Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.
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β-hairpin-mediated formation of structurally distinct multimers of neurotoxic prion peptidesPrionsChanging a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers.The prion protein modulates A-type K+ currents mediated by Kv4.2 complexes through dipeptidyl aminopeptidase-like protein 6Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.Dissecting trait heterogeneity: a comparison of three clustering methods applied to genotypic dataGerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases.Neurodegeneration in humans caused by prionsGerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.Genetic studies in human prion diseases.Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoformConservation of infectivity in purified fibrillary extracts of scrapie-infected hamster brain after sequential enzymatic digestion or polyacrylamide gel electrophoresisCreutzfeldt-Jakob disease and the eye. I. Background and patient management.Biological network inferences for a protection mechanism against familial Creutzfeldt-Jakob disease with E200K pathogenic mutation.Familial conformational diseases and dementias.Prions.Comparative analysis of the Shadoo gene between cattle and buffalo reveals significant differences.Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene.Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP genePrion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphismPresymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases.Inherited prion diseases.Etiology and pathogenesis of prion diseases.Deletion in prion protein gene in a Moroccan familyAmyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders.Host Determinants of Prion Strain Diversity Independent of Prion Protein Genotype.Molecular biology and pathology of scrapie and the prion diseases of humans.Molecular biology and transgenetics of prion diseases.Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.Heterologous PrP molecules interfere with accumulation of protease-resistant PrP in scrapie-infected murine neuroblastoma cellsSulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells.Three hamster species with different scrapie incubation times and neuropathological features encode distinct prion proteins.A Japanese family with a variant of Gerstmann-Sträussler-Scheinker disease.Neurotoxic species in prion disease: a role for PrP isoforms?The search for scrapie agent nucleic acidRecombinant scrapie-like prion protein of 106 amino acids is soluble.Heterozygous inhibition in prion infection: the stone fence modelPrion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
P2860
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P2860
Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.
description
1989 nî lūn-bûn
@nan
1989 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@ast
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@en
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@nl
type
label
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@ast
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@en
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@nl
prefLabel
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@ast
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@en
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@nl
P2093
P1476
Pro----leu change at position ...... Gerstmann-Sträussler syndrome.
@en
P2093
P304
P356
10.1016/0006-291X(89)92317-6
P407
P577
1989-09-01T00:00:00Z