Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Zhengjing, Lu"'
Publikováno v:
Genes and Diseases, Vol 11, Iss 6, Pp 101118- (2024)
Externí odkaz:
https://doaj.org/article/a0d3cbfdbc7f4b988e2092f065d7d4d2
Autor:
Zhengjing Lu, Xiaolin Wang, Jun Feng, Wenjia Chai, Wei Wang, Qixin Wang, Shen Yang, Wei Yang, Yan Su, Wenjun Mou, Yun Peng, Huanmin Wang, Jingang Gui
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Pediatric hepatoblastoma (HB) is the most common primary liver malignancy in infants and children. With great diversity and plasticity, tumor-infiltrating neutrophils were one of the most determining factors for poor prognosis in many malignant tumor
Externí odkaz:
https://doaj.org/article/8bc29f9b080242078fe347246ac9becc
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
Autor:
Shusen Chen MD, Yu Shi MD, Zhengjing Lu MD, Mingwei Wang MD, Longfei Cong MD, Baixia Yang MD, Xudong Chen MD, Jing Cai MD, Xi Yang MD, PhD
Publikováno v:
Cancer Control, Vol 28 (2021)
Objective: Esophageal carcinosarcoma (ECS) is a rare malignant tumor that accounts for only 0.5%-2.8% of all esophageal malignancies. As most current studies are case reports, the relationship between clinical features and prognosis remains controver
Externí odkaz:
https://doaj.org/article/e9358c5bd9894ff68da590b09bec7292
Autor:
Zhengjing Lu, Xiaolin Wang, Jun Feng, Wenjia Chai, Wei Wang, Qixin Wang, Shen Yang, Wei Yang, Yan Su, Wenjun Mou, Yun Peng, Huanmin Wang, Jingang Gui
Publikováno v:
Frontiers in Immunology; 2024, p1-17, 17p
Autor:
Wenjia Chai, Xiaolin Wang, Zhengjing Lu, Shihan Zhang, Wei Wang, Hui Wang, Chenghao Chen, Wei Yang, Haiyan Cheng, Huanmin Wang, Jun Feng, Shen Yang, Qiliang Li, Wenqi Song, Fang Jin, Hui Zhang, Yan Su, Jingang Gui
Publikováno v:
Clinical Immunology. 250:109322
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
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
Autor:
Baixia Yang, Xi Yang, Zhengjing Lu, Shusen Chen, Yu Shi, Xudong Chen, Longfei Cong, Mingwei Wang, Jing Cai
Publikováno v:
Cancer Control, Vol 28 (2021)
Cancer Control : Journal of the Moffitt Cancer Center
Cancer Control : Journal of the Moffitt Cancer Center
Objective: Esophageal carcinosarcoma (ECS) is a rare malignant tumor that accounts for only 0.5%-2.8% of all esophageal malignancies. As most current studies are case reports, the relationship between clinical features and prognosis remains controver
Publikováno v:
Thrombosis research. 198