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The Biochemical Journal|March 26, 2008
Correctors promote folding of the CFTR in the endoplasmic reticulumTip W Loo, M Claire Bartlett, David M ClarkePharmaceutical Biology|March 22, 2017
Identification of highly potent α-glucosidase inhibitory and antioxidant constituents from Zizyphus rugosa bark: enzyme kinetic and molecular docking studies with active metabolitesJirapast Sichaem, Thammarat Aree, Kiattisak Lugsanangarm, et al.Natural Product Communications|August 19, 2016
A New Non-glucosidic Iridoid from the Roots of Strychnos nux-blandaJirapast Sichaem, Suttira Khumkratok, Pongpun Siripong, et al.Theriogenology|March 4, 2025
Seasonal effect on farrowing duration in sows within a temporarily confined farrowing system under tropical climatesTip-Apa Akkhaphan, Rafa Boonprakob, Alexander Grahofer, et al.Porcine Health Management|June 11, 2025
Ultrasound examination of the uterine diameter and the uterine blood vessels size in temporarily confined sows in the postpartal period- a pilot studyTip-Apa Akkhaphan, Preechaphon Taechamaeteekul, Alexander Grahofer, et al.The Journal of Biological Chemistry|August 12, 2003
Simultaneous binding of two different drugs in the binding pocket of the human multidrug resistance P-glycoproteinTip W Loo, M Claire Bartlett, David M ClarkeMolecular Pharmaceutics|July 21, 2005
Disulfiram metabolites permanently inactivate the human multidrug resistance P-glycoproteinTip W Loo, M Claire Bartlett, David M ClarkeNatural Product Research|March 31, 2007
9-epi-Viridiol, a novel cytotoxic furanosteroid from soil fungus Trichoderma virensPreecha Phuwapraisirisan, Jakaphan Rangsan, Pongpun Siripong, et al.Natural Product Research|November 22, 2008
Complete NMR assignment and absolute configuration of feronielloside, a new acetylcholinesterase inhibitor from Feroniella lucidaChalouyluk Phoopichayanun, Preecha Phuwapraisirisan, Santi Tip-Pyang, et al.The Journal of Biological Chemistry|September 13, 2007
Suppressor mutations in the transmembrane segments of P-glycoprotein promote maturation of processing mutants and disrupt a subset of drug-binding sitesTip W Loo, M Claire Bartlett, David M ClarkePageof 70