Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Shangjin Gong"'
Autor:
Weilong Zou, Zhanjie Fang, Yu Feng, Shangjin Gong, Ziqiang Li, Meng Li, Yong Sun, Xiuyan Ruan, Xiangdong Fang, Hongzhu Qu, Haiyang Li
Publikováno v:
BMC Cancer, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Background Patients with primary multifocal hepatocellular carcinoma (HCC) have a poor prognosis and often experience a high rate of treatment failure. Multifocal HCC is mainly caused by intrahepatic metastasis (IM), and though portal vein t
Externí odkaz:
https://doaj.org/article/2ab88a413e504fe3ad1f9be2e847df9e
Autor:
Yuanyuan Han, Ling Huang, Man Zhou, Xiaoyu Tan, Shangjin Gong, Zhaojun Zhang, Tingting Jin, Xiangdong Fang, Yankai Jia, S. W. Huang
Publikováno v:
Hematology, Vol 27, Iss 1, Pp 263-273 (2022)
Background The reactivation of fetal γ-globin expression is an effective strategy for ameliorating the clinical symptoms of β-hemoglobinopathies. However, the mechanism of globin switching, especially the roles of long non-coding RNAs (lncRNAs) in
Externí odkaz:
https://doaj.org/article/2bf29f90c73f4007a9cc2b8277ef27d9
Publikováno v:
Genomics, Proteomics & Bioinformatics. 19:358-376
There is an imbalance between the supply and demand of functional red blood cells (RBCs) in clinical applications. This imbalance can be addressed by regenerating RBCs using several in vitro methods. Induced pluripotent stem cells (iPSCs) can handle
Autor:
Xiaoyu Tan, Ling Huang, Li Hu, Man Zhou, Wenqiu Zhang, Juan Liu, Yankai Jia, Yuanyuan Han, Shangjin Gong, Zhaojun Zhang, Tingting Jin, Shengwen Huang, Xiangdong Fang
Background: β-thalassemia and sickle cell disease (SCD) are chronic hemolytic anemias caused by mutation or deletion of the β-globin gene. Reactivation of fetal γ-globin gene (HBG) expression can ameliorate the clinical course of β-hemoglobinopat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79d537021d40f5086cff587308064cfe
https://doi.org/10.21203/rs.3.rs-45443/v2
https://doi.org/10.21203/rs.3.rs-45443/v2
Autor:
Yuanyuan Han, Ling Huang, Man Zhou, Shangjin Gong, Zhaojun Zhang, Tingting Jin, Juan Liu, Li Hu, Wenqiu Zhang, Xiangdong Fang, Yankai Jia, Shengwen Huang
Background: β-thalassemia and sickle cell disease (SCD) are chronic hemolytic anemias caused by mutation or deletion of the β-globin gene. Reactivation of fetal γ-globin gene (HBG) expression can ameliorate the clinical course of β-hemoglobinopat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5b086b74cd78864c1183095c216011d
https://doi.org/10.21203/rs.3.rs-45443/v1
https://doi.org/10.21203/rs.3.rs-45443/v1
There is an imbalance between the supply and demand of functional red blood cells (RBCs) in clinical applications. This imbalance can be addressed by regenerating RBCs using several in vitro methods. Induced pluripotent stem cells (iPSCs) can handle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::656617fd8c1e64564923a75cbee31bcd