Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain (Q28511651)

25 January 2017

title

Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain (English)

1 reference

AT rich interactive domain 4B (RBP1-like)

25 January 2017

main subject

1 reference

AT rich interactive domain 4A (RBP1-like)

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Mei-Yi Wu

1 reference

25 January 2017

Ting-Fen Tsai

series ordinal

1 reference

25 January 2017

Arthur L. Beaudet

series ordinal

1 reference

25 January 2017

publication date

15 October 2006

1 reference

25 January 2017

1 reference

25 January 2017

1 reference

25 January 2017

1 reference

25 January 2017

page(s)

2859–2870

1 reference

DNA-binding properties of ARID family proteins

25 January 2017

cites work

1 reference

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Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes

19 March 2017

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The imprinting mechanism of the Prader-Willi/Angelman regional control center

19 March 2017

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Parent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center

19 March 2017

1 reference

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RBP1 recruits the mSIN3-histone deacetylase complex to the pocket of retinoblastoma tumor suppressor family proteins found in limited discrete regions of the nucleus at growth arrest

19 March 2017

1 reference

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Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain

19 March 2017

1 reference

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Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins

19 March 2017

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RBP1 recruits both histone deacetylase-dependent and -independent repression activities to retinoblastoma family proteins

19 March 2017

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19 March 2017

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19 March 2017

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Methylation of histone H4 lysine 20 controls recruitment of Crb2 to sites of DNA damage

19 March 2017

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7 April 2017

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Rb targets histone H3 methylation and HP1 to promoters

7 April 2017

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Mice deficient for Rb are nonviable and show defects in neurogenesis and haematopoiesis

7 April 2017

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The Prader-Willi/Angelman imprinted domain and its control center

29 September 2017

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Imprinting defects on human chromosome 15.

29 September 2017

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Tumour suppressor retinoblastoma protein Rb: a transcriptional regulator

29 September 2017

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Reversing histone methylation

29 September 2017

1 reference

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Nomenclature of the ARID family of DNA-binding proteins

29 September 2017

1 reference

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Epigenetics and human disease

29 September 2017

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The retinoblastoma tumour suppressor in development and cancer

29 September 2017

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DNA methylation and genomic imprinting: insights from cancer into epigenetic mechanisms

29 September 2017

1 reference

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RBP1L1, a retinoblastoma-binding protein-related gene encoding an antigenic epitope abundantly expressed in human carcinomas and normal testis

29 September 2017

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Association of acetylated histones with paternally expressed genes in the Prader--Willi deletion region

29 September 2017

1 reference

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Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome.

29 September 2017

1 reference

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Cytotoxic T lymphocytes that recognize decameric peptide sequences of retinoblastoma binding protein 1 (RBP-1) associated with human breast cancer.

29 September 2017

1 reference

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Recognition of an epitope of a breast cancer antigen by human antibody

29 September 2017

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RBP1 induces growth arrest by repression of E2F-dependent transcription

29 September 2017

1 reference

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Imprinting-mutation mechanisms in Prader-Willi syndrome

29 September 2017

1 reference

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Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern

29 September 2017

1 reference

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Genomic imprinting of the human serotonin-receptor (HTR2) gene involved in development of retinoblastoma

29 September 2017

1 reference

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Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

29 September 2017

1 reference

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Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

29 September 2017

1 reference

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Mouse imprinting defect mutations that model Angelman syndrome.

2 June 2018

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Role of the RB1 family in stabilizing histone methylation at constitutive heterochromatin

27 November 2018

1 reference

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Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells.

27 November 2018

1 reference

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Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice

27 November 2018

1 reference

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The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1619944

Structure and function correlations at the imprinted mouse Snrpn locus

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1619944

A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp

27 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/17043311

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1101/GAD.1452206

1 reference

1 reference

1 reference

1 reference