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Volumn 55, Issue 12, 2002, Pages 1293-1310

The mitochondrial organelle and the heart;La mitocondria y el corazón

Author keywords

Apoptosis; Cardiotoxicity; Dilated cardiomyopathy; Gene therapy; Hypertrophic cardiomyopathy; Ischemic cardiomyopathy; Mitochondria; Stem cells

Indexed keywords

ALCOHOL; ASCORBIC ACID; DOXORUBICIN; MITOCHONDRIAL DNA; RIBOFLAVIN; THIAMINE; VITAMIN K GROUP;

EID: 1942512393     PISSN: 03008932     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0300-8932(02)76802-4     Document Type: Review
Times cited : (38)

References (157)
  • 3
    • 0030920779 scopus 로고    scopus 로고
    • Mitochondrial DNA maintenance in vertebrates
    • Shadel GS, Clayton DA. Mitochondrial DNA maintenance in vertebrates. Annu Rev Biochem 1997;66:409-35.
    • (1997) Annu. Rev. Biochem. , vol.66 , pp. 409-435
    • Shadel, G.S.1    Clayton, D.A.2
  • 4
    • 85047677277 scopus 로고
    • Developmental changes in energy substrate use by the heart
    • Lopaschuk GD, Collins-Nakai RL, Itoi T. Developmental changes in energy substrate use by the heart. Cardiovasc Res 1992; 26:1172-80.
    • (1992) Cardiovasc. Res. , vol.26 , pp. 1172-1180
    • Lopaschuk, G.D.1    Collins-Nakai, R.L.2    Itoi, T.3
  • 5
    • 0034007338 scopus 로고    scopus 로고
    • Coordinate regulation of metabolic enzyme encoding genes during cardiac development and following carvedilol therapy in spontaneously hypertensive rats
    • Sack MN, Harrington LS, Jonassen AK, Mjos OD, Yellon DM. Coordinate regulation of metabolic enzyme encoding genes during cardiac development and following carvedilol therapy in spontaneously hypertensive rats. Cardiovasc Drugs Ther 2000; 14:31-9.
    • (2000) Cardiovasc. Drugs Ther. , vol.14 , pp. 31-39
    • Sack, M.N.1    Harrington, L.S.2    Jonassen, A.K.3    Mjos, O.D.4    Yellon, D.M.5
  • 6
    • 0028943364 scopus 로고
    • Mitochondrial carnitine palmitoyltransferase I isoform switching in the developing rat heart
    • Brown NF, Weis BC, Husti JE, Foster DW, McGarry JD. Mitochondrial carnitine palmitoyltransferase I isoform switching in the developing rat heart. J Biol Chem 1995;270:8952-7.
    • (1995) J. Biol. Chem. , vol.270 , pp. 8952-8957
    • Brown, N.F.1    Weis, B.C.2    Husti, J.E.3    Foster, D.W.4    McGarry, J.D.5
  • 7
    • 0034972285 scopus 로고    scopus 로고
    • Differential regulation of carnitine palmitoyltransferase-I gene isoforms (CPT-I alpha and CPT-I beta) in the rat heart
    • Cook GA, Edwards TL, Jansen MS, Bahouth SW, Wilcox HG, Park EA. Differential regulation of carnitine palmitoyltransferase-I gene isoforms (CPT-I alpha and CPT-I beta) in the rat heart. J Mol Cell Cardiol 2001;33:317-29.
    • (2001) J. Mol. Cell Cardiol. , vol.33 , pp. 317-329
    • Cook, G.A.1    Edwards, T.L.2    Jansen, M.S.3    Bahouth, S.W.4    Wilcox, H.G.5    Park, E.A.6
  • 8
    • 0032993685 scopus 로고    scopus 로고
    • Co-expression in rat heart and skeletal muscle of four genes coding for proteins implicated in long-chain fatty acid uptake
    • Van Nieuwenhoven FA, Willemsen PH, Van der Vusse GJ, Glatz JF. Co-expression in rat heart and skeletal muscle of four genes coding for proteins implicated in long-chain fatty acid uptake. Int J Biochem Cell Biol 1999;31:489-98.
    • (1999) Int. J. Biochem. Cell Biol. , vol.31 , pp. 489-498
    • Van Nieuwenhoven, F.A.1    Willemsen, P.H.2    Van der Vusse, G.J.3    Glatz, J.F.4
  • 9
    • 0033921426 scopus 로고    scopus 로고
    • Developmental changes in regulation of mitochondrial respiration by ADP and creatine in rat heart in vivo
    • Tiivel T, Kadaya L, Kuznetsov A, Kaambre T, Peet N, Sikk P, et al. Developmental changes in regulation of mitochondrial respiration by ADP and creatine in rat heart in vivo. Mol Cell Biochem 2000;208:119-28.
    • (2000) Mol. Cell Biochem. , vol.208 , pp. 119-128
    • Tiivel, T.1    Kadaya, L.2    Kuznetsov, A.3    Kaambre, T.4    Peet, N.5    Sikk, P.6
  • 10
    • 0026095968 scopus 로고
    • Functional development of the creatine kinase system in perinatal rabbit heart
