Showing results (211-220 of 355) with videos related to
Sort By:
Pageof 36
Ebiomedicine|July 14, 2023
Dose imbalance of DYRK1A kinase causes systemic progeroid status in Down syndrome by increasing the un-repaired DNA damage and reducing LaminB1 levelsAoife Murray, Gillian Gough, Ana Cindrić, et al.Plos Genetics|June 9, 2009
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrationsMelanie Kolz, Toby Johnson, Serena Sanna, et al.Journal of Human Immunity|June 1, 2026
Human germline biallelic loss-of-function OSMR variants cause severe allergic diseaseSimran Samra, Mehul Sharma, Julia Körholz, et al.Atherosclerosis|December 19, 2009
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individualsIris M Heid, Peter Henneman, Andrew Hicks, et al.Nature Communications|June 13, 2015
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levelsHarmen H M Draisma, René Pool, Michael Kobl, et al.The European Respiratory Journal|December 7, 2013
Telomere length in circulating leukocytes is associated with lung function and diseaseEva Albrecht, Elina Sillanpää, Stefan Karrasch, et al.Nature Medicine|June 28, 2020
Publisher Correction: Building an international consortium for tracking coronavirus health statusEran Segal, Feng Zhang, Xihong Lin, et al.Aging|July 23, 2020
Blood DNA methylation sites predict death risk in a longitudinal study of 12, 300 individualsElena Colicino, Riccardo Marioni, Cavin Ward-Caviness, et al.Nature Communications|March 7, 2015
Whole-genome sequence-based analysis of thyroid functionPeter N Taylor, Eleonora Porcu, Shelby Chew, et al.Human Reproduction (Oxford, England)|December 5, 2023
Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundityHamdi Mbarek, Scott D Gordon, David L Duffy, et al.Pageof 36