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The Journal of Pathology|July 12, 2017
Hepatocellular carcinoma-associated single-nucleotide variants and deletions identified by the use of genome-wide high-throughput analysis of hepatitis B virusWen-Chun Liu, I-Chin Wu, Yen-Chien Lee, et al.Biorxiv : the Preprint Server for Biology|April 27, 2026
Single-cell full-length transcriptome of human lung reveals genetic effects on isoform regulation beyond gene-level expressionBolun Li, Thong Luong, Elelta Sisay, et al.Leukemia|July 11, 2025
A genome-wide association study identifies an African-specific locus on chromosome 21q22.12 associated with Burkitt lymphoma risk and survivalDiptavo Dutta, Mateus H Gouveia, Bryan R Gorman, et al.Research Square|May 25, 2026
A high-penetrance intergenic variant at 9p21 confers melanoma susceptibilityMaria Teresa Landi, Linh Bui-Raborn, Lorenza Pastorino, et al.Medrxiv : the Preprint Server for Health Sciences|July 20, 2021
Genetic regulation of <i>OAS1</i> nonsense-mediated decay underlies association with risk of severe COVID-19A Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.Nature Genetics|July 14, 2022
Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestriesA Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.Pageof 12