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Genetic Epidemiology|October 13, 2018
Prediction of treatment response in rheumatoid arthritis patients using genome-wide SNP dataSvetlana Cherlin, Darren Plant, John C Taylor, et al.Genes|September 5, 2019
Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart DiseaseAlessandro Testori, Vito A Lasorsa, Flora Cimmino, et al.Journal of the American Society of Nephrology : JASN|December 5, 2009
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric refluxHeather J Cordell, Rebecca Darlay, Pimphen Charoen, et al.Scandinavian Journal of Gastroenterology|May 5, 2012
Fine mapping and replication of genetic risk loci in primary sclerosing cholangitisBrijesh Srivastava, George F Mells, Heather J Cordell, et al.Genes and Immunity|July 24, 2015
CTLA-4 as a genetic determinant in autoimmune Addison's diseaseA S B Wolff, A L Mitchell, H J Cordell, et al.Genes and Immunity|July 9, 2003
Genetic susceptibility to visceral leishmaniasis in The Sudan: linkage and association with IL4 and IFNGR1H S Mohamed, M E Ibrahim, E N Miller, et al.International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|November 11, 1999
The tissue distribution of the human beta3-adrenoceptor studied using a monoclonal antibody: direct evidence of the beta3-adrenoceptor in human adipose tissue, atrium and skeletal muscleP D Chamberlain, K H Jennings, F Paul, et al.Heart (British Cardiac Society)|October 13, 2010
Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variantsHelen R Griffin, Ana Töpf, Elise Glen, et al.Genes and Immunity|January 22, 2004
Genome-wide scans for leprosy and tuberculosis susceptibility genes in BraziliansE N Miller, S E Jamieson, C Joberty, et al.Journal of Medical Genetics|September 28, 2014
Factors determining penetrance in familial atypical haemolytic uraemic syndromeFrancis H Sansbury, Heather J Cordell, Coralie Bingham, et al.Pageof 27