Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome.
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SUT-2 potentiates tau-induced neurotoxicity in Caenorhabditis elegansThe prion protein gene in humans revisited: lessons from a worldwide resequencing studyProbing the role of structural features of mouse PrP in yeast by expression as Sup35-PrP fusionsPrion Fibrillization Is Mediated by a Native Structural Element That Comprises Helices H2 and H3Increased interleukin-17 in the cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease: a case-control study of rapidly progressive dementiaOvine reference materials and assays for prion genetic testing.Neurodegeneration in humans caused by prionsGenetic studies in human prion diseases.Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.Experimental verification of a traceback phenomenon in prion infection.Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.Creutzfeldt-Jakob disease and the eye. I. Background and patient management.Familial conformational diseases and dementias.Pathogenic mutations in the hydrophobic core of the human prion protein can promote structural instability and misfolding.Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases.Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology?Prion diseases: from molecular biology to intervention strategies.Etiology and pathogenesis of prion diseases.Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders.Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform.Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob diseaseA Japanese family with a variant of Gerstmann-Sträussler-Scheinker disease.Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes.Deciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein.Systematic investigation of predicted effect of nonsynonymous SNPs in human prion protein gene: a molecular modeling and molecular dynamics study.The structure of human prions: from biology to structural models-considerations and pitfalls.Hereditary Human Prion Diseases: an Update.Pathogenic mutations in the glycosylphosphatidylinositol signal peptide of PrP modulate its topology in neuroblastoma cells.Evidence that the 127-164 region of prion proteins has two equi-energetic conformations with beta or alpha features.Gerstmann-Sträussler-Scheinker disease and the Indiana kindred.Prion protein transgenes and the neuropathology in prion diseases.Defining the limits of prion disease.Nucleation of amyloidogenesis in infectious and noninfectious amyloidoses of brain.The genetics and transgenetics of human prion disease.The nature of the scrapie agent: the virus theory.Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt-Jakob disease: a reliability and agreement studyPrion protein amyloidosis.Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prionsCo-occurrence of types 1 and 2 PrP(res) in sporadic Creutzfeldt-Jakob disease MM1.
P2860
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P2860
Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome.
description
1993 nî lūn-bûn
@nan
1993 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի մարտին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@ast
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@en
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@nl
type
label
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@ast
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@en
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@nl
prefLabel
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@ast
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@en
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@nl
P2093
P356
P1476
Novel missense variants of pri ...... Gerstmann-Sträussler syndrome.
@en
P2093
P304
P356
10.1006/BBRC.1993.1275
P407
P577
1993-03-01T00:00:00Z