Marked aging‐related decline in efficiency of oxidative phosphorylation in human skin fibroblasts
暂无分享,去创建一个
[1] H. Westerblad,et al. Increased mitochondrial mass in mitochondrial myopathy mice , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[2] G. Attardi. Role of mitochondrial DNA in human aging. , 2002, Mitochondrion.
[3] M. L. Genova,et al. Control of oxidative phosphorylation by Complex I in rat liver mitochondria: implications for aging. , 2002, Biochimica et biophysica acta.
[4] J. Aiken,et al. Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia , 2001, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[5] C. Elger,et al. Flux control of cytochrome c oxidase in human skeletal muscle. , 2000, The Journal of biological chemistry.
[6] M. L. Genova,et al. Mitochondrial bioenergetics in aging. , 2000, Biochimica et biophysica acta.
[7] K. Nair,et al. Effects of Aging on Mitochondrial DNA Copy Number and Cytochromec Oxidase Gene Expression in Rat Skeletal Muscle, Liver, and Heart* , 2000, The Journal of Biological Chemistry.
[8] G. Attardi,et al. Brief Communication: Role of Nuclear Background and in vivo Environment in Variable Segregation Behavior of the Aging-Dependent T414G Mutation at Critical Control Site for Human Fibroblast mtDNA Replication , 1999, Somatic cell and molecular genetics.
[9] N. Bresolin,et al. Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication. , 1999, Science.
[10] S. Papa,et al. Low Reserve of Cytochrome c Oxidase Capacity in Vivo in the Respiratory Chain of a Variety of Human Cell Types* , 1998, The Journal of Biological Chemistry.
[11] Y. Kagawa,et al. Nuclear-recessive Mutations of Factors Involved in Mitochondrial Translation Are Responsible for Age-related Respiration Deficiency of Human Skin Fibroblasts* , 1998, The Journal of Biological Chemistry.
[12] R. G. Allen,et al. Development and Age-associated Differences in Electron Transport Potential and Consequences for Oxidant Generation* , 1997, The Journal of Biological Chemistry.
[13] J. M. Izquierdo,et al. Mitochondrial Biogenesis in the Liver during Development and Oncogenesis , 1997, Journal of bioenergetics and biomembranes.
[14] B. Ames,et al. Mitochondrial decay in hepatocytes from old rats: membrane potential declines, heterogeneity and oxidants increase. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[15] G. Attardi,et al. In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[16] S. Papa. Mitochondrial oxidative phosphorylation changes in the life span. Molecular aspects and physiopathological implications. , 1996, Biochimica et biophysica acta.
[17] N. Bresolin,et al. Aging-dependent Functional Alterations of Mitochondrial DNA (mtDNA) from Human Fibroblasts Transferred into mtDNA-less Cells* , 1996, The Journal of Biological Chemistry.
[18] S. Papa,et al. Ageing is associated in females with a decline in the content and activity on the b-c1 complex in skeletal muscle mitochondria. , 1996, Biochimica et biophysica acta.
[19] W. Kunz,et al. Oxygraphic evaluation of mitochondrial function in digitonin-permeabilized mononuclear cells and cultured skin fibroblasts of patients with chronic progressive external ophthalmoplegia. , 1995, Biochemical and molecular medicine.
[20] N. Bresolin,et al. Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers. , 1994, American journal of human genetics.
[21] S. Papa,et al. Decline with age of the respiratory chain activity in human skeletal muscle. , 1994, Biochimica et biophysica acta.
[22] G. Attardi,et al. Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles , 1994, Molecular and cellular biology.
[23] Y. Kagawa,et al. Nuclear but not mitochondrial genome involvement in human age-related mitochondrial dysfunction. Functional integrity of mitochondrial DNA from aged subjects. , 1994, The Journal of biological chemistry.
[24] D. Price,et al. Age‐Dependent Impairment of Mitochondrial Function in Primate Brain , 1993, Journal of neurochemistry.
[25] A. Martinuzzi,et al. Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[26] J. Müller‐Höcker. Cytochrome c oxidase deficient fibres in the limb muscle and diaphragm of man without muscular disease: An age-related alteration , 1990, Journal of the Neurological Sciences.
[27] Y. Wei,et al. Liver mitochondrial respiratory functions decline with age. , 1989, Biochemical and biophysical research communications.
[28] J. Müller‐Höcker,et al. Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study. , 1989, The American journal of pathology.
[29] Edward Byrne,et al. DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING , 1989, The Lancet.
[30] Michael P. King,et al. Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA , 1988, Cell.
[31] J. Erickson,et al. Variation among human 28S ribosomal RNA genes. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[32] S. Goldstein,et al. Mitochondrial DNA in mortal and immortal human cells. Genome number, integrity, and methylation. , 1983, The Journal of biological chemistry.
[33] A. Feinberg,et al. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.
[34] M. M. Bradford. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.
[35] P. Seibel,et al. Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly , 2005, Virchows Archiv A.
[36] G. Attardi,et al. In vivo measurements of respiration control by cytochrome c oxidase and in situ analysis of oxidative phosphorylation. , 2001, Methods in cell biology.
[37] A. Chomyn. In vivo labeling and analysis of human mitochondrial translation products. , 1996, Methods in enzymology.
[38] T. Ozawa,et al. Age-related decrease in respiratory muscle mitochondrial function in rats. , 1992, American journal of respiratory cell and molecular biology.