(Q40511076)

English

Glycosylation deficiency at either one of the two glycan attachment sites of cellular prion protein preserves susceptibility to bovine spongiform encephalopathy and scrapie infections.

scientific article published on 23 September 2004

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Glycosylation deficiency at either one of the two glycan attachment sites of cellular prion protein preserves susceptibility to bovine spongiform encephalopathy and scrapie infections (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

prion protein family

0 references

1 reference

based on heuristic

inferred from title

Armin Saalmüller

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Hermann M. Schätzl

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

author name string

Erdmute Neuendorf

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Artur Weber

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Kurt Reifenberg

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Eberhardt Pfaff

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Martin Hermann Groschup

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

language of work or name

0 references

publication date

23 September 2004

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

279

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

51

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

53306-53316

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15448157%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Identification of a protein that purifies with the scrapie prion.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Scrapie prion protein contains a phosphatidylinositol glycolipid

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

A protease-resistant protein is a structural component of the scrapie prion.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Molecular cloning and complete sequence of prion protein cDNA from mouse brain infected with the scrapie agent

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Site-specific characterization of the N-linked glycans of murine prion protein by high-performance liquid chromatography/electrospray mass spectrometry and exoglycosidase digestions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Asparagine-linked glycosylation of the scrapie and cellular prion proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

PrPc glycoform heterogeneity as a function of brain region: implications for selective targeting of neurons by prion strains

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Selective neuronal targeting in prion disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Molecular analysis of bovine spongiform encephalopathy and scrapie strain variation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Glycosylation differences between the normal and pathogenic prion protein isoforms

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Glycosylation influences cross-species formation of protease-resistant prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Synthesis and trafficking of prion proteins in cultured cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Intracellular accumulation of the cellular prion protein after mutagenesis of its Asn-linked glycosylation sites

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Expression of unglycosylated mutated prion protein facilitates PrP(Sc) formation in neuroblastoma cells infected with different prion strains

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Prion protein and species barriers in the transmissible spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Overcoming interference to retroviral superinfection results in amplified expression and transmission of cloned genes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

How N-linked oligosaccharides affect glycoprotein folding in the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

The role of N-glycans in the secretory pathway.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Transmissible and genetic prion diseases share a common pathway of neurodegeneration

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

The role of N-glycosylation in the targeting and activity of the GLYT1 glycine transporter

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Role of individual N-linked glycosylation sites in the function and intracellular transport of the human alpha folate receptor.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Inhibition of N-glycan processing alters axonal transport of synaptic glycoproteins in vivo.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Structural and functional analysis of the canine histamine H2 receptor by site-directed mutagenesis: N-glycosylation is not vital for its action.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Role of the proteasome in membrane extraction of a short-lived ER-transmembrane protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Intracellular targeting of the proteasome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410796200

21 January 2018

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q40511076&oldid=1496004871"