Showing results (551-560 of 1,240) with videos related to
Sort By:
Pageof 124
Cancer Research|December 18, 2004
Specific recognition and killing of glioblastoma multiforme by interleukin 13-zetakine redirected cytolytic T cellsKanwarpal S Kahlon, Christine Brown, Laurence J N Cooper, et al.In Silico Biology|June 23, 2006
In silico discrimination of single nucleotide polymorphisms and pathological mutations in human gene promoter regions by means of local DNA sequence context and regularityImtiaz A Khan, Matthew Mort, Paul R Buckland, et al.Human Genetics|December 29, 2000
Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regionsM Krawczak, N A Chuzhanova, P D Stenson, et al.Global Pediatric Health|January 28, 2021
Effects of the FDA Codeine Safety Investigation on Racial and Geographic Disparities in Opioid Prescribing after Pediatric Tonsillectomy and/or AdenoidectomyAmy Lawrence, Jennifer N Cooper, Katherine J Deans, et al.JAMA|September 23, 2010
Association of telomere length of peripheral blood leukocytes with hematopoietic relapse, malignant transformation, and survival in severe aplastic anemiaPhillip Scheinberg, James N Cooper, Elaine M Sloand, et al.The Journal of Thoracic and Cardiovascular Surgery|January 1, 1977
Studies of the effects of hypothermia on regional myocardial blood flow and metabolism during cardiopulmonary bypass. I. The adequately perfused beating, fibrillating, and arrested heartG D Buckberg, J R Brazier, R L Nelson, et al.The Journal of Surgical Research|August 16, 2017
Perioperative blood transfusion and complications in children undergoing surgery for solid tumorsDani O Gonzalez, Jennifer N Cooper, Erica Mantell, et al.Journal of Urban Health : Bulletin of the New York Academy of Medicine|June 16, 2010
Pharmacy participation in non-prescription syringe sales in Los Angeles and San Francisco counties, 2007Erin N Cooper, Chaka Dodson, Thomas J Stopka, et al.Human Mutation|May 28, 2011
Monozygotic twins discordant for neurofibromatosis type 1 due to a postzygotic NF1 gene mutationJulia Vogt, Jürgen Kohlhase, Susanne Morlot, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
Compound heterozygosity for two novel mutations (1203insG/Y1456X) in the von Willebrand factor gene causing type 3 von Willebrand diseaseF Xie, X Wang, D N Cooper, et al.Pageof 124