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Communications Biology|December 14, 2020
Nasopharyngeal carcinoma MHC region deep sequencing identifies HLA and novel non-HLA TRIM31 and TRIM39 lociLvwen Ning, Josephine Mun-Yee Ko, Valen Zhuoyou Yu, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 21, 2016
Whole-exome sequencing identifies multiple loss-of-function mutations of NF-κB pathway regulators in nasopharyngeal carcinomaHong Zheng, Wei Dai, Arthur Kwok Leung Cheung, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 9, 2016
Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinomaWei Dai, Hong Zheng, Arthur Kwok Leung Cheung, et al.
American Journal of Human Genetics|June 23, 2023
High-throughput identification of regulatory elements and functional assays to uncover susceptibility genes for nasopharyngeal carcinomaTong-Min Wang, Ruo-Wen Xiao, Yong-Qiao He, et al.
The Journal of Clinical Investigation|January 2, 2025
Whole-exome sequencing association study reveals genetic effects on tumor microenvironment components in nasopharyngeal carcinomaYanni Zeng, Chun-Ling Luo, Guo-Wang Lin, et al.
Journal of the National Cancer Institute|September 6, 2022
Whole-Exome Sequencing Study of Familial Nasopharyngeal Carcinoma and Its Implication for Identifying High-Risk IndividualsTong-Min Wang, Yong-Qiao He, Wen-Qiong Xue, et al.
Nature Communications|April 13, 2022
A polygenic risk score for nasopharyngeal carcinoma shows potential for risk stratification and personalized screeningYong-Qiao He, Tong-Min Wang, Mingfang Ji, et al.
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