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Human Genomics|February 1, 2023
Genome-wide allele and haplotype-sharing patterns suggested one unique Hmong-Mein-related lineage and biological adaptation history in Southwest ChinaGuanglin He, Jiawen Wang, Lin Yang, et al.Human Genomics|February 11, 2023
Integrated analysis of RNA methylation regulators crosstalk and immune infiltration for predictive and personalized therapy of diabetic nephropathyJia Li, Dongwei Liu, Jingjing Ren, et al.Human Genomics|December 10, 2025
Recurrent somatic copy number alterations in resected cerebral cavernous malformationsAndrew K Ressler, Evon Debose-Scarlett, Amanda Fuenzalida, et al.Human Genomics|December 6, 2025
Genome-wide methylation profiles of primary and matched distant metastasis: insights from the Dutch Early-Stage melanoma (D-ESMEL) studyJasper Ouwerkerk, Thamila Kerkour, Antien Mooyaart, et al.Human Genomics|November 20, 2012
Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitusZohreh Rahimi, Reza Nourozi-Rad, Ziba Rahimi, et al.Human Genomics|January 11, 2014
On the stability of the Bayenv method in assessing human SNP-environment associationsLily M Blair, Julie M Granka, Marcus W FeldmanHuman Genomics|January 23, 2014
A survey of software for genome-wide discovery of differential splicing in RNA-Seq dataJoan E HooperHuman Genomics|March 12, 2015
Rapid detection of genetic mutations in individual breast cancer patients by next-generation DNA sequencingSuqin Liu, Hongjiang Wang, Lizhi Zhang, et al.Human Genomics|June 28, 2020
Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discoveryClaudia De Masi, Paola Spitalieri, Michela Murdocca, et al.Pageof 112