Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD
Tu, Chaofeng, Nie, Hongchuan, Meng, Lanlan, Wang, Weili, Li, Haiyu, Yuan, Shimin, Cheng, Dehua, He, Wenbin, Liu, Gang, Du, Juan, Gong, Fei, Lu, Guangxiu, Lin, Ge, Zhang, Qianjun, Tan, Yue-Qiu
Published in Human genetics (01.02.2020)
Published in Human genetics (01.02.2020)
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Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations
Wang, Weili, Tu, Chaofeng, Nie, Hongchuan, Meng, Lanlan, Li, Yong, Yuan, Shimin, Zhang, Qianjun, Du, Juan, Wang, Junpu, Gong, Fei, Fan, Liqing, Lu, Guang-Xiu, Lin, Ge, Tan, Yue-Qiu
Published in Journal of medical genetics (01.11.2019)
Published in Journal of medical genetics (01.11.2019)
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Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans
Tan, Yue-Qiu, Tu, Chaofeng, Meng, Lanlan, Yuan, Shimin, Sjaarda, Calvin, Luo, Aixiang, Du, Juan, Li, Wen, Gong, Fei, Zhong, Changgao, Deng, Han-Xiang, Lu, Guangxiu, Liang, Ping, Lin, Ge
Published in Genetics in medicine (01.05.2019)
Published in Genetics in medicine (01.05.2019)
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Establishment of trimester-specific reference intervals of serum lipids and the associations with pregnancy complications and adverse perinatal outcomes: a population-based prospective study
Lu, Yifan, Jia, Zhaoxia, Su, Shaofei, Han, Lican, Meng, Lanlan, Tang, Guodong, Wang, Jing, Zhang, Chunhong, Xie, Xin, Zhang, Yi, Zhang, Yue, Zhai, Yanhong, Cao, Zheng
Published in Annals of medicine (Helsinki) (01.01.2021)
Published in Annals of medicine (Helsinki) (01.01.2021)
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CEP112 coordinates translational regulation of essential fertility genes during spermiogenesis through phase separation in humans and mice
Zhang, Xueguang, Huang, Gelin, Jiang, Ting, Meng, Lanlan, Li, Tongtong, Zhang, Guohui, Wu, Nan, Chen, Xinyi, Zhao, Bingwang, Li, Nana, Wu, Sixian, Guo, Junceng, Zheng, Rui, Ji, Zhiliang, Xu, Zhigang, Wang, Zhenbo, Deng, Dong, Tan, Yueqiu, Xu, Wenming
Published in Nature communications (30.09.2024)
Published in Nature communications (30.09.2024)
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Diverse associations observed between pregnancy complications and RBC or plasma folates determined by an in-house developed LC-MS/MS method
Xu, Zhengwen, Li, Youran, Liu, Ying, Liu, Shengmin, Zhang, Lin, Wang, Jing, Su, Shaofei, Liu, Lin, Meng, Lanlan, Zhu, Hongyuan, Sun, Jingru, Shao, Lijun, Li, Lin, Zhai, Yanhong, Li, Guanghui, Cao, Zheng
Published in Annals of medicine (Helsinki) (12.12.2023)
Published in Annals of medicine (Helsinki) (12.12.2023)
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Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia
Wang, Ying, Tu, Chaofeng, Nie, Hongchuan, Meng, Lanlan, Li, Dongyan, Wang, Weili, Zhang, Huan, Lu, Guangxiu, Lin, Ge, Tan, Yue-Qiu, Du, Juan
Published in Journal of assisted reproduction and genetics (01.04.2020)
Published in Journal of assisted reproduction and genetics (01.04.2020)
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Delivery prediction by quantitative analysis of four steroid metabolites with liquid chromatography tandem mass spectrometry in asymptomatic pregnant women
Meng, Lanlan, Su, Shaofei, Li, Lin, Liu, Shengmin, Li, Youran, Liu, Ying, Lu, Yifan, Xu, Zhengwen, Liu, Lin, He, Qixin, Zheng, Yuanyuan, Liu, Xiaowei, Cong, Yuting, Zhai, Yanhong, Zhao, Zhen, Cao, Zheng
Published in Annals of medicine (Helsinki) (31.12.2022)
Published in Annals of medicine (Helsinki) (31.12.2022)
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Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia
Wang, Yurong, Liu, Ling, Tan, Chen, Meng, Guiquan, Meng, Lanlan, Nie, Hongchuan, Du, Juan, Lu, Guang-Xiu, Lin, Ge, He, Wen-Bin, Tan, Yue-Qiu
Published in Frontiers in genetics (05.08.2022)
Published in Frontiers in genetics (05.08.2022)
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Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly
