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Ai-Wen Yang

Showing results (1-10 of 4) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 28, 2021
Elevated GFAP isoform expression promotes protein aggregation and compromises astrocyte functionNi-Hsuan Lin, Ai-Wen Yang, Chih-Hsuan Chang, et al.
Molecular Biology of the Cell|May 5, 2022
Effects of Alexander disease-associated mutations on the assembly and organization of GFAP intermediate filamentsAi-Wen Yang, Ni-Hsuan Lin, Ting-Hung Yeh, et al.
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.
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.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 28, 2021
Elevated GFAP isoform expression promotes protein aggregation and compromises astrocyte functionNi-Hsuan Lin, Ai-Wen Yang, Chih-Hsuan Chang, et al.
Molecular Biology of the Cell|May 5, 2022
Effects of Alexander disease-associated mutations on the assembly and organization of GFAP intermediate filamentsAi-Wen Yang, Ni-Hsuan Lin, Ting-Hung Yeh, et al.
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.
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.
Pageof 1