|1.||Brown, Rachel C: 3 articles (06/2010 - 05/2004)|
|2.||Wang, Jian: 2 articles (07/2005 - 06/2005)|
|3.||Sylvester, J T: 2 articles (07/2005 - 06/2005)|
|4.||Weigand, Letitia: 2 articles (07/2005 - 06/2005)|
|5.||Shimoda, Larissa A: 2 articles (07/2005 - 06/2005)|
|6.||Davis, Thomas P: 2 articles (02/2005 - 05/2004)|
|7.||Song, M: 1 article (07/2014)|
|8.||Yu, S P: 1 article (07/2014)|
|9.||Chen, D: 1 article (07/2014)|
|10.||Chang, Hsien-Chang: 1 article (03/2013)|
01/01/2009 - "NFAT nuclear translocation was significantly enhanced by hypoxia, which was dependent on SOCE and sensitive to SOC inhibitor SKF96365 (SKF), as well as cGMP analogue, 8-brom-cGMP. "
07/01/2005 - "At concentrations that blocked CCE and [Ca(2+)](i) responses to hypoxia in PASMC, SKF-96365 and NiCl(2) prevented and reversed HPV but did not alter pressor responses to KCl. "
06/01/2005 - "These effects, as well as the increased [Ca2+]i caused by hypoxia in PASMCs perfused with normal salt solutions, were blocked by the SOCC antagonists SKF-96365, NiCl2, and LaCl3 at concentrations that inhibited CCE >80% but did not alter [Ca2+]i responses to 60 mM KCl. "
01/01/2010 - "Antagonists for TRPC, 2APB and SKF96365, significantly reduced hypoxia-induced [Ca2+]i elevation by almost 60%. "
12/31/2008 - "Blockage of TRPCs by 2APB and SKF96365 could significantly reduce hypoxia-mediated [Ca2+]i elevation. "
08/16/1993 - "SK&F 96365, a reported receptor-operated Ca2+ channel blocker, inhibited the growth of U-373 MG human astrocytoma and SK-N-MC human neuroblastoma cell lines in a dose-dependent manner. "
08/01/2010 - "SK&F 96365 was used in a Neuroblastoma (Neuro-2a) cell based assay to determine the production of maitotoxin-like (MTX-like) compounds in two strains of Gambierdiscus spp. A 2.5 hour assay was effective for the detection of the MTX-induced toxic effects with a concentration that inhibited 50% cell viability (IC(50)) equivalent to 3.38 nM MTX. "
06/01/1996 - "Since muscarinic acetylcholine receptor-mediated phosphoinositide turnover shows a marked dependence on factors affecting cytosolic Ca2+ concentration, the effects of SK & F 96365 on the coupling of muscarinic receptors to the phosphoinositide hydrolysis were examined in human neuroblastoma SH-SY5Y and rat cerebellar granule cells. "
06/01/1996 - "SK & F 96365 inhibits carbachol-induced phosphoinositide turnover in human neuroblastoma SH-SY5Y and rat cerebellar granule cells."
|5.||Burkitt Lymphoma (Burkitt's Lymphoma)
|5.||Calcium Channels (Calcium Channel)
|7.||Protein Isoforms (Isoforms)
|10.||Endothelin-1 (Endothelin 1)