Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease (Q36174780)

12 August 2017

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

1 reference

12 August 2017

0 references

1 reference

10

J J Hauw

0 references

Shu Chen

2

object named as

S G Chen

1 reference

12 August 2017

P Parchi

1

0 references

Herbert Budka

object named as

H Budka

6

0 references

Pierluigi Gambetti

12

object named as

P Gambetti

1 reference

12 August 2017

P Brown

3

1 reference

12 August 2017

W Zou

4

1 reference

12 August 2017

S Capellari

5

1 reference

12 August 2017

J Hainfellner

7

1 reference

12 August 2017

P F Reyes

8

1 reference

12 August 2017

G T Golden

9

1 reference

12 August 2017

D C Gajdusek

11

1 reference

12 August 2017

language of work or name

English

0 references

publication date

1 July 1998

1 reference

Proceedings of the National Academy of Sciences of the United States of America

12 August 2017

1 reference

12 August 2017

95

1 reference

12 August 2017

14

1 reference

12 August 2017

8322-8327

1 reference

A transmembrane form of the prion protein in neurodegenerative disease

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Prion protein amyloidosis

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Familial cerebral amyloidosis and spongiform encephalopathy

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Molecular biology of prion diseases

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

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

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease.

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Isolation and structural studies of the intact scrapie agent protein.

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Spongiform encephalopathy transmitted experimentally from Creutzfeldt-Jakob and familial Gerstmann-Sträussler-Scheinker diseases.

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

Clinical and molecular genetic study of a large German kindred with Gerstmann-Straussler-Scheinker syndrome

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20974

2 July 2018

Typing prion isoforms.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.14.8322

Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.14.8322

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.14.8322

First experimental transmission of fatal familial insomnia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.14.8322

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)

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.14.8322

New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.14.8322

Allelic origin of the abnormal prion protein isoform in familial prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.14.8322

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.14.8322

[Conference at the Salpêtrière. June 1989. Progressive instability of gait, dysphagia and dysphonia, paraparesis with amyotrophy and mental deterioration in a 56-year-old man]

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9653185

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.95.14.8322

1 reference

12 August 2017

0 references

1 reference

12 August 2017

1 reference