Renming Hu
Fudan University
13 Papers
234 Citations
Renming Hu is an academic researcher from Fudan University. The author has contributed to research in topics: Kinetochore & Spindle apparatus. The author has an hindex of 10, co-authored 13 publications. Previous affiliations of Renming Hu include Ruijin Hospital.
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Papers
Human NUF2 Interacts With Centromere-Associated Protein E and Is Essential for a Stable Spindle Microtubule-Kinetochore Attachment
Dan Liu,Xia Ding,Xia Ding,Jian Du,Xin Cai,Xin Cai,Yuejia Huang,Tarsha Ward,Andrew P. Shaw,Yong Yang,Yong Yang,Renming Hu,Changjiang Jin,Xuebiao Yao,Xuebiao Yao +14 more
TL;DR: It is shown that Homo sapiens (Hs) NUF2 is required for stable kinetochore localization of centromere-associated protein E (CENP-E) in HeLa cells and that depletion of HsNUF2 caused aberrant chromosome segregation.
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Phosphorylation of HsMis13 by Aurora B Kinase Is Essential for Assembly of Functional Kinetochore
Yong Yang,Yong Yang,Fang Wu,Tarsha Ward,Feng Yan,Feng Yan,Quan Wu,Quan Wu,Zhaoyang Wang,Tanisha McGlothen,Wei Peng,Tianpa You,Mingkuan Sun,Mingkuan Sun,Taixing Cui,Renming Hu,Zhen Dou,Zhen Dou,Jingde Zhu,Wei Xie,Wei Xie,Zihe Rao,Xia Ding,Xia Ding,Xuebiao Yao +24 more
TL;DR: It is shown that HsMis13 phosphorylation by Aurora B is required for organizing a stable bi-oriented microtubule kinetochore attachment that is essential for faithful chromosome segregation in mitosis.
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Human NUF2 Interacts with Centromere-associated Protein E and Is Essential for a Stable Spindle
Dan Liu,Xia Ding,Jian Du,Xin Cai,Yuejia Huang,Tarsha Ward,Andrew W. Shaw,Yong Yang,Renming Hu,Changjiang Jin,Xuebiao Yao +10 more
- 01 Jan 2007
TL;DR: In this paper, the authors show that HsNUF2 is required for stable kinetochore localization of centromere-associated protein E (CENP-E) in HeLa cells.
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Phospho-regulation of HsCdc14A By Polo-like kinase 1 is essential for mitotic progression.
Kai Yuan,Kai Yuan,Haiying Hu,Haiying Hu,Zhen Guo,Zhen Guo,Guosheng Fu,Andrew P. Shaw,Renming Hu,Xuebiao Yao,Xuebiao Yao +10 more
TL;DR: It is proposed that PLK1-HsCdc14A interaction provides a temporal regulation of HsCDC14A in chromosome segregation during mitosis through an auto-inhibitory mechanism via its intra-molecular association.
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A complex heterozygous mutation of His373Leu and Asp487–Ser488–Phe489 deletion in human cytochrome P450c17 causes 17α-hydroxylase/17,20-lyase deficiency in three Chinese sisters
Jie Qiao,Renming Hu,Peng Yongde,Huai-Dong Song,Yi-Wen Peng,Guo-Feng Gao,Jian-Hua Hao,Nan-Ying Hu,Man-Yin Xu,Jia-Lun Chen +9 more
TL;DR: The mother and the brother have been demonstrated to be carriers of deletion mutation through restriction enzyme analysis, and the first report of the molecular genetic study of 17alpha-hydroxylase/17,20-lyase deficiency in mainland China with a novel compound heterozygous mutation.
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