ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating-Reference-Cited by-同舟云学术

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

Published:2004-03-21 Issue:4 Volume:36 Page:382-387
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Bienengraeber Martin,Olson Timothy M,Selivanov Vitaliy A,Kathmann Eva C,O'Cochlain Fearghas,Gao Fan,Karger Amy B,Ballew Jeffrey D,Hodgson Denice M,Zingman Leonid V,Pang Yuan-Ping,Alekseev Alexey E,Terzic Andre

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1329.pdf

Reference29 articles.

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2. Inagaki, N. et al. A family of sulfonylurea receptors determines the pharmacological properties of ATP-sensitive K+ channels. Neuron 16, 1011– 1017 (1996).

3. Bienengraeber, M. et al. ATPase activity of the sulfonylurea receptor: A catalytic function for the KATP channel complex. FASEB J. 14, 1943– 1952 (2000).

4. Matsuo, M., Tanabe, K., Kioka, N., Amachi, T. & Ueda, K. Different binding properties and affinities for ATP and ADP among sulfonylurea receptor subtypes, SUR1, SUR2A, and SUR2B. J. Biol. Chem. 275, 28757– 28763 (2000).

5. Zingman, L.V. et al. Signaling in channel/enzyme multimers: ATPase transitions in SUR module gate ATP-sensitive K+ conductance. Neuron 31, 233– 245 (2001).

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