendency for Spontaneous Redifferentiation

21 January 2018

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Hippocampal development and neural stem cell maintenance require Sox2-dependent regulation of Shh.

21 January 2018

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Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns

21 January 2018

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CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression

21 January 2018

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Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features

21 January 2018

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The Notch ligand Jagged1 is required for inner ear sensory development.

21 January 2018

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Long-term tripotent differentiation capacity of human neural stem (NS) cells in adherent culture

21 January 2018

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The genome-wide dynamics of the binding of Ldb1 complexes during erythroid differentiation

21 January 2018

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A transgenic mouse line that retains Cre recombinase activity in mature oocytes irrespective of the cre transgene transmission

21 January 2018

1 reference

Two-step cross-linking method for identification of NF-kappaB gene network by chromatin immunoprecipitation.

21 January 2018

1 reference

Genome-wide identification of in vivo protein-DNA binding sites from ChIP-Seq data

21 January 2018

1 reference

ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis

21 January 2018

1 reference

12 December 2020

Temporal bone histopathologic findings in Alagille's syndrome

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12 December 2020

The value of prior knowledge in discovering motifs with MEME

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12 December 2020

The EGF receptor-sox2-EGF receptor feedback loop positively regulates the self-renewal of neural precursor cells

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12 December 2020

Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans

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12 December 2020