(Q39961980)

15 September 2017

title

PrP mutants with different numbers of octarepeat sequences are more susceptible to the oxidative stress (English)

1 reference

15 September 2017

Run An

1

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15 September 2017

Chenfang Dong

2

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15 September 2017

Yanjun Lei

3

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15 September 2017

Lu Han

4

1 reference

15 September 2017

Ping Li

5

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15 September 2017

Jianming Chen

6

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15 September 2017

Guirong Wang

7

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15 September 2017

Qi Shi

8

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15 September 2017

Chen Gao

9

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15 September 2017

Huiying Jiang

10

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15 September 2017

Wei Zhou

11

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15 September 2017

Jun Han

12

1 reference

15 September 2017

Yonglie Chu

13

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15 September 2017

Xiaoping Dong

14

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15 September 2017

publication date

13 July 2008

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Science in China. Series C: Life Sciences

15 September 2017

published in

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15 September 2017

volume

51

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15 September 2017

issue

7

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15 September 2017

page(s)

630-639

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https://scigraph.springernature.com/pub.10.1007/s11427-008-0062-4

15 September 2017

exact match

0 references

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Prion protein interconversions and the transmissible spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Self-replication and scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Scrapie prions: a three-dimensional model of an infectious fragment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

The cellular prion protein binds copper in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Copper stimulates endocytosis of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Prion protein expression and superoxide dismutase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Oxidative stress hypothesis in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Alteration of free radical metabolism in the brain of mice infected with scrapie agent

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Aberrant metal binding by prion protein in human prion disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Recombinant neural protein PrP can bind with both recombinant and native apolipoprotein E in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Removal of the glycosylation of prion protein provokes apoptosis in SF126.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Study on interaction between microtubule associated protein tau and prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Prions prevent neuronal cell-line death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Prion protein-deficient neurons reveal lower glutathione reductase activity and increased susceptibility to hydrogen peroxide toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Copper-catalyzed oxidation of the recombinant SHa(29-231) prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Measurement of striatal H2O2 by microdialysis following global forebrain ischemia and reperfusion in the rat: correlation with the cytotoxic potential of H2O2 in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

Reactive oxygen species-mediated beta-cleavage of the prion protein in the cellular response to oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-008-0062-4

10.1007/S11427-008-0062-4

21 January 2018

Identifiers

DOI

1 reference

15 September 2017

1 reference