Showing results (1-10 of 39) with videos related to
Sort By:
Pageof 4
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 29, 2021
[Analysis of C2ORF71 gene variant in a Chinese patient with retinitis pigmentosa]Man Liu, Yilu Lu, Yongxin MaGene|May 18, 2017
Congenital adrenal hyperplasia due to 11-hydroxylase deficiency-Compound heterozygous mutations of a prevalent and two novel CYP11B1 mutationsChongjuan Gu, Hao Tan, Junbao Yang, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 6, 2019
[Mutation analysis of a family affected with isolated proteinuria]Zhao Yang, Chongjuan Gu, Xulei Zheng, et al.Biomed Research International|November 7, 2017
Decreased Plasma COMP and Increased Plasma CTX-II Levels in a Chinese Pseudoachondroplasia Family with Novel <i>COMP</i> MutationChongjuan Gu, Zhao Yang, Hao Tan, et al.Journal of Cellular and Molecular Medicine|May 18, 2019
PIWIL1 suppresses circadian rhythms through GSK3β-induced phosphorylation and degradation of CLOCK and BMAL1 in cancer cellsHao Tan, Yingchuan Zhu, Xulei Zheng, et al.Cell Death & Disease|March 21, 2018
PIWIL2 suppresses Siah2-mediated degradation of HDAC3 and facilitates CK2α-mediated HDAC3 phosphorylationYingying Zhang, Xulei Zheng, Hao Tan, et al.Molecular Genetics & Genomic Medicine|August 29, 2025
Unraveling CBS Mutations and Their Clinical Impact in a Chinese Family With Classical HomocystinuriaJingfei Zhang, Xinyu Lin, Xinmei Liu, et al.Genes & Genomics|July 30, 2020
Identification of two rare mutations c.1318G>A and c.6438+2T>G in a Chinese DMD family as genetic markersYingchuan Zhu, Lijun Yang, Tengjiao Ma, et al.Cell Biology International|June 3, 2010
Sp1 plays an important role in regulating the transcription of ZNF313Xiaolin Liao, Wenqian Deng, Yilu Lu, et al.Reproduction (Cambridge, England)|July 21, 2007
A microarray for microRNA profiling in mouse testis tissuesNaihong Yan, Yilu Lu, Huaqin Sun, et al.Pageof 4