Altered prion protein glycosylation in the aging mouse brain (Q38307048)

2 September 2017

title

Altered prion protein glycosylation in the aging mouse brain (English)

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2 September 2017

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Angeline Xi-Hua Goh

1

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2 September 2017

Chaoyang Li

series ordinal

2

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2 September 2017

Man-Sun Sy

series ordinal

3

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2 September 2017

Boon-Seng Wong

series ordinal

4

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2 September 2017

language of work or name

English

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publication date

27 November 2006

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Journal of Neurochemistry

2 September 2017

published in

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2 September 2017

volume

100

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2 September 2017

issue

3

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2 September 2017

page(s)

841-854

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Glycosylation-related gene expression in prion diseases: PrPSc accumulation in scrapie infected GT1 cells depends on beta-1,4-linked GalNAc-4-SO4 hyposulfation.

2 September 2017

cites work

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Roles, regulation, and mechanism of polysialic acid function during neural development

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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Prion diseases of humans and animals: their causes and molecular basis

21 January 2018

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Asparagine-linked glycosylation of the scrapie and cellular prion proteins

21 January 2018

1 reference

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

21 January 2018

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Prion protein glycosylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.04268.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.04268.X

Increased levels of insulin and insulin-like growth factor-1 hybrid receptors and decreased glycosylation of the insulin receptor alpha- and beta-subunits in scrapie-infected neuroblastoma N2a cells

21 January 2018

1 reference

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Heterogeneity of normal prion protein in two- dimensional immunoblot: presence of various glycosylated and truncated forms.

21 January 2018

1 reference

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Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type

21 January 2018

1 reference

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Novel antibody-lectin enzyme-linked immunosorbent assay that distinguishes prion proteins in sporadic and variant cases of Creutzfeldt-Jakob disease

21 January 2018

1 reference

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Biochemical fingerprints of prion infection: accumulations of aberrant full-length and N-terminally truncated PrP species are common features in mouse prion disease

21 January 2018

1 reference

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21 January 2018

Typing prion isoforms.

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

21 January 2018

1 reference

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21 January 2018

1 reference

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Glycosylation differences between the normal and pathogenic prion protein isoforms

21 January 2018

1 reference

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Prion glycoprotein: structure, dynamics, and roles for the sugars

21 January 2018

1 reference

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Molecular mass, biochemical composition, and physicochemical behavior of the infectious form of the scrapie precursor protein monomer

21 January 2018

1 reference

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Developmental expression of the cellular prion protein in elongating axons.

21 January 2018

1 reference

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Altered glycosylation of acetylcholinesterase in Creutzfeldt-Jakob disease.

21 January 2018

1 reference

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Scrapie prion protein contains a phosphatidylinositol glycolipid

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

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Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.04268.X

Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.04268.X

Copper refolding of prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.04268.X

Prion protein expression in different species: analysis with a panel of new mAbs

21 January 2018

1 reference

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10.1111/J.1471-4159.2006.04268.X

21 January 2018

Identifiers

DOI

1 reference

release_sblluj4psrfndhoyq76xwbyl34

2 September 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/sblluj4psrfndhoyq76xwbyl34

mapped directly with Wikidata item

24 November 2022

based on heuristic

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