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Nature Genetics|July 14, 1998
A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patientsF Cucca, J V Goy, Y Kawaguchi, et al.
The Journal of Investigative Dermatology|November 11, 2011
Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effectSara J Brown, Karin Kroboth, Aileen Sandilands, et al.
Annals of the Rheumatic Diseases|May 8, 2010
Association between anti-tumour necrosis factor treatment response and genetic variants within the TLR and NF{kappa}B signalling pathwaysCatherine Potter, Heather J Cordell, Anne Barton, et al.
The Journal of Clinical Endocrinology and Metabolism|October 24, 2009
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibilityAnna L Mitchell, Heather J Cordell, Rachel Soemedi, et al.
Clinical Endocrinology|October 4, 2018
Analysis of BAFF gene polymorphisms in UK Graves' disease patientsLaura C Lane, Kathleen R Allinson, Katy Campbell, et al.
Clinical Journal of the American Society of Nephrology : CJASN|March 29, 2011
Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bankHeather J Lambert, Aisling Stewart, Ambrose M Gullett, et al.
The American Journal of Pathology|June 11, 1999
Biochemical detection of novel anaplastic lymphoma kinase proteins in tissue sections of anaplastic large cell lymphomaK Pulford, B Falini, J Cordell, et al.
Scientific Reports|September 3, 2020
Heritability of haemodynamics in the ascending aortaKathryn A McGurk, Benjamin Owen, William D Watson, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Genetic variants associated with myocardial infarction risk factors in over 8000 individuals from five ethnic groups: The INTERHEART Genetics StudySonia S Anand, Changchun Xie, Guillaume Paré, et al.
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