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Bioorganic & Medicinal Chemistry Letters|September 18, 2007
Neutral 5-substituted 4-anilinoquinazolines as potent, orally active inhibitors of erbB2 receptor tyrosine kinasePeter Ballard, Bernard C Barlaam, Robert H Bradbury, et al.Genomics|March 15, 2001
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesiaL Bartoloni, J L Blouin, A K Maiti, et al.Circulation. Cardiovascular Genetics|December 8, 2017
Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive CardiomyopathyNathan R Tucker, Micheal A McLellan, Dongjian Hu, et al.Hepatology (Baltimore, Md.)|July 7, 2021
A Mammalian Target of Rapamycin-Perilipin 3 (mTORC1-Plin3) Pathway is essential to Activate Lipophagy and Protects Against HepatosteatosisMarina Garcia-Macia, Adrián Santos-Ledo, Jack Leslie, et al.Journal of Virology|January 10, 2025
Modulation of cytokeratin and cytokine/chemokine expression following influenza virus infection of differentiated human tonsillar epithelial cellsS Scott Perry, David C Brice, Ahmed Atef Sakr, et al.Bioorganic & Medicinal Chemistry Letters|November 9, 2011
Discovery, optimisation and in vivo evaluation of novel GPR119 agonistsKaty J Brocklehurst, Anders Broo, Roger J Butlin, et al.Diabetologia|November 6, 2010
Effects of fenofibrate on renal function in patients with type 2 diabetes mellitus: the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) StudyT M E Davis, R Ting, J D Best, et al.American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses|September 1, 2021
Survey of Nurses' Experiences Applying The Joint Commission's Medication Management Titration StandardsJudy E Davidson, Neal Doran, Amber Petty, et al.Human Molecular Genetics|October 24, 2002
The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitroMichel Guipponi, Grégoire Vuagniaux, Marie Wattenhofer, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 7, 2009
Aire-deficient C57BL/6 mice mimicking the common human 13-base pair deletion mutation present with only a mild autoimmune phenotypeFrançois-Xavier Hubert, Sarah A Kinkel, Pauline E Crewther, et al.Pageof 203