Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Huanying Ren"'
Autor:
Huanying Ren, Jingyi Feng, Minglin Hong, Zhuang Liu, Daniel Muteb Muyey, Yaofang Zhang, Zhifang Xu, Yanhong Tan, Fanggang Ren, Jianmei Chang, Xiuhua Chen, Hongwei Wang
Publikováno v:
Molecular and Cellular Probes, Vol 76, Iss , Pp 101966- (2024)
Platelet-derived growth factor receptor β (PDGFRβ) plays a crucial role in murine haematopoiesis. Baicalein (BAI), a naturally occurring flavonoid, can alleviate disease damage through anti-oxidative, anti-apoptotic, and anti-inflammatory mechanism
Externí odkaz:
https://doaj.org/article/0ce9c1d6d4114930a644bb9f9815d1a6
Autor:
Huanying Ren, Minglin Hong, Jingyi Feng, Zhuanghui Hao, Xian Chen, Fengting Liang, Wei Wei, Xuelan Liang, Hongwei Wang, Xiuhua Chen
Publikováno v:
Biomolecules & Biomedicine (2024)
In this study, we analyzed GATA2 mutations (GATA2mut) and co-mutations in 166 Chinese patients with cytogenetically normal acute myeloid leukemia. This was done through targeted next-generation sequencing of 34 genes associated with myeloid leukemia.
Externí odkaz:
https://doaj.org/article/ef0004cc267e4c25974894977b27b49a
Autor:
Yefang Kang, Xiuhua Chen, Fang Fang, Hongwei Wang, Huanying Ren, Daniel Muteb Muyey, Jing Xu, Yanhong Tan, Zhifang Xu
Publikováno v:
International Journal of Laboratory Hematology. 43:1491-1500
Introduction GATA binding protein 2 (GATA2) gene, involved in progression of hematologic malignancies and various solid tumors, is a susceptibility gene for inherited acute myeloid leukemia (AML). However, the influence of its single-nucleotide polym
Autor:
Chuchu Tian, Fang Fang, Wenzheng Guo, Yefang Kang, Daniel Muteb Muyey, Jing Xu, Lingli Zhang, Huanying Ren, Xiuhua Chen, Hongwei Wang, Yanhong Tan, Zhifang Xu, Jiaxuan Wang
Publikováno v:
International Journal of Laboratory Hematology. 43:1424-1431
INTRODUCTION CEBPA mutation is a common mutation in normal karyotype AML. CEBPAdm AML has been recognized as a separate entity, but there is still controversy to the prognosis of CEBPAsm patients. METHODS A total of 151 newly diagnosed cytogeneticall