Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Shaojuan Gu"'
Autor:
Shaojuan Gu, Huarong Yang, Yong Qi, Xiong Deng, Le Zhang, Yi Guo, Qing Huang, Jing Li, Xiaoliu Shi, Zhi Song, Hao Deng
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e66526 (2013)
Wilson's disease (WD) is an autosomal recessive inherited disorder caused by mutations in the ATPase Cu(2+) transporting beta polypeptide gene (ATP7B). The detailed metabolism of copper-induced pathology in WD is still unknown. Gene mutations as well
Externí odkaz:
https://doaj.org/article/85a4439d02cd4b3da98e2590870b2b17
Publikováno v:
Experimental Brain Research. 241:1585-1598
Publikováno v:
Digestion. 99:319-326
Background: Wilson’s disease (WD) is an autosomal recessive disease, which is characterized by an excessive copper accumulation in the liver and brain, leading to subsequent hepatic and/or neurological disorders. The causative gene for WD has been
Autor:
Bingqi Wang, Shaojuan Gu, Yi Guo, Yuan Wu, Hongbo Xu, Wen Zheng, Pengzhi Hu, Anjie Lu, Yan Yang, Hao Deng, Lamei Yuan
Publikováno v:
Journal of Cellular and Molecular Medicine
GNE myopathy is a rare, recessively inherited, early adult‐onset myopathy, characterized by distal and proximal muscle degeneration which often spares the quadriceps. It is caused by mutations in the UDP‐N‐acetylglucosamine 2‐epimerase/N‐ac
Publikováno v:
Digestion. 99(4)
Wilson's disease (WD) is an autosomal recessive disease, which is characterized by an excessive copper accumulation in the liver and brain, leading to subsequent hepatic and/or neurological disorders. The causative gene for WD has been identified as
Autor:
Jian Guan, Mingyang Liu, Xin Li, Liangrui Zhou, Xueyu Dong, Wei Dai, Yu Xia, Tao Yang, Shaojuan Guo, Xingqi Li, Yehua Han, Yufeng Luo
Publikováno v:
Journal of Bio-X Research, Vol 5, Iss 4, Pp 181-196 (2022)
Objective:. To explore the antitumor and potential off-target effects of systemically delivered cholesterol-conjugated let-7a mimics (Chol-let-7a) and control mimics (Chol-miRCtrl) on hepatocellular carcinoma in vivo. Methods:. The antitumor effects
Externí odkaz:
https://doaj.org/article/50261826130141d393c957e6a997f2b3
Publikováno v:
The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology. 25
Background/Aims: Copper is an essential trace element that serves as an important catalytic cofactor for cuproenzymes, carrying out major biological functions in growth and development. Although Wilson’s disease (WD) is unquestionably caused by mut
Autor:
Shaojuan Gu, Zhi Song, Hongbo Xu, Yongxiang Zhao, Lina Gong, Anding Zhu, Lamei Yuan, Hao Deng
Publikováno v:
Neuroscience Letters. 543:69-71
Growing evidences show that genetic abnormalities play an important role in the etiopathogenesis of Parkinson disease (PD). At least 18 genetic loci and 13 disease-related genes for parkinsonism have been identified. Recently, the p.Ala502Val and p.A
Publikováno v:
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. 38(11)
To determine the effect of Parkinson's disease-weight bearing exercise for better balance (PD-WEBB) exercise on balance impairment and falls in people with Parkinson's disease (PD).A single-blind, randomized controlled clinical trial was conducted. T
Publikováno v:
Journal of Clinical Neurology (Seoul, Korea)
BackgroundzzVogt-Koyanagi-Harada (VKH) disease is characterized by bilateral granulomatous uveitis with neurologic, auditory, and dermatologic manifestations. However, acute myelitis complicating VKH disease has rarely been reported. Case ReportzzA 5