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Clinica Chimica Acta; International Journal of Clinical Chemistry|February 16, 2011
A novel frame-shift mutation of GLI3 causes non-syndromic and complex digital anomalies in a Chinese familyFeng Cheng, Xin Ke, Ming Lv, et al.Gene|May 21, 2018
Genetic variants of TREML2 are associated with HLA-B27-positive ankylosing spondylitisYuan Feng, Yaqiang Hong, Xin Zhang, et al.BMC Medicine|August 4, 2020
Hypomethylation in HBV integration regions aids non-invasive surveillance to hepatocellular carcinoma by low-pass genome-wide bisulfite sequencingHaikun Zhang, Peiling Dong, Shicheng Guo, et al.Frontiers in Genetics|February 4, 2022
PDE4B Proposed as a High Myopia Susceptibility Gene in Chinese PopulationFuxin Zhao, Wei Chen, Hui Zhou, et al.Carcinogenesis|May 31, 2021
TGFB3 downregulation causing chordomagenesis and its tumor suppression role maintained by Smad7Liang Wang, Xiaonan Guan, Qingtao Hu, et al.Journal of Medical Genetics|December 15, 2020
Dysfunction of VIPR2 leads to myopia in humans and miceFuxin Zhao, Qihang Li, Wei Chen, et al.Human Genetics|September 19, 2017
Genome-wide compound heterozygote analysis highlights alleles associated with adult height in EuropeansKaiyin Zhong, Gu Zhu, Xiaoxi Jing, et al.Scientific Data|July 20, 2024
A panel sequencing dataset of peripheral blood gene variations in pan-cancerYanxia Liu, Jie Liu, Shouwei Zhang, et al.Hepatology International|February 27, 2020
Noninvasive chimeric DNA profiling identifies tumor-originated HBV integrants contributing to viral antigen expression in liver cancerWei Chen, Ke Zhang, Peiling Dong, et al.BMC Musculoskeletal Disorders|June 3, 2024
Causal impact of DNA methylation on refracture in elderly individuals with osteoporosis - a prospective cohort studyBingtao Wen, Yaning Zhang, Jianhua He, et al.Pageof 12