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Behavioural Brain Research|March 23, 2026
Progressive gait and motor deficits in a rat model of Alexander diseaseRobert F Berman, Matthew R Matson, Angelica M Bachman, et al.
Cells|April 13, 2023
STAT3 Drives GFAP Accumulation and Astrocyte Pathology in a Mouse Model of Alexander DiseaseTracy L Hagemann, Sierra Coyne, Alder Levin, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 1, 2024
Plasma concentrations of glial fibrillary acidic protein, neurofilament light, and tau in Alexander diseaseNicholas J Ashton, Guglielmo Di Molfetta, Kübra Tan, et al.
Molecular and Cellular Neurosciences|October 24, 2006
The potassium channels Kv1.5 and Kv1.3 modulate distinct functions of microgliaUlrike Pannasch, Katrin Färber, Christiane Nolte, et al.
Human Mutation|April 11, 2012
Splice site, frameshift, and chimeric GFAP mutations in Alexander diseaseDaniel Flint, Rong Li, Lital S Webster, et al.
The American Journal of Pathology|December 7, 2007
Protection against human immunodeficiency virus type 1 Tat neurotoxicity by Ginkgo biloba extract EGb 761 involving glial fibrillary acidic proteinWei Zou, Byung Oh Kim, Betty Y Zhou, et al.
Plos One|January 18, 2024
Large-scale gene expression changes in APP/PSEN1 and GFAP mutation models exhibit high congruence with Alzheimer's diseaseStephen C Gammie, Albee Messing, Mason A Hill, et al.
BMC Biology|October 11, 2007
Sleep in Kcna2 knockout miceChristopher L Douglas, Vladyslav Vyazovskiy, Teresa Southard, et al.
Molecular Biology of the Cell|November 1, 2016
The role of gigaxonin in the degradation of the glial-specific intermediate filament protein GFAPNi-Hsuan Lin, Yu-Shan Huang, Puneet Opal, et al.
Molecular and Cellular Neurosciences|June 23, 2006
The effects of a dominant connexin32 mutant in myelinating Schwann cellsLinda Jo Bone Jeng, Rita J Balice-Gordon, Albee Messing, et al.
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