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

Roseline Godbout

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author name string

Graham S Banting

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Orr Barak

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Tanya M Ames

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Amanda C Burnham

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Melanie D Kardel

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Neil S Cooch

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Courtney E Davidson

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Heather E McDermid

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Ramin Shiekhattar

What does 'chromatin remodeling' mean?

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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

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issue

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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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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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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 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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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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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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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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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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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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