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Science (New York, N.Y.)|December 1, 2012
An exon splice enhancer primes IGF2:IGF2R binding site structure and function evolutionChristopher Williams, Hans-Jürgen Hoppe, Dellel Rezgui, et al.Biorxiv : the Preprint Server for Biology|October 14, 2020
Making the invisible enemy visibleTristan Croll, Kay Diederichs, Florens Fischer, et al.Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|October 26, 2023
Preliminary investigation of a significant national Cryptosporidium exceedance in the United Kingdom, August 2023 and ongoingLewis Peake, Thomas Inns, Christopher Jarvis, et al.Ticks and Tick-Borne Diseases|January 7, 2026
Mapping ticks (Acari: Argasidae, Ixodidae) and informing local public action: Insights from the United Kingdom Tick Surveillance Scheme (2021-2024)Kayleigh M Hansford, Faye V Brown, Sarah M Biddlecombe, et al.Journal of Medicinal Chemistry|December 3, 2014
Design and nuclear magnetic resonance (NMR) structure determination of the second extracellular immunoglobulin tyrosine kinase A (TrkAIg2) domain construct for binding site elucidation in drug discoveryDebbie K Shoemark, Christopher Williams, Mark S Fahey, et al.Epidemiology and Infection|December 26, 2024
National outbreak of Shiga toxin-producing Escherichia coli O145:H28 associated with pre-packed sandwiches, United Kingdom, May-June 2024Orlagh Quinn, Yanshi, Grace King, et al.Blood|June 24, 2005
Activity of the tyrosine kinase inhibitor PKC412 in a patient with mast cell leukemia with the D816V KIT mutationJason Gotlib, Caroline Berubé, Joseph D Growney, et al.Nature Chemical Biology|September 24, 2013
A conserved motif flags acyl carrier proteins for β-branching in polyketide synthesisAnthony S Haines, Xu Dong, Zhongshu Song, et al.Science (New York, N.Y.)|July 7, 2010
Terrestrial gross carbon dioxide uptake: global distribution and covariation with climateChristian Beer, Markus Reichstein, Enrico Tomelleri, et al.Human Molecular Genetics|February 13, 2014
Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defectsAlexandros Onoufriadis, Amelia Shoemark, Miriam Schmidts, et al.Pageof 38