(Q35800381)

10 August 2017

Inducible overexpression of wild-type prion protein in the muscles leads to a primary myopathy in transgenic mice (English)

1 reference

10 August 2017

0 references

1 reference

12

Shu G Chen

1 reference

10 August 2017

15

Pierluigi Gambetti

1 reference

10 August 2017

Shenghai Huang

1

1 reference

10 August 2017

Jingjing Liang

2

1 reference

10 August 2017

Mengjie Zheng

3

1 reference

10 August 2017

Xinyi Li

4

1 reference

10 August 2017

Meiling Wang

5

1 reference

10 August 2017

Ping Wang

6

1 reference

10 August 2017

Difernando Vanegas

7

1 reference

10 August 2017

Di Wu

8

1 reference

10 August 2017

Bikram Chakraborty

9

1 reference

10 August 2017

Arthur P Hays

10

1 reference

10 August 2017

Ken Chen

11

1 reference

10 August 2017

Stephanie Booth

13

1 reference

10 August 2017

Mark Cohen

14

1 reference

10 August 2017

Qingzhong Kong

16

1 reference

10 August 2017

language of work or name

English

0 references

publication date

9 April 2007

1 reference

Proceedings of the National Academy of Sciences of the United States of America

10 August 2017

6

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

10 August 2017

104

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10 August 2017

16

1 reference

10 August 2017

6800-6805

1 reference

Accumulation of prion protein in muscle fibers of experimental chloroquine myopathy: in vivo model for deposition of prion protein in non-neuronal tissues

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

The molecular era of myology

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

Doppel-induced cerebellar degeneration in transgenic mice

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

Internalization of mammalian fluorescent cellular prion protein and N-terminal deletion mutants in living cells

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

The disintegrins ADAM10 and TACE contribute to the constitutive and phorbol ester-regulated normal cleavage of the cellular prion protein

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

Phorbol ester-regulated cleavage of normal prion protein in HEK293 human cells and murine neurons

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

Mice devoid of PrP are resistant to scrapie

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

Prion protein biosynthesis in scrapie-infected and uninfected neuroblastoma cells

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

Amyloid filaments in inclusion body myositis. Novel findings provide insight into nature of filaments

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

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

11 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0608885104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0608885104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0608885104

Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0608885104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0608885104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0608885104

Essential role of the prion protein N terminus in subcellular trafficking and half-life of cellular prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0608885104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0608885104

Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

Prion protein is abnormally accumulated in inclusion-body myositis

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871865

Temporal, spatial, and cell type-specific control of Cre-mediated DNA recombination in transgenic mice

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17420473

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A prion protein cycles between the cell surface and an endocytic compartment in cultured neuroblastoma cells

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17420473

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0608885104

1 reference

10 August 2017

0 references

1 reference

10 August 2017

PubMed publication ID

17420473

1 reference