Mitochondrial biology, degenerative diseases and aging

BioFactors

Volumn 7, Issue 3, 1998, Pages 187-190

  Wallace, Douglas C ^a   Brown, Michael D ^a   Melov, Simon ^a   Graham, Brett ^a   Lott, Marie ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; MITOCHONDRIAL ENZYME;

AGE; AGING; ANIMAL MODEL; BIOENERGY; CONFERENCE PAPER; DEGENERATIVE DISEASE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTRON TRANSPORT; GENE MUTATION; HUMAN; MITOCHONDRIAL RESPIRATION; MOUSE; MUTATION; NONHUMAN; OXIDATIVE PHOSPHORYLATION; PRIORITY JOURNAL;

ANIMALIA;

EID: 0031921725     PISSN: 09516433     EISSN: None     Source Type: Journal    
DOI: 10.1002/biof.5520070303     Document Type: Conference Paper

References (9)

1. S. DiMauro and E. Bonilla, Mitochondrial encephalomyopathies, in: The Molecular and Genetic Basis of Neurological Disease, R.N. Rosenberg, S.B. Prusiner, S. DiMauro and R.L. Barchi, eds, Butterworth-Heinemann, Boston, 1997, pp. 201-235.
2. B. Graham, K. Waymire, B. Cottrell, I.A. Trounce, G.R. MacGregor and D.C. Wallace, A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/skeletal muscle isoform of the adenine nucleotide translocator, Nature Genet. 16 (1997), 226-234.
3. Y. Li, T.-T. Huang, E.J. Carlson, S. Melov, P.C. Ursell, J.L. Olson, L.J. Noble, M.P. Yoshimura, C. Berger, P.H. Chan, D.C. Wallace and C.J. Epstein, Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase, Nature Genet. 11 (1995), 376-381.
4. S. Melov, D. Hinerfeld, L. Esposito and D.C. Wallace, Multi-organ characterization of mitochondrial genomic rearrangements in ad libitum and caloric restricted mice show striking somatic mitochondrial DNA rearrangements with age, Nucleic Acids Res. 25(5) (1997), 974-982.
5. G. Schatz, The protein import system of mitochondria, J. Biol. Chem. 271(50) (1996), 31 763-31 766.
6. E.A. Schon, The mitochondrial genome, in: The Molecular and Genetic Basis of Neurological Disease, R.N. Rosenberg, S.B. Prusiner, S. DiMauro and R.L. Barchi, eds, Butterworth-Heinemann, Boston, 1997, pp. 189-200.
7. J.M. Shoffner and D.C. Wallace, Oxidative phosphorylation diseases, in: Metabolic and Molecular Basis of Inherited Diseases, C.R. Scriver, A.L. Beaudet, W.S. Sly and D. Valle, eds, 7th edn, McGraw-Hill, 1995, pp. 1535-1609.
8. D.C. Wallace, Mitochondrial DNA mutations and bioenergetic defects in aging and degenerative diseases, in: The Molecular and Genetic Basis of Neurological Disease, R.N. Rosenberg, S.B. Prusiner, S. DiMauro and R.L. Barchi, eds, Butterworth-Heinemann, Boston, 1997, pp. 237-269.
9. D.C. Wallace, M.D. Brown and M.T. Lott, Mitochondrial genetics, in: Emery and Rimoin's Principle and Practice of Medical Genetics, Rimoin et al., eds, 3rd edn, Churchill Livingstone Publishers, 1996.