Zobrazeno 21 - 30
of 75
pro vyhledávání: '"Haigang Ren"'
Autor:
Haigang, Ren, Guanghui, Wang
Publikováno v:
Advances in experimental medicine and biology. 1207
Lysosomal storage disorders (LSDs) are one of the most common human genetic metabolic diseases caused by gene mutations. Up to now, more than 70 LSDs have been identified and mainly divided into five categories. LSDs are mainly caused by defects in t
Publikováno v:
Advances in experimental medicine and biology. 1207
Polyglutamine (polyQ) disease is a type of fatal neurodegenerative disease caused by an expansion of CAG repeats in a specific gene, resulting in a protein with an abnormal polyQ fragment. The age of onset and the degree of pathological deterioration
Publikováno v:
Experimental and Therapeutic Medicine
Circadian rhythm serves an essential role in numerous physiological functions. Circadian oscillations are organized by circadian clock components at the molecular level. The precision of the circadian clock is controlled by transcriptional-translatio
Publikováno v:
Aging Cell
Accumulation of PINK1 on the outer mitochondrial membrane (OMM) is necessary for PINK‐mediated mitophagy. The proton ionophores, like carbonyl cyanide m‐chlorophenylhydrazone (CCCP) and carbonyl cyanide‐4‐(trifluoromethoxy)phenylhydrazone (FC
Publikováno v:
Autophagy: Biology and Diseases ISBN: 9789811542718
Polyglutamine (polyQ) disease is a type of fatal neurodegenerative disease caused by an expansion of CAG repeats in a specific gene, resulting in a protein with an abnormal polyQ fragment. The age of onset and the degree of pathological deterioration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6751b6215a33f90674854fd7879dafa
https://doi.org/10.1007/978-981-15-4272-5_9
https://doi.org/10.1007/978-981-15-4272-5_9
Autor:
Guanghui Wang, Haigang Ren
Publikováno v:
Autophagy: Biology and Diseases ISBN: 9789811542718
Lysosomal storage disorders (LSDs) are one of the most common human genetic metabolic diseases caused by gene mutations. Up to now, more than 70 LSDs have been identified and mainly divided into five categories. LSDs are mainly caused by defects in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a7de06afa312be25f5999d335c58df5
https://doi.org/10.1007/978-981-15-4272-5_5
https://doi.org/10.1007/978-981-15-4272-5_5
Publikováno v:
Neuroscience Bulletin. 33:685-694
Parkinson’s disease (PD) is the most common neurodegenerative movement disorder. Mutations in the DJ-1, including L166P, are responsible for recessive early-onset PD. Many lines of evidence have shown that L166P is not only a loss-of-function mutan
Autor:
An-Ping Feng, Lu Liu, Yonghong Zhang, Xiao Li, Wen-Zhu Hu, Lei Zhang, Hui Shen, Haigang Ren, Wei-Wen Kong, Yun Huang, Hong-Wen Deng, Chen Fang, Wen Zhao, Yu-Fang Pei, Qing Tian, Xin-Yi You
Publikováno v:
Obesity. 25:757-764
OBJECTIVE Body fat mass (BFM) is more homogeneous and accurate than body total mass in measuring obesity but has rarely been studied. Aiming to uncover the genetic basis of fat-induced obesity, a genome-wide association meta-analysis of BFM, after ad
Autor:
Guanghui Wang, Haigang Ren, Zhuangli Guo, Lengqiu Guo, Xuechu Zhen, Xiaoqing Luo, Shui Yang, Rui Liang
Publikováno v:
Neuroscience Letters. 635:44-50
Sleep, particularly rapid eye movement (REM) sleep, is implicated in the consolidation of emotional memories. In the present study, we investigated the protective effects of a phosphodiesterase 10A (PDE10A) inhibitor MP-10 on deficits in long-term fe
Autor:
Guanghui Wang, Haigang Ren, Shun Zhang, Hongyang Sun, Xingyun Xu, Chenchen Mu, Dan Wu, Zongbing Hao, Rui Wang
Publikováno v:
Neurosci Bull
GGGGCC repeat expansions in the C9ORF72 gene are the most common cause of amyotrophic lateral sclerosis and frontotemporal dementia (c9ALS/FTD). It has been reported that hexanucleotide repeat expansions in C9ORF72 produce five dipeptide repeat (DPR)