A novel human disease with abnormal prion protein sensitive to protease (Q24648865)

Ermias D Belay

11

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James R Burke

James R Burke

15

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Thomas Wisniewski

Thomas Wisniewski

17

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Dennis W. Dickson

Dennis W Dickson

18

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Pierluigi Gambetti

1

Pierluigi Gambetti

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Lawrence B. Schonberger

12

Lawrence B Schonberger

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author name string

Zhiqian Dong

2

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Jue Yuan

3

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Xiangzhu Xiao

4

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Mengjie Zheng

5

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Amer Alshekhlee

6

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Rudy Castellani

7

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Mark Cohen

8

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D Gonzalez-Romero

10

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Karen Marder

13

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Carrie Harris

14

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Thomas Montine

16

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Claudio Soto

19

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Christine M Hulette

20

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James A Mastrianni

21

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Qingzhong Kong

22

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Wen-Quan Zou

Deciphering the genetic basis of Alzheimer's disease

23

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language of work or name

English

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publication date

June 2008

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published in

Annals of Neurology

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volume

63

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issue

6

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page(s)

697-708

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cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Exogenous induction of cerebral beta-amyloidogenesis is governed by agent and host

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Eight prion strains have PrP(Sc) molecules with different conformations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prions

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Prion detection by an amyloid seeding assay.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Accumulation of prion protein in the brain that is not associated with transmissible disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Diagnosis of human prion disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Mutant PrPSc conformers induced by a synthetic peptide and several prion strains

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Antibody to DNA detects scrapie but not normal prion protein

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Sporadic and familial CJD: classification and characterisation.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Protease-sensitive scrapie prion protein in aggregates of heterogeneous sizes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Genetic influence on the structural variations of the abnormal prion protein

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Transmissible and genetic prion diseases share a common pathway of neurodegeneration

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

A transmembrane form of the prion protein in neurodegenerative disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Comparison of four staining methods on the detection of neuritic plaques

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

An aggregation-specific enzyme-linked immunosorbent assay: detection of conformational differences between recombinant PrP protein dimers and PrP(Sc) aggregates

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Biological evidence that scrapie agent has an independent genome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Isolation and characterization of a proteinase K-sensitive PrPSc fraction.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Characterization of proteinase K-resistant N- and C-terminally truncated PrP in Nor98 atypical scrapie.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2767200

Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18571782

12 December 2020

inferred from PubMed ID database lookup

Scrapie produced experimentally in goats with special reference to the clinical syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18571782

12 December 2020

inferred from PubMed ID database lookup

Temporary and permanent modifications to a single strain of mouse scrapie on transmission to rats and hamsters

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18571782

12 December 2020

inferred from PubMed ID database lookup

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANA.21420

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1002/ANA.21420

1 reference

2527421

2527421

1 reference

1 reference

1 reference