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Current Atherosclerosis Reports|May 21, 2008
Common and rare alleles as causes of complex phenotypesConstantin PolychronakosDiabetes|April 23, 2008
Association analysis of type 2 diabetes Loci in type 1 diabetesHui-Qi Qu, Struan F A Grant, Jonathan P Bradfield, et al.Diabetes|December 29, 2006
Genetic control of alternative splicing in the TAP2 gene: possible implication in the genetics of type 1 diabetesHui-Qi Qu, Yang Lu, Luc Marchand, et al.Hormone Research|February 18, 2003
Impact of the human genome project on pediatric endocrinologyConstantin PolychronakosJournal of Medical Genetics|September 14, 2012
Gene expression as a quantitative trait: what about translation?Constantin PolychronakosEuropean Journal of Pharmacology|April 18, 2012
Screening for novel lead compounds increasing insulin expression in medullary thymic epithelial cellsXiu-Ying Yang, Dina Levi, Houria Ounissi-Benkalha, et al.Human Molecular Genetics|April 10, 2010
In silico replication of the genome-wide association results of the Type 1 Diabetes Genetics ConsortiumHui-Qi Qu, Jonathan P Bradfield, Quan Li, et al.European Journal of Endocrinology|November 26, 2002
Parental genomic imprinting in endocrinopathiesConstantin Polychronakos, Asterios KukuvitisNature Reviews. Genetics|October 19, 2011
Understanding type 1 diabetes through genetics: advances and prospectsConstantin Polychronakos, Quan LiIslets|July 14, 2011
RFX6 is needed for the development and maintenance of the β-cell phenotypeNadine Taleb, Constantin PolychronakosPageof 20