α2A- and α2C-Adrenergic Receptors Form Homo- and Heterodimers: The Heterodimeric State Impairs Agonist-Promoted GRK Phosphorylation and β-Arrestin Recruitment-Reference-Cited by-同舟云学术

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α2A- and α2C-Adrenergic Receptors Form Homo- and Heterodimers: The Heterodimeric State Impairs Agonist-Promoted GRK Phosphorylation and β-Arrestin Recruitment

Published:2006-03-22 Issue:15 Volume:45 Page:4760-4767
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Small Kersten M.¹,Schwarb Mary Rose¹,Glinka Clare¹,Theiss Cheryl T.¹,Brown Kari M.¹,Seman Carrie A.¹,Liggett Stephen B.¹

Affiliation:

1. Department of Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267, and Cardiopulmonary Genomics Program, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland 21201

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi052074z

Reference36 articles.

Cited by 64 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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