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Transboundary and Emerging Diseases|July 4, 2020
COVID-19 drug repurposing: Summary statistics on current clinical trials and promising untested candidatesJ Wes Ulm, Stanley F NelsonCurrent Opinion in Neurology|September 11, 2015
What can Duchenne Connect teach us about treating Duchenne muscular dystrophy?Richard T Wang, Stanley F NelsonEMBO Molecular Medicine|April 17, 2023
RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesisSamantha Wong, Yu Xuan Tan, Abigail Yi Ting Loh, et al.Genome Medicine|October 27, 2017
Next-generation mapping: a novel approach for detection of pathogenic structural variants with a potential utility in clinical diagnosisHayk Barseghyan, Wilson Tang, Richard T Wang, et al.The New England Journal of Medicine|June 11, 2020
Disseminated Coccidioidomycosis Treated with Interferon-γ and DupilumabMonica Tsai, Timothy J Thauland, Alden Y Huang, et al.American Journal of Human Genetics|December 7, 2010
Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signalingJing Tian, Ling Ling, Mohammad Shboul, et al.BMC Bioinformatics|June 26, 2010
Local alignment of generalized k-base encoded DNA sequenceNils Homer, Stanley F Nelson, Barry MerrimanBMC Bioinformatics|June 11, 2009
Local alignment of two-base encoded DNA sequenceNils Homer, Barry Merriman, Stanley F NelsonPlos One|November 13, 2009
BFAST: an alignment tool for large scale genome resequencingNils Homer, Barry Merriman, Stanley F NelsonBMC Medical Genetics|June 3, 2014
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencingSamuel P Strom, Reymundo Lozano, Hane Lee, et al.Pageof 32