Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Misheng, Zhao"'
Autor:
Quanqiang Wang, Misheng Zhao, Tianyu Zhang, Bingxin Zhang, Ziwei Zheng, Zhili Lin, Shujuan Zhou, Dong Zheng, Zixing Chen, Sisi Zheng, Yu Zhang, Xuanru Lin, Rujiao Dong, Jingjing Chen, Honglan Qian, Xudong Hu, Yan Zhuang, Qianying Zhang, Songfu Jiang, Yongyong Ma
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Background: One particular type of cellular death that is known as ferroptosis is caused by the excessive lipid peroxidation. It is a regulated form of cell death that can affect the response of the tumor cells. Currently, it is not known if the pres
Externí odkaz:
https://doaj.org/article/44a57cfb69eb499abfc82f17c168aba3
Autor:
Xiaomin Yu, Qingyun Zheng, Yun He, Dandan Yu, Guolin Chang, Cheng Chen, Laixi Bi, Jia Lv, Misheng Zhao, Xiangyang Lin, Liqing Zhu
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
ObjectiveTo determine whether gut microbiota, fatty metabolism and cytokines were associated with immune thrombocytopenia (ITP).MethodsIn total, 29 preliminarily diagnosed ITP patients and 33 healthy volunteers were enrolled. Fecal bacterial were ana
Externí odkaz:
https://doaj.org/article/4ac6f33f41484fb9995a2cf81ac855d9
Autor:
Xiaomin Yu, Qingyun Zheng, Yun He, Dandan Yu, Guolin Chang, Cheng Chen, Laixi Bi, Jia Lv, Misheng Zhao, Xiangyang Lin, Liqing Zhu
Publikováno v:
Frontiers in medicine. 9
ObjectiveTo determine whether gut microbiota, fatty metabolism and cytokines were associated with immune thrombocytopenia (ITP).MethodsIn total, 29 preliminarily diagnosed ITP patients and 33 healthy volunteers were enrolled. Fecal bacterial were ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a0a981ccea86ec7e1f02eda1fda91e8
https://pubmed.ncbi.nlm.nih.gov/35665326
https://pubmed.ncbi.nlm.nih.gov/35665326
Autor:
Mingshan Wang, Han Wang, Liqing Zhu, Shenmeng Gao, Dandan Yu, Liangliang Pan, Bin Zhou, Zhefeng Lou, Misheng Zhao, Xiaoli Chen, Wenli Xia
Publikováno v:
Journal of Thrombosis and Thrombolysis. 46:211-218
Hypodysfibrinogenemia is the least frequently reported congenital fibrinogen disorder, characterized by both quantity and quality defects of fibrinogen. In this study, we investigated the molecular basis of hypodysfibrinogenemia in a Chinese family.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89ab843b6fbd83532975bf8c84f83bb2
https://doi.org/10.1007/s11239-018-1678-2
https://doi.org/10.1007/s11239-018-1678-2
Autor:
Liqing, Zhu, Misheng, Zhao, Xiaoli, Cheng, Dandan, Yu, Xiaolong, Li, Fei, Xu, Jinguo, Wang, Mingshan, Wang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 35(2)
To explore the genetic basis for a Chinese pedigree affected with congenital hypofibrinogenamia.Peripheral blood samples were collected from 9 members from the pedigree. Routine coagulation tests including activated partial thromboplastin time (APTT)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::25147838f6d1c950a1ed3b02e511f1f0
https://pubmed.ncbi.nlm.nih.gov/29652987
https://pubmed.ncbi.nlm.nih.gov/29652987
Autor:
Liqing, Zhu, Misheng, Zhao, Jie, Lin, Yingyu, Wang, Haixiao, Xie, Yaosheng, Xie, Hongxiang, Ding, Mingshan, Wang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 32(6)
To explore the molecular pathogenesis and clinical phenotypes in 10 probands with inherited fibrinogen (Fg) deficiency.The diagnosis of hereditary Fg deficiency was validated by prothrombin time (PT), thrombin time (TT), Fg activity (Fg:C) and Fg ant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f7a63e8b825796fdba7d26bebbd4b06
https://pubmed.ncbi.nlm.nih.gov/26663050
https://pubmed.ncbi.nlm.nih.gov/26663050
Autor:
Yingyu Wang, Yaosheng Xie, Hongxiang Ding, Misheng Zhao, Xiuping Hao, Haixiao Xie, Liqing Zhu, Mingshan Wang
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 25(8)
Congenital hypofibrinogenemia is a rare disorder caused by heterozygous mutations in the fibrinogen genes. The aim of this study was to elucidate the molecular defects in two unrelated families with hypofibrinogenemia. The proband from family A was a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f9e95bba5c47454b3fe0215256aef7a
https://pubmed.ncbi.nlm.nih.gov/24914742
https://pubmed.ncbi.nlm.nih.gov/24914742
Autor:
Misheng Zhao, Mingshan Wang, Zhefeng Lou, Xiaoli Chen, Dandan Yu, Xiaolong Li, Wenli Xia, Han Wang, Shenmeng Gao, Liqing Zhu
Publikováno v:
Hämostaseologie; 2018, Vol. 38 Issue 1, p43-48, 6p