(Q35122347)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

review article

1 reference

title

A murine model of a familial prion disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

0 references

1 reference

1

1 reference

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3 November 2019

Roberto Chiesa

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

author name string

Bettina Drisaldi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Elena Quaglio

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Antonio Migheli

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Pedro Piccardo

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Bernardino Ghetti

7

1 reference

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3 November 2019

publication date

1 March 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

Clinics in laboratory medicine

3 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

23

1 reference

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3 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

page(s)

175-186

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

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

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Neurological illness in transgenic mice expressing a prion protein with an insertional mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Nerve growth factor-induced differentiation does not alter the biochemical properties of a mutant prion protein expressed in PC12 cells

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

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

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

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%2FS0272-2712%2802%2900069-0

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%2FS0272-2712%2802%2900069-0

7 January 2021

Prion proteins carrying pathogenic mutations are resistant to phospholipase cleavage of their glycolipid anchors

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

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%2FS0272-2712%2802%2900069-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Neuronal apoptosis in fatal familial insomnia

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Neuronal cell death in scrapie-infected mice is due to apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Neuronal apoptosis in Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Detection of apoptosis in murine scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

Prion diseases: what is the neurotoxic molecule?

1 reference

https://api.crossref.org/works/10.1016%2FS0272-2712%2802%2900069-0

7 January 2021

10.1016/S0272-2712(02)00069-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733431%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference