Bcl-2-Protein Family as Modulators of IP


Journal

Cold Spring Harbor perspectives in biology
ISSN: 1943-0264
Titre abrégé: Cold Spring Harb Perspect Biol
Pays: United States
ID NLM: 101513680

Informations de publication

Date de publication:
01 04 2020
Historique:
pubmed: 11 9 2019
medline: 3 8 2021
entrez: 11 9 2019
Statut: epublish

Résumé

The pro- and antiapoptotic proteins belonging to the B-cell lymphoma-2 (Bcl-2) family exert a critical control over cell-death processes by enabling or counteracting mitochondrial outer membrane permeabilization. Beyond this mitochondrial function, several Bcl-2 family members have emerged as critical modulators of intracellular Ca

Identifiants

pubmed: 31501195
pii: cshperspect.a035089
doi: 10.1101/cshperspect.a035089
pmc: PMC7111250
pii:
doi:

Substances chimiques

BCL2L1 protein, human 0
Inositol 1,4,5-Trisphosphate Receptors 0
MCL1 protein, human 0
Myeloid Cell Leukemia Sequence 1 Protein 0
Proto-Oncogene Proteins c-bcl-2 0
VDAC1 protein, human 0
bcl-X Protein 0
Voltage-Dependent Anion Channel 1 EC 1.6.-
Calcium SY7Q814VUP

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM072804
Pays : United States
Organisme : NINDS NIH HHS
ID : R21 NS106968
Pays : United States
Organisme : NIDCR NIH HHS
ID : R01 DE014756
Pays : United States

Informations de copyright

Copyright © 2020 Cold Spring Harbor Laboratory Press; all rights reserved.

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Auteurs

Hristina Ivanova (H)

Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine, KU Leuven, B-3000 Leuven, Belgium.

Tim Vervliet (T)

Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine, KU Leuven, B-3000 Leuven, Belgium.

Giovanni Monaco (G)

Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine, KU Leuven, B-3000 Leuven, Belgium.

Lara E Terry (LE)

Department of Pharmacology and Physiology, School of Medicine and Dentistry, University of Rochester, Rochester, New York 14642.

Nicolas Rosa (N)

Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine, KU Leuven, B-3000 Leuven, Belgium.

Mariah R Baker (MR)

Department of Biochemistry and Molecular Biology, McGovern Medical School at The University of Texas Health Science Center at Houston, Structural Biology Imaging Center, Houston, Texas 77030.

Jan B Parys (JB)

Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine, KU Leuven, B-3000 Leuven, Belgium.

Irina I Serysheva (II)

Department of Biochemistry and Molecular Biology, McGovern Medical School at The University of Texas Health Science Center at Houston, Structural Biology Imaging Center, Houston, Texas 77030.

David I Yule (DI)

Department of Pharmacology and Physiology, School of Medicine and Dentistry, University of Rochester, Rochester, New York 14642.

Geert Bultynck (G)

Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine, KU Leuven, B-3000 Leuven, Belgium.

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Classifications MeSH