Showing results (681-690 of 888) with videos related to
Sort By:
Pageof 89
Stem Cell Research|May 23, 2020
Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen programKanika Kanchan, Kruthika Iyer, Lisa R Yanek, et al.Journal of Clinical Lipidology|October 15, 2022
Guidance for the diagnosis and treatment of hypolipidemia disordersCindy Bredefeld, M Mahmood Hussain, Maurizio Averna, et al.Diabetes|April 25, 2009
Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1qInga Prokopenko, Eleftheria Zeggini, Robert L Hanson, et al.Genome Biology|January 5, 2021
Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrualDiana L Cousminer, Yadav Wagley, James A Pippin, et al.Nature Genetics|February 10, 2009
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants, Sekar Kathiresan, Benjamin F Voight, et al.Biorxiv : the Preprint Server for Biology|June 22, 2026
PanKbase Integrated Single-Cell Map: A Comprehensive Atlas of Human Pancreatic IsletsHa T H Vu, Han Sun, Parul Kudtarkar, et al.Nature Genetics|September 4, 2007
A common variant of HMGA2 is associated with adult and childhood height in the general populationMichael N Weedon, Guillaume Lettre, Rachel M Freathy, et al.Science Translational Medicine|January 14, 2021
Kidney disease genetic risk variants alter lysosomal beta-mannosidase (MANBA) expression and disease severityXiangchen Gu, Hongliu Yang, Xin Sheng, et al.Nature Genetics|January 18, 2006
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetesStruan F A Grant, Gudmar Thorleifsson, Inga Reynisdottir, et al.Human Molecular Genetics|June 9, 2016
Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathyElizabeth E Palmer, Kelsey E Jarrett, Rani K Sachdev, et al.Pageof 89