Ikaros-CtIP interactions do not require C-terminal binding protein and participate in a deacetylase-independent mode of repression (Q28215092)

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scientific article (publication date: 28 June 2002)

Language	Label	Description	Also known as
English	Ikaros-CtIP interactions do not require C-terminal binding protein and participate in a deacetylase-independent mode of repression	scientific article (publication date: 28 June 2002)

Statements

scholarly article

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Ikaros-CtIP interactions do not require C-terminal binding protein and participate in a deacetylase-independent mode of repression (English)

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author name string

Joseph Koipally

1

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Katia Georgopoulos

2

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language of work or name

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publication date

28 June 2002

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Journal of Biological Chemistry

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277

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26

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23143-9

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Ikaros, an early lymphoid-specific transcription factor and a putative mediator for T cell commitment

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https://api.crossref.org/works/10.1074%2FJBC.M202079200

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Aiolos, a lymphoid restricted transcription factor that interacts with Ikaros to regulate lymphocyte differentiation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Helios, a novel dimerization partner of Ikaros expressed in the earliest hematopoietic progenitors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Helios, a T cell-restricted Ikaros family member that quantitatively associates with Ikaros at centromeric heterochromatin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Eos: a novel member of the Ikaros gene family expressed predominantly in the developing nervous system

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

The lymphoid transcription factor LyF-1 is encoded by specific, alternatively spliced mRNAs derived from the Ikaros gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

The Ikaros gene is required for the development of all lymphoid lineages

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Selective defects in the development of the fetal and adult lymphoid system in mice with an Ikaros null mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Defects in hemopoietic stem cell activity in Ikaros mutant mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Pre-T cell receptor (TCR) and TCR-controlled checkpoints in T cell differentiation are set by Ikaros

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Unconventional potentiation of gene expression by Ikaros

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Repression by Ikaros and Aiolos is mediated through histone deacetylase complexes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Transcriptional repression: the long and the short of it.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Sin meets NuRD and other tails of repression.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

The corepressor N-CoR and its variants RIP13a and RIP13Delta1 directly interact with the basal transcription factors TFIIB, TAFII32 and TAFII70.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Transcriptional repression by the SMRT-mSin3 corepressor: multiple interactions, multiple mechanisms, and a potential role for TFIIB.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Mechanism of transcriptional repression of E2F by the retinoblastoma tumor suppressor protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

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Molecular cloning and characterization of a cellular phosphoprotein that interacts with a conserved C-terminal domain of adenovirus E1A involved in negative modulation of oncogenic transformation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Interaction between a cellular protein that binds to the C-terminal region of adenovirus E1A (CtBP) and a novel cellular protein is disrupted by E1A through a conserved PLDLS motif

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

MEF-2 function is modified by a novel co-repressor, MITR

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

The CtBP family: enigmatic and enzymatic transcriptional co-repressors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

CtBP, an unconventional transcriptional corepressor in development and oncogenesis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

A mechanism for Rb/p130-mediated transcription repression involving recruitment of the CtBP corepressor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Binding of CtIP to the BRCT repeats of BRCA1 involved in the transcription regulation of p21 is disrupted upon DNA damage

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Linking the Rb and polycomb pathways

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Emerging roles of BRCA1 in transcriptional regulation and DNA repair

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Nuclear localization and cell cycle-specific expression of CtIP, a protein that associates with the BRCA1 tumor suppressor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

The LIM domain protein LMO4 interacts with the cofactor CtIP and the tumor suppressor BRCA1 and inhibits BRCA1 activity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

The C-terminal (BRCT) domains of BRCA1 interact in vivo with CtIP, a protein implicated in the CtBP pathway of transcriptional repression

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Functional link of BRCA1 and ataxia telangiectasia gene product in DNA damage response

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Effect of DNA damage on a BRCA1 complex

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Ikaros DNA-binding proteins direct formation of chromatin remodeling complexes in lymphocytes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Ikaros interactions with CtBP reveal a repression mechanism that is independent of histone deacetylase activity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Mad proteins contain a dominant transcription repression domain.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Rb interacts with histone deacetylase to repress transcription

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Identification of a transcriptional repressor related to the noncatalytic domain of histone deacetylases 4 and 5

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202079200

21 January 2018

Identifiers

10.1074/JBC.M202079200

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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