(Q39972640)

16 September 2017

title

Adenoviral-mediated Rybp expression promotes tumor cell-specific apoptosis (English)

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16 September 2017

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1 reference

R L Novak

1

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16 September 2017

A C Phillips

series ordinal

2

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16 September 2017

publication date

13 June 2008

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16 September 2017

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16 September 2017

volume

15

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16 September 2017

issue

11

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16 September 2017

page(s)

713-722

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https://scigraph.springernature.com/pub.10.1038/cgt.2008.25

16 September 2017

exact match

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Cancer-specific toxicity of apoptin is independent of death receptors but involves the loss of mitochondrial membrane potential and the release of mitochondrial cell-death mediators by a Nur77-dependent pathway

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Human death effector domain-associated factor interacts with the viral apoptosis agonist Apoptin and exerts tumor-preferential cell killing.

21 January 2018

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RYBP, a new repressor protein that interacts with components of the mammalian Polycomb complex, and with the transcription factor YY1

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Genome regulation by polycomb and trithorax proteins

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Interaction of YY1 with E2Fs, mediated by RYBP, provides a mechanism for specificity of E2F function

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YEAF1/RYBP and YAF-2 are functionally distinct members of a cofactor family for the YY1 and E4TF1/hGABP transcription factors

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The E2F6 transcription factor is a component of the mammalian Bmi1-containing polycomb complex

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Rybp/DEDAF is required for early postimplantation and for central nervous system development

21 January 2018

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https://api.crossref.org/works/10.1038%2FCGT.2008.25

Rybp, a polycomb complex-associated protein, is required for mouse eye development

21 January 2018

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https://api.crossref.org/works/10.1038%2FCGT.2008.25

The death effector domain-associated factor plays distinct regulatory roles in the nucleus and cytoplasm.

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The death effector domain protein family

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inferred from DOI database lookup

7 January 2021

based on heuristic

The Drosophila RYBP gene functions as a Polycomb-dependent transcriptional repressor

1 reference

https://api.crossref.org/works/10.1038%2FCGT.2008.25

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/CGT.2008.25

1 reference

16 September 2017

1 reference