Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Wenxu, Chen"'
Publikováno v:
BMC Primary Care, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background In 2010, China launched a rural-oriented tuition-waived medical education (RTME) programme to train more general practitioners (GPs) to meet the needs of the rural health workforce. Motivating and maintaining GPs is an important c
Externí odkaz:
https://doaj.org/article/3c7fa6e1415043c4b5fd1b923a8a8b4c
Autor:
Yiyang Zhang, Lianghe Lu, Zhangping He, Zhishen Xu, Zhicheng Xiang, Run-Cong Nie, Wenping Lin, Wenxu Chen, Jie Zhou, Yixin Yin, Juanjuan Xie, Youcheng Zhang, Xueyi Zheng, Tianchen Zhu, Xiaoxia Cai, Peng Li, Xue Chao, Mu-Yan Cai
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundSerum C-reactive protein (CRP) is a biomarker of an acute inflammatory response and has been successfully used as a prognostic predictor for several malignancies. However, the clinicopathological significance of CRP levels in hepatocellular
Externí odkaz:
https://doaj.org/article/bd498e708e034c7495a6f6aabc175f07
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Metformin is one of the most widely prescribed hypoglycemic drugs and has the potential to treat many diseases. More and more evidence shows that metformin can regulate the function of macrophages in atherosclerosis, including reducing the differenti
Externí odkaz:
https://doaj.org/article/4cea14c4276647f99c5e1927ac0f44d0
Autor:
Mu-Yan Cai, Connor E. Dunn, Wenxu Chen, Bose S. Kochupurakkal, Huy Nguyen, Lisa A. Moreau, Geoffrey I. Shapiro, Kalindi Parmar, David Kozono, Alan D. D’Andrea
Publikováno v:
Cell Reports, Vol 30, Iss 7, Pp 2402-2415.e5 (2020)
Summary: Cells deficient in ataxia telangiectasia mutated (ATM) are hypersensitive to ionizing radiation and other anti-cancer agents that induce double-strand DNA breaks. ATM inhibitors may therefore sensitize cancer cells to these agents. Some canc
Externí odkaz:
https://doaj.org/article/6bb81879c78a40209c975837c5b87fc5
Autor:
Sheng Liu, Hui Gao, Lei Zhang, Xiaojun Feng, Aizong Shen, Lingli Li, Wenxu Chen, Yadi Geng, Suowen Xu, Yanan Wang
Publikováno v:
Aging (Albany NY)
Sirtuin 3 (SIRT3) is a type III histone deacetylase that inhibits cardiac hypertrophy. It is mainly localized in the mitochondria and is thus implicated in mitochondrial metabolism. Recent studies have shown that SIRT3 can also accumulate in the nucl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1b6eb8f2e9ed5e230bd97ba4826488a
https://doi.org/10.18632/aging.102862
https://doi.org/10.18632/aging.102862
Autor:
David Kozono, Bose Kochupurakkal, Lisa A. Moreau, Connor E. Dunn, Huy V. Nguyen, Wenxu Chen, Geoffrey I. Shapiro, Mu-Yan Cai, Alan D. D'Andrea, Kalindi Parmar
Publikováno v:
Cell Reports, Vol 30, Iss 7, Pp 2402-2415.e5 (2020)
Cell Rep
Cell Rep
Summary: Cells deficient in ataxia telangiectasia mutated (ATM) are hypersensitive to ionizing radiation and other anti-cancer agents that induce double-strand DNA breaks. ATM inhibitors may therefore sensitize cancer cells to these agents. Some canc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b24684492783aafc829c3d635e3f8651
http://www.sciencedirect.com/science/article/pii/S2211124720300772
http://www.sciencedirect.com/science/article/pii/S2211124720300772
Publikováno v:
The International Journal of Advanced Manufacturing Technology. 104:2827-2838
Effectively improving the precision and surface quality simultaneously is the goal of manufacturing technology. Due to the excellent surface quality of machined workpieces, electrochemical mechanical machining (ECMM) has been widely used as a polishi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69751a09f99e2336be96149d6f659a2e
https://doi.org/10.1007/s00170-019-04135-w
https://doi.org/10.1007/s00170-019-04135-w
Publikováno v:
The Tohoku Journal of Experimental Medicine. 242:173-181
Multiple osteochondromas (MO) is one of the most common benign bone tumors in humans with an autosomal dominant hereditary mode. MO is a genetic heterogeneity disease with variable number and size of osteochondromas, as well as changeable number and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e626590e83b3a7213c88c53e4b72e78
https://doi.org/10.1620/tjem.242.173
https://doi.org/10.1620/tjem.242.173
Publikováno v:
International Journal of Oncology
The molecular mechanism of hereditary multiple exostoses (HME) remains ambiguous and a limited number of studies have investigated the pathogenic mechanism of mutations in patients with HME. In the present study, a novel heterozygous splice mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f77d0191b11aae3f15afa908f09b707
https://doi.org/10.3892/ijo.2019.4688
https://doi.org/10.3892/ijo.2019.4688
Publikováno v:
The Tohoku journal of experimental medicine. 242(3)
Multiple osteochondromas (MO) is one of the most common benign bone tumors in humans with an autosomal dominant hereditary mode. MO is a genetic heterogeneity disease with variable number and size of osteochondromas, as well as changeable number and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f1b2575fb96f0e70e9939b1d83e1efec
https://pubmed.ncbi.nlm.nih.gov/28690282
https://pubmed.ncbi.nlm.nih.gov/28690282