(Q38601340)

English

Mutant prion protein D202N associated with familial prion disease is retained in the endoplasmic reticulum and forms 'curly' intracellular aggregates

scientific article published on January 2007

In more languages

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

Mutant prion protein D202N associated with familial prion disease is retained in the endoplasmic reticulum and forms 'curly' intracellular aggregates (English)

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

prion protein family

0 references

endoplasmic reticulum

0 references

author name string

Yaping Gu

1

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

Susamma Verghese

2

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

Sharmila Bose

3

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

Maradumane Mohan

4

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

Neena Singh

5

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

publication date

1 January 2007

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

Journal of Molecular Neuroscience

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

32

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

1

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

90-96

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

https://scigraph.springernature.com/pub.10.1007/s12031-007-0023-6

0 references

New insights into prion structure and toxicity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

6 September 2017

Mammalian prion biology: one century of evolving concepts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

6 September 2017

Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

6 September 2017

Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

6 September 2017

Prion protein-deficient neurons reveal lower glutathione reductase activity and increased susceptibility to hydrogen peroxide toxicity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

6 September 2017

The disulfide isomerase Grp58 is a protective factor against prion neurotoxicity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

14 September 2017

Doxycycline and protein folding agents rescue the abnormal phenotype of familial CJD H187R in a cell model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

14 September 2017

Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

23 June 2018

Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

31 August 2018

Cell surface accumulation of a truncated transmembrane prion protein in Gerstmann-Straussler-Scheinker disease P102L.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

31 August 2018

Lack of prion protein expression results in a neuronal phenotype sensitive to stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2394189

31 August 2018

Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/17873292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prion Protein Aggregation Reverted by Low Temperature in Transfected Cells Carrying a Prion Protein Gene Mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17873292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12031-007-0023-6

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

4 September 2017

ResearchGate publication ID

0 references

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