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Movement Disorders : Official Journal of the Movement Disorder Society|May 7, 2020
Recessively-Inherited Adult-Onset Alexander Disease Caused by a Homozygous Mutation in the GFAP GeneMu-Hui Fu, Yung-Yee Chang, Ni-Hsuan Lin, et al.Oxidative Medicine and Cellular Longevity|February 13, 2020
Chlorella sorokiniana Extract Prevents Cisplatin-Induced Myelotoxicity In Vitro and In VivoShyh-Horng Lin, Ming-Han Li, Kai-An Chuang, et al.Journal of Alzheimer'S Disease Reports|February 13, 2023
Neuroprotective Effects of a Multi-Herbal Extract on Axonal and Synaptic Disruption in Vitro and Cognitive Impairment in VivoNi-Hsuan Lin, Angela Goh, Shyh-Horng Lin, et al.European Journal of Human Genetics : EJHG|March 5, 2022
A novel in-frame GFAP p.E138_L148del mutation in Type II Alexander disease with atypical phenotypesYou-Ri Kang, So-Hyun Lee, Ni-Hsuan Lin, et al.Science Translational Medicine|November 17, 2021
Antisense therapy in a rat model of Alexander disease reverses GFAP pathology, white matter deficits, and motor impairmentTracy L Hagemann, Berit Powers, Ni-Hsuan Lin, et al.BMC Neurology|September 9, 2017
Aggregation-prone GFAP mutation in Alexander disease validated using a zebrafish modelSo-Hyun Lee, Tai-Seung Nam, Kun-Hee Kim, et al.Elife|November 5, 2019
Site-specific phosphorylation and caspase cleavage of GFAP are new markers of Alexander disease severityRachel A Battaglia, Adriana S Beltran, Samed Delic, et al.Pageof 4