Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia (Q33952856)

30 July 2017

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title

Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia (English)

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sporadic Creutzfeldt-Jakob disease

30 July 2017

0 references

1 reference

3

Gambetti P

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30 July 2017

Parchi P

1

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30 July 2017

Capellari S

series ordinal

2

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30 July 2017

publication date

1 July 2000

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Microscopy Research and Technique

30 July 2017

published in

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30 July 2017

volume

50

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30 July 2017

issue

1

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30 July 2017

page(s)

16-25

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Fatal familial insomnia: a new Austrian family

30 July 2017

cites work

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Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

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Identification of a protein that purifies with the scrapie prion

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21 January 2018

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21 January 2018

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Cerebral metabolism in fatal familial insomnia: relation to duration, neuropathology, and distribution of protease-resistant prion protein

21 January 2018

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Fatal familial insomnia and the widening spectrum of prion diseases

21 January 2018

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

21 January 2018

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Gerstmann-Sträussler-Scheinker disease and the Indiana kindred

21 January 2018

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

21 January 2018

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PrP genotype and agent effects in scrapie: change in allelic interaction with different isolates of agent in sheep, a natural host of scrapie

21 January 2018

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The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype

21 January 2018

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A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.

21 January 2018

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Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters

21 January 2018

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Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease.

21 January 2018

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Prion protein conformation in a patient with sporadic fatal insomnia

21 January 2018

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The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred

21 January 2018

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Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

21 January 2018

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

21 January 2018

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Fatal familial insomnia in a new Italian kindred

21 January 2018

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

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Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

21 January 2018

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Regional distribution of protease-resistant prion protein in fatal familial insomnia

21 January 2018

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Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

21 January 2018

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21 January 2018

Typing prion isoforms.

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Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease

21 January 2018

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A subtype of sporadic prion disease mimicking fatal familial insomnia.

21 January 2018

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Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred).

21 January 2018

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Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.

21 January 2018

1 reference

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A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.

21 January 2018

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Novel proteinaceous infectious particles cause scrapie

21 January 2018

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21 January 2018

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The nosology of Creutzfeldt-Jakob disease and conditions related to the accumulation of PrPCJD in the nervous system

21 January 2018

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Fatal familial insomnia: genetic, neuropathologic, and biochemical study of a patient from a new Italian kindred

21 January 2018

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The paraffin-embedded tissue blot detects PrP(Sc) early in the incubation time in prion diseases

21 January 2018

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Regional mapping of prion proteins in brain

21 January 2018

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Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

21 January 2018

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A new variant of Creutzfeldt-Jakob disease in the UK.

21 January 2018

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Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease.

21 January 2018

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Phenotypic variability in fatal familial insomnia (D178N-129M) genotype

21 January 2018

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Straining the prion hypothesis

21 January 2018

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Early pathologic and biochemical changes in Creutzfeldt-Jakob disease: study of brain biopsies

21 January 2018

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BSE and prions: uncertainties about the agent

21 January 2018

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Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein gene.

21 January 2018

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Molecular pathology of fatal familial insomnia

21 January 2018

1 reference

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Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

21 January 2018

1 reference

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10.1002/1097-0029(20000701)50:1<16::AID-JEMT4>3.0.CO;2-Y

21 January 2018

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DOI

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30 July 2017

1 reference