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Current Diabetes Reports|March 24, 2004
Animal models of spontaneous autoimmune diabetes: notes on their relevance to the human diseaseConstantin PolychronakosPediatric Endocrinology Reviews : PER|January 31, 2006
Genetic variation and health; towards individualized medicineConstantin PolychronakosCurrent Atherosclerosis Reports|May 21, 2008
Common and rare alleles as causes of complex phenotypesConstantin PolychronakosHormone 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 PolychronakosBMJ Open Diabetes Research & Care|October 17, 2020
tRNA methyltransferase 10 homologue A (<i>TRMT10A</i>) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephalyHu Lin, Xuelian Zhou, Xuefeng Chen, 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 14