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Knowledge and Information Systems|May 20, 2026
Automated biomedical hypothesis generation with time-aware hypergraph contrastive learningAmir Hassan Shariatmadari, Sikun Guo, Nathan C Sheffield, et al.The Journal of Clinical Investigation|November 1, 1992
Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patientsE Freneaux, V C Sheffield, L Molin, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
The phenotype in Norwegian patients with Bardet-Biedl syndrome with mutations in the BBS4 geneRuth Riise, Kristina Tornqvist, Alan F Wright, et al.Human Molecular Genetics|January 10, 2012
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypesQihong Zhang, Seongjin Seo, Kevin Bugge, et al.Journal of Pharmacy Practice|January 17, 2018
Pain Assessment Documentation After Opioid Administration at a Community Teaching HospitalMegan E Phillips, Rod A Gilmore, Melody C Sheffield, et al.Progress in Retinal and Eye Research|December 20, 2021
Retinal ciliopathies through the lens of Bardet-Biedl Syndrome: Past, present and futureBharatendu Chandra, Moon Ley Tung, Ying Hsu, et al.American Journal of Pharmaceutical Education|May 17, 2008
Influences on pharmacy students' decision to pursue a doctor of pharmacy degreeDouglas C Anderson, Melody C Sheffield, Angela Massey Hill, et al.Human Molecular Genetics|September 1, 1996
Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D)V Ionasescu, C Searby, V C Sheffield, et al.Plos One|February 15, 2018
Genotypic and phenotypic characterization of the Sdccag8Tn(sb-Tyr)2161B.CA1C2Ove mouse modelKatie Weihbrecht, Wesley A Goar, Calvin S Carter, et al.Clinical Orthopaedics and Related Research|January 23, 2009
Evaluation of CAND2 and WNT7a as candidate genes for congenital idiopathic clubfootWilliam Shyy, Frederick Dietz, Matthew B Dobbs, et al.Pageof 41