Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Manlv Wei"'
Autor:
Zhengjing Lu, Lauriane Nikuze, Zhoulin Zhong, Fang Li, Fuyong Zhang, Kairong Liang, Manlv Wei, Hongying Wei
Publikováno v:
Platelets, Vol 31, Iss 3, Pp 355-359 (2020)
Glanzmann thrombasthenia (GT) is an inherited disorder of platelet aggregation resulting from quantitative and/or qualitative abnormalities of the glycoprotein IIb/IIIa complex. We analyzed the expression of GPIIb/IIIa and the gene sequencing in two
Externí odkaz:
https://doaj.org/article/c68a5802dfc1440c8cd406e4de89ffb0
Publikováno v:
Blood Coagulation & Fibrinolysis
Congenital factor VII deficiency (FVIID) is a rare F7 gene mutation causing bleeding disorder inherited in an autosomal recessive manner. In this study, we aimed to identify genetic defects and analyze their relationships with phenotype in three Chin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::676123c1db52f8d2adc9652112b4f3aa
https://doi.org/10.1097/mbc.0000000000001022
https://doi.org/10.1097/mbc.0000000000001022
Autor:
Jiali Jiang, Junli Zhou, Lauriane Nikuze, Hongying Wei, Manlv Wei, Sanjeev Singh, Yuping Li, Jinxia Jiang, Lifang Huang
Publikováno v:
Scandinavian Journal of Immunology. 95
Wiskott-Aldrich syndrome (WAS) also called the eczema-thrombocytopenia-immunodeficiency syndrome is a primary immunodeficiency disease with X-linked recessive inheritance caused by mutations in the WAS protein (WASp) gene and characterized by thrombo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf3754ad8c000630997b3545453880bc
https://doi.org/10.1111/sji.13115
https://doi.org/10.1111/sji.13115
Autor:
Yali Zhou, Guiping Liao, Jing Li, Manlv Wei, Linan Lu, Jingting Luo, Xiuren Jin, Shijie Yang, Lei Yang, Tianhong Zhou, Jie Huang, Yaopeng Chen, Xiaolin Yin
Publikováno v:
Mediterranean Journal of Hematology & Infectious Diseases; 2023, Vol. 15 Issue 1, p1-6, 6p
Autor:
Kairong Liang, Fang Li, Manlv Wei, Zhoulin Zhong, Fuyong Zhang, Zhengjing Lu, Lauriane Nikuze, Hongying Wei
Publikováno v:
Platelets. 31:355-359
Glanzmann thrombasthenia (GT) is an inherited disorder of platelet aggregation resulting from quantitative and/or qualitative abnormalities of the glycoprotein IIb/IIIa complex. We analyzed the expression of GPIIb/IIIa and the gene sequencing in two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65c3bcb05622237f58043f5cd6fd3eb9
https://doi.org/10.1080/09537104.2019.1615614
https://doi.org/10.1080/09537104.2019.1615614
Autor:
Zhengjing, Lu, Lauriane, Nikuze, Zhoulin, Zhong, Fang, Li, Fuyong, Zhang, Kairong, Liang, Manlv, Wei, Hongying, Wei
Publikováno v:
Platelets. 31(3)
Glanzmann thrombasthenia (GT) is an inherited disorder of platelet aggregation resulting from quantitative and/or qualitative abnormalities of the glycoprotein IIb/IIIa complex. We analyzed the expression of GPIIb/IIIa and the gene sequencing in two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c8c746dbd3bb5d509c562593608726ae
https://pubmed.ncbi.nlm.nih.gov/31088191
https://pubmed.ncbi.nlm.nih.gov/31088191
Publikováno v:
Blood Coagulation & Fibrinolysis; Jul2021, Vol. 32 Issue 5, p340-343, 4p