(Q48381755)

English

Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders.

scientific article published on 10 September 2012

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders. (English)

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

prion protein family

0 references

neurodegeneration

1 reference

based on heuristic

inferred from title

Yassmine Chebaro

7

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

object named as

Katell Peoc'h

1

0 references

Etienne Levavasseur

2

object named as

Etienne Levavasseur

1 reference

Europe PubMed Central

11 February 2018

Jean-Jacques Hauw

13

object named as

Jean-Jacques Hauw

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

author name string

Emilien Delmont

3

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Alfonso De Simone

4

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Isabelle Laffont-Proust

5

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Nicolas Privat

6

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Céline Chapuis

8

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Pierre Bedoucha

9

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Jean-Philippe Brandel

10

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Annie Laquerriere

11

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Jean-Louis Kemeny

12

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Michel Borg

14

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Human Rezaei

15

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Philippe Derreumaux

16

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Jean-Louis Laplanche

17

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Stéphane Haïk

18

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

publication date

10 September 2012

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

Human Molecular Genetics

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

21

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

5417-5428

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

26

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Novel proteinaceous infectious particles cause scrapie

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

The state of the prion

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

The prion's elusive reason for being

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

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/10.1093%2FHMG%2FDDS377

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Gerstmann-Sträussler-Scheinker disease and the Indiana kindred

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Diversity in prion protein oligomerization pathways results from domain expansion as revealed by hydrogen/deuterium exchange and disulfide linkage

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Estimating prion concentration in fluids and tissues by quantitative PMCA.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

In vitro generation of infectious scrapie prions.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrPSc.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Effects of human PrPSc type and PRNP genotype in an in-vitro conversion assay

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Crossing the species barrier by PrP(Sc) replication in vitro generates unique infectious prions.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Molecular model of prion transmission to humans

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Cell-free propagation of prion strains.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Genetic prion disease: the EUROCJD experience.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

NMR solution structure of the human prion protein

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Scrapie prion protein structural constraints obtained by limited proteolysis and mass spectrometry

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Neurotoxic and gliotrophic activity of a synthetic peptide homologous to Gerstmann-Sträussler-Scheinker disease amyloid protein.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Glimepiride reduces the expression of PrPc, prevents PrPSc formation and protects against prion mediated neurotoxicity in cell lines

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

High yield purification and physico-chemical properties of full-length recombinant allelic variants of sheep prion protein linked to scrapie susceptibility

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

GROMACS: A message-passing parallel molecular dynamics implementation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Structural and hydration properties of the partially unfolded states of the prion protein

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Ultra-efficient replication of infectious prions by automated protein misfolding cyclic amplification.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

The oligomerization properties of prion protein are restricted to the H2H3 domain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS377

21 January 2018

Identifiers

10.1093/HMG/DDS377

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/22965875

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48381755&oldid=1936372482"