(Q28219319)

GOA release 2020-03-11

9

Pierre Jouannet

0 references

Katell Peoc'h

object named as

Katell Peoc'h

1

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Sylvain Lehmann

object named as

Sylvain Lehmann

5

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author name string

Catherine Serres

2

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Yveline Frobert

3

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Caroline Martin

4

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Stephanie Chasseigneaux

6

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Veronique Sazdovitch

7

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Jacques Grassi

8

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Jean-Marie Launay

10

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Jean-Louis Laplanche

Journal of Biological Chemistry

11

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language of work or name

English

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publication date

8 November 2002

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published in

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volume

277

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page(s)

43071-8

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issue

45

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cites work

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Doppel-induced cerebellar degeneration in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

The cellular prion protein binds copper in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Prion infection impairs the cellular response to oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Prions prevent neuronal cell-line death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Signal transduction through prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Nearly ubiquitous tissue distribution of the scrapie agent precursor protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

The PrP-like protein Doppel gene in sheep and cattle: cDNA sequence and expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Two different neurodegenerative diseases caused by proteins with similar structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Expression and structural characterization of the recombinant human doppel protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Selective identification and differentiation of N- and O-linked oligosaccharides in glycoproteins by liquid chromatography-mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

A mutant prion protein displays an aberrant membrane association when expressed in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

A new method for predicting signal sequence cleavage sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Absence of the prion protein homologue Doppel causes male sterility

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Cell-to-cell transfer of glycosylphosphatidylinositol-anchored membrane proteins during sperm maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

GPI-anchored complement regulatory proteins in seminal plasma. An analysis of their physical condition and the mechanisms of their binding to exogenous cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Functional processing of fertilin: evidence for a critical role of proteolysis in sperm maturation and activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Metal ions and prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Expression of doppel in the CNS of mice does not modulate transmissible spongiform encephalopathy disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Glycosyl Phosphatidylinositol-Anchored Ceruloplasmin Is Expressed by Rat Sertoli Cells and Is Concentrated in Detergent-Insoluble Membrane Fractions1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Identification of a novel gene encoding a PrP-like protein expressed as chimeric transcripts fused to PrP exon 1/2 in ataxic mouse line with a disrupted PrP gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

B lymphocytes and neuroinvasion

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

New insight into abnormal prion protein using monoclonal antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200

Male-specific modification of human CD52

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206357200