Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Yaosheng, Xie"'
Publikováno v:
Turkish Journal of Hematology, Vol 41, Iss 1, Pp 66-68 (2024)
Externí odkaz:
https://doaj.org/article/d99413f87f104be592550e48d9242adf
Autor:
Xin Wei, Weifeng Yao, Huiping Li, Jingjing Qian, Yaosheng Xie, Zhuo Zhang, Hong Lu, Liang Shi, Xiangyang Lin
Publikováno v:
Gastroenterology Research and Practice, Vol 2019 (2019)
Purpose. Pancreatitis can lead to systemic inflammatory response, but the relationship between lymphocyte changes and patients with pancreatitis remains unclear. In this study, we evaluated the feedback function of changes in peripheral lymphocyte su
Externí odkaz:
https://doaj.org/article/4382d43a20cc426bb2d0df1fd371707d
Autor:
Manlin Zeng, Kaiqi Jia, Haixiao Xie, Yaosheng Xie, Lihong Yang, Yuan Chen, Yanhui Jin, Mingshan Wang
Publikováno v:
Indian Journal of Hematology and Blood Transfusion.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b65a7359cdbadedbeb80c3b24808f00
https://doi.org/10.1007/s12288-023-01666-x
https://doi.org/10.1007/s12288-023-01666-x
Autor:
Jiajin Zhu, Liyan Zhou, Yuxiang Gong, Yaosheng Xie, Xiaoqing Yi, Wenhe Wu, Yuping Deng, Mingshan Wang
Publikováno v:
Blood Coagulation & Fibrinolysis. 32:513-518
To explore the causative mutation for autosomal recessive inheritance factor V (FV) deficiency in a Chinese family. Relative coagulation indexes and the FV antigen were tested by the one-stage clotting method and ELISA, respectively. At the same time
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9f303d6d6e95e96cae8b0becc347cb4
https://doi.org/10.1097/mbc.0000000000001056
https://doi.org/10.1097/mbc.0000000000001056
Autor:
Xinyuan Chen, Lianfeng Wu, Weifeng Yao, Xin Wei, Hong Lu, Jingjing Qian, Jingjing Guan, Xiangyang Lin, Xiaoyuan Liu, Zhuo Zhang, Liling Chen, Yujie Jiang, Yaosheng Xie
Publikováno v:
The Indian Journal of Pediatrics. 88:113-119
To study the dynamic change of peripheral lymphocyte subsets and its clinical value in children with infectious mononucleosis (IM). Thirty-six pediatric patients with IM, 19 children with IM-like symptoms but lacking the serological pattern compatibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a2b60b11f4cf96f1795f54888a369f2
https://doi.org/10.1007/s12098-020-03319-7
https://doi.org/10.1007/s12098-020-03319-7
Autor:
Xiangyang Lin, Hong Lu, Liang Shi, Weifeng Yao, Xin Wei, Jingjing Qian, Huiping Li, Zhuo Zhang, Yaosheng Xie
Publikováno v:
Gastroenterology Research and Practice
Gastroenterology Research and Practice, Vol 2019 (2019)
Gastroenterology Research and Practice, Vol 2019 (2019)
Purpose. Pancreatitis can lead to systemic inflammatory response, but the relationship between lymphocyte changes and patients with pancreatitis remains unclear. In this study, we evaluated the feedback function of changes in peripheral lymphocyte su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6951b4e3047758733cfb39966e1a8328
https://doi.org/10.1155/2019/7568410
https://doi.org/10.1155/2019/7568410
Autor:
Shasha Luo, Mingshan Wang, Siqi Liu, Qiyu Xu, Yaosheng Xie, Lihong Yang, Xiaolong Li, Yanhui Jin
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 31(8)
The aim of this study was to elucidate the molecular defects in a Chinese family with dysfibrinogenemia. The fibrinogen activity was measured by the one-stage clotting method. The fibrinogen antigen was measured with immunoturbidimetry. The fibrinoge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b30e4614ca4c72c0683adf6928b1c4a
https://pubmed.ncbi.nlm.nih.gov/32833807
https://pubmed.ncbi.nlm.nih.gov/32833807
A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patient
Autor:
Siqi Liu, Yaosheng Xie, Haixiao Xie, Xiaolong Li, Shasha Luo, Lihong Yang, Yanhui Jin, Mingshan Wang
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 31(1)
To explore the phenotype and genotype of a Chinese family with hereditary factor V deficiency. Routine blood coagulation indexes were detected by one-stage clotting method, whereas factor V antigen was detected by ELISA. All exons and intron-exon bou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d31eaae6960328449866df11e18050b4
https://pubmed.ncbi.nlm.nih.gov/31789663
https://pubmed.ncbi.nlm.nih.gov/31789663
A novel heterozygous mutation (γ IIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.
Autor:
Shasha Luo, Qiyu Xu, Yaosheng Xie, Xiaolong Li, Yanhui Jin, Lihong Yang, Siqi Liu, Mingshan Wang
Publikováno v:
Blood Coagulation & Fibrinolysis; Dec2020, Vol. 31 Issue 8, p569-574, 6p
Autor:
Siqi Liu, Shasha Luo, Lihong Yang, Yanhui Jin, Haixiao Xie, Yaosheng Xie, Xiaolong Li, Mingshan Wang
Publikováno v:
Blood Coagulation & Fibrinolysis; Jan2020, Vol. 31 Issue 1, p71-76, 6p