(Q48308927)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883727%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

Neurological illness in transgenic mice expressing a prion protein with an insertional mutation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883727%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

0 references

1 reference

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8 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883727%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

P Piccardo

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883727%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

B Ghetti

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883727%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

language of work or name

English

0 references

publication date

1 December 1998

1 reference

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8 December 2019

1 reference

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8 December 2019

volume

1 reference

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8 December 2019

issue

1 reference

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8 December 2019

page(s)

1339-1351

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883727%20AND%20SRC:MED&resulttype=core&format=json

Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent

8 December 2019

cites work

1 reference

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7 January 2021

A vector for expressing foreign genes in the brains and hearts of transgenic mice

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Allelic origin of the abnormal prion protein isoform in familial prion diseases

1 reference

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7 January 2021

Structural clues to prion replication

1 reference

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7 January 2021

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Identification of intermediate steps in the conversion of a mutant prion protein to a scrapie-like form in cultured cells

1 reference

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7 January 2021

Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

1 reference

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7 January 2021

Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features

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7 January 2021

The structure and biosynthesis of glycosyl phosphatidylinositol protein anchors

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease

1 reference

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7 January 2021

Processing of a cellular prion protein: identification of N- and C-terminal cleavage sites.

1 reference

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7 January 2021

The prion folding problem.

1 reference

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7 January 2021

A transmembrane form of the prion protein in neurodegenerative disease

1 reference

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7 January 2021

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

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7 January 2021

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

1 reference

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7 January 2021

Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene.

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

7 January 2021

Mutant and infectious prion proteins display common biochemical properties in cultured cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

7 January 2021

A wild-type prion protein does not acquire properties of the scrapie isoform when coexpressed with a mutant prion protein in cultured cells

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

7 January 2021

Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix

1 reference

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7 January 2021

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

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7 January 2021

A dementing illness associated with a novel insertion in the prion protein gene

1 reference

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7 January 2021

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1 reference

7 January 2021

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

7 January 2021

Abnormal properties of prion protein with insertional mutations in different cell types

1 reference

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

1 reference

7 January 2021

Prion Protein Biology

1 reference

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7 January 2021

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

1 reference

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7 January 2021

A chemical modification that makes glycoinositol phospholipids resistant to phospholipase C cleavage: fatty acid acylation of inositol

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

7 January 2021

Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

7 January 2021

Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980653-4

7 January 2021

Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions

1 reference

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7 January 2021

Prion Protein Aggregation Reverted by Low Temperature in Transfected Cells Carrying a Prion Protein Gene Mutation

1 reference

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7 January 2021

Scrapie prion protein contains a phosphatidylinositol glycolipid

1 reference

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7 January 2021

Differential release of cellular and scrapie prion proteins from cellular membranes by phosphatidylinositol-specific phospholipase C.

1 reference

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7 January 2021

Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice

1 reference

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7 January 2021

Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins

1 reference

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7 January 2021

MK-801 neurotoxicity in male mice: histologic effects and chronic impairment in spatial learning

1 reference

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7 January 2021

10.1016/S0896-6273(00)80653-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883727%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9883727%20AND%20SRC:MED&resulttype=core&format=json