Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Wen Ming Xu"'
Autor:
Wen Ming Xu, Jing Chen, Hui Chen, Rui Ying Diao, Kin Lam Fok, Jian Da Dong, Ting Ting Sun, Wen Ying Chen, Mei Kuen Yu, Xiao Hu Zhang, Lai Ling Tsang, Ann Lau, Qi Xian Shi, Qing Hua Shi, Ping Bo Huang, Hsiao Chang Chan
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19120 (2011)
Cystic fibrosis (CF) is the most common life-limiting recessive genetic disease among Caucasians caused by mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) with over 95% male patients infertile. However, whether CFTR mutati
Externí odkaz:
https://doaj.org/article/bc77bb3475134ff0999ec90d0ddb04e2
Autor:
Qin Zeng, Kai Wang, Wei-xin Liu, Jiu-zhi Zeng, Xing-lan Li, Qing-feng Zhang, Shang-qing Ren, Wen-ming Xu
Publikováno v:
BMC Medical Education, Vol 23, Iss 1, Pp 1-12 (2023)
Abstract Background Simulation is an increasingly used novel method for the education of medical professionals. This study aimed to systematically review the efficacy of high-fidelity (HF) simulation compared with low-fidelity (LF) simulation or no s
Externí odkaz:
https://doaj.org/article/02500a64ba744368b8289dbc2476ca40
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:
Kang-Kang Yu, Kun Li, Hao-Yuan Wang, Xiao-Liang Li, Si-Xian Wu, Wen-Ming Xu, Yan-Hong Liu, Chuan-Fang Wu, Xiao-Qi Yu, Jin-Ku Bao
Publikováno v:
Analytical Chemistry; 7/23/2024, Vol. 96 Issue 29, p11915-11922, 8p
Publikováno v:
Neural Regeneration Research, Vol 14, Iss 11, Pp 1977-1985 (2019)
HECT, UBA and WWE domain-containing 1 (Huwe1), an E3 ubiquitin ligase involved in the ubiquitin-proteasome system, is widely expressed in brain tissue. Huwe1 is involved in the turnover of numerous substrates, including p53, Mcl-1, Cdc6 and N-myc, th
Externí odkaz:
https://doaj.org/article/fc31117268a943208042c8558cff37f2
Publikováno v:
Structures. 49:365-376
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e493b3255ebe7bf821d35a4997d0d8b
https://doi.org/10.1016/j.istruc.2022.10.098
https://doi.org/10.1016/j.istruc.2022.10.098
Autor:
Hui Lin, Peng Xiao, Rui-Qian Bu, Shengchao Guo, Zhao Yang, Daopeng Yuan, Zhong-Liang Zhu, Chuan-Xin Zhang, Qing-Tao He, Chao Zhang, Yu-Qi Ping, Ru-Jia Zhao, Chuan-Shun Ma, Chang-Hao Liu, Xiao-Ning Zhang, Dan Jiang, Shaohui Huang, Yue-Tong Xi, Dao-Lai Zhang, Chen-Yang Xue, Bai-Sheng Yang, Jian-Yuan Li, Hao-Cheng Lin, Xu-Hui Zeng, Han Zhao, Wen-Ming Xu, Fan Yi, Zhongmin Liu, Jin-Peng Sun, Xiao Yu
Publikováno v:
Nature Chemical Biology. 18:1196-1203
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b4731d217e1c6493f1433b86a842ba9
https://doi.org/10.1038/s41589-022-01084-6
https://doi.org/10.1038/s41589-022-01084-6
Publikováno v:
Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition. 53(6)
Preeclampsia gravely threatens the health of mothers and infants. At present, treatment based on the relevant mechanisms of pathogenesis is still not available, and there is no independent reliable clinical index for early prediction of preeclampsia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5efb4cbda3e4ea33bc723cef8657c03b
https://pubmed.ncbi.nlm.nih.gov/36443045
https://pubmed.ncbi.nlm.nih.gov/36443045
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.
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-known
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::806176092bd1026107bad743f88fabba
https://pubmed.ncbi.nlm.nih.gov/35665694
https://pubmed.ncbi.nlm.nih.gov/35665694
Publikováno v:
Molecular Medicine Reports
Autophagy and the ubiquitin proteasome system (UPS) are two major protein degradation pathways involved in brain ischemia. Autophagy can compensate for UPS impairment‑induced cellular dysfunction. HECT, UBA and WWE domain containing E3 ubiquitin pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2442977baac61fff571374f51dfda07a
http://europepmc.org/articles/PMC7646962
http://europepmc.org/articles/PMC7646962