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Nature|April 3, 2024
The variation and evolution of complete human centromeresGlennis A Logsdon, Allison N Rozanski, Fedor Ryabov, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2026
A segmental duplication-mediated deletion leads to neocentromere formation in orangutansLuciana De Gennaro, DongAhn Yoo, Letizia Pistacchia, et al.
Journal of Medicinal Chemistry|August 16, 1996
Nonpeptidal P2 ligands for HIV protease inhibitors: structure-based design, synthesis, and biological evaluationA K Ghosh, J F Kincaid, D E Walters, et al.
Science (New York, N.Y.)|October 19, 2019
Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genesPingHsun Hsieh, Mitchell R Vollger, Vy Dang, et al.
Biorxiv : the Preprint Server for Biology|April 27, 2026
Long-read MitoScope reveals tissue-resolved somatic mitochondrial variation and landscape of nuclear-embedded mitochondrial sequencesChristina Zakarian, Joshua D Smith, Chee Hong Wong, et al.
Nature Biotechnology|December 8, 2020
Fully phased human genome assembly without parental data using single-cell strand sequencing and long readsDavid Porubsky, Peter Ebert, Peter A Audano, et al.
Nature Communications|April 18, 2026
Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversionDavid Porubsky, DongAhn Yoo, Nidhi Koundinya, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2026
S1PR3 mediates glial stimulated tumor invasion in response to interstitial fluid flowR Chase Cornelison, Samantha Howerton, Kinsley M Tate, et al.
Genome Biology|August 12, 2020
An evolutionary driver of interspersed segmental duplications in primatesStuart Cantsilieris, Susan M Sunkin, Matthew E Johnson, et al.
American Journal of Human Genetics|March 15, 2022
Familial long-read sequencing increases yield of de novo mutationsMichelle D Noyes, William T Harvey, David Porubsky, et al.
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