(Q46694094)

24 December 2017

title

Chemically induced accumulation of GAGs delays PrP(Sc) clearance but prolongs prion disease incubation time (English)

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24 December 2017

main subject

prion protein family

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author name string

Tehila Mayer-Sonnenfeld

1

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24 December 2017

Dana Avrahami

2

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24 December 2017

Yael Friedman-Levi

3

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24 December 2017

Ruth Gabizon

4

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24 December 2017

publication date

19 March 2008

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24 December 2017

Cellular and Molecular Neurobiology

published in

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24 December 2017

volume

28

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24 December 2017

issue

7

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24 December 2017

page(s)

1005-1015

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24 December 2017

https://scigraph.springernature.com/pub.10.1007/s10571-008-9274-1

exact match

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cites work

Drug-induced lysosomal storage of sulphated glycosaminoglycans

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10571-008-9274-1

Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10571-008-9274-1

Up-regulation of cathepsin B and cathepsin L activities in scrapie-infected mouse Neuro2a cells

21 January 2018

1 reference

12 December 2020

The biochemical basis for mucopolysaccharidoses and mucolipidoses

1 reference

12 December 2020

Quinoline derivatives are therapeutic candidates for transmissible spongiform encephalopathies

1 reference

12 December 2020

Mefloquine, an antimalaria drug with antiprion activity in vitro, lacks activity in vivo

1 reference

12 December 2020

Glycosaminoglycans and beta-amyloid, prion and tau peptides in neurodegenerative diseases

1 reference

12 December 2020

Copper binding to PrPC may inhibit prion disease propagation

1 reference

12 December 2020

Prions and the lymphoreticular system.

1 reference

12 December 2020

The anti-prion activity of Congo red. Putative mechanism

1 reference

12 December 2020

Combined alcian blue and silver staining of subnanogram quantities of proteoglycans and glycosaminoglycans in sodium dodecyl sulfate-polyacrylamide gels.

1 reference

12 December 2020

Drug-induced lysosomal storage of sulfated glycosaminoglycans in cultured bovine and human fibroblasts

1 reference

12 December 2020

PrPSc incorporation to cells requires endogenous glycosaminoglycan expression

1 reference

12 December 2020

Retrovirally transduced bone marrow has a therapeutic effect on brain in the mouse model of mucopolysaccharidosis IIIB.

1 reference

12 December 2020

Prion diseases and the spleen

1 reference

12 December 2020

The potential role of lysosomes in tissue distribution of weak bases

1 reference

12 December 2020

Dextran Sulphate 500 Delays and Prevents Mouse Scrapie by Impairment of Agent Replication in Spleen

1 reference

12 December 2020

Potent inhibition of scrapie prion replication in cultured cells by bis-acridines

1 reference

12 December 2020

Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding

1 reference

12 December 2020

Opposite effects of dextran sulfate 500, the polyene antibiotic MS-8209, and Congo red on accumulation of the protease-resistant isoform of PrP in the spleens of mice inoculated intraperitoneally with the scrapie agent

1 reference

12 December 2020

Sulphate polyanions prolong the incubation period of scrapie-infected hamsters.

1 reference

12 December 2020

Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells

1 reference

12 December 2020

The metabolism of glycosaminoglycans is impaired in prion diseases.

1 reference

12 December 2020

Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie-associated prion protein accumulation

1 reference

12 December 2020

Acridine Orange, a precipitant for sulfated glycosaminoglycans, causes mucopolysaccharidosis in cultured fibroblasts

1 reference

12 December 2020

Upregulation of the genes encoding lysosomal hydrolases, a perforin-like protein, and peroxidases in the brains of mice affected with an experimental prion disease

1 reference

12 December 2020

Uptake and neuritic transport of scrapie prion protein coincident with infection of neuronal cells.

1 reference

12 December 2020

Lysosomal storage of sulfated glycosaminoglycans in cultured fibroblasts exposed to immunostimulatory acridine derivatives

1 reference

12 December 2020

Lysosomes as key organelles in the pathogenesis of prion encephalopathies

1 reference

12 December 2020

The tilorone-induced mucopolysaccharidosis in rats. Biochemical investigations

1 reference

12 December 2020

Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease

1 reference

12 December 2020

Activated microglia in cortex of mouse models of mucopolysaccharidoses I and IIIB

1 reference

12 December 2020

Evaluation of quinacrine treatment for prion diseases

1 reference

12 December 2020

Human prion diseases: epidemiology and integrated risk assessment

1 reference

12 December 2020

Screening test for urinary glycosaminoglycans and differentiation of various mucopolysaccharidoses

1 reference

12 December 2020

Purified prion proteins and scrapie infectivity copartition into liposomes

1 reference

12 December 2020

Immunolocalization of heparan sulfate proteoglycans to the prion protein amyloid plaques of Gerstmann-Straussler syndrome, Creutzfeldt-Jakob disease and scrapie

1 reference

12 December 2020

Infectivity of scrapie prions bound to a stainless steel surface

1 reference

12 December 2020

Heparin oligosaccharides that pass the blood-brain barrier inhibit beta-amyloid precursor protein secretion and heparin binding to beta-amyloid peptide.

1 reference

12 December 2020

The most infectious prion protein particles.

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12 December 2020

Cell-free formation of protease-resistant prion protein.

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12 December 2020

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

1 reference

12 December 2020

The antimalarials quinacrine and chloroquine induce weak lysosomal storage of sulphated glycosaminoglycans in cell culture and in vivo

1 reference

12 December 2020

Drug-induced lysosomal storage of sulfated glycosaminoglycans. Studies on the underlying structure-activity relationships.

1 reference

12 December 2020

Heparin-like molecules bind differentially to prion-proteins and change their intracellular metabolic fate

1 reference

12 December 2020

Prion urine comprises a glycosaminoglycan-light chain IgG complex that can be stained by Congo red.

1 reference

12 December 2020

Quinacrine does not prolong survival in a murine Creutzfeldt-Jakob disease model

1 reference

12 December 2020

Prion Protein Biology

1 reference

12 December 2020

Copaxone interferes with the PrP Sc-GAG interaction.

1 reference

12 December 2020

Methods for analysis of urinary glycosaminoglycans

1 reference

12 December 2020

Heparan sulfate is a cellular receptor for purified infectious prions.

1 reference

12 December 2020

Time course of the tilorone-induced lysosomal accumulation of sulphated glycosaminoglycans in cultured fibroblasts

1 reference

12 December 2020

10.1007/S10571-008-9274-1

Identifiers

DOI

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24 December 2017

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24 December 2017