(Q48114589)

8 February 2018

title

Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patients (English)

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8 February 2018

sporadic Creutzfeldt-Jakob disease

main subject

prion protein family

0 references

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9

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8 February 2018

author name string

Cardone F

1

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8 February 2018

Liu QG

2

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8 February 2018

Petraroli R

3

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8 February 2018

Ladogana A

4

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8 February 2018

D'Alessandro M

5

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8 February 2018

Arpino C

6

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8 February 2018

Di Bari M

7

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8 February 2018

Macchi G

8

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8 February 2018

publication date

1 August 1999

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8 February 2018

published in

Brain Research Bulletin

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8 February 2018

volume

49

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8 February 2018

issue

6

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8 February 2018

page(s)

429-433

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8 February 2018

Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation)

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1 reference

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7 January 2021

Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent

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7 January 2021

Scrapie associated PrP accumulation and its prevention: insights from cell culture

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7 January 2021

Truncated forms of the human prion protein in normal brain and in prion diseases.

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7 January 2021

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

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7 January 2021

New variant Creutzfeldt-Jakob disease in France

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7 January 2021

The nature of the scrapie agent: the virus theory

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7 January 2021

A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Asparagine-linked glycosylation of the scrapie and cellular prion proteins

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7 January 2021

A rapid and efficient method to enrich SAF-protein from scrapie brains of hamsters

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7 January 2021

Biochemical differences among scrapie-associated fibrils support the biological diversity of scrapie agents

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7 January 2021

Molecular analysis of bovine spongiform encephalopathy and scrapie strain variation

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7 January 2021

Separation and properties of cellular and scrapie prion proteins

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7 January 2021

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

1 reference

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7 January 2021

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

1 reference

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7 January 2021

Typing prion isoforms.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Creutzfeldt-Jakob disease after non-commercial dura mater graft

1 reference

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7 January 2021

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

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7 January 2021

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7 January 2021

Recent Italian FFI cases.

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7 January 2021

Polymorphisms of the Prion Protein gene in italian patients with Creutzfeldt-Jakob disease

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7 January 2021

Biochemical typing of scrapie strains

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Detection of proteinase-resistant protein (PrP) in small brain tissue samples from Creutzfeldt-Jakob disease patients.

1 reference

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7 January 2021

10.1016/S0361-9230(99)00077-5

Identifiers

DOI

1 reference

8 February 2018

1 reference

8 February 2018