Lu, Shuai, Gu, Yayun, Wu, Yifei, Yang, Shenmin, Li, Chenmeijie, Meng, Lanlan, Yuan, Wenwen, Jiang, Tao, Zhang, Xin, Li, Yang, Wang, Cheng, Liu, Mingxi, Ye, Lan, Guo, Xuejiang, Shen, Hongbing, Yang, Xiaoyu, Tan, Yueqiu, Hu, Zhibin
Published in Cell discovery (16.11.2021)
Published in Cell discovery (16.11.2021)
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ZnCl2-Promoted One-Pot Three-Component Synthesis of Multisubstituted Thiazolo[4,5-b]pyridines and Thieno[2,3-b:4,5-b′]dipyridines
Luo, Laichun, Meng, Lanlan, Peng, Yangqiu, Xing, Yongning, Sun, Qi, Ge, Zemei, Li, Runtao
Published in European journal of organic chemistry (01.01.2015)
Published in European journal of organic chemistry (01.01.2015)
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Establishment of trimester-specific reference intervals of renal function tests and their predictive values in pregnant complications and perinatal outcomes: A population-based cohort study
Han, Lican, Liu, Lin, Meng, Lanlan, Su, Shaofei, Lu, Yifan, Xu, Zhengwen, Tang, Guodong, Wang, Jing, Zhu, Hongyuan, Zhang, Yue, Zhai, Yanhong, Cao, Zheng
Published in Practical laboratory medicine (01.11.2023)
Published in Practical laboratory medicine (01.11.2023)
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DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice
Zhou, Shushu, Yuan, Shimin, Zhang, Jintao, Meng, Lanlan, Zhang, Xin, Liu, Siyu, Lu, Guangxiu, Lin, Ge, Liu, Mingxi, Tan, Yue-Qiu
Published in Signal transduction and targeted therapy (10.01.2023)
Published in Signal transduction and targeted therapy (10.01.2023)
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Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella
Meng, Lanlan, Liu, Qiang, Tan, Chen, Xu, Xilin, He, Wenbin, Hu, Tongyao, Tu, Chaofeng, Li, Yong, Du, Juan, Zhang, Qianjun, Lu, Guangxiu, Fan, Li-Qing, Lin, Ge, Nie, Hongchuan, Zhang, Huan, Tan, Yue-Qiu
Published in Frontiers in cell and developmental biology (01.06.2023)
Published in Frontiers in cell and developmental biology (01.06.2023)
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Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression
Tu, Chaofeng, Wen, Junfei, Wang, Weili, Zhu, Qifan, Chen, Ying, Cheng, Jianglu, Li, Zeye, Meng, Lanlan, Li, Yong, He, Wenbin, Tan, Chen, Xie, Chunbo, Fu, Shao-Mei, Du, Juan, Lu, Guangxiu, Lin, Ge, Gou, Lan-Tao, Tan, Yue-Qiu
Published in Cell discovery (22.08.2023)
Published in Cell discovery (22.08.2023)
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Serum peptidomic screening identified circulating peptide biomarkers predictive for preeclampsia
Zhao, Shenglong, Yin, Chenghong, Zhai, Yanhong, Jia, Zhaoxia, Su, Shaofei, Lu, Yifan, Meng, Lanlan, Li, Chunbo, Liu, Xiang, Cong, Yuting, Li, Youran, Liu, Ying, Chen, Lu, Wang, Jing, Xu, Zhengwen, Zheng, Yuanyuan, Sun, Zhi, Luo, Ruben Y., Yu, Xiaobo, Yang, He S., Liu, Xiaowei, Zhao, Zhen, Cao, Zheng
Published in Frontiers in cardiovascular medicine (11.10.2022)
Published in Frontiers in cardiovascular medicine (11.10.2022)
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Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature
Li, Haiyu, Du, Juan, Li, Wen, Cheng, Dehua, He, Wenbin, Yi, Duo, Xiong, Bo, Yuan, Shimin, Tu, Chaofeng, Meng, Lanlan, Luo, Aixiang, Lin, Ge, Lu, Guangxiu, Tan, Yue-Qiu
Published in Molecular cytogenetics (05.02.2018)
Published in Molecular cytogenetics (05.02.2018)
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Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia
Xie, Chunbo, Wang, Weili, Tu, Chaofeng, Meng, Lanlan, Lu, Guangxiu, Lin, Ge, Lu, Lin-Yu, Tan, Yue-Qiu
Published in Human reproduction update (02.11.2022)
Published in Human reproduction update (02.11.2022)
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Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development
Zhang, Guohui, Li, Dongyan, Tu, Chaofeng, Meng, Lanlan, Tan, Yueqiu, Ji, Zhiliang, Cheng, Jiao, Lu, Guangxiu, Lin, Ge, Zhang, Huan, Sun, Jinpeng, Wang, Mingwei, Du, Juan, Xu, Wenming
Published in Human molecular genetics (27.12.2021)
Published in Human molecular genetics (27.12.2021)
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