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The Journal of Physiology|March 3, 2023
Short-term high-fat diet feeding of mice suppresses catecholamine-stimulated Ca<sup>2+</sup> signalling in hepatocytes and intact liverRobert P Brumer, Juliana C Corrêa-Velloso, Samantha J Thomas, et al.The Journal of Pharmacology and Experimental Therapeutics|July 29, 2011
Bromoenol lactone inhibits voltage-gated Ca2+ and transient receptor potential canonical channelsSaikat Chakraborty, Zachary C Berwick, Paula J Bartlett, et al.American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|December 21, 2007
Prior hypoglycemia enhances glucose responsiveness in some ventromedial hypothalamic glucosensing neuronsLing Kang, Nicole M Sanders, Ambrose A Dunn-Meynell, et al.The Journal of Biological Chemistry|August 28, 2020
The genetic Ca<sup>2+</sup> sensor GCaMP3 reveals multiple Ca<sup>2+</sup> stores differentially coupled to Ca<sup>2+</sup> entry in the human malaria parasite <i>Plasmodium falciparum</i>Lucas Borges-Pereira, Samantha J Thomas, Amanda Laizy Dos Anjos E Silva, et al.Science Signaling|June 26, 2014
Reliable encoding of stimulus intensities within random sequences of intracellular Ca2+ spikesKevin Thurley, Stephen C Tovey, Gregor Moenke, et al.Aging Cell|January 22, 2010
A mutant telomerase defective in nuclear-cytoplasmic shuttling fails to immortalize cells and is associated with mitochondrial dysfunctionOlga A Kovalenko, Matthieu J Caron, Perihan Ulema, et al.Current Topics in Medicinal Chemistry|February 1, 2017
InsP3 Signaling in Apicomplexan ParasitesCelia R S Garcia, Eduardo Alves, Pedro H S Pereira, et al.Journal of Medicinal Chemistry|March 8, 2002
Novel 4-anilinoquinazolines with C-7 basic side chains: design and structure activity relationship of a series of potent, orally active, VEGF receptor tyrosine kinase inhibitorsLaurent F Hennequin, Elaine S E Stokes, Andrew P Thomas, et al.Malaria Journal|February 14, 2025
Unravelling the mode of action of the Tres Cantos Antimalarial Set (TCAMS): investigating the mechanism of potent antimalarial compounds potentially targeting the human serotonin receptorBenedito Matheus Dos Santos, Lenna Rosanie Cordero Mallaupoma, Mateus Fila Pecenin, et al.Cancer Research|February 29, 2012
AZD4547: an orally bioavailable, potent, and selective inhibitor of the fibroblast growth factor receptor tyrosine kinase familyPaul R Gavine, Lorraine Mooney, Elaine Kilgour, et al.Pageof 7