Glial fibrillary acidic protein filaments can tolerate the incorporation of assembly-compromised GFAP-delta, but with consequences for filament organization and alphaB-crystallin association.
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Alexander diseaseDysfunctions of neuronal and glial intermediate filaments in diseaseThe potential of pathological protein fragmentation in blood-based biomarker development for dementia - with emphasis on Alzheimer's diseaseDevelopmental splicing deregulation in leukodystrophies related to EIF2B mutationsThe specificity of the interaction between αB-crystallin and desmin filaments and its impact on filament aggregation and cell viability.GFAP isoforms control intermediate filament network dynamics, cell morphology, and focal adhesions.Alternative mRNA splicing from the glial fibrillary acidic protein (GFAP) gene generates isoforms with distinct subcellular mRNA localization patterns in astrocytes.Specific human astrocyte subtype revealed by affinity purified GFAP antibody; unpurified serum cross-reacts with neurofilament-L in AlzheimerIntermediate filaments take the heat as stress proteins.Characterization of a panel of monoclonal antibodies recognizing specific epitopes on GFAP.Defective glial maturation in vanishing white matter disease.Alexander disease causing mutations in the C-terminal domain of GFAP are deleterious both to assembly and network formation with the potential to both activate caspase 3 and decrease cell viability.Computational characterization of 3' splice variants in the GFAP isoform family.GFAP isoforms in adult mouse brain with a focus on neurogenic astrocytes and reactive astrogliosis in mouse models of Alzheimer disease.GFAPδ expression in glia of the developmental and adolescent mouse brain.Identification of a novel nonsense mutation in the rod domain of GFAP that is associated with Alexander disease.Withaferin A effectively targets soluble vimentin in the glaucoma filtration surgical model of fibrosis.Neurological diseases as primary gliopathies: a reassessment of neurocentrismLoss of the androgen receptor cofactor p44/WDR77 induces astrogliosis.Evolution of the vertebrate beaded filament protein, Bfsp2; comparing the in vitro assembly properties of a "tailed" zebrafish Bfsp2 to its "tailless" human orthologueIdentification and cytoprotective function of a novel nestin isoform, Nes-S, in dorsal root ganglia neurons.Foveolar Müller Cells of the Pied Flycatcher: Morphology and Distribution of Intermediate Filaments Regarding Cell TransparencySubventricular zone neural progenitors from rapid brain autopsies of elderly subjects with and without neurodegenerative disease.Cytoarchitecture of the lateral ganglionic eminence and rostral extension of the lateral ventricle in the human fetal brainIsolation of neural progenitor cells from the human adult subventricular zone based on expression of the cell surface marker CD271Emerging role of autophagy in pediatric neurodegenerative and neurometabolic diseases.Glial fibrillary acidic protein exhibits altered turnover kinetics in a mouse model of Alexander disease.Intermediate filament transcription in astrocytes is repressed by proteasome inhibition.Quantum mechanism of light transmission by the intermediate filaments in some specialized optically transparent cells.Alexander Disease Mutations Produce Cells with Coexpression of Glial Fibrillary Acidic Protein and NG2 in Neurosphere Cultures and Inhibit Differentiation into Mature OligodendrocytesGFAPδ/GFAPα ratio directs astrocytoma gene expression towards a more malignant profile.Antisense suppression of glial fibrillary acidic protein as a treatment for Alexander disease.Type III Intermediate Filaments Desmin, Glial Fibrillary Acidic Protein (GFAP), Vimentin, and Peripherin.Down-regulated GFAPα: a major player in heavy metal induced astrocyte damage.A histopathological diagnostic marker for human spinal astrocytoma: expression of glial fibrillary acidic protein-δ.
P2860
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P2860
Glial fibrillary acidic protein filaments can tolerate the incorporation of assembly-compromised GFAP-delta, but with consequences for filament organization and alphaB-crystallin association.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Glial fibrillary acidic protei ...... alphaB-crystallin association.
@en
type
label
Glial fibrillary acidic protei ...... alphaB-crystallin association.
@en
prefLabel
Glial fibrillary acidic protei ...... alphaB-crystallin association.
@en
P2093
P2860
P356
P1476
Glial fibrillary acidic protei ...... alphaB-crystallin association.
@en
P2093
Elly M Hol
Jacqueline Sluijs
Jinte Middeldorp
Ming-Der Perng
Roy A Quinlan
Shu-Fang Wen
Terry Gibbon
P2860
P304
P356
10.1091/MBC.E08-03-0284
P577
2008-08-06T00:00:00Z