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Human Genomics|March 1, 2023
Computational network analysis of host genetic risk variants of severe COVID-19Sakhaa B Alsaedi, Katsuhiko Mineta, Xin Gao, et al.Human Genomics|February 28, 2025
Genetic insights into cardiac conduction disorders from genome-wide association studiesBingxun Li, Hongxuan Xu, Lin WuHuman Genomics|February 26, 2025
Exploring the hepatic-ophthalmic axis through immune modulation and cellular dynamics in diabetic retinopathy and non-alcoholic fatty liver diseaseShuyan Zhang, Jiajun Wu, Leilei Wang, et al.Human Genomics|February 25, 2025
Proteome-wide Mendelian randomization identifies causal plasma proteins in prostate cancer developmentJian Wu, Zitong Yang, Jiafeng Ding, et al.Human Genomics|February 23, 2025
The comprehensive potential of AQP1 as a tumor biomarker: evidence from kidney neoplasm cohorts, cell experiments and pan-cancer analysisYifan Liu, Donghao Lyu, Yuntao Yao, et al.Human Genomics|November 6, 2024
Development of oxidative stress- and ferroptosis-related prognostic signature in gastric cancer and identification of CDH19 as a novel biomarkerShibo Wang, Siyi Zhang, Xiaoxuan Li, et al.Human Genomics|November 19, 2024
Global transcriptome modulation by xenobiotics: the role of alternative splicing in adaptive responses to chemical exposuresAndrew J Annalora, Jacki L Coburn, Antony Jozic, et al.Human Genomics|December 5, 2024
An analysis of mitochondrial variation in cardiomyopathy patients from the 100,000 genomes cohort: m.4300A>G as a cause of genetically elusive hypertrophic cardiomyopathyLuis R Lopes, William L Macken, Seth Du Preez, et al.Human Genomics|November 22, 2024
Advancing understanding of human variability through toxicokinetic modeling, in vitro-in vivo extrapolation, and new approach methodologiesAnna Kreutz, Xiaoqing Chang, Helena T Hogberg, et al.Human Genomics|March 13, 2025
The CFTR K464N variant in fetuses potential increases premature birth risk in Chinese familiesJingping Li, Lingyun Zhang, Fangfang Xi, et al.Pageof 112