Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Hai-ting Chen"'
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 109, Iss , Pp 1211-1220 (2019)
The study was designed to determine the safety and pharmacokinetics of intraocular crocetin and examine whether crocetin inhibits the development of proliferative vitreoretinopathy (PVR) in a rabbit model. In the toxicity study, the right eyes of rab
Externí odkaz:
https://doaj.org/article/b07b8320c9364ea3a7f18365c3430b24
Autor:
Xiao-Huan Zou, Dong-Ping Chen, Bing-Cong Hong, Yao-Bin Liu, Lu-Lu Lai, Xin-Xin Guo, Chang-Yun Liu, Ji-Dong Peng, Jing-Hui Lai, Hui-Zhen Su, Qing-Yang Yao, Hua-Song Lin, Yu-Ying Zhao, Xiao-Pei Lu, Hong-Xia Fu, Yao Xiangping, Dan-Qin Huang, Wan-Jin Chen, Pan Lin, Chong Wang, Yu-Chun Deng, Xiao-Qun Zhu, Hai-Liang Lin, Yan-Fang Niu, Xue-Jiao Chen, Yong-Kun Li, Ning Wang, Hai-Ting Chen, Gen-Bin Huang
Publikováno v:
Human Mutation. 40:392-403
Primary familial brain calcification (PFBC) is a rare neurodegenerative disorder with four causative genes (SLC20A2, PDGFRB, PDGFB, and XPR1) that have been identified. Here, we aim to describe the mutational spectrum of four causative genes in a ser
Publikováno v:
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
BACKGROUND This study aimed to explore the effects of plumbagin (PLB) on epithelial-to-mesenchymal transition in retinal pigment epithelial (RPE) cells and in proliferative vitreoretinopathy (PVR) rabbit models. MATERIAL AND METHODS Rabbit RPE cells
Publikováno v:
European Journal of Pharmacology. 815:391-398
Retinal pigment epithelial (RPE) cells, the major cell type in the fibrotic membrane of proliferative vitreoretinopathy, display enhanced proliferative and migratory capacities and epithelial-mesenchymal transition (EMT). In this study, we investigat
Autor:
Jing-Hui Lai, Yao-Bin Liu, Xin-Xin Guo, Chong Wang, Hai-Ting Chen, Hui-Zhen Su, Miao Zhao, Yao Xiangping, Wan-Jin Chen, En-Lin Dong, Ning Wang
Publikováno v:
Cell and Tissue Research. 370:267-273
Primary familial brain calcification (PFBC) is a neuropsychiatric disorder characterized by bilateral cerebral calcification with diverse neurologic or psychiatric symptoms. Recently, XPR1 variation has accounted for PFBC as another new causative gen
Autor:
Jing-Hui Lai, Qi-Jie Zhang, Wan-Jin Chen, Yao Xiangping, Hui-Zhen Su, Hai-Ting Chen, Ning Wang, En-Lin Dong, Chong Wang, Xin-Xin Guo
Publikováno v:
Journal of Human Genetics. 62:697-701
Four causative genes, including solute carrier family 20 member 2 (SLC20A2), platelet-derived growth factor receptor b (PDGFRB), platelet-derived growth factor b (PDGFB)and xenotropic and polytropic retrovirus receptor 1 (XPR1), have been identified
Autor:
Hui-Zhen Su, Ying-Qian Lu, Yao Xiangping, Yao-Bin Liu, Xin-Xin Guo, Ning Wang, Hai-Ting Chen, Wan-Jin Chen, Miao Zhao, Chong Wang, Jing-Hui Lai
Publikováno v:
Gene. 597:17-22
Background Until recently, primary familial brain calcification (PFBC) has been determined by four genes, SLC20A2 , PDGFRB , PDGFB and XPR1 . No studies have been carried out to analyze the gene mutation of PDGFB in Chinese population. Objective To s
Publikováno v:
IOP Conference Series: Earth and Environmental Science. 510:062005
Regional urban connection is mainly reflected in the connection between transportation and economy. Using accessibility and improved gravity model, this paper studies the traffic and economic relations and spatial pattern analysis among districts and
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 109, Iss, Pp 1211-1220 (2019)
The study was designed to determine the safety and pharmacokinetics of intraocular crocetin and examine whether crocetin inhibits the development of proliferative vitreoretinopathy (PVR) in a rabbit model. In the toxicity study, the right eyes of rab
Publikováno v:
BMC Complementary and Alternative Medicine
BMC Complementary and Alternative Medicine, Vol 18, Iss 1, Pp 1-10 (2018)
BMC Complementary and Alternative Medicine, Vol 18, Iss 1, Pp 1-10 (2018)
Background This study aimed to explore the effects of plumbagin (PLB) on ARPE-19 cells and underlying mechanism. Methods Cultured ARPE-19 cells were treated with various concentrations (0, 5, 15, and 25 μM) of PLB for 24 h or with 15 μM PLB for 12,