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Journal of Cell Science|April 21, 2005
Alexander-disease mutation of GFAP causes filament disorganization and decreased solubility of GFAPVictoria C Hsiao, Rujin Tian, Heather Long, et al.
Molecular Biology of the Cell|August 8, 2008
Glial fibrillary acidic protein filaments can tolerate the incorporation of assembly-compromised GFAP-delta, but with consequences for filament organization and alphaB-crystallin associationMing-Der Perng, Shu-Fang Wen, Terry Gibbon, et al.
International Journal of Molecular Sciences|August 29, 2024
Development of Fusion-Based Assay as a Drug Screening Platform for Nipah Virus Utilizing Baculovirus Expression Vector SystemIndah Permata Sari, Christopher Llynard D Ortiz, Lee-Wei Yang, et al.
American Journal of Human Genetics|July 11, 2006
The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27Ming Der Perng, Mu Su, Shu Fang Wen, et al.
Medicina (Kaunas, Lithuania)|December 23, 2022
The Relationship between Obesity-Related Factors and Graves' Orbitopathy: A Pilot StudyChing Lu, Chao-Lun Lai, Chih-Man Yang, et al.
Medical Education|July 19, 2026
Applying Transformative Learning Theory to Compare Role Transition in Undergraduate-Entry and Post-Baccalaureate Medical StudentsSin-Yee Patty Kwong, Hui-Ting Wang, Shiuan-Ruey Yu, et al.
Plos One|January 1, 2015
Granulocyte colony-stimulating factor reduces fibrosis in a mouse model of chronic pancreatitisWey-Ran Lin, Tzung-Hai Yen, Siew-Na Lim, et al.
Oxidative Medicine and Cellular Longevity|November 29, 2017
Rhinacanthin C Alleviates Amyloid-β Fibrils' Toxicity on Neurons and Attenuates Neuroinflammation Triggered by LPS, Amyloid-β, and Interferon-γ in Glial CellsKai-An Chuang, Ming-Han Li, Ni-Hsuan Lin, et al.
The FEBS Journal|January 27, 2005
R120G alphaB-crystallin promotes the unfolding of reduced alpha-lactalbumin and is inherently unstableTeresa M Treweek, Agata Rekas, Robyn A Lindner, et al.
European Journal of Human Genetics : EJHG|April 24, 2014
Identification of a novel nonsense mutation in the rod domain of GFAP that is associated with Alexander diseaseTai-Seung Nam, Jin Hee Kim, Chi-Hsuan Chang, et al.
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