Zobrazeno 1 - 8
of 8
pro vyhledávání: '"J L, Shevell"'
Autor:
Gregory J. Kaczorowski, V F King, John P. Felix, J L Shevell, I. R. C. Bick, Robert S. Slaughter, Maria L. Garcia
Publikováno v:
Biochemistry. 31:11793-11800
Bis(benzylisoquinoline) alkaloids block Ca2+ uptake through the L-type Ca2+ channel and modulate binding of ligands to four distinct sites (dihydropyridine, benzothiazepine, aralkylamine, and (diphenylbutyl)piperidine) in the Ca2+ entry blocker recep
Autor:
Maria L. Garcia, J L Shevell, Robert S. Slaughter, V F King, Gregory J. Kaczorowski, Raymond J. Winquist, Guilherme Suarez-Kurtz
Publikováno v:
ResearcherID
Three structural classes of commonly used amiloride analogs, molecules derivatized at the terminal guanidino-nitrogen, the five-position pyrazinoyl-nitrogen, or di-substituted at both of these positions, inhibit binding of the L-type Ca2+ channel mod
Autor:
M L, Garcia, V F, King, J L, Shevell, R S, Slaughter, G, Suarez-Kurtz, R J, Winquist, G J, Kaczorowski
Publikováno v:
The Journal of biological chemistry. 265(7)
Three structural classes of commonly used amiloride analogs, molecules derivatized at the terminal guanidino-nitrogen, the five-position pyrazinoyl-nitrogen, or di-substituted at both of these positions, inhibit binding of the L-type Ca2+ channel mod
Autor:
Robert S. Slaughter, John P. Felix, J L Shevell, Gregory J. Kaczorowski, V. Frank King, Maria L. Garcia
Publikováno v:
Calcium Transport and Intracellular Calcium Homeostasis ISBN: 9783642839795
Voltage-dependent Ca2+ channels have been identified in both electrically excitable and non-excitable cells. Several distinct types of Ca2+ channels have been detected in these preparations. Perhaps the best characterized channel, in terms of its pha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cf173e893e065549608043986134b1c
https://doi.org/10.1007/978-3-642-83977-1_6
https://doi.org/10.1007/978-3-642-83977-1_6
Publikováno v:
Journal of Biological Chemistry. 264:5633-5641
Fluspirilene binds with high affinity to a single class of sites in purified porcine cardiac sarcolemmal membrane vesicles at a Kd of 0.6 nM and a Bmax that is in approximately 1:1 stoichiometry with other Ca2+ entry blocker receptors. Fluspirilene b
Publikováno v:
Plant Pathogenic Bacteria ISBN: 9789401080903
This study employed cotton lines developed by breeding genes for resistance to bacterial blight into the susceptible background of cultivar Ac 44. Leaves of Ac 44 and of lines containing resistance genes B2, B3, b7, or BN, or a combination of these p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd3803f4528feffdf03d320b4146a0a6
https://doi.org/10.1007/978-94-009-3555-6_126
https://doi.org/10.1007/978-94-009-3555-6_126
Publikováno v:
Biochemistry. 28(9)
Membrane vesicles which exhibit high levels of Nai-dependent Ca2+ uptake have been prepared from either porcine or bovine aortic smooth muscle. These membranes are identified as being of sarcolemmal origin by enrichment of marker activities associate
Publikováno v:
The Journal of biological chemistry. 264(10)
Fluspirilene binds with high affinity to a single class of sites in purified porcine cardiac sarcolemmal membrane vesicles at a Kd of 0.6 nM and a Bmax that is in approximately 1:1 stoichiometry with other Ca2+ entry blocker receptors. Fluspirilene b