Literature DB >> 8516847

Mitochondrial diseases: genotype versus phenotype.

D C Wallace1.   

Abstract

Recently, a variety of degenerative diseases have been attributed to mutations in mitochondrial DNA. Even though these mutations are inherited and present throughout the body, they frequently cause late-onset, tissue-specific disease. This may be explained by a combination of the tissue-specific accumulation of somatic mtDNA mutations with age and the variation between tissues in the expression of nuclear genes that encode mitochondrial functions.

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Year:  1993        PMID: 8516847     DOI: 10.1016/0168-9525(93)90207-x

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  28 in total

1.  Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy.

Authors:  B Melegh; L Seress; T Bedekovics; G Kispál; B Sümegi; K Trombitás; K Méhes
Journal:  J Inherit Metab Dis       Date:  1999-10       Impact factor: 4.982

2.  Tissue variation in the control of oxidative phosphorylation: implication for mitochondrial diseases.

Authors:  R Rossignol; T Letellier; M Malgat; C Rocher; J P Mazat
Journal:  Biochem J       Date:  2000-04-01       Impact factor: 3.857

3.  Effect of 'binary mitochondrial heteroplasmy' on respiration and ATP synthesis: implications for mitochondrial diseases.

Authors:  B Korzeniewski; M Malgat; T Letellier; J P Mazat
Journal:  Biochem J       Date:  2001-08-01       Impact factor: 3.857

4.  Identification of mitochondrial deficiency using principal component analysis.

Authors:  G Durrieu; T Letellier; J Antoch; J M Deshouillers; M Malgat; J P Mazat
Journal:  Mol Cell Biochem       Date:  1997-09       Impact factor: 3.396

5.  Theoretical studies on the control of oxidative phosphorylation in muscle mitochondria: application to mitochondrial deficiencies.

Authors:  B Korzeniewski; J P Mazat
Journal:  Biochem J       Date:  1996-10-01       Impact factor: 3.857

6.  The investigation of mitochondrial respiratory chain disease.

Authors:  A A Morris; M J Jackson; L A Bindoff; D M Turnbull
Journal:  J R Soc Med       Date:  1995-04       Impact factor: 5.344

7.  Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic mice.

Authors:  I Nelson; S Gerasimov; C Marsac; P Lestienne; P Boursot
Journal:  Mamm Genome       Date:  1993-11       Impact factor: 2.957

8.  Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseases.

Authors:  P Seibel; J Trappe; G Villani; T Klopstock; S Papa; H Reichmann
Journal:  Nucleic Acids Res       Date:  1995-01-11       Impact factor: 16.971

Review 9.  Creatine metabolism and the consequences of creatine depletion in muscle.

Authors:  M Wyss; T Wallimann
Journal:  Mol Cell Biochem       Date:  1994 Apr-May       Impact factor: 3.396

10.  Effect of enzyme deficiencies on oxidative phosphorylation: from isolated mitochondria to intact tissues. Theoretical studies.

Authors:  Bernard Korzeniewski
Journal:  Mol Biol Rep       Date:  2002       Impact factor: 2.316

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