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Human Molecular Genetics|July 1, 1992
Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2M J Dixon, J Dixon, D Raskova, et al.RNA (New York, N.Y.)|October 17, 2003
RNA-protein interactions promote asymmetric sorting of the ASH1 mRNA ribonucleoprotein complexGraydon B Gonsalvez, Katrina A Lehmann, Derek K Ho, et al.Society of General Physiologists Series|January 1, 1987
Mechanisms involved in receptor-mediated changes of intracellular Ca2+ in liverJ R Williamson, C A Hansen, A Verhoeven, et al.The Journal of Allergy and Clinical Immunology|November 7, 1999
Identifying genes predisposing to atopic eczemaS Forrest, K Dunn, K Elliott, et al.Human Genetics|September 1, 1990
The incidence of delta F508 CF mutation, and associated haplotypes, in a sample of English CF familiesE K Watson, E S Mayall, L Simova, et al.Journal of Molecular Biology|July 19, 2011
Single-molecule studies reveal that DEAD box protein DDX1 promotes oligomerization of HIV-1 Rev on the Rev response elementRae M Robertson-Anderson, Jun Wang, Stephen P Edgcomb, et al.Trials|August 25, 2017
Using routinely recorded data in the UK to assess outcomes in a randomised controlled trial: The Trials of AccessG A Powell, L J Bonnett, C Tudur-Smith, et al.The Annals of Pharmacotherapy|August 11, 2017
Iatrogenic Opioid Withdrawal in Critically Ill Patients: A Review of Assessment Tools and ManagementAda W Chiu, Sofia Contreras, Sangeeta Mehta, et al.Lancet (London, England)|February 20, 1988
Genetic differences between cystic fibrosis with and without meconium ileusE Mornet, B Simon-Bouy, J L Serre, et al.Trials|March 19, 2013
MOMENT--Management of Otitis Media with Effusion in Cleft Palate: protocol for a systematic review of the literature and identification of a core outcome set using a Delphi surveyNicola L Harman, Iain A Bruce, Peter Callery, et al.Pageof 196