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Proceedings of the National Academy of Sciences of the United States of America|June 17, 2015
Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter geneTao Cai, Liu Yang, Wanshi Cai, et al.
Nucleic Acids Research|October 14, 2016
TET1 modulates H4K16 acetylation by controlling auto-acetylation of hMOF to affect gene regulation and DNA repair functionJianing Zhong, Xianfeng Li, Wanshi Cai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 6, 2015
Lysosomal storage disease in the brain: mutations of the β-mannosidase gene identified in autosomal dominant nystagmusPing Yu, Yun Cui, Wanshi Cai, et al.
Biochemical and Biophysical Research Communications|August 10, 2010
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese familiesJuanjuan Zhang, Xiangtian Zhou, Jian Zhou, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|November 6, 2018
Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencingJinyu Wu, Ping Yu, Xin Jin, et al.
Nature Medicine|August 27, 2025
Allogeneic CD19-targeting T cells for treatment-refractory systemic lupus erythematosus: a phase 1 trialXiaobing Wang, Yi Zhang, Huimin Wang, et al.
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