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Current Opinion in Genetics & Development|June 30, 2020
The frontiers of sequencing in undiagnosed neurodevelopmental diseasesHane Lee, Stanley F NelsonBMC Medical Genomics|June 15, 2018
Calculating the statistical significance of rare variants causal for Mendelian and complex disordersAliz R Rao, Stanley F NelsonTransboundary 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 NelsonFrontiers in Cell and Developmental Biology|September 4, 2023
Elucidation of bioinformatic-guided high-prospect drug repositioning candidates for DMD via Swanson linking of target-focused latent knowledge from text-mined categorical metadataJ Wes Ulm, Florian Barthélémy, Stanley F NelsonBMC Bioinformatics|January 8, 2011
SeqWare Query Engine: storing and searching sequence data in the cloudBrian D O'Connor, Barry Merriman, Stanley F NelsonNature Reviews. Neuroscience|September 21, 2004
DNA-microarray analysis of brain cancer: molecular classification for therapyPaul S Mischel, Timothy F Cloughesy, Stanley F NelsonCancer Biology & Therapy|July 25, 2003
Molecular analysis of glioblastoma: pathway profiling and its implications for patient therapyPaul S Mischel, Stanley F Nelson, Timothy F CloughesyMethods in Molecular Biology (Clifton, N.J.)|September 2, 2018
Validation and Detection of Exon Skipping Boosters in DMD Patient Cell Models and mdx MouseFlorian Barthelemy, Dereck Wang, Stanley F Nelson, et al.BMC Cancer|February 6, 2013
Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemiaVivian Y Chang, Giuseppe Basso, Kathleen M Sakamoto, et al.Pageof 26