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American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
G3 (Bethesda, Md.)|August 8, 2023
Genome Report: chromosome-scale genome assembly of the African spiny mouse (Acomys cahirinus)Elizabeth Dong Nguyen, Vahid Nikoonejad Fard, Bernard Y Kim, et al.
Communications Biology|August 26, 2024
Single-cell analysis of chromatin and expression reveals age- and sex-associated alterations in the human heartDavid F Read, Gregory T Booth, Riza M Daza, et al.
Biorxiv : the Preprint Server for Biology|July 14, 2025
Differential cell signaling testing for cell-cell communication inference from single-cell data by dominoSignalJacob T Mitchell, Orian Stapleton, Kavita Krishnan, et al.
American Journal of Human Genetics|May 11, 2015
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3Jessica X Chong, Lindsay C Burrage, Anita E Beck, et al.
Neuron|January 14, 2023
Machine learning dissection of human accelerated regions in primate neurodevelopmentSean Whalen, Fumitaka Inoue, Hane Ryu, et al.
American Journal of Human Genetics|August 6, 2013
Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissectionsDong-chuan Guo, Ellen Regalado, Darren E Casteel, et al.
Nature|April 13, 2012
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutationsBrian J O'Roak, Laura Vives, Santhosh Girirajan, et al.
Influenza and Other Respiratory Viruses|June 22, 2023
Respiratory syncytial virus and other respiratory virus infections in residents of homeless shelters - King County, Washington, 2019-2021Denise J McCulloch, Julia H Rogers, Yongzhe Wang, et al.
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