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BMJ Open|July 12, 2015
Emergency supply of prescription-only medicines to patients by community pharmacists: a mixed methods evaluation incorporating patient, pharmacist and GP perspectivesCharles W Morecroft, Adam J Mackridge, Elizabeth C Stokes, et al.Oncogene|January 11, 2007
Selective inhibition of MEK1/2 reveals a differential requirement for ERK1/2 signalling in the regulation of HIF-1 in response to hypoxia and IGF-1K M Sutton, S Hayat, N-M Chau, et al.Molecular & Cellular Proteomics : MCP|February 29, 2012
The role of chaperone-subunit usher domain interactions in the mechanism of bacterial pilus biogenesis revealed by ESI-MSBethny Morrissey, Aneika C Leney, Ana Toste Rêgo, et al.Journal of Innovation in Health Informatics|November 7, 2018
SMASH! The Salford medication safety dashboardRichard Williams, Richard Keers, Wouter T Gude, et al.Journal of Technology and Science Education|August 8, 2022
CONTEXTUALIZING TECHNOLOGY IN THE CLASSROOM VIA REMOTE ACCESS: USING SPACE EXPLORATION THEMES AND SCANNING ELECTRON MICROSCOPY AS TOOLS TO PROMOTE ENGAGEMENT IN GEOLOGY/CHEMISTRY EXPERIMENTSBrandon Rodriguez, Veronica Jaramillo, Vanessa Wolf, et al.BMJ Open|September 5, 2023
Protocol for the Paediatric Otorrhoea Study (POSt): a multi-methods study to understand the burden of paediatric otorrhoea in the UKElliot Heward, James Dempsey, Judith Lunn, et al.Diabetologia|May 29, 2002
Human calcium/calmodulin-dependent protein kinase II gamma gene (CAMK2G): cloning, genomic structure and detection of variants in subjects with type II diabetesA L Gloyn, M Desai, A Clark, et al.British Journal of Haematology|January 13, 2009
CD4(+)CD25(+)FoxP3(+) regulatory T cells are increased whilst CD3(+)CD4(-)CD8(-)alphabetaTCR(+) Double Negative T cells are decreased in the peripheral blood of patients with multiple myeloma which correlates with disease burdenSylvia Feyler, Marie von Lilienfeld-Toal, Sarah Jarmin, et al.Archives of Disease in Childhood|July 1, 1981
Nesidioblastosis of the pancreas: definition of the syndrome and the management of the severe neonatal hyperinsulinaemic hypoglycaemiaA Aynsley-Green, J M Polak, S R Bloom, et al.The Journal of Clinical Investigation|October 6, 2000
Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1H Huopio, F Reimann, R Ashfield, et al.Pageof 185