Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Journal of the National Cancer Institute|July 10, 2019
The Role of APAL/ST8SIA6-AS1 lncRNA in PLK1 Activation and Mitotic Catastrophe of Tumor CellsMan-Li Luo, Jingjing Li, Liping Shen, et al.
Plos Genetics|August 21, 2019
NKILA represses nasopharyngeal carcinoma carcinogenesis and metastasis by NF-κB pathway inhibitionWei Zhang, Qiannan Guo, Guoying Liu, et al.
Oncotarget|September 18, 2015
NBAT1 suppresses breast cancer metastasis by regulating DKK1 via PRC2Pengnan Hu, Junjun Chu, Yanqing Wu, et al.
Molecular Medicine Reports|November 9, 2017
Prenatal diagnosis and genetic counseling for Waardenburg syndrome type I and II in Chinese familiesLi Wang, Litao Qin, Tao Li, et al.
Clinical Transplantation|April 4, 2023
Association of fasting blood glucose variability with all-cause mortality in heart transplant recipientsQiang Zheng, Xing Liu, Hongwen Lan, et al.
Bioorganic & Medicinal Chemistry Letters|December 24, 2013
Design, synthesis and in vitro cytotoxicity evaluation of 5-(2-carboxyethenyl)isatin derivatives as anticancer agentsKailin Han, Yao Zhou, Fengxi Liu, et al.
Biomed Research International|October 9, 2015
Long Noncoding RNA Expression Signatures of Metastatic Nasopharyngeal Carcinoma and Their Prognostic ValueWei Zhang, Lin Wang, Fang Zheng, et al.
Frontiers in Nutrition|November 3, 2025
Sex differences in the association between the uric acid to high density lipoprotein cholesterol ratio and mild cognitive impairment in patients with type 2 diabetes mellitusYafen Chu, Li Wang, Qiannan Guo, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 22, 2022
[Application of genomic copy number variation detection technology in prenatal diagnosis of 7617 pregnant women with serological screening abnormalities during the second trimester of pregnancy]Jia Huang, Dong Wu, Yue Gao, et al.
Human Genomics|April 9, 2026
Integrated multiomics profiling of amniotic fluid exosomes reveals dysregulated lipid and protein signatures in fetal 22q11.2 deletion syndromeHai Xiao, Tao Li, Mengting Zhang, et al.
Pageof 6