(Q33952856)

30 July 2017

1 reference

title

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

1 reference

sporadic Creutzfeldt-Jakob disease

30 July 2017

0 references

1 reference

3

Gambetti P

1 reference

30 July 2017

Parchi P

1

1 reference

30 July 2017

Capellari S

series ordinal

2

1 reference

30 July 2017

publication date

1 July 2000

1 reference

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

1 reference

30 July 2017

page(s)

16-25

1 reference

Fatal familial insomnia: a new Austrian family

30 July 2017

cites work

1 reference

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

21 January 2018

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Identification of a protein that purifies with the scrapie prion.

21 January 2018

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Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy.

21 January 2018

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The disease characteristics of different strains of scrapie in Sinc congenic mouse lines: implications for the nature of the agent and host control of pathogenesis

21 January 2018

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Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent

21 January 2018

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Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases).

21 January 2018

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Mice devoid of PrP are resistant to scrapie

21 January 2018

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Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.

21 January 2018

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Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

21 January 2018

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Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

21 January 2018

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https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Scrapie in mice. Agent-strain differences in the distribution and intensity of grey matter vacuolation.

21 January 2018

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Unconventional Viruses and the Origin and Disappearance of Kuru

21 January 2018

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https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Fatal familial insomnia and the widening spectrum of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Gerstmann-Sträussler-Scheinker disease and the Indiana kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Prion protein conformation in a patient with sporadic fatal insomnia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Fatal familial insomnia in a new Italian kindred.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

21 January 2018

Typing prion isoforms.

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

A subtype of sporadic prion disease mimicking fatal familial insomnia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Novel proteinaceous infectious particles cause scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Regional mapping of prion proteins in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Straining the prion hypothesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

BSE and prions: uncertainties about the agent

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

Molecular pathology of fatal familial insomnia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0029%2820000701%2950%3A1%3C16%3A%3AAID-JEMT4%3E3.0.CO%3B2-Y

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

21 January 2018

Identifiers

DOI

1 reference

30 July 2017

1 reference