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American Journal of Medical Genetics|June 22, 1999
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3G A Bellus, M J Bamshad, K A Przylepa, et al.Journal of Consulting and Clinical Psychology|September 12, 2001
Cognitive-behavioral therapy to reduce weight concerns improves smoking cessation outcome in weight-concerned womenK A Perkins, M D Marcus, M D Levine, et al.Molecular Pharmaceutics|September 27, 2013
Quantitative prediction of renal transporter-mediated clinical drug-drug interactionsBo Feng, Susan Hurst, Yasong Lu, et al.Drug Metabolism Reviews|September 2, 2024
Drug transporters in drug disposition - highlights from the year 2023Paresh P Chothe, Upendra A Argikar, Pallabi Mitra, et al.Clinical Genetics|October 9, 2012
The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLAF S Ong, H Vakil, Y Xue, et al.Drug Metabolism Reviews|July 25, 2025
Drug transporters in drug disposition - highlights from the year 2024Philip Sandoval, Pallabi Mitra, Upendra A Argikar, et al.The AAPS Journal|May 20, 2014
Mechanism-based pharmacokinetic modeling to evaluate transporter-enzyme interplay in drug interactions and pharmacogenetics of glyburideManthena V S Varma, Renato J Scialis, Jian Lin, et al.Biopharmaceutics & Drug Disposition|September 3, 2013
Quantitative assessment of the contribution of sodium-dependent taurocholate co-transporting polypeptide (NTCP) to the hepatic uptake of rosuvastatin, pitavastatin and fluvastatinYi-an Bi, Xi Qiu, Charles J Rotter, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|August 1, 1988
Neurodevelopmental readiness for adolescence: studies of an assessment instrument for 9- to 14-year-old childrenM D Levine, L Rappaport, T Fenton, et al.American Journal of Human Genetics|February 1, 1991
High-resolution linkage mapping for susceptibility genes in human polygenic disease: insulin-dependent diabetes mellitus and chromosome 11qR N Hyer, C Julier, J D Buckley, et al.Pageof 34