(Q40010724)

16 September 2017

title

ARC is a critical cardiomyocyte survival switch in doxorubicin cardiotoxicity (English)

1 reference

16 September 2017

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Junfeng An

1

1 reference

16 September 2017

Peifeng Li

2

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16 September 2017

Jincheng Li

3

1 reference

16 September 2017

Rainer Dietz

4

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16 September 2017

Stefan Donath

5

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16 September 2017

publication date

13 January 2009

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Journal of Molecular Medicine

16 September 2017

published in

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16 September 2017

volume

87

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16 September 2017

issue

4

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16 September 2017

page(s)

401-410

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https://scigraph.springernature.com/pub.10.1007/s00109-008-0434-z

16 September 2017

exact match

0 references

cites work

A mechanistic role for cardiac myocyte apoptosis in heart failure

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00109-008-0434-Z

Mitochondrial dysfunction is an early indicator of doxorubicin-induced apoptosis

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00109-008-0434-Z

Humanin peptide suppresses apoptosis by interfering with Bax activation

21 January 2018

1 reference

12 December 2020

Hsp10 and Hsp60 modulate Bcl-2 family and mitochondria apoptosis signaling induced by doxorubicin in cardiac muscle cells.

1 reference

12 December 2020

Insulin-like growth factor I modulates induction of apoptotic signaling in H9C2 cardiac muscle cells

1 reference

12 December 2020

Doxorubicin induces apoptosis by activation of caspase-3 in cultured cardiomyocytes in vitro and rat cardiac ventricles in vivo.

1 reference

12 December 2020

Apoptosis repressor with caspase recruitment domain is required for cardioprotection in response to biomechanical and ischemic stress

1 reference

12 December 2020

Myocytes die by multiple mechanisms in failing human hearts

1 reference

12 December 2020

Mitochondrial membrane permeabilisation by Bax/Bak

1 reference

12 December 2020

The apoptosis inhibitor ARC undergoes ubiquitin-proteasomal-mediated degradation in response to death stimuli: identification of a degradation-resistant mutant

1 reference

12 December 2020

Ubiquitination and degradation of the anti-apoptotic protein ARC by MDM2.

1 reference

12 December 2020

Doxorubicin-induced cardiomyopathy

1 reference

12 December 2020

The protective roles of nitric oxide and superoxide dismutase in adriamycin-induced cardiotoxicity

1 reference

12 December 2020

14-3-3 Interacts directly with and negatively regulates pro-apoptotic Bax

1 reference

12 December 2020

ARC, an inhibitor of apoptosis expressed in skeletal muscle and heart that interacts selectively with caspases

1 reference

12 December 2020

The apoptotic regulatory protein ARC (apoptosis repressor with caspase recruitment domain) prevents oxidant stress-mediated cell death by preserving mitochondrial function

1 reference

12 December 2020

Phosphorylation by protein kinase CK2: a signaling switch for the caspase-inhibiting protein ARC

1 reference

12 December 2020

Bcl-xl reduces doxorubicin-induced myocardial damage but fails to control cardiac gene downregulation

1 reference

12 December 2020

p53 initiates apoptosis by transcriptionally targeting the antiapoptotic protein ARC

1 reference

12 December 2020

Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death

1 reference

12 December 2020

Pro-apoptotic cascade activates BID, which oligomerizes BAK or BAX into pores that result in the release of cytochrome c.

1 reference

12 December 2020

Cytoprotective membrane-permeable peptides designed from the Bax-binding domain of Ku70.

1 reference

12 December 2020

Inhibition of both the extrinsic and intrinsic death pathways through nonhomotypic death-fold interactions

1 reference

12 December 2020

10.1007/S00109-008-0434-Z

Identifiers

DOI

1 reference

release_ziihi3lle5d6zp6butguwtvtg4

16 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ziihi3lle5d6zp6butguwtvtg4

24 November 2022

mapped directly with Wikidata item

1 reference