CECR2, a protein involved in neurulation, forms a novel chromatin remodeling complex with SNF2L (Q24337637)

GOA release 2020-03-11

1 reference

CECR2, histone acetyl-lysine reader

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

8

Roseline Godbout

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author name string

Graham S Banting

1

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Orr Barak

2

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Tanya M Ames

3

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Amanda C Burnham

4

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Melanie D Kardel

5

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Neil S Cooch

6

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Courtney E Davidson

7

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Heather E McDermid

9

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Ramin Shiekhattar

What does 'chromatin remodeling' mean?

10

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language of work or name

English

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publication date

15 February 2005

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published in

Human Molecular Genetics

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volume

14

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issue

4

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page(s)

513-24

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cites work

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Chromatin remodeling by ATP-dependent molecular machines.

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Syndromes of disordered chromatin remodeling

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Human diseases with underlying defects in chromatin structure and modification.

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ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome

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Growth retardation and premature aging phenotypes in mice with disruption of the SNF2-like gene, PASG

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Biological functions of the ISWI chromatin remodeling complex NURF.

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The ISWI chromatin-remodeling protein is required for gene expression and the maintenance of higher order chromatin structure in vivo

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ISWI, a member of the SWI2/SNF2 ATPase family, encodes the 140 kDa subunit of the nucleosome remodeling factor

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ACF, an ISWI-containing and ATP-utilizing chromatin assembly and remodeling factor

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Chromatin-remodelling factor CHRAC contains the ATPases ISWI and topoisomerase II.

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Cloning and mapping of SMARCA5 encoding hSNF2H, a novel human homologue of Drosophila ISWI

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Cloning and characterization of the murine Imitation Switch (ISWI) genes: differential expression patterns suggest distinct developmental roles for Snf2h and Snf2l

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Cloning of human and bovine homologs of SNF2/SWI2: a global activator of transcription in yeast S. cerevisiae

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The ISWI ATPase Snf2h is required for early mouse development

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A family of chromatin remodeling factors related to Williams syndrome transcription factor

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Requirement of RSF and FACT for transcription of chromatin templates in vitro

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WSTF-ISWI chromatin remodeling complex targets heterochromatic replication foci

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NoRC--a novel member of mammalian ISWI-containing chromatin remodeling machines

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HuCHRAC, a human ISWI chromatin remodelling complex contains hACF1 and two novel histone-fold proteins

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A chromatin remodelling complex that loads cohesin onto human chromosomes

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Isolation of human NURF: a regulator of Engrailed gene expression

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Analysis of the cat eye syndrome critical region in humans and the region of conserved synteny in mice: a search for candidate genes at or near the human chromosome 22 pericentromere

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Sequence analysis of LRPPRC and its SEC1 domain interaction partners suggests roles in cytoskeletal organization, vesicular trafficking, nucleocytosolic shuttling, and chromosome activity

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Binding of Acf1 to DNA involves a WAC motif and is important for ACF-mediated chromatin assembly

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Bromodomain: an acetyl-lysine binding domain

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Function and selectivity of bromodomains in anchoring chromatin-modifying complexes to promoter nucleosomes.

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Deciphering the transcriptional histone acetylation code for a human gene

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The genetic basis of mammalian neurulation.

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AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice

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Folic acid prevents exencephaly in Cited2 deficient mice

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Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice

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Functional analysis of the subunits of the chromatin assembly factor RSF

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An ACF1-ISWI chromatin-remodeling complex is required for DNA replication through heterochromatin

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Hepatitis B virus pX interacts with HBXAP, a PHD finger protein to coactivate transcription

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Functional differences between the human ATP-dependent nucleosome remodeling proteins BRG1 and SNF2H

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Catalytic activity of the yeast SWI/SNF complex on reconstituted nucleosome arrays.

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Neural tube defects: a review of human and animal studies on the etiology of neural tube defects

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Curly tail: a 50-year history of the mouse spina bifida model

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Exencephaly in a subset of animals heterozygous for AP-2alpha mutation

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Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

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Homeotic transformations in the mouse induced by overexpression of a human Hox3.3 transgene

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Preparation of extracts from higher eukaryotes

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Normal mouse strains differ in the site of initiation of closure of the cranial neural tube

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Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

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Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice.

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A genetic risk factor for mouse neural tube defects: defining the embryonic basis

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