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Plos One|June 23, 2012
MiR-137 targets estrogen-related receptor alpha and impairs the proliferative and migratory capacity of breast cancer cellsYuanyin Zhao, Yuping Li, Guiyu Lou, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 6, 2017
[Phenotypic and genetic analysis of a child carrying a 17q11.2 microdeletion]Hongdan Wang, Zhanqi Feng, Ke Yang, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 2, 2023
[Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene]Wenyu Zhang, Na Qi, Liangjie Guo, et al.Journal of Biochemistry|February 19, 2008
Transcriptional regulation of the human PNRC promoter by NFY in HepG2 cellsYan Zhang, Bin Chen, Yuping Li, et al.Plos One|September 20, 2014
HBx inhibits CYP2E1 gene expression via downregulating HNF4α in human hepatoma cellsHongming Liu, Guiyu Lou, Chongyi Li, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 9, 2018
[Identification of a novel EXT1 mutation in a pedigree affected with hereditary multiple exostosis]Guiyu Lou, Ke Yang, Litao Qin, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 12, 2020
[Identification of SPAST gene variant in a pedigree affected with hereditary spastic paraplegia type 4]Na Qi, Mingming Ma, Ke Yang, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 29, 2021
[Analysis of a Chinese pedigree affected with dyschromatosis symmetrica hereditaria due to a novel variant of ADAR gene]Ke Yang, Qiaofang Hou, Yuwei Zhang, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 22, 2022
[Genetic analysis and prenatal diagnosis of a Chinese pedigree affected with Usher syndrome due to novel compound heterozygous variants of PCDH15 gene]Ke Yang, Yuwei Zhang, Guiyu Lou, et al.Frontiers in Genetics|September 11, 2023
Functional analysis of a novel nonsense variant c.91A>T of the TRAPPC2 gene in a Chinese family with X-linked recessive autosomal spondyloepiphyseal dysplasia tardaGuiyu Lou, Yuanyin Zhao, Huiru Zhao, et al.Pageof 5