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Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|January 6, 2016
Association of well-characterized lung cancer lncRNA polymorphisms with lung cancer susceptibility and platinum-based chemotherapy responseWei-Jing Gong, Ji-Ye Yin, Xiang-Ping Li, et al.Biomedical Chromatography : BMC|August 16, 2013
A high-throughput inhibition screening of major human cytochrome P450 enzymes using an in vitro cocktail and liquid chromatography-tandem mass spectrometryChong-Zhen Qin, Xian Ren, Zhi-Rong Tan, et al.Journal of Cancer|November 28, 2019
CLEC4M is associated with poor prognosis and promotes cisplatin resistance in NSCLC patientsLi-Ming Tan, Xi Li, Cheng-Feng Qiu, et al.Journal of Hazardous Materials|July 22, 2021
Reductive soil disinfestation attenuates antibiotic resistance genes in greenhouse vegetable soilsChen Yanlong, Yang Kejian, Ye Yin, et al.Clinical Chemistry and Laboratory Medicine|November 1, 2007
Impact of rosiglitazone on the expression of beta3-AR in the stable cell lines expressed beta3-AR geneXin Zhao, Min-Yu Hu, Qiong Huang, et al.Scientific Reports|July 19, 2017
Genetic Polymorphisms and Platinum-based Chemotherapy Treatment Outcomes in Patients with Non-Small Cell Lung Cancer: A Genetic Epidemiology Study Based Meta-analysisLi-Ming Tan, Cheng-Feng Qiu, Tao Zhu, et al.Pediatric Surgery International|November 20, 2025
The essential role of cytoskeleton and ciliary abnormalities in the development of congenital pulmonary airway malformationsTianqi Zhu, Xinyao Meng, Qingxuan Hu, et al.Molecular Vision|May 23, 2015
Mutation analysis in 129 genes associated with other forms of retinal dystrophy in 157 families with retinitis pigmentosa based on exome sequencingYan Xu, Liping Guan, Xueshan Xiao, et al.Acta Pharmacologica Sinica|March 4, 2015
Association of positively selected eIF3a polymorphisms with toxicity of platinum-based chemotherapy in NSCLC patientsJi-ye Yin, Xiang-guang Meng, Chen-yue Qian, et al.International Journal of Molecular Medicine|June 11, 2014
Exome sequencing reveals CHM mutations in six families with atypical choroideremia initially diagnosed as retinitis pigmentosaShiqiang Li, Liping Guan, Shaohua Fang, et al.Pageof 28