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Circulation|April 3, 2020
Reduced Apolipoprotein M and Adverse Outcomes Across the Spectrum of Human Heart FailureJulio A Chirinos, Lei Zhao, Yi Jia, et al.Circulation. Genomic and Precision Medicine|September 1, 2020
Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery DiseaseAkihiro Nomura, Connor A Emdin, Hong Hee Won, et al.Cell Reports|October 19, 2022
SARS-CoV-2 infections elicit higher levels of original antigenic sin antibodies compared with SARS-CoV-2 mRNA vaccinationsElizabeth M Anderson, Shuk Hang Li, Moses Awofolaju, et al.American Journal of Human Genetics|June 18, 2019
Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human LiverMinal Çalışkan, Elisabetta Manduchi, H Shanker Rao, et al.Cell Stem Cell|February 2, 2021
Pathogenic LMNA variants disrupt cardiac lamina-chromatin interactions and de-repress alternative fate genesParisha P Shah, Wenjian Lv, Joshua H Rhoades, et al.Circulation. Cardiovascular Genetics|March 26, 2016
Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United States: Data From the CASCADE-FH RegistryEmil M deGoma, Zahid S Ahmad, Emily C O'Brien, et al.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.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.Pageof 75