Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Xiao‐qiong Wei"'
Autor:
Fan‐lian Zeng, Xiao‐yan Wang, Ya‐wen Hu, Zhen Wang, Ya Li, Jing Hu, Jia‐dong Yu, Pei Zhou, Xiu Teng, Hong Zhou, Hua‐ping Zheng, Fu‐lei Zhao, Lin‐na Gu, Cheng‐cheng Yue, Shu‐wen Chen, Juan Cheng, Yan Hao, Qi‐xiang Zhao, Chen Zhang, Song Zou, Zhong‐lan Hu, Xiao‐qiong Wei, Xiao Liu, Guo‐lin Li, Nong‐yu Huang, Wen‐ling Wu, Yi‐fan Zhou, Wei Li, Kaijun Cui, Jiong Li
Publikováno v:
MedComm, Vol 4, Iss 2, Pp n/a-n/a (2023)
Abstract Interleukin 37 (IL‐37), a member of the IL‐1 family, is considered a suppressor of innate and adaptive immunity and, hence is a regulator of tumor immunity. However, the specific molecular mechanism and role of IL‐37 in skin cancer rem
Externí odkaz:
https://doaj.org/article/1535f09d5e044e6890b874393ac6084f
Autor:
Zhen Wang, Fan-lian Zeng, Ya-wen Hu, Xiao-yan Wang, Fu-lei Zhao, Pei Zhou, Jing Hu, Yuan-yuan Xiao, Zhong-lan Hu, Ming-feng Guo, Xiao-qiong Wei, Xiao Liu, Nong-yu Huang, Jun Zhang, Shu-wen Chen, Juan Cheng, Hua-ping Zheng, Hong Zhou, Qi-xiang Zhao, Chen Zhang, Yan Hao, Song Zou, Yi-yue Gui, Jia-dong Yu, Lin-na Gu, Cheng-cheng Yue, Hao-zhou Zhang, Wen-ling Wu, Yi-fan Zhou, Xi-kun Zhou, Guo-bo Shen, Xiu Teng, Jiong Li
Publikováno v:
Signal Transduction and Targeted Therapy, Vol 7, Iss 1, Pp 1-17 (2022)
Abstract Interleukin-37b (hereafter called IL-37) was identified as fundamental inhibitor of natural and acquired immunity. The molecular mechanism and function of IL-37 in colorectal cancer (CRC) has been elusive. Here, we found that IL-37 transgeni
Externí odkaz:
https://doaj.org/article/b3a08cf291cf4f77bb99a84ceb4e72a7
Publikováno v:
Chinese Nursing Research. 3(4):162-167
Objective To develop a new curriculum for a master's degree in nursing and provide a reference for nursing education in China. Methods After a comprehensive literature review and item consolidation, an expert panel developed the initial version of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::497cc752234ac4a6fd778dc1459a15f2
Autor:
Yu-Peng, Liu, Yan-Yan, Ma, Tong-Fei, Wu, Qiao, Wang, Qing-Peng, Kong, Xiao-Qiong, Wei, Yao, Zhang, Jin-Qing, Song, Xing-Zhi, Chang, Yue-Hua, Zhang, Jiang-Xi, Xiao, Yan-Ling, Yang
Publikováno v:
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics. 14(8)
This study reviews a case of mitochondrial respiratory chain complex I deficiency due to the 10191TC mutation in mitochondrial ND3 gene. The previously healthy boy progressively presented with blepharoptosis, weakness, epilepsy and motor regression a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3e7a1b4135295d60d588fd936c3ff09
https://pubmed.ncbi.nlm.nih.gov/22898272
https://pubmed.ncbi.nlm.nih.gov/22898272
Publikováno v:
Zhonghua er ke za zhi = Chinese journal of pediatrics. 47(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::79c4f05f01cd82875089a1b7700c98ab
https://pubmed.ncbi.nlm.nih.gov/19573469
https://pubmed.ncbi.nlm.nih.gov/19573469
Autor:
Xiao-Qiong, Wei, Qing-Peng, Kong, Yao, Zhang, Yan-Ling, Yang, Xing-Zhi, Chang, Yu, Qi, Zhao-Yue, Qi, Jiang-Xi, Xiao, Jiong, Qin, Xi-Ru, Wu
Publikováno v:
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics. 11(5)
Leigh syndrome is a genetically heterogeneous disease caused by defects in enzymes involved in aerobic energy metabolism and the Krebs', cycle. Mitonchondrial complex I deficiency is a main cause of Leigh syndrome. In this study, a Chinese child with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::198e7223223324fa3e92540c4635ffe2
https://pubmed.ncbi.nlm.nih.gov/19470250
https://pubmed.ncbi.nlm.nih.gov/19470250