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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 1, 2007
Biphenyl 2,3',4,5',6-pentakisphosphate, a novel inositol polyphosphate surrogate, modulates Ca2+ responses in rat hepatocytesFabrice Vandeput, Laurent Combettes, Stephen J Mills, et al.
The Journal of Biological Chemistry|December 1, 2011
The C terminus of Bax inhibitor-1 forms a Ca2+-permeable channel poreGeert Bultynck, Santeri Kiviluoto, Nadine Henke, et al.
Plos One|October 19, 2013
Alpha-helical destabilization of the Bcl-2-BH4-domain peptide abolishes its ability to inhibit the IP3 receptorGiovanni Monaco, Elke Decrock, Koen Nuyts, et al.
Scientific Reports|April 16, 2015
Ryanodine receptors are targeted by anti-apoptotic Bcl-XL involving its BH4 domain and Lys87 from its BH3 domainTim Vervliet, Irma Lemmens, Elien Vandermarliere, et al.
The EMBO Journal|December 20, 2003
Regulation of InsP3 receptor activity by neuronal Ca2+-binding proteinsNael Nadif Kasri, Anthony M Holmes, Geert Bultynck, et al.
Pflugers Archiv : European Journal of Physiology|November 7, 2013
Polycystin-1 but not polycystin-2 deficiency causes upregulation of the mTOR pathway and can be synergistically targeted with rapamycin and metforminDjalila Mekahli, Jean-Paul Decuypere, Eva Sammels, et al.
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