Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sabina Kuperschmidt"'
Autor:
Michel Lazdunski, John P. Adelman, Gary V. Desir, Jonathan Robbins, Stephan Grissmer, Heike Wulff, Gail A. Robertson, Manuel Covarriubias, Douglas A. Bayliss, David McKinnon, Bernardo Rudy, Henry A. Lester, Andreas Karschin, Aguan Wei, David E. Clapham, Kiyoshi Furuichi, Maria L. Garcia, Randy S. Wymore, Barry Ganetzky, K. George Chandy, Michael C. Sanguinetti, Lily Yeh Jan, Jayashree Aiyar, Yoshihisa Kurachi, Walter Stuehmer, Florian Lesage, Colin G. Nichols, Ita O'Kelly, Sabina Kuperschmidt, Michael M. Tamkun, George A. Gutman, Susumu Seino, Carol A. Vandenberg, Donghee Kim
Publikováno v:
Pharmacological Reviews. 55:575-578
This summary article presents an overview of the molecular relationships among the voltage-gated sodium channels and a standard nomenclature for them, which is derived from the IUPHAR Compendium of Voltage-Gated Ion Channels. The complete Compendium,
Autor:
Gary V. Desir, I. T. A. O'kelly, David McKinnon, Kiyoshi Furuichi, Maria L. Garcia, Bernardo Rudy, Jonathan Robbins, Lily Yeh Jan, John P. Adelman, Jayashree Aiyar, David E. Clapham, Florian Lesage, Michel Lazdunski, Stephan Grissmer, Manuel Covarriubias, Randy S. Wymore, Heike Wulff, Gail A. Robertson, George A. Gutman, Michael C. Sanguinetti, Aguan Wei, Carol A. Vandenberg, Susumu Seino, Douglas A. Bayliss, Sabina Kuperschmidt, Michael M. Tamkun, Colin G. Nichols, Henry A. Lester, Walter Stuehmer, Barry Ganetzky, K. George Chandy, Yoshihisa Kurachi, Donghee Kim, Andreas Karschin
Publikováno v:
Pharmacological reviews. 55(4)
This summary article presents an overview of the molecular relationships among the voltage-gated potassium channels and a standard nomenclature for them, which is derived from the IUPHAR Compendium of Voltage-Gated Ion Channels.1 The complete Compend
Autor:
Antoon F.M. Moorman, Anne Jarry, Piet A.J. de Boer, Yann Péréon, Dan M. Roden, Sophie Demolombe, Diego Franco, Denis Escande, Sabina Kuperschmidt
Publikováno v:
American journal of physiology. Cell physiology, 280(2), C359-C372. American Physiological Society
Scopus-Elsevier
Scopus-Elsevier
KCNQ1 is the human gene responsible in most cases for the long QT syndrome, a genetic disorder characterized by anomalies in cardiac repolarization leading to arrhythmias and sudden death. KCNQ1 encodes a pore-forming K+channel subunit termed KvLQT1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdce3d9bbc2e263d062f5ccd42cf37d5
https://pure.amc.nl/en/publications/differential-expression-of-kvlqt1-and-its-regulator-isk-in-mouse-epithelia(824a8136-b367-41ad-9023-9164a5f06738).html
https://pure.amc.nl/en/publications/differential-expression-of-kvlqt1-and-its-regulator-isk-in-mouse-epithelia(824a8136-b367-41ad-9023-9164a5f06738).html
Autor:
A, Gutman George, George, Chandy K, P, Adelman John, Jayashree, Aiyar, A, Bayliss Douglas, E, Clapham David, Manuel, Covarriubias, V, Desir Gary, Kiyoshi, Furuichi, Barry, Ganetzky, L, Garcia Maria, Stephan, Grissmer, Y, Jan Lily, Andreas, Karschin, Donghee, Kim, Sabina, Kuperschmidt, Yoshihisa, Kurachi, Michel, Lazdunski, Florian, Lesage, A, Lester Henry, David, McKinnon, G, Nichols Colin, Ita, O'Kelly, Jonathan, Robbins, A, Robertson Gail, Bernardo, Rudy, Michael, Sanguinetti, Susumu, Seino, Walter, Stuehmer, Micha, Tamkun
Publikováno v:
Pharmacological Reviews; December 2003, Vol. 55 Issue: 4 p583-6, 4p