Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Hong-Chao Jiang"'
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-6 (2023)
Abstract Background Retinitis pigmentosa is a group of rare hereditary retinal dystrophy diseases that lead to difficulty seeing at night, progressive loss of peripheral field vision (tunnel vision), and eventual loss of central vision. However, a ge
Externí odkaz:
https://doaj.org/article/5af79e3792b5402cb83c91f6d79d0fb5
Autor:
Jing Ma, Ken Lin, Hong‐chao Jiang, Yanli Yang, Yu Zhang, Guilian Yang, Hao Sun, Cheng Ming, Xianyun Bi, Tiesong Zhang, Biao Ruan
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Abstract Background To analyze the clinical phenotypes and genetic variants of a Chinese family with Waardenburg syndrome (WS) and to explore the possible molecular pathogenesis of WS. Methods The clinical data from a patient and his family were coll
Externí odkaz:
https://doaj.org/article/93f6baa2a37d446fae611f367ca155e0
Publikováno v:
Cellular Physiology and Biochemistry, Vol 32, Iss 5, Pp 1247-1254 (2013)
Background/Aims: Copper is an essential trace element for normal cellular function and contributes to critical physiological or pathological processes. The aim of the study was to investigate the effects of copper on vascular tone of rat mesenteric a
Externí odkaz:
https://doaj.org/article/0ba5e3328e414ae7b16db8de25691ef2
Publikováno v:
World Journal of Clinical Cases. 10:5463-5469
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a349e62955e0adc9bc57bc3bc3303e9
https://doi.org/10.12998/wjcc.v10.i16.5463
https://doi.org/10.12998/wjcc.v10.i16.5463
Autor:
Qiangming Sun, Zhao Canchun, Weiwei Nan, Qiu Lijuan, Huang Tilong, Jiaolian Tang, Zhang Zhen, Shulan Shi, Ming Yu, Kui Liyue, Li Xue, Bailing Zhou, Hong-Chao Jiang
Publikováno v:
Oncology Reports
Semaphorin 4D (Sema4D) is highly expressed in a variety of tumors and is associated with high invasion, poor prognosis and poor therapeutic response. However, the expression and role of Sema4D in leukemia remains unclear. The present study investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca642db2c5f4845c04158fa9834b66a0
https://doi.org/10.3892/or.2021.7952
https://doi.org/10.3892/or.2021.7952
Autor:
Zhen Zhang, Yi-shuang Xiao, Hong-chao Jiang, Ru Sheng, Li Tang, XIAO-Hong Yang, Huai-yu Gu, Wen-Ji He, Jing Ma
Background : Familial exudative vitreoretinopathy (FEVR) is a rare inherited retinal disorder characterized by the failure of peripheral retinal vascularization at birth. FEVR can cause further pathological changes, such as neovascularization, exudat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be5700434210d34ec7bdca3c0c3dd907
https://doi.org/10.21203/rs.2.20941/v1
https://doi.org/10.21203/rs.2.20941/v1
Autor:
Yanli Yang, Hong-Chao Jiang, Xianyun Bi, Tiesong Zhang, Jing Ma, Ken Lin, Cheng Ming, Gui-Lian Yang, Yu Zhang, Biao Ruan, Hao Sun
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Background To analyze the clinical phenotypes and genetic variants of a Chinese family with Waardenburg syndrome (WS) and to explore the possible molecular pathogenesis of WS. Methods The clinical data from a patient and his family were collected. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9829befb14d216c27f9a8028551798c7
http://europepmc.org/articles/PMC6625151
http://europepmc.org/articles/PMC6625151
Autor:
Zhen Zhang, Hao Sun, Mei‑Hua Sun, Biao Ruan, Yang Xiao, Ying‑Qin Gao, Cheng Ming, Tie‑Song Zhang, Hong‑Chao Jiang, Li‑Ping Zhao, Zheng‑Cai Li, Jing Ma, Guo‑Li Wu
Publikováno v:
Molecular medicine reports. 19(3)
Waardenburg syndrome type 2 (WS2) is a rare genetic disorder, characterized by bright blue eyes, moderate to profound hearing loss and pigmental abnormalities of the hair and skin. Between 10 and 20 mutations in the SRY‑box 10 (SOX10) gene were pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d244600eb7d858471f56c76dc136074
https://pubmed.ncbi.nlm.nih.gov/30628718
https://pubmed.ncbi.nlm.nih.gov/30628718
Autor:
Shan-Liang Li, Hong-Chao Jiang, Qi Li, Ming-Yu Liu, Ying Zhang, Yu-Hong Li, Chao-Wei Hu, De-Li Dong, Wei Han
Publikováno v:
Pflügers Archiv - European Journal of Physiology. 466:2049-2057
Cardiac T-type Ca(2+) channels are reexpressed in atrial and ventricular myocytes under various pathological conditions such as post-myocardial infarction, hypertrophy, and heart failure, but relatively little is known about the mechanisms. Our previ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0a3c0f7c3fc073a622ae0364a6ccc83
https://doi.org/10.1007/s00424-014-1459-5
https://doi.org/10.1007/s00424-014-1459-5
Autor:
Jing Ma, Ken Lin, Hong-chao Jiang, Yanli Yang, Yu Zhang, Guilian Yang, Hao Sun, Cheng Ming, Xianyun Bi, Tiesong Zhang, Biao Ruan
Publikováno v:
Molecular Genetics & Genomic Medicine. 7:e00853
The cover image based on Original Article A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I by Jing Ma et al., DOI: 10.1002/mgg3.798. [Image: see text]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53af527ad48250f4be31bed02afcb57a
https://doi.org/10.1002/mgg3.853
https://doi.org/10.1002/mgg3.853