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American Journal of Human Genetics|August 1, 1997
Spectrum of mutations in the Batten disease gene, CLN3P B Munroe, H M Mitchison, A M O'Rawe, et al.Genomics|February 12, 1998
Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody diseaseA Odermatt, P E Taschner, S W Scherer, et al.The Journal of Clinical Endocrinology and Metabolism|June 8, 2006
A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptorM J E Walenkamp, H J van der Kamp, A M Pereira, et al.The Pharmacogenomics Journal|August 10, 2016
Irinotecan-induced toxicity pharmacogenetics: an umbrella review of systematic reviews and meta-analysesJ M Campbell, M D Stephenson, E Bateman, et al.JBI Database of Systematic Reviews and Implementation Reports|August 18, 2016
Effectiveness of allied health therapy in the symptomatic management of progressive supranuclear palsy: a systematic reviewErica Tilley, James McLoughlin, Simon A Koblar, et al.Developmental Biology|July 1, 1988
Signal transduction, chemotaxis, and cell aggregation in Dictyostelium discoideum cells without myosin heavy chainD J Peters, D A Knecht, W F Loomis, et al.Journal of Cell Science|December 1, 1991
Abberant chemotaxis and differentiation in Dictyostelium mutant fgdC with a defective regulation of receptor-stimulated phosphoinositidase CA A Bominaar, F Kesbeke, B E Snaar-Jagalska, et al.Cancer Chemotherapy and Pharmacology|May 5, 2016
Methotrexate-induced toxicity pharmacogenetics: an umbrella review of systematic reviews and meta-analysesJared M Campbell, Emma Bateman, Matthew D Stephenson, et al.Worldviews on Evidence-Based Nursing|July 28, 2018
An International Educational Training Course for Conducting Systematic Reviews in Health Care: The Joanna Briggs Institute's Comprehensive Systematic Review Training ProgramCindy Stern, Zac Munn, Kylie Porritt, et al.Nature Genetics|June 30, 2001
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosisO T Njajou, N Vaessen, M Joosse, et al.Pageof 24