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Nature|April 24, 2025
Human de novo mutation rates from a four-generation pedigree referenceDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.Biorxiv : the Preprint Server for Biology|August 16, 2024
A familial, telomere-to-telomere reference for human de novo mutation and recombination from a four-generation pedigreeDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.Immunity|November 17, 2016
Epigenomic Profiling of Human CD4+ T Cells Supports a Linear Differentiation Model and Highlights Molecular Regulators of Memory DevelopmentPawel Durek, Karl Nordström, Gilles Gasparoni, et al.Frontiers in Immunology|January 22, 2025
Magnitude and dynamics of the T-cell response to SARS-CoV-2 infection at both individual and population levelsThomas M Snyder, Rachel M Gittelman, Mark Klinger, et al.Medrxiv : the Preprint Server for Health Sciences|August 15, 2020
Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population LevelsThomas M Snyder, Rachel M Gittelman, Mark Klinger, et al.Human Molecular Genetics|August 3, 2013
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodelingDagmar Wieczorek, Nina Bögershausen, Filippo Beleggia, et al.Biorxiv : the Preprint Server for Biology|September 26, 2025
A complete diploid human genome benchmark for personalized genomicsNancy F Hansen, Nathan Dwarshuis, Hyun Joo Ji, et al.Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.Science (New York, N.Y.)|March 31, 2022
The complete sequence of a human genomeSergey Nurk, Sergey Koren, Arang Rhie, et al.Biorxiv : the Preprint Server for Biology|August 1, 2026
HPRC2: A human pangenome reference with near-complete coverage of common genetic variationJulian K Lucas, Prajna Hebbar, Wen-Wei Liao, et al.Pageof 17