Ming-der Perng
101 Kuang Fu 2 Road
Hsinchu, TNQ 30013, Taiwan
Hsinchu, TNQ 30013, Taiwan
Last Updated: 09/26/2026
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Found 23 publications
Synergistic Effects of Glial Fibrillary Acidic Protein Mutation and Overexpression in the Pathogenesis of Alexander Disease.
Journal: International journal of molecular sciences
Published: April 13, 2026
Applying Transformative Learning Theory to Compare Role Transition in Undergraduate-Entry and Post-Baccalaureate Medical Students.
Journal: Medical education
Published: December 30, 2025
Experimental Approaches for Biochemical Analysis of Glial Fibrillary Acidic Protein and Its Disease-associated Variants.
Journal: Journal of visualized experiments : JoVE
Published: December 15, 2025
Phenotypic and molecular characterization of a recurrent SPTAN1 mutation causing SPG91.
Journal: Molecular biology reports
Published: March 29, 2025
Deletions in Glial Fibrillary Acidic Protein Leading to Alterations in Intermediate Filament Assembly and Network Formation.
Journal: International journal of molecular sciences
Published: December 08, 2024
Development of Fusion-Based Assay as a Drug Screening Platform for Nipah Virus Utilizing Baculovirus Expression Vector System.
Journal: International journal of molecular sciences
Published: June 06, 2024
Glial fibrillary acidic protein is pathologically modified in Alexander disease.
Journal: The Journal of biological chemistry
Published: February 16, 2024
The Relationship between Obesity-Related Factors and Graves' Orbitopathy: A Pilot Study.
Journal: Medicina (Kaunas, Lithuania)
Published: November 04, 2022
Neuroprotective Effects of a Multi-Herbal Extract on Axonal and Synaptic Disruption in Vitro and Cognitive Impairment in Vivo.
Journal: Journal of Alzheimer's disease reports
Published: August 04, 2022
Effects of Alexander disease-associated mutations on the assembly and organization of GFAP intermediate filaments.
Journal: Molecular biology of the cell
Published: May 05, 2022
Antisense therapy in a rat model of Alexander disease reverses GFAP pathology, white matter deficits, and motor impairment.
Journal: Science translational medicine
Published: November 17, 2021
A novel in-frame GFAP p.E138_L148del mutation in Type II Alexander disease with atypical phenotypes.
A novel in-frame GFAP p.E138_L148del mutation in Type II Alexander disease with atypical phenotypes.
Journal: European journal of human genetics : EJHG
Published: July 30, 2021
Last Updated: 09/26/2026