Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
about
Propagation of tau pathology: hypotheses, discoveries, and yet unresolved questions from experimental and human brain studies.Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases.Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.Beta-amyloid oligomers and cellular prion protein in Alzheimer's disease.Tau, prions and Aβ: the triad of neurodegeneration.Immunomodulation for prion and prion-related diseases.Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.Translation of the prion protein mRNA is robust in astrocytes but does not amplify during reactive astrocytosis in the mouse brainMeningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G)Activation of the unfolded protein response and granulovacuolar degeneration are not common features of human prion pathology.Selective vulnerability to neurodegenerative disease: the curious case of Prion Protein.Frontotemporal dementia: implications for understanding Alzheimer disease.Prion disease: a tale of folds and strains.Molecular morphology and toxicity of cytoplasmic prion protein aggregates in neuronal and non-neuronal cells.The prionoses and other conformational disorders.Report about four novel mutations in the prion protein gene.Influence of mutations associated with familial prion-related encephalopathies on biological activity of prion protein peptides.Tau pathology in Creutzfeldt-Jakob disease revisited.iPS Cell Cultures from a Gerstmann-Sträussler-Scheinker Patient with the Y218N PRNP Mutation Recapitulate tau Pathology.Pathological phenotype in familial neurodegenerative disease: implications for families and therapeutic constructsDetection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [F]Flortaucipir PETAn autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid
P2860
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P2860
Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
@en
type
label
Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
@en
prefLabel
Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
@en
P2093
P2860
P356
P1476
Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
@en
P2093
B Frangione
F Tagliavini
G Giaccone
M R Farlow
S R Dlouhy
P2860
P2888
P356
10.1007/BF02778006
P577
1994-02-01T00:00:00Z
P6179
1046716753