Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Zi-Xuan Ding"'
Autor:
Qian Wang, Hai-ping Dai, Dan-dan Liu, Jun-dan Xie, Hong Yao, Zi-xuan Ding, Ting-ting Tao, Su-ning Chen, Ri Zhang
Publikováno v:
Leukemia Research Reports, Vol 14, Iss , Pp 100229- (2020)
Myelodysplastic/myeloproliferative neoplasm, unclassifiable (MDS/MPN-U) is a rare but heterogeneous subtype of MDS/MPN, with no specific genetic alterations and standard treatments. ASXL1, SRSF2, TET2, JAK2 and NRAS are commonly mutated in MDS/MPN-U.
Externí odkaz:
https://doaj.org/article/d7abbc2e37684b93a53f5b9ad05c2e74
Autor:
Song-Bai Liu, Hao-Jie Dong, Xie-Bing Bao, Qiao-Cheng Qiu, Hong-Zhi Li, Hong-Jie Shen, Zi-Xuan Ding, Chao Wang, Xiao-Ling Chu, Jing-Qiu Yu, Tao Tao, Zheng Li, Xiao-Wen Tang, Su-Ning Chen, De-Pei Wu, Ling Li, Sheng-Li Xue
Publikováno v:
Haematologica, Vol 104, Iss 1 (2019)
Externí odkaz:
https://doaj.org/article/065f8d7b68f048f6806242096bf62788
Autor:
Hui-Peng Song, Ming-Yue Zhao, Zhi-Li Xu, Jia-Nuo Zhang, Wen-Yu Wang, Zi-Xuan Ding, Ying Wang, Li-Bin Zhan, Xi Chen, Ruo-Nan Li, Yue-Hua Chen
Publikováno v:
Natural Product Communications; Aug2024, Vol. 19 Issue 8, p1-13, 13p
Autor:
Wen-Juan, Wang, Jun-Dan, Xie, Hong, Yao, Zi-Xuan, Ding, Ai-Rui, Jiang, Liang, Ma, Hong-Jie, Shen, Su-Ning, Chen
Publikováno v:
Clinical Genetics. 103:67-78
Hereditary spherocytosis (HS) is the most common type of hereditary erythrocyte membrane disease and has varied phenotypic features and genetic patterns. We herein performed a retrospective study of 94 patients with HS and aimed to investigate the ge
Publikováno v:
Materials Science Forum. 1032:147-151
The milling experiments were conducted carried out which Ti-6Al-4V alloys with different amount of hydrogen permeating were processed, in order to explore various problem in the machining process of hydrogenated titanium alloy. The main cutting force
Publikováno v:
2021 IEEE 9th International Conference on Information, Communication and Networks (ICICN).
Publikováno v:
Advanced Optical Materials. 10:2270087
Publikováno v:
Optics Communications. 520:128458
Autor:
Ming Xie, Ming-Yue Zhao, Rui Hu, Hui-Yang Sun, Xin-Tong Han, Yue-Hua Chen, Zi-Xuan Ding, Xin Zhang, Hua Guo, Hong-He Xiao, Hui Zhang, Wei-Hong Yuan, Ting-Guo Kang, Hui-Peng Song, Xin-Yi Xu, An Chang
Publikováno v:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 1181
Lead compound is an important concept for modern drug discovery. In this study, a new concept of lead chemome and an efficient strategy to discover lead chemome were proposed. Compared with the concept of lead compound, lead chemome can provide not o
Publikováno v:
Hemoglobin. 45(1)
β-Thalassemia (β-thal) is an inherited blood disorder characterized by reduced or absent synthesis of the β chains of hemoglobin (Hb). Although more than 900 β-globin gene mutations around the world have been identified, here we report a novel mu