(Q37711146)

English

Mitochondrial dysfunction in some oxidative stress-related genetic diseases: Ataxia-Telangiectasia, Down Syndrome, Fanconi Anaemia and Werner Syndrome

scientific article published on 18 March 2010

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

1 reference

Europe PubMed Central

Mitochondrial dysfunction in some oxidative stress-related genetic diseases: Ataxia-Telangiectasia, Down Syndrome, Fanconi Anaemia and Werner Syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

object named as

Ana Lloret

2

0 references

Giuseppe Castello

object named as

Giuseppe Castello

8

0 references

David Le Couteur

object named as

David G Le Couteur

6

0 references

Victoria Cogger

5

object named as

Victoria C Cogger

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

author name string

Federico V Pallardó

1

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

Michel Lebel

3

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

Marco d'Ischia

4

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

Maria Nicola Gadaleta

7

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

Giovanni Pagano

9

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

publication date

18 March 2010

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

401-419

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

https://scigraph.springernature.com/pub.10.1007/s10522-010-9269-4

0 references

Fanconi anemia and its diagnosis

1 reference

https://api.crossref.org/works/10.1007%2FS10522-010-9269-4

21 January 2018

SSC1, an essential member of the yeast HSP70 multigene family, encodes a mitochondrial protein

1 reference

https://api.crossref.org/works/10.1007%2FS10522-010-9269-4

21 January 2018

A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

1 reference

https://api.crossref.org/works/10.1007%2FS10522-010-9269-4

21 January 2018

Aging: a theory based on free radical and radiation chemistry

1 reference

https://api.crossref.org/works/10.1007%2FS10522-010-9269-4

21 January 2018

Vitamin E at high doses improves survival, neurological performance, and brain mitochondrial function in aging male mice

1 reference

https://api.crossref.org/works/10.1007%2FS10522-010-9269-4

21 January 2018

The Werner syndrome protein affects the expression of genes involved in adipogenesis and inflammation in addition to cell cycle and DNA damage responses.

1 reference

https://api.crossref.org/works/10.1007%2FS10522-010-9269-4

21 January 2018

Identifiers

10.1007/S10522-010-9269-4

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q37711146&oldid=2179404731"