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

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

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31 January 2017

1

Erik Engelen

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31 January 2017

3

Jan Christian Bryne

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31 January 2017

6

Maaike Moen

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31 January 2017

10

Dick H. W. Dekkers

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31 January 2017

14

Sjaak Philipsen

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31 January 2017

19

Raymond A. Poot

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31 January 2017

Umut Akinci

2

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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

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

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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

43

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31 January 2017

6

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31 January 2017

607–611

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31 January 2017

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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

1 reference

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

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

21 April 2017

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

21 April 2017

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CHD7 cooperates with PBAF to control multipotent neural crest formation

21 April 2017

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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

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

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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

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

21 January 2018

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Mutations in SOX2 cause anophthalmia

21 January 2018

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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

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

21 January 2018

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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