(Q30327252)

18 June 2017

title

Glycosylation of prions and its effects on protein conformation relevant to amino acid mutations. (English)

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18 June 2017

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Wong NK

1

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18 June 2017

Renouf DV

series ordinal

2

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18 June 2017

Lehmann S

series ordinal

3

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18 June 2017

Hounsell EF

series ordinal

4

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18 June 2017

publication date

1 April 2000

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Journal of Molecular Graphics & Modelling

18 June 2017

published in

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18 June 2017

volume

18

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18 June 2017

issue

2

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18 June 2017

page(s)

126-34, 163-5

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Further purification and characterization of scrapie prions

18 June 2017

cites work

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Blockade of glycosylation promotes acquisition of scrapie-like properties by the prion protein in cultured cells

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

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NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

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NMR structure of the mouse prion protein domain PrP(121-231)

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Prion protein NMR structure and familial human spongiform encephalopathies

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

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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

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Conformational studies of the backbone (poly-N-acetyllactosamine) and the core region sequences of O-linked carbohydrate chains

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Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.

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7 January 2021

A Mutant Prion Protein Displays an Aberrant Membrane Association When Expressed in Cultured Cells

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7 January 2021

Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease

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7 January 2021

Familial spongiform encephalopathy associated with a novel prion protein gene mutation

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Glycosylation of microtubule-associated protein tau: an abnormal posttranslational modification in Alzheimer's disease

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7 January 2021

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7 January 2021

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7 January 2021

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

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7 January 2021

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7 January 2021

Effect of the D178N Mutation and the Codon 129 Polymorphism on the Metabolism of the Prion Protein

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7 January 2021

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

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7 January 2021

10.1016/S1093-3263(00)00044-9

Identifiers

DOI

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18 June 2017

1 reference