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American Journal of Public Health|December 14, 2017
No Equity, No Triple Aim: Strategic Proposals to Advance Health Equity in a Volatile Policy EnvironmentGeoffrey W Wilkinson, Alan Sager, Sara Selig, et al.Human Molecular Genetics|February 11, 2010
African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic AmericansDoron M Behar, Saharon Rosset, Shay Tzur, et al.Cell|June 24, 2004
Regulation of murine telomere length by Rtel: an essential gene encoding a helicase-like proteinHao Ding, Mike Schertzer, Xiaoli Wu, et al.Journal of Acquired Immune Deficiency Syndromes (1999)|March 16, 2007
Early response to highly active antiretroviral therapy in HIV-1-infected Kenyan childrenDalton C Wamalwa, Carey Farquhar, Elizabeth M Obimbo, et al.Plos One|December 24, 2010
Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutationStephanie K Mewborn, Megan J Puckelwartz, Fida Abuisneineh, et al.Journal of Human Genetics|May 13, 2021
RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric functionNadra Samra, Shir Toubiana, Hilde Yttervik, et al.Human Molecular Genetics|December 8, 2025
Missense substitutions in the BTB domain of ZBTB24 can lead to protein instability and cause ICF2 syndromeOr Givol, Ido S Han, Francesco Cecere, et al.Pigment Cell & Melanoma Research|August 13, 2014
Biology of advanced uveal melanoma and next steps for clinical therapeuticsJason J Luke, Pierre L Triozzi, Kyle C McKenna, et al.The Journal of Experimental Medicine|July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defectsAmos J Simon, Atar Lev, Yong Zhang, et al.Pigment Cell & Melanoma Research|October 7, 2023
Proceedings from the Melanoma Research Foundation Mucosal Melanoma Meeting (December 16, 2022, New York, USA)Alexander Z Wei, Lanyi N Chen, Marlana Orloff, et al.Pageof 4