Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Hsing‐Jung Lai"'
Autor:
Hsin‐Hsiung Chen, Chia‐Yang Lin, Ya‐Ju Han, Yun‐Hsin Huang, Yi‐Hsiang Liu, Wan‐En Hsu, Li‐Kai Tsai, Hsing‐Jung Lai, Yeou‐Ping Tsao, Hsiang‐Po Huang, Show‐Li Chen
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 15, Iss 6, Pp 2559-2573 (2024)
ABSTRACT Background Nuclear receptor interaction protein (NRIP) is versatile and engages with various proteins to execute its diverse biological function. NRIP deficiency was reported to cause small myofibre size in adult muscle regeneration, indicat
Externí odkaz:
https://doaj.org/article/50fa6166eeac479199cfac2eb4e0c6f6
Autor:
Hsin-Hsiung Chen, Hsin-Tung Yeo, Yun-Hsin Huang, Li-Kai Tsai, Hsing-Jung Lai, Yeou-Ping Tsao, Show-Li Chen
Publikováno v:
Skeletal Muscle, Vol 14, Iss 1, Pp 1-18 (2024)
Abstract Background Amyotrophic lateral sclerosis (ALS) is characterized by progressive motor neuron (MN) degeneration, leading to neuromuscular junction (NMJ) dismantling and severe muscle atrophy. The nuclear receptor interaction protein (NRIP) fun
Externí odkaz:
https://doaj.org/article/e80c578ac91c4c2aa3db510bbe57fac1
Autor:
Lan-Hsin Nancy Lee, Chen-Syuan Huang, Ren-Wei Wang, Hsing-Jung Lai, Chih-Ching Chung, Ya-Chin Yang, Chung-Chin Kuo
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-18 (2022)
Abstract The success of deep brain stimulation (DBS) therapy indicates that Parkinson’s disease is a brain rhythm disorder. However, the manifestations of the erroneous rhythms corrected by DBS remain to be established. We found that augmentation o
Externí odkaz:
https://doaj.org/article/cec89dbfc8e649e9b18d9c133d238015
Autor:
Lan-Hsin Nancy Lee, Chen-Syuan Huang, Hsiang-Hao Chuang, Hsing-Jung Lai, Cheng-Kai Yang, Ya-Chin Yang, Chung-Chin Kuo
Publikováno v:
Journal of Biomedical Science, Vol 28, Iss 1, Pp 1-14 (2021)
Abstract Parkinson’s disease (PD), or paralysis agitans, is a common neurodegenerative disease characterized by dopaminergic deprivation in the basal ganglia because of neuronal loss in the substantia nigra pars compacta. Clinically, PD apparently
Externí odkaz:
https://doaj.org/article/a2c28b5807c342768294b0a2fb44bca7
Autor:
Hsing-Jung Lai, Kuan-Chih Huang, Yun-Chieh Liang, Kuo-Liong Chien, Ming-Jen Lee, Sung-Tsang Hsieh, Chi-Chao Chao, Chih-Chao Yang
Publikováno v:
Journal of the Formosan Medical Association, Vol 119, Iss 3, Pp 693-700 (2020)
Background: The cardiac manifestations of late-onset hereditary transthyretin amyloidosis with p.A97S variant have not been extensively studied, and the prognostic factors remain unclear. Methods: The clinical profile, echocardiography, and ECG of pa
Externí odkaz:
https://doaj.org/article/59b0c59c701348f6a0f4b5c37887327b
Publikováno v:
Biomedicines, Vol 9, Iss 1, p 51 (2021)
Paramyotonia congenita (PMC) is a rare hereditary skeletal muscle disorder. The major symptom, muscle stiffness, is frequently induced by cold exposure and repetitive exercise. Mutations in human SCN4A gene, which encodes the α-subunit of Nav1.4 cha
Externí odkaz:
https://doaj.org/article/2dd6696533bb474e892f7ddcf687778e
Publikováno v:
PLoS Biology, Vol 14, Iss 9, p e1002561 (2016)
The Nav1.7 channel critically contributes to the excitability of sensory neurons, and gain-of-function mutations of this channel have been shown to cause inherited erythromelalgia (IEM) with neuropathic pain. In this study, we report a case of a seve
Externí odkaz:
https://doaj.org/article/f9eda9a3366840c9a06f462d7e2b23f3
Autor:
Hsing-Jung Lai, Ya-Wen Chiang, Chih-Chao Yang, Sung-Tsang Hsieh, Chi-Chao Chao, Ming-Jen Lee, Chung-Chin Kuo
Publikováno v:
PLoS ONE, Vol 10, Iss 11, p e0141935 (2015)
Familial amyloid polyneuropathy (FAP) caused by a mutation in transthyretin (TTR) gene is an autosomal dominant inherited disorder. The aim of this study is to explore the pathophysiological mechanism of FAP. We prospectively recruited 12 pauci-sympt
Externí odkaz:
https://doaj.org/article/a5109d18384c4e50919d72875e8e1ec0
Autor:
Hsing-Jung Lai, 賴幸蓉
101
The objective of this study is to explore whether the corporate governance is different between family firms and non-family firms and further examine the endogenous relations among firm performance, risk and liabilities during the period 200
The objective of this study is to explore whether the corporate governance is different between family firms and non-family firms and further examine the endogenous relations among firm performance, risk and liabilities during the period 200
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/x7fhgx
Autor:
Hsin-Hsiung Chen, Ya-Ju Han, Tung-Chien Wu, Won-Shin Yen, Tzu-Yun Lai, Po-Han Wei, Li-Kai Tsai, Hsing-Jung Lai, Yeou-Ping Tsao, Show-Li Chen
To investigate the role of nuclear receptor interaction protein (NRIP) in myoblast fusion, both the primary myoblasts from muscle-specific NRIP-knockout mice and NRIP-null C2C12 cells (KO19 cells) exhibited a significant deficit in the fusion index d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acbebab8e56811ddc728e08ac28c2a44
https://doi.org/10.1101/2022.06.14.496213
https://doi.org/10.1101/2022.06.14.496213