Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Xingshen Zhu"'
Autor:
Yanwei Sha, Wensheng Liu, Xianjing Huang, Yang Li, Zhiyong Ji, Libin Mei, Shaobin Lin, Shuangbo Kong, Jinhua Lu, Lingyuan Kong, Xingshen Zhu, Zhongxian Lu, Lu Ding
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)
Abstract Background Asthenozoospermia (AZS), also known as asthenospermia, is characterized by reduced motility of ejaculated spermatozoa and is detected in more than 40% of infertile patients. Because the proportion of progressive spermatozoa in sev
Externí odkaz:
https://doaj.org/article/a164ac7377024dd392954c218e481de9
Autor:
Yanwei Sha, Xingshen Zhu, Wensheng Liu, Xiaoyu Yang, Xiaoli Wei, Xiaoya Zhang, Bowen Tang, Xiong Wang, Yifeng Wang
Publikováno v:
Clinical Genetics. 100:280-291
Non-obstructive azoospermia (NOA) is the most severe form of male infertility, and it is primarily associated with genetic defects. We performed whole-exome sequencing of 236 patients with NOA and identified a homozygous pathogenic variant of autopha
Autor:
Na Li, Fu-Xing Zhang, Yanwei Sha, Rongfeng Wu, Youzhu Li, Xiaoli Wei, Yifeng Wang, Xiaoya Zhang, Zhongxian Lu, Xingshen Zhu, Wensheng Liu, Ya-Ling Tang
Publikováno v:
Asian Journal of Andrology
Asian Journal of Andrology, Vol 24, Iss 1, Pp 67-72 (2022)
Asian Journal of Andrology, Vol 24, Iss 1, Pp 67-72 (2022)
Acephalic spermatozoa syndrome is a rare type of teratozoospermia that severely impairs the reproductive ability of male patients, and genetic defects have been recognized as the main cause of acephalic spermatozoa syndrome. Spermatogenesis and centr
Autor:
Na Li, Wensheng Liu, Dekun Zhou, Xiaoli Wei, Xiaohong Yan, Xingshen Zhu, Youzhu Li, Qicai Liu, Zhongxian Lu, Fu-Xing Zhang, Yingpu Tian
Publikováno v:
Journal of Clinical Pathology. 75:201-204
BackgroundThe zona pellucida (ZP) of human oocytes plays essential protective roles in sperm–egg interactions during fertilisation and embryo development. ZP4-null female rabbits exhibit a thin and irregular ZP, which severely impairs embryo develo
Autor:
Huiliang Zhou, Xingshen Zhu, Wensheng Liu, Xinzong Zhang, Mingxiang Weng, Yanwei Sha, Yankun Sha, Yifeng Wang
Publikováno v:
Clinical Genetics. 99:443-448
Multiple morphological abnormalities of the sperm flagella (MMAF) is a severe type of teratozoospermia. In this study, whole-exome sequencing was conducted on 55 patients with MMAF, and biallelic mutations of CFAP58 were identified in two patients. T
Publikováno v:
Clinical Genetics. 96:385-393
Male patients with multiple morphological abnormalities of the sperm flagella (MMAF) are infertile and exhibit absent, short, coiled, bent and/or irregular sperm flagella. Mutations in the SPEF2 gene reduce sperm motility and cause sperm tail defects
Autor:
Xiaoli Wei, Jing Chen, Vladimir Isachenko, Zhongxian Lu, Youzhu Li, Yanwei Sha, Xingshen Zhu, Wensheng Liu, Xiaoya Zhang
Publikováno v:
Clinical geneticsREFERENCES. 100(4)
Oligo-astheno-teratozoospermia (OAT) is a common cause of male infertility, and most of idiopathic OAT patients are thought to be caused by genetic defects. Here, we recruited 38 primary infertile patients with the OAT phenotype and 40 adult men with
Autor:
Xingshen Zhu, Huiliang Zhou, He-jia Yuan, Xiaoya Zhang, Xiong Wang, Hua-yu Lian, Jie Chen, Zhongxian Lu, Yunge Tang, Yanwei Sha, Weibing Qin, Wei Yan, Yuan-qing Cui, Xinzhong Zhang
BackgroundMultiple morphological anomalies of the sperm flagella (MMAF) is a term used to describe abnormalities in sperm morphology, which lead to primary infertility in males. Intracytoplasmic sperm injection (ICSI) is an effective treatment for MM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::744fb18f2a5bc358088b3c776e9d56de
https://doi.org/10.21203/rs.3.rs-279593/v1
https://doi.org/10.21203/rs.3.rs-279593/v1