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Diabetologia|June 14, 2015
Heritability of thyroid peroxidase autoantibody levels in type 1 diabetes: evidence from discordant twin pairsBin Wang, Mohammed I Hawa, Frühling V Rijsdijk, et al.
Plos One|November 19, 2010
Genome-wide analysis of copy number variation in type 1 diabetesBritney L Grayson, Mary Ellen Smith, James W Thomas, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 22, 2008
Presence of de novo mutations in autosomal dominant polycystic kidney disease patients without family historyBerenice Reed, Kim McFann, William J Kimberling, et al.
Plos One|November 9, 2013
Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathyNzali Campbell, Gianfranco Sinagra, Kenneth L Jones, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2013
NLRP1 haplotypes associated with vitiligo and autoimmunity increase interleukin-1β processing via the NLRP1 inflammasomeCecilia B Levandowski, Christina M Mailloux, Tracey M Ferrara, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 2009
Homozygosity of the polymorphism MICA5.1 identifies extreme risk of progression to overt adrenal insufficiency among 21-hydroxylase antibody-positive patients with type 1 diabetesTaylor M Triolo, Erin E Baschal, Taylor K Armstrong, et al.
Human Molecular Genetics|March 26, 2002
Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3-p32.2Asem Alkhateeb, Gary L Stetler, William Old, et al.
Journal of Autoimmunity|January 20, 2016
Hypomethylation within gene promoter regions and type 1 diabetes in discordant monozygotic twinsEmon Elboudwarej, Michael Cole, Farren B S Briggs, et al.
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