Wen Li
Central South University
35 Papers
52 Citations
Wen Li is an academic researcher from Central South University. The author has contributed to research in topics: Mutation (genetic algorithm) & Gene mutation. The author has an hindex of 9, co-authored 35 publications. Previous affiliations of Wen Li include National Health and Family Planning Commission & Brock University.
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Papers
A highly homozygous and parthenogenetic human embryonic stem cell line derived from a one-pronuclear oocyte following in vitro fertilization procedure
TL;DR: The first successful derivation of a human homozygous ESC line (chHES-32) from a one-pronuclear oocyte following routine in vitro fertilization treatment is reported, indicating that 'unwanted' one- pronuclear oocytes might be a potential source for humanhomozygous and parthenogenetic ESCs.
HLA-Matching Potential of an Established Human Embryonic Stem Cell Bank in China
Ge Lin,Yubin Xie,Qi Ouyang,Xiaobing Qian,Pingyuan Xie,Xiaoying Zhou,Bo Xiong,Yue-Qiu Tan,Wen Li,Leiyu Deng,Jing Zhou,Di Zhou,Lili Du,De-Hua Cheng,Yi Liao,Yifan Gu,Shuoping Zhang,Tiancheng Liu,Yi Sun,Guangxiu Lu +19 more
TL;DR: Document S1.
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Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans
Yue-Qiu Tan,Chaofeng Tu,Chaofeng Tu,Lanlan Meng,Lanlan Meng,Shimin Yuan,Shimin Yuan,Calvin Sjaarda,Aixiang Luo,Aixiang Luo,Juan Du,Juan Du,Wen Li,Wen Li,Fei Gong,Fei Gong,Chang-gao Zhong,Chang-gao Zhong,Han Xiang Deng,Guangxiu Lu,Ping Liang,Ge Lin,Ge Lin +22 more
TL;DR: TDRD7 causing CC is identified as a new pathogenic gene for male azoospermia in human, with an autosomal recessive mode of inheritance.
91
Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella.
Chaofeng Tu,Hongchuan Nie,Lanlan Meng,Shimin Yuan,Wen-Bin He,Aixiang Luo,Haiyu Li,Wen Li,Juan Du,Guangxiu Lu,Ge Lin,Yue-Qiu Tan +11 more
TL;DR: Three men with primary infertility due to multiple morphological abnormalities of the sperm flagella from two unrelated Han Chinese families are described and novel recessive mutations in DNAH6 are identified as a cause of MMAF.
Novel FOXL2 mutations cause blepharophimosis‐ptosis‐epicanthus inversus syndrome with premature ovarian insufficiency
Xiao-Wen Yang,Wen-Bin He,Fei Gong,Wen Li,Xiurong Li,Chang-gao Zhong,Guangxiu Lu,Ge Lin,Juan Du,Yue-Qiu Tan +9 more
TL;DR: Blepharophimosis‐ptosis‐epicanthus inversus syndrome (BPES) is a malformation of the eyelids and Forkhead Box L2 (FOXL2) is the only gene known to be associated with BPES.
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