Zobrazeno 1 - 10
of 195
pro vyhledávání: '"Yue-qiu Tan"'
Autor:
Jihong Guo, Wen-Bin He, Lei Dai, Fen Tian, Zhenqing Luo, Fang Shen, Ming Tu, Yu Zheng, Liu Zhao, Chen Tan, Yongteng Guo, Lan-Lan Meng, Wei Liu, Mei Deng, Xinghan Wu, Yu Peng, Shuju Zhang, Guang-Xiu Lu, Ge Lin, Hua Wang, Yue-Qiu Tan, Yongjia Yang
Publikováno v:
HGG Advances, Vol 5, Iss 1, Pp 100256- (2024)
Summary: In this study, we report on mosaic variegated aneuploidy (MVA) syndrome with tetraploidy and predisposition to infertility in a family. Sequencing analysis identified that the CEP192 biallelic variants (c.1912C>T, p.His638Tyr and c.5750A>G,
Externí odkaz:
https://doaj.org/article/67694e929e9e453aa535bdd7f4b671dc
Autor:
Chaofeng Tu, Junfei Wen, Weili Wang, Qifan Zhu, Ying Chen, Jianglu Cheng, Zeye Li, Lanlan Meng, Yong Li, Wenbin He, Chen Tan, Chunbo Xie, Shao-Mei Fu, Juan Du, Guangxiu Lu, Ge Lin, Lan-Tao Gou, Yue-Qiu Tan
Publikováno v:
Cell Discovery, Vol 9, Iss 1, Pp 1-4 (2023)
Externí odkaz:
https://doaj.org/article/92c27d42277248d084a41b9625dd8223
Autor:
Jian-Wen Hou, Xiao-Liang Li, Li Wang, Cong-Ling Dai, Na Li, Xiao-Hui Jiang, Yue-Qiu Tan, Er-Po Tian, Qin-Tong Li, Wen-Ming Xu
Publikováno v:
Asian Journal of Andrology, Vol 25, Iss 1, Pp 58-65 (2023)
Congenital bilateral absence of the vas deferens (CBAVD) is observed in 1%–2% of males presenting with infertility and is clearly associated with cystic fibrosis transmembrane conductance regulator (CFTR) mutations. CFTR is one of the most well-kno
Externí odkaz:
https://doaj.org/article/d93b4c6cd9634101bfe5a260da361346
Autor:
Shushu Zhou, Shimin Yuan, Jintao Zhang, Lanlan Meng, Xin Zhang, Siyu Liu, Guangxiu Lu, Ge Lin, Mingxi Liu, Yue-Qiu Tan
Publikováno v:
Signal Transduction and Targeted Therapy, Vol 8, Iss 1, Pp 1-4 (2023)
Externí odkaz:
https://doaj.org/article/b5dba3d508ab40b0949c78d5315dfa2f
Publikováno v:
Asian Journal of Andrology, Vol 25, Iss 5, Pp 643-645 (2023)
Male infertility is a major reproductive disorder, which is clinically characterized by highly heterogeneous phenotypes of abnormal sperm count or quality. To date, five male patients with biallelic loss-of-function (LOF) variants of PARN-like ribonu
Externí odkaz:
https://doaj.org/article/36823caca8214b5f8c8a1c2e434993fb
Autor:
Pingyuan Xie, Shuoping Zhang, Yifang Gu, Bo Jiang, Liang Hu, Yue-qiu Tan, Yaxin Yao, Yi Tang, Anqi Wan, Sufen Cai, Yangyun Zou, Guangxiu Lu, Cheng Wan, Fei Gong, Sijia Lu, Ge Lin
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-10 (2022)
Abstract Background Previous studies suggested that non-invasive preimplantation genetic testing (niPGT) for intracytoplasmic sperm injection (ICSI) blastocysts can be used to identify chromosomal ploidy and chromosomal abnormalities. Here, we report
Externí odkaz:
https://doaj.org/article/1c78f14e53564791aa6df3b6aea654d4
Autor:
Lanlan Meng, Qiang Liu, Chen Tan, Xilin Xu, Wenbin He, Tongyao Hu, Chaofeng Tu, Yong Li, Juan Du, Qianjun Zhang, Guangxiu Lu, Li-Qing Fan, Ge Lin, Hongchuan Nie, Huan Zhang, Yue-Qiu Tan
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Introduction: Tracing the genetic causes for male infertility due to asthenoteratozoospermia has revealed at least 40 causative genes, which provides valuable reference for the genetic testing of asthenoteratozoospermia in clinical practice. To ident
Externí odkaz:
https://doaj.org/article/c51f175f0fcd493dab1ac8eeaa88c2c0
Autor:
Dong-Yan Li, Xiao-Xuan Yang, Chao-Feng Tu, Wei-Li Wang, Lan-Lan Meng, Guang-Xiu Lu, Yue-Qiu Tan, Qian-Jun Zhang, Juan Du
Publikováno v:
Asian Journal of Andrology, Vol 24, Iss 4, Pp 359-366 (2022)
Spermiogenesis is a complex and tightly regulated process, consisting of acrosomal biogenesis, condensation of chromatin, flagellar assembly, and disposal of extra cytoplasm. Previous studies have reported that sperm flagellar 2 (SPEF2) deficiency ca
Externí odkaz:
https://doaj.org/article/ef7599ad93e6460984f29901b6aa9b33
Autor:
Yurong Wang, Ling Liu, Chen Tan, Guiquan Meng, Lanlan Meng, Hongchuan Nie, Juan Du, Guang-Xiu Lu, Ge Lin, Wen-Bin He, Yue-Qiu Tan
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Infertility is a global health concern. MEIOB has been found to be associated with premature ovarian insufficiency (POI) and non-obstructive azoospermia (NOA), but its variants have not been reported in Chinese patients. The aim of this s
Externí odkaz:
https://doaj.org/article/65a1368ddce549be97d248cb97243b58
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Reciprocal translocations are the most common structural chromosome rearrangements and may be associated with reproductive problems. Therefore, the objective of this study was to analyze factors that can influence meiotic segregation patterns in blas
Externí odkaz:
https://doaj.org/article/96722a37b3fc4f1ba141aad9aa1217c2