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Human Genomics|July 25, 2023
CVD-associated SNPs with regulatory potential reveal novel non-coding disease genesChaonan Zhu, Nina Baumgarten, Meiqian Wu, et al.Human Genomics|July 17, 2023
Whole-genome sequencing and functional annotation of pathogenic Paraconiothyrium brasiliense causing human cellulitisHaibing Liu, Yue Zhang, Jianguo ChenHuman Genomics|July 28, 2023
Mitochondrial genome study in blood of maternally inherited ALS casesSarah J Brockmann, Eva Buck, Tiziana Casoli, et al.Human Genomics|July 24, 2023
COVID-19 annual update: a narrative reviewMichela Biancolella, Vito Luigi Colona, Lucio Luzzatto, et al.Human Genomics|June 16, 2023
Evaluation of a genetic risk score computed using human chromosomal-scale length variation to predict breast cancerCharmeine Ko, James P BrodyHuman Genomics|June 11, 2023
Systems genetics identifies miRNA-mediated regulation of host response in COVID-19T Gjorgjieva, A Chaloemtoem, T Shahin, et al.Human Genomics|June 24, 2026
Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case reportSatoshi Hara, Tomohiko Sato, Osamu Shimokawa, et al.Human Genomics|December 10, 2021
A regulatory miRNA-mRNA network is associated with transplantation response in acute kidney injuryDuan Guo, Yu Fan, Ji-Rong Yue, et al.Human Genomics|June 19, 2026
Dynamic responses in the human methylome to exertional heat exhaustion, heat injury, and heat strokeBrandon M Roberts, Ruoting Yang, Kari C Goodwin, et al.Human Genomics|May 23, 2025
CLPP Gene Variants Causing Perrault Syndrome Type 3 in Han Chinese Families: A Genotype-Phenotype StudyXicui Long, Bingqian Yang, Wei Wang, et al.Pageof 112