(Q48343268)

10 February 2018

title

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

1 reference

10 February 2018

0 references

1 reference

10 February 2018

Marco Prinz

object named as

Marco Prinz

1 reference

10 February 2018

author name string

Philipp Meier

1 reference

10 February 2018

Nicolas Genoud

1 reference

10 February 2018

Manuela Maissen

1 reference

10 February 2018

Thomas Rülicke

1 reference

10 February 2018

Andreas Zurbriggen

1 reference

10 February 2018

Alex J Raeber

1 reference

10 February 2018

language of work or name

English

0 references

publication date

1 April 2003

1 reference

10 February 2018

published in

Cell

1 reference

10 February 2018

volume

113

1 reference

10 February 2018

issue

1 reference

10 February 2018

page(s)

49-60

1 reference

10 February 2018

Prions and the immune system: a journey through gut, spleen, and nerves

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Interventional strategies against prion diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Prions: health scare and biological challenge.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Non-genetic propagation of strain-specific properties of scrapie prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

CHARMM: A program for macromolecular energy, minimization, and dynamics calculations

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

High prion and PrPSc levels but delayed onset of disease in scrapie-inoculated mice heterozygous for a disrupted PrP gene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Mice devoid of PrP are resistant to scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

The binding affinity of human IgG for its high affinity Fc receptor is determined by multiple amino acids in the CH2 domain and is modulated by the hinge region

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

A soluble chimeric form of the L1 glycoprotein stimulates neurite outgrowth

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Disrupted splenic architecture, but normal lymph node development in mice expressing a soluble lymphotoxin-beta receptor-IgG1 fusion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Binding of disease-associated prion protein to plasminogen.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Prion protein is secreted in soluble forms in the epididymal fluid and proteolytically processed and transported in seminal plasma.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Efficient lymphoreticular prion propagation requires PrP(c) in stromal and hematopoietic cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

A crucial role for B cells in neuroinvasive scrapie.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Complement facilitates early prion pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Cell-free formation of protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Mechanism of scrapie replication

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Unusual topogenic sequence directs prion protein biogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Temporary inactivation of follicular dendritic cells delays neuroinvasion of scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Temporary depletion of complement component C3 or genetic deficiency of C1q significantly delays onset of scrapie.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Plasminogen binds to disease-associated prion protein of multiple species

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Impaired prion replication in spleens of mice lacking functional follicular dendritic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Characterization of detergent-insoluble complexes containing the cellular prion protein and its scrapie isoform

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

PrP27-30 is a normal soluble prion protein fragment released by human platelets

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Dominant-negative inhibition of prion replication in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Molecular biology of prion diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Measurement of the scrapie agent using an incubation time interval assay

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Attempts to restore scrapie prion infectivity after exposure to protein denaturants

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

No propagation of prions in mice devoid of PrP.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Structural features of human immunoglobulin G that determine isotype-specific differences in complement activation

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

7 January 2021

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900201-0

1 reference

7 January 2021

10.1016/S0092-8674(03)00201-0

Identifiers

DOI

1 reference

10 February 2018

1 reference

10 February 2018