Anchoring proteins for protein kinase C: a means for isozyme selectivity-Reference-Cited by-同舟云学术

Anchoring proteins for protein kinase C: a means for isozyme selectivity

Published:1998-01 Issue:1 Volume:12 Page:35-42
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Mochly‐Rosen Daria¹,Gordon Adrienne S.²

Affiliation:

1. Department of Molecular PharmacologyStanford UniversitySchool of Medicine Stanford California 94305–5332 USA

2. Department of Neurology and Cellular and Molecular PharmacologyErnest Gallo Clinic and Research CenterProgram in NeuroscienceCenter for the Neurobiology of AddictionUniversity of California San Francisco California 94110 USA

Funder

National Institutes of Health

American Cancer Society

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fsb2fasebj.12.1.35

Reference56 articles.

1. Protein kinase C — a family affair

2. Intracellular Signaling by Hydrolysis of Phospholipids and Activation of Protein Kinase C

3. PKCμ, is a novel, atypical member of the protein kinase C family;Johannes F.‐J.;J. Biol. Chem.,1994

4. Molecular cloning and characterization of protein kinase D: a target for diacylglycerol and phorbol esters with a distinctive catalytic domain.

5. A carboxy-terminal deletion mutant of protein kinase C beta II inhibits insulin-stimulated 2-deoxyglucose uptake in L6 rat skeletal muscle cells

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