(Q44184780)

English

Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA.

scientific article published in October 2002

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA. (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

mitochondrial DNA

0 references

author name string

Stefan Vielhaber

1

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Dmitry A Varlamov

2

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Tatiana A Kudina

3

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Rolf Schröder

4

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Karen Kappes-Horn

5

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Christian E Elger

6

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Martina Seibel

7

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Peter Seibel

8

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Wolfram S Kunz

9

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

publication date

1 October 2002

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Journal of Neuropathology & Experimental Neurology

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

61

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

885-895

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

The myoclonic epilepsy and ragged-red fiber mutation provides new insights into human mitochondrial function and genetics

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

Pathophysiology of the MELAS 3243 transition mutation

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

Bioenergetic consequences of accumulating the common 4977-bp mitochondrial DNA deletion

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

No correlation between muscle A3243G mutation load and mitochondrial function in vivo

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.10.885

21 January 2018

Identifiers

10.1093/JNEN/61.10.885

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

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=Q44184780&oldid=2155136285"