(Q40842489)

24 September 2017

1 reference

title

Mutations and polymorphisms in the prion protein gene (English)

1 reference

24 September 2017

0 references

Palmer MS

1

1 reference

PubMed ID

8364585

24 September 2017

Collinge J

series ordinal

2

1 reference

24 September 2017

1 January 1993

1 reference

24 September 2017

1 reference

24 September 2017

2

1 reference

24 September 2017

168-173

1 reference

24 September 2017

3

1 reference

Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene

24 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

A prion protein variant in a family with the telencephalic form of Gerstmann-Straussler-Scheinker syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

Aminoacid polymorphism in human prion protein and age at death in inherited prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

The molecular genetics of familial Creutzfeldt-Jakob disease in France

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

1 reference

7 January 2021

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Diversity of oligosaccharide structures linked to asparagines of the scrapie prion protein

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Identical mutation in unrelated patients with Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Deletion in prion protein gene in a Moroccan family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Human prion protein cDNA: molecular cloning, chromosomal mapping, and biological implications

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

A dementing illness associated with a novel insertion in the prion protein gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Deletions in the prion protein gene are not associated with CJD.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Molecular biology of prion diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Localization of a human gene homologous to the PrP gene on the p arm of chromosome 20 and detection of PrP-related antigens in normal human brain

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Scrapie prion protein contains a phosphatidylinositol glycolipid

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

1 reference

7 January 2021

A PvuII RFLP detected in the human prion protein (PrP) gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020303

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380020303

1 reference

24 September 2017

1 reference

PubMed ID

8364585