Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hong-Qiao Wei"'
Autor:
Huan Shi, Xin-Yu LI, Yao Chen, Xing Zhang, Yong Wu, Zi-Xuan Wang, Pan-Hong Chen, Hui-Qi Dai, Ji Feng, Sayantan Chatterjee, Zhong-Jie Li, Xiao-Wei Huang, Hong-Qiao Wei, Jigang Wang, Guo-Dong Lu, Jing Zhou
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2021)
Externí odkaz:
https://doaj.org/article/cc8665ca544d48428889c5153815915e
Autor:
Huan Shi, Xin-Yu Li, Yao Chen, Xing Zhang, Yong Wu, Zi-Xuan Wang, Pan-Hong Chen, Hui-Qi Dai, Ji Feng, Sayantan Chatterjee, Zhong-Jie Li, Xiao-Wei Huang, Hong-Qiao Wei, Jigang Wang, Guo-Dong Lu, Jing Zhou
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Acute myeloid leukemia (AML) is an aggressive haematological malignancy characterized by highly proliferative accumulation of immature and dysfunctional myeloid cells. Quercetin (Qu), one kind of flavonoid, exhibits anti-cancer property in multiple t
Externí odkaz:
https://doaj.org/article/5ad835bf88714b44abbbfb06642a6d7d
Autor:
Haiyang Wang, Juncai Pu, Xiaotong Zhang, Hong Qiao Wei, Lanxiang Liu, Wei Zhou, Xuechen Rao, Chanjuan Zhou, Tingjia Chai, Ying Yu, Peng Xie, Wenxia Li, Hanping Zhang, Benhua Zeng
Publikováno v:
Neuropsychiatric Disease and Treatment. 16:761-769
Introduction Recently, an increasing number of studies have focused on commensal microbiota. These microorganisms have been suggested to impact human health and disease. However, only a small amount of data exists to support the assessment of the in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c170ed6baa1276435b637a9c0dc3746
https://doi.org/10.2147/ndt.s236541
https://doi.org/10.2147/ndt.s236541
Autor:
Hong Qiao Wei, Wen Sheng Lu, Yi Yuan Huang, Jing Xian, Yufeng Deng, Yuan Heng Huang, Qin Huang
Publikováno v:
Biochemical and Biophysical Research Communications. 486:218-223
Caveolin-3 (CAV3) is a muscle specific protein that plays an important role in maintaining muscle health and glucose homeostasis in vivo. A novel autosomal dominant form of LGMD-1C in humans is due to a P104L mutation within the coding sequence of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20aff8ab82b0ee6ac3d04c50459f1e7c
https://doi.org/10.1016/j.bbrc.2017.02.072
https://doi.org/10.1016/j.bbrc.2017.02.072