Inhibition of adenylyl cyclase isoforms V and VI by various G βγ subunits

Author:

Bayewitch Michael L.1,Avidor‐Reiss Tomer1,Levy Rivka1,Pfeuffer Thomas1,Nevo Igal2,Simonds William F.2,Vogel Zvi3

Affiliation:

1. Department of NeurobiologyThe Weizmann Institute of Science Rehovot 76100 Israel

2. Department of Physiological Chemistry IIUniversity of Düsseldorf Düsseldorf D‐40225 Germany

3. Metabolic Diseases BranchNIDDKNational Institutes of Health Bethesda Maryland 20892 USA

Funder

National Institute on Drug Abuse

German-Israeli Foundation for Scientific Research and Development

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Reference41 articles.

1. μ–Opioid receptors inhibit dopamine‐stimulated activity of type V adenylyl cyclase but enhance dopamine‐stimulated activity of type VII adenylyl cyclase;Yoshimura M.;Mol. Pharmacol.,1996

2. Complexity and Diversity of Mammalian Adenylyl Cyclases

3. Inhibition of Adenylyl Cyclase by G iα

4. Adenylate cyclases: critical foci in neuronal signaling

5. Hormonal stimulation of adenylyl cyclase through Gi-protein βγ subunits

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