(Q37356800)

19 August 2017

Disruption of Doppel prevents neurodegeneration in mice with extensive Prnp deletions (English)

1 reference

19 August 2017

1 reference

Stefan Freigang

6

0 references

Axel Behrens

object named as

Axel Behrens

2

0 references

Adriano Aguzzi

object named as

Adriano Aguzzi

7

0 references

author name string

Nicolas Genoud

1

1 reference

19 August 2017

Gino Miele

3

1 reference

19 August 2017

Dimitri Robay

4

1 reference

19 August 2017

Frank L Heppner

5

1 reference

19 August 2017

language of work or name

English

0 references

publication date

8 March 2004

1 reference

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

19 August 2017

6

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

19 August 2017

101

1 reference

19 August 2017

12

1 reference

19 August 2017

4198-4203

1 reference

Shadoo, a new protein highly conserved from fish to mammals and with similarity to prion protein

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

NMR structure of the human doppel protein

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

An evolutionary basis for scrapie disease: identification of a fish prion mRNA.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Absence of the prion protein homologue Doppel causes male sterility

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Small is not beautiful: antagonizing functions for the prion protein PrP(C) and its homologue Dpl.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Doppel-induced cerebellar degeneration in transgenic mice

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue Doppel

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Prions: health scare and biological challenge.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Two different neurodegenerative diseases caused by proteins with similar structures

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Expression and structural characterization of the recombinant human doppel protein

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Doppel is an N-glycosylated, glycosylphosphatidylinositol-anchored protein. Expression in testis and ectopic production in the brains of Prnp(0/0) mice predisposed to Purkinje cell loss

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Perspectives: neurobiology. PrP's double causes trouble

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Mice devoid of PrP are resistant to scrapie

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Prion protein gene variation among primates

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Expression of truncated PrP targeted to Purkinje cells of PrP knockout mice causes Purkinje cell death and ataxia

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Prevention of scrapie pathogenesis by transgenic expression of anti-prion protein antibodies.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Physiological expression of the gene for PrP-like protein, PrPLP/Dpl, by brain endothelial cells and its ectopic expression in neurons of PrP-deficient mice ataxic due to Purkinje cell degeneration

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Cellular isoform of the scrapie agent protein participates in lymphocyte activation

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384718

No propagation of prions in mice devoid of PrP.

26 June 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

The black cat/white cat principle of signal integration in bacterial promoters

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

NEUROBIOLOGY:PrP's Double Causes Trouble

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

cDNA sequence and tissue expression of Fugu rubripes prion protein-like: a candidate for the teleost orthologue of tetrapod PrPs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

Molecular cloning of the cDNA coding for Xenopus laevis prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

A C-terminal-truncated PrP Isoform Is Present in Mature Sperm

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

Cannibals and garbage piles

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

Monoclonal antibodies inhibit prion replication and delay the development of prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

cDNA cloning of turtle prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

Immunolocalization of the cellular prion protein in normal brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

Engineering chromosomes in mice through targeted meiotic recombination (TAMERE)

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

Cre expression in primary spermatocytes: a tool for genetic engineering of the germ line

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

T‐lymphocyte activation and the cellular form of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0400131101

21 January 2018

Identifiers

DOI

10.1073/PNAS.0400131101

1 reference

19 August 2017

0 references

1 reference

19 August 2017

PubMed publication ID

15007175

1 reference