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Li-Lin Du

Showing results (91-100 of 107) with videos related to

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Nature Communications|March 3, 2019
Systematic analysis reveals the prevalence and principles of bypassable gene essentialityJun Li, Hai-Tao Wang, Wei-Tao Wang, et al.
G3 (Bethesda, Md.)|December 1, 2021
Perturbation of kinetochore function using GFP-binding protein in fission yeastDa-Jie Deng, Qian-Cheng Xia, Guo-Song Jia, et al.
Human Genetics|October 18, 2002
The prevalence of connexin 26 ( GJB2) mutations in the Chinese populationXue Zhong Liu, Xia Juan Xia, Xiao Mei Ke, et al.
Plos Biology|September 10, 2014
Fission yeast Pxd1 promotes proper DNA repair by activating Rad16XPF and inhibiting Dna2Jia-Min Zhang, Xiao-Man Liu, Yue-He Ding, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 2024
A meiotic driver hijacks an epigenetic reader to disrupt mitosis in noncarrier offspringYu Hua, Jianxiu Zhang, Man-Yun Yang, et al.
The EMBO Journal|November 19, 2025
S-phase PARylation of microprotein RSMC enhances the function of Sororin in sister chromatid cohesionMeiqian Jiang, Jiaxin Zhang, Jiankun He, et al.
Molecular & Cellular Proteomics : MCP|April 20, 2025
Global analysis of protein and small-molecule substrates of ubiquitin-like proteins (UBLs)Guang-Can Shao, Zhen-Lin Chen, Shan Lu, et al.
Molecular & Cellular Proteomics : MCP|March 5, 2026
Correction: Global Analysis of Protein and Small-Molecule Substrates of Ubiquitin-Like ProteinsGuang-Can Shao, Zhen-Lin Chen, Shan Lu, et al.
Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.
Human Genetics|December 4, 2008
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Xue-Zhong Liu, Yongyi Yuan, Denise Yan, et al.
Pageof 11

Showing results (91-100 of 107) with videos related to

Sort By:
Pageof 11
Nature Communications|March 3, 2019
Systematic analysis reveals the prevalence and principles of bypassable gene essentialityJun Li, Hai-Tao Wang, Wei-Tao Wang, et al.
G3 (Bethesda, Md.)|December 1, 2021
Perturbation of kinetochore function using GFP-binding protein in fission yeastDa-Jie Deng, Qian-Cheng Xia, Guo-Song Jia, et al.
Human Genetics|October 18, 2002
The prevalence of connexin 26 ( GJB2) mutations in the Chinese populationXue Zhong Liu, Xia Juan Xia, Xiao Mei Ke, et al.
Plos Biology|September 10, 2014
Fission yeast Pxd1 promotes proper DNA repair by activating Rad16XPF and inhibiting Dna2Jia-Min Zhang, Xiao-Man Liu, Yue-He Ding, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 2024
A meiotic driver hijacks an epigenetic reader to disrupt mitosis in noncarrier offspringYu Hua, Jianxiu Zhang, Man-Yun Yang, et al.
The EMBO Journal|November 19, 2025
S-phase PARylation of microprotein RSMC enhances the function of Sororin in sister chromatid cohesionMeiqian Jiang, Jiaxin Zhang, Jiankun He, et al.
Molecular & Cellular Proteomics : MCP|April 20, 2025
Global analysis of protein and small-molecule substrates of ubiquitin-like proteins (UBLs)Guang-Can Shao, Zhen-Lin Chen, Shan Lu, et al.
Molecular & Cellular Proteomics : MCP|March 5, 2026
Correction: Global Analysis of Protein and Small-Molecule Substrates of Ubiquitin-Like ProteinsGuang-Can Shao, Zhen-Lin Chen, Shan Lu, et al.
Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.
Human Genetics|December 4, 2008
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Xue-Zhong Liu, Yongyi Yuan, Denise Yan, et al.
Pageof 11