Prion protein conformation in a patient with sporadic fatal insomnia (Q33863178)

29 July 2017

Prion protein conformation in a patient with sporadic fatal insomnia (English)

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29 July 2017

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7

S B Prusiner

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29 July 2017

J A Mastrianni

1

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29 July 2017

R Nixon

2

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29 July 2017

R Layzer

3

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29 July 2017

G C Telling

4

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29 July 2017

D Han

5

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29 July 2017

S J DeArmond

6

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29 July 2017

language of work or name

English

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publication date

1 May 1999

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The New England Journal of Medicine

29 July 2017

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29 July 2017

340

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21

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29 July 2017

1630-1638

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A cellular gene encodes scrapie PrP 27-30 protein

29 July 2017

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Mutations and polymorphisms in the prion protein gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Separation and properties of cellular and scrapie prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Fatal familial insomnia: clinical and pathologic study of five new cases

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Prion disease (PrP-A117V) presenting with ataxia instead of dementia

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Clinical and genetic studies of fatal familial insomnia.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Regional mapping of prion proteins in brain

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Analysis of the prion protein gene in thalamic dementia

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Fatal familial insomnia: a seventh family.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Typing prion isoforms.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Pathologic conformations of prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

[18F]FDG PET in fatal familial insomnia: the functional effects of thalamic lesions.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Selective neuronal targeting in prion disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: first report from Japan

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Eight prion strains have PrP(Sc) molecules with different conformations

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJM199905273402104

Identifiers

DOI

10.1056/NEJM199905273402104

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29 July 2017

1 reference