about
Astrocytes promote myelination in response to electrical impulsesAlexander diseaseThe multifaceted role of astrocytes in regulating myelinationPrecursor cell biology and the development of astrocyte transplantation therapies: lessons from spinal cord injuryAlexander disease in a dog: case presentation of electrodiagnostic, magnetic resonance imaging and histopathologic findings with review of literatureThe origin of Rosenthal fibers and their contributions to astrocyte pathology in Alexander diseaseAlexander's disease: clinical, pathologic, and genetic features.Megalencephalic leukoencephalopathy with subcortical cysts.Protein expression profile in the differentiation of rat bone marrow stromal cells into Schwann cell-like cells.CDK5-induced p-PPARγ(Ser 112) downregulates GFAP via PPREs in developing rat brain: effect of metal mixture and troglitazone in astrocytes.Autophagy induced by Alexander disease-mutant GFAP accumulation is regulated by p38/MAPK and mTOR signaling pathways.GFAP mutations, age at onset, and clinical subtypes in Alexander diseaseIntermediate filaments and vesicular membrane traffic: the odd couple's first dance?ngs (notochord granular surface) gene encodes a novel type of intermediate filament family protein essential for notochord maintenance in zebrafish.Giant axonal neuropathy-associated gigaxonin mutations impair intermediate filament protein degradation.Splice site, frameshift, and chimeric GFAP mutations in Alexander diseaseDon't fence me in: harnessing the beneficial roles of astrocytes for spinal cord repair.Composition of Rosenthal Fibers, the Protein Aggregate Hallmark of Alexander DiseaseUnraveling pathology in juvenile Alexander disease: serial quantitative MR imaging and spectroscopy of white matter.Astrocyte phenotypes and their relationship to myelination.ASTROCYTES: EMERGING STARS IN LEUKODYSTROPHY PATHOGENESIS.Neuroglial alterations in the zebrafish brain exposed to cadmium chloride.Explaining intermediate filament accumulation in giant axonal neuropathyA case of infantile Alexander disease accompanied by infantile spasms diagnosed by DNA analysis.Unusual variants of Alexander's disease.Gene expression analysis in mice with elevated glial fibrillary acidic protein and Rosenthal fibers reveals a stress response followed by glial activation and neuronal dysfunction.Infantile-onset Alexander disease: a genetically proven case with mild clinical course in a 6-year-old Indian boy.A Rosenthal fiber encephalomyelopathy resembling Alexander's disease in 3 sheep.
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
GFAP mutations in Alexander disease.
@ast
GFAP mutations in Alexander disease.
@en
GFAP mutations in Alexander disease.
@nl
type
label
GFAP mutations in Alexander disease.
@ast
GFAP mutations in Alexander disease.
@en
GFAP mutations in Alexander disease.
@nl
prefLabel
GFAP mutations in Alexander disease.
@ast
GFAP mutations in Alexander disease.
@en
GFAP mutations in Alexander disease.
@nl
P2093
P1476
GFAP mutations in Alexander disease.
@en
P2093
Albee Messing
James E Goldman
Michael Brenner
P304
P356
10.1016/S0736-5748(02)00019-9
P577
2002-06-01T00:00:00Z