Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Haojuan Wu"'
Autor:
Ying Shen, Feng Zhang, Fuping Li, Xiaohui Jiang, Yihong Yang, Xiaoliang Li, Weiyu Li, Xiang Wang, Juan Cheng, Mohan Liu, Xueguang Zhang, Guiping Yuan, Xue Pei, Kailai Cai, Fengyun Hu, Jianfeng Sun, Lanzhen Yan, Li Tang, Chuan Jiang, Wenling Tu, Jinyan Xu, Haojuan Wu, Weiqi Kong, Shuying Li, Ke Wang, Kai Sheng, Xudong Zhao, Huanxun Yue, Xiaoyu Yang, Wenming Xu
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Multiple morphological abnormalities of the sperm flagella (MMAF) is a cause of male infertility. Here the authors identify homozygous nonsense mutations of the glutamine rich 2 (QRICH2) gene in two MMAF patients from 2 consanguineous families and sh
Externí odkaz:
https://doaj.org/article/7f434c531ab1482fa370de4f562ac05c
Autor:
Juan Cheng, Haojuan Wu, Huawei Liu, Hua Li, Hua Zhu, Yongmei Zhou, Hongxia Li, Wenming Xu, Jiang Xie
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
The hippocampus is a region in which neurogenesis persists and retains substantial plasticity throughout lifespan. Accumulating evidences indicate an important role of androgens and androgenic signaling in the regulation of offspring hippocampal neur
Externí odkaz:
https://doaj.org/article/7a805f9de4a94ce39ada1675256ead44
Autor:
Ying Shen, Feng Zhang, Fuping Li, Xiaohui Jiang, Yihong Yang, Xiaoliang Li, Weiyu Li, Xiang Wang, Juan Cheng, Mohan Liu, Xueguang Zhang, Guiping Yuan, Xue Pei, Kailai Cai, Fengyun Hu, Jianfeng Sun, Lanzhen Yan, Li Tang, Chuan Jiang, Wenling Tu, Jinyan Xu, Haojuan Wu, Weiqi Kong, Shuying Li, Ke Wang, Kai Sheng, Xudong Zhao, Huanxun Yue, Xiaoyu Yang, Wenming Xu
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)
In the original version of this Article, the Acknowledgements section omitted the National Key Research and Development Program of China (SQ2018YFC1003603).
Externí odkaz:
https://doaj.org/article/2e058d40aa02446eb35d673743c52c06
Autor:
Juan Cheng, Xiang Wang, Wenming Xu, Andras Dinnyes, Jiang Xie, Xueguang Zhang, Juan Li, Baoshan Xu, Yan Liang, Haojuan Wu
Autistic spectrum disorder (ASD) is a complex neurodevelopmental disorder. The copy number variation (CNV) of genes in the X-chromosome is speculated to play a critical role in ASD. The HECT, UBA and WWE domain containing the E3 ubiquitin protein lig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd8e568641f181ba7977998648acbc01
https://doi.org/10.21203/rs.3.rs-404499/v1
https://doi.org/10.21203/rs.3.rs-404499/v1
Autor:
Mohan Liu, J. Xu, Fuping Li, Lanzhen Yan, Weiqi Kong, Fengyun Hu, Wenming Xu, Xudong Zhao, Xiaoyu Yang, Xue Pei, Jianfeng Sun, Xueguang Zhang, Feng Zhang, Xiang Wang, Ying Shen, Xiaoliang Li, Guiping Yuan, Huanxun Yue, Li Tang, Chuan Jiang, Haojuan Wu, Weiyu Li, Shuying Li, Yihong Yang, Wenling Tu, Juan Cheng, Kailai Cai, Kai Sheng, Xiaohui Jiang, Ke Wang
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)
Nature Communications
Nature Communications
Aberrant sperm flagella impair sperm motility and cause male infertility, yet the genes which have been identified in multiple morphological abnormalities of the flagella (MMAF) can only explain the pathogenic mechanisms of MMAF in a small number of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e01a64b65daf1674a49a079f5681583
https://doi.org/10.1038/s41467-019-10313-x
https://doi.org/10.1038/s41467-019-10313-x
Autor:
Ke Wang, Xiaohui Jiang, Jianfeng Sun, Kai Sheng, Li Tang, Feng Zhang, Chuan Jiang, Xue Pei, Weiyu Li, Lanzhen Yan, Ying Shen, Mohan Liu, Juan Cheng, Wenling Tu, Xiang Wang, Haojuan Wu, Huanxun Yue, Shuying Li, Weiqi Kong, Fengyun Hu, Xueguang Zhang, Xiaoyu Yang, Xudong Zhao, J. Xu, Wenming Xu, Kailai Cai, Fuping Li, Guiping Yuan, Xiaoliang Li, Yihong Yang
Publikováno v:
Nature Communications
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Aberrant sperm flagella impair sperm motility and cause male infertility, yet the genes which have been identified in multiple morphological abnormalities of the flagella (MMAF) can only explain the pathogenic mechanisms of MMAF in a small number of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7240d528861bd065f3bd7b88e232dfb5
https://doi.org/10.1038/s41467-018-08182-x
https://doi.org/10.1038/s41467-018-08182-x