Literature DB >> 10066162

Mitochondrial diseases in man and mouse.

D C Wallace1.   

Abstract

Over the past 10 years, mitochondrial defects have been implicated in a wide variety of degenerative diseases, aging, and cancer. Studies on patients with these diseases have revealed much about the complexities of mitochondrial genetics, which involves an interplay between mutations in the mitochondrial and nuclear genomes. However, the pathophysiology of mitochondrial diseases has remained perplexing. The essential role of mitochondrial oxidative phosphorylation in cellular energy production, the generation of reactive oxygen species, and the initiation of apoptosis has suggested a number of novel mechanisms for mitochondrial pathology. The importance and interrelationship of these functions are now being studied in mouse models of mitochondrial disease.

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Year:  1999        PMID: 10066162     DOI: 10.1126/science.283.5407.1482

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  743 in total

1.  Replication and preferential inheritance of hypersuppressive petite mitochondrial DNA.

Authors:  D M MacAlpine; J Kolesar; K Okamoto; R A Butow; P S Perlman
Journal:  EMBO J       Date:  2001-04-02       Impact factor: 11.598

2.  Stability of the mitochondrial genome requires an amino-terminal domain of yeast mitochondrial RNA polymerase.

Authors:  Y Wang; G S Shadel
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

3.  A causal link between respiration and senescence in Podospora anserina.

Authors:  E Dufour; J Boulay; V Rincheval; A Sainsard-Chanet
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-11       Impact factor: 11.205

4.  EMBO WORKSHOP REPORT: Molecular and cellular gerontology Serpiano, Switzerland, September 18-22, 1999.

Authors:  C Brack; G Lithgow; H Osiewacz; O Toussaint
Journal:  EMBO J       Date:  2000-05-02       Impact factor: 11.598

Review 5.  Disorders related to mitochondrial membranes: pathology of the respiratory chain and neurodegeneration.

Authors:  S Di Donato
Journal:  J Inherit Metab Dis       Date:  2000-05       Impact factor: 4.982

6.  Outer mitochondrial membrane permeability can regulate coupled respiration and cell survival.

Authors:  M G Vander Heiden; N S Chandel; X X Li; P T Schumacker; M Colombini; C B Thompson
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

7.  Microphotometric analysis of NADH-tetrazolium reductase deficiency in fibroblasts of patients with Leber hereditary optic neuropathy.

Authors:  S Malik; H Sudoyo; S Marzuki
Journal:  J Inherit Metab Dis       Date:  2000-11       Impact factor: 4.982

8.  Transmitochondrial mice: proof of principle and promises.

Authors:  M Hirano
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-16       Impact factor: 11.205

Review 9.  Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.

Authors:  A Brega; J Narula; E Arbustini
Journal:  J Nucl Cardiol       Date:  2001 Jan-Feb       Impact factor: 5.952

10.  The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method.

Authors:  D G Murdock; N C Christacos; D C Wallace
Journal:  Nucleic Acids Res       Date:  2000-11-01       Impact factor: 16.971

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