Zobrazeno 1 - 10
of 22
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36493897fe738aee0a565d470551c40c
https://doi.org/10.1111/cge.13995
https://doi.org/10.1111/cge.13995
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c85ac7157c90a917992b49c3ace1b2d4
http://europepmc.org/articles/PMC8788604
http://europepmc.org/articles/PMC8788604
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12fd256bca1246e442ffc14f96c5ae52
https://doi.org/10.1136/jclinpath-2020-207170
https://doi.org/10.1136/jclinpath-2020-207170
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c2ca5d67efb5ac3c793da07bc194589
https://doi.org/10.1111/cge.13898
https://doi.org/10.1111/cge.13898
Autor:
Xiaoli Wei, Youzhu Li, Qicai Liu, Wensheng Liu, Xiaohong Yan, Xingshen Zhu, Dekun Zhou, Yingpu Tian, Fuxing Zhang, Na Li, Zhongxian Lu
Publikováno v:
Journal of Clinical Pathology; Mar2022, Vol. 75 Issue 3, p201-204, 4p
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4b0af873674d3b335907cbd96dfe713
https://doi.org/10.1111/cge.13602
https://doi.org/10.1111/cge.13602
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb8ffb3aa7b483078bc894855542ad18
https://pubmed.ncbi.nlm.nih.gov/34096614
https://pubmed.ncbi.nlm.nih.gov/34096614