Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Hong-qiong Yang"'
Autor:
Hong-qiong Yang, Aihua Gong, Suraj K. George, Xiaomeng Jiang, Min Xu, Hongmei Huang, Zhijun Jiao, Youli Zhang
Publikováno v:
Cancer Letters. 369:124-133
Drug resistance in gastric cancer largely results from the gastric cancer stem cells (GCSCs), which could be targeted to improve the efficacy of chemotherapy. In this study, we identified a subpopulation of GCSCs enriched in holoclones that expressed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62c65a98e4908084a76be4939ca300e5
https://doi.org/10.1016/j.canlet.2015.08.005
https://doi.org/10.1016/j.canlet.2015.08.005
Publikováno v:
Zhonghua zhong liu za zhi [Chinese journal of oncology]. 35(3)
To dynamically investigate the morphology of human gastric cancer SGC-7901 cell clones, and then compare the tumorigenic ability of different clones in order to identify the tumor stem cell clones.Clones derived from gastric cancer SGC-7901 cells wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::68969bdba8def1d2cbb8ece18780bb8b
https://pubmed.ncbi.nlm.nih.gov/23879994
https://pubmed.ncbi.nlm.nih.gov/23879994
Autor:
Hiroshi Hiai, Jun A. Takahashi, Haruhiko Kikuchi, Nozomu Murai, Masakazu Hatanaka, Hong-Qiong Yang, Tetsuya Ueba, Manabu Fukumoto
Publikováno v:
Journal of Neurosurgery. 85:1072-1077
✓ Basic fibroblast growth factor (bFGF) is mitogenic to neuroectoderm- and mesoderm-derived cells and is a potent angiogenic factor. Abundant amounts of this factor and its receptor are detected in human glioma tissues and cells, and bFGF in glioma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa2b60edbb55ab936181196e087f94f7
https://doi.org/10.3171/jns.1996.85.6.1072
https://doi.org/10.3171/jns.1996.85.6.1072
Publikováno v:
Journal of Biological Chemistry. 269:24430-24436
Calpastatin is a widely distributed endogenous inhibitor protein specifically acting on calpain (Ca(2+)-dependent proteinase) and is known to interact with the calmodulin-like domain (CaMLD) of the proteinase in a Ca(2+)-dependent fashion. The calpas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deac826231e889dd6ffd3e52690ff584
https://doi.org/10.1016/s0021-9258(19)51102-4
https://doi.org/10.1016/s0021-9258(19)51102-4
Publikováno v:
Journal of Biological Chemistry. 269:18977-18984
Calpain requires Ca2+ both for proteolysis of its substrates and for interaction with its endogenous inhibitor, calpastatin. Although calmodulin-like domains (CaMLDs) of large and small subunits of calpain have been suggested to be the sites for Ca(2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a3061bfc21d92774b11c1152bda1262
https://doi.org/10.1016/s0021-9258(17)32262-7
https://doi.org/10.1016/s0021-9258(17)32262-7
Publikováno v:
The Journal of Biochemistry. 113:591-599
Calpain requires Ca2+ for both proteolysis of its substrates and interaction with its endogenous inhibitor, calpastatin. The mechanism of inhibition of calpain by calpastatin has remained unsolved, although Nishimura and Goll [J. Biol. Chem. 266, 118
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa543a4f6f8905e3dc29bc28d072ca0b
https://doi.org/10.1093/oxfordjournals.jbchem.a124088
https://doi.org/10.1093/oxfordjournals.jbchem.a124088
Publikováno v:
Journal of Biological Chemistry. 267:8437-8442
Calpastatin, a specific inhibitor of calpain, consists of a unique N-terminal domain (domain L) and four repetitive calpain-inhibition domains (domains 1-4). Calpastatin cDNA of human was reported to have two deletions in domains L and 1, as compared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1955277158cc469137e58ecb6392da7d
https://doi.org/10.1016/s0021-9258(18)42463-5
https://doi.org/10.1016/s0021-9258(18)42463-5
Autor:
Cun Guo, Zhenghong Li, Fan Ye, Fa-qiang Zhang, Zhen Wang, Chun-tong Ying, Jian-lun Yang, Hong-qiong Yang, Guang-jun Liu
Publikováno v:
SPIE Proceedings.
Fast neutron radiography offers means to inspect thick hydrogenous materials because of high penetration depth of fast neutrons. Further more, quasi monoenergetic neutrons is relatively easy to obtain by neutron generators and it is helpful for densi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::147061fa0b89edb164b782ecf750f95f
https://doi.org/10.1117/12.725151
https://doi.org/10.1117/12.725151
Autor:
Maggie C. Louie, Hongwu Chen, Hong Qiong Yang, Wei Xu, June X. Zou, Hsing Jien Kung, Ai Hong Ma
The androgen receptor, like other nuclear receptors, activates target genes by binding to hormone-responsive enhancers. Here we demonstrate that androgen induces robust recruitment of androgen receptor, members of the p160 coactivator family, and CRE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a12e7f3dfaf4af08c784ee0d048f8ee
https://europepmc.org/articles/PMC151322/
https://europepmc.org/articles/PMC151322/
Autor:
JianGen Gong, Massimo Levrero, William G. Kaelin, Jean Y. J. Wang, Hong-Qiong Yang, Gerry Melino, Antonio Costanzo
Cancer chemotherapeutic agents such as cisplatin exert their cytotoxic effect by inducing DNA damage and activating programmed cell death (apoptosis). The tumour-suppressor protein p53 is an important activator of apoptosis. Although p53-deficient ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08c4ece25b496aa3a4992ff03ce85100
http://hdl.handle.net/11573/438336
http://hdl.handle.net/11573/438336