Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Chen Liang"'
Autor:
Pierpaolo Ala, Miroslav P. Milev, Shinsuke Maruyama, Adnan Y. Manzur, D. Chambers, Nadine McCrea, Pinki Munot, Michael Sacher, Rahul Phadke, Wen-Chen Liang, Phil Cox, Lucy Feng, Helen Roper, Francesco Muntoni, Caroline Sewry, Ichizo Nishino, Irina Zaharieva, Tamas Marton, N Ragge, Silvia Torelli
Publikováno v:
BASE-Bielefeld Academic Search Engine
Background: TRAPPC11, a subunit of the transport protein particle (TRAPP) complex is important for complex integrity and anterograde membrane transport from the endoplasmic reticulum (ER) to the ER-Golgi intermediate compartment. Several individuals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14ad39104e58b2b52877ee6b43f6b38a
https://doi.org/10.21203/rs.3.rs-31937/v1
https://doi.org/10.21203/rs.3.rs-31937/v1
Autor:
Ichizo Nishino, Yuh-Jyh Jong, Po-Ching Chou, Yukiko K. Hayashi, Chia-Cheng Hung, Yi-Ning Su, Wen-Chen Liang, Tsu-Min Kan, Wan-Zi Chen
Publikováno v:
Journal of the Neurological Sciences. 362:304-308
Limb-girdle muscular dystrophy type 2D (LGMD2D), an autosomal-recessive inherited LGMD, is caused by the mutations in SGCA. SGCA encodes alpha-sarcoglycan (SG) that forms a heterotetramer with other SGs in the sarcolemma, and comprises part of the dy
Publikováno v:
Neuromuscular Disorders. 22:331-338
This study aimed to evaluate muscle involvement pattern and correlate the lesions on muscle imaging with clinical features and D4Z4 fragment size in 24 patients with facioscapulohumeral muscular dystrophy (FSHD). The grading of the muscle image detec
Autor:
Y. C. Chen, S. N. Yang, Yuh-Jyh Jong, Jan-Gowth Chang, Y. C. Wu, S. M. Wu, Yi-Hsin Yang, Tai-Heng Chen, Yining Huang, H. H. Mai, Haiyan Wang, Wen-Chen Liang
Publikováno v:
Neurology. 75:2190-2197
Objective: The purpose of this study was to evaluate the safety and efficacy of hydroxyurea (HU) in spinal muscular atrophy (SMA) in a randomized, double-blind, placebo-controlled trial. Methods: Twenty-eight patients with type 2 SMA and 29 patients
Autor:
Hui-Yi Wang, Jan-Gowth Chang, Yun-Huei Ju, Yung-Fu Chang, Yuh-Jyh Jong, Chung-Yee Yuo, Wen-Chen Liang, Yi Ching Chen, Shyh-Shin Chiou
Publikováno v:
Journal of the Neurological Sciences. 268:87-94
Background: Spinal muscular atrophy (SMA) is a degenerative motor neuron disease caused by homozygous mutations of the survival motor neuron 1 (SMN1) gene. Effective treatment for SMA is unavailable at present. The aim of this study was to investigat