    • Hoerter JA, Kuznetsov A, Ventura-Clapier R. Functional development of the creatine kinase system in perinatal rabbit heart. Circ Res 1991;69:665-76.
    • (1991) Circ. Res. , vol.69 , pp. 665-676
    • Hoerter, J.A.1    Kuznetsov, A.2    Ventura-Clapier, R.3
  • 12
    • 0034306267 scopus 로고    scopus 로고
    • Mitochondria, oxygen free radicals, disease and ageing
    • Raha S, Robinson BH. Mitochondria, oxygen free radicals, disease and ageing. Trends Biochem Sci 2000;25:502-8.
    • (2000) Trends Biochem. Sci. , vol.25 , pp. 502-508
    • Raha, S.1    Robinson, B.H.2
  • 13
    • 0035968183 scopus 로고    scopus 로고
    • Modulation of mitochondrial function by hydrogen peroxide
    • Nulton-Persson AC, Szweda LI. Modulation of mitochondrial function by hydrogen peroxide. J Biol Chem 2001;276:23357-61.
    • (2001) J. Biol. Chem. , vol.276 , pp. 23357-23361
    • Nulton-Persson, A.C.1    Szweda, L.I.2
  • 14
    • 0025272543 scopus 로고
    • Age-related changes in the activity of the pyruvate carrier and in the lipid composition in rat-heart mitochondria
    • Paradies G, Ruggiero FM. Age-related changes in the activity of the pyruvate carrier and in the lipid composition in rat-heart mitochondria. Biochim Biophys Acta 1990;1016:207-21.
    • (1990) Biochim. Biophys. Acta , vol.1016 , pp. 207-221
    • Paradies, G.1    Ruggiero, F.M.2
  • 17
    • 0024337077 scopus 로고
    • Age-dependent decrease of carnitine content in muscle of mice and humans
    • Costell M, O'Connor JE, Grisolia S. Age-dependent decrease of carnitine content in muscle of mice and humans. Biochem Biophys Res Commun 1989 161:1135-43.
    • (1989) Biochem. Biophys. Res. Commun. , vol.161 , pp. 1135-1143
    • Costell, M.1    O'Connor, J.E.2    Grisolia, S.3
  • 18
    • 0024541837 scopus 로고
    • Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases
    • Linnane AW, Marzuki S, Ozawa T, Tanaka M. Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases. Lancet 1989;1:642-5.
    • (1989) Lancet , vol.1 , pp. 642-645
    • Linnane, A.W.1    Marzuki, S.2    Ozawa, T.3    Tanaka, M.4
  • 19
    • 0025758425 scopus 로고
    • Age-dependent increase in deleted mitochondrial DNA in the human heart:possible contributory factor in presbycardia
    • Hattori K, Tanaka M, Sugiyama S, Obayashi T, Ito T, Satake T, et al. Age-dependent increase in deleted mitochondrial DNA in the human heart:possible contributory factor in presbycardia. Am Heart J 1991;121:1735-42.
    • (1991) Am. Heart J. , vol.121 , pp. 1735-1742
    • Hattori, K.1    Tanaka, M.2    Sugiyama, S.3    Obayashi, T.4    Ito, T.5    Satake, T.6
  • 20
    • 0024366601 scopus 로고
    • Cytochrome-c-oxidase deficient cardiomyocytes in the human heart -an age-related phenomenon. A histochemical ultracytochemical study
    • Muller-Hocker J. Cytochrome-c-oxidase deficient cardiomyocytes in the human heart -an age-related phenomenon. A histochemical ultracytochemical study. Am J Pathol 1989;134:1167-73.
    • (1989) Am. J. Pathol. , vol.134 , pp. 1167-1173
    • Muller-Hocker, J.1
  • 22
    • 0034682963 scopus 로고    scopus 로고
    • Aging is associated with increased lipid peroxidation in human hearts, but not with mitochondrial respiratory chain enzyme defects
    • Miro O, Casademont J, Casals E, Perea M, Urbano-Márquez A, Rustin P, et al. Aging is associated with increased lipid peroxidation in human hearts, but not with mitochondrial respiratory chain enzyme defects. Cardiovasc Res 2000;47:624-31.
    • (2000) Cardiovasc. Res. , vol.47 , pp. 624-631
    • Miro, O.1    Casademont, J.2    Casals, E.3    Perea, M.4    Urbano-Márquez, A.5    Rustin, P.6
  • 23
    • 0034960785 scopus 로고    scopus 로고
    • Mitochondrial dysfunction in cardiac disease: Ischemia -reperfusion, aging, and heart failure
    • Lesnefsky EJ, Moghaddas S, Tandler B, Kerner J, Hoppel CL. Mitochondrial dysfunction in cardiac disease: ischemia -reperfusion, aging, and heart failure. J Mol Cell Cardiol 2001;33: 1065-89.
    • (2001) J. Mol. Cell Cardiol. , vol.33 , pp. 1065-1089
    • Lesnefsky, E.J.1    Moghaddas, S.2    Tandler, B.3    Kerner, J.4    Hoppel, C.L.5
  • 24
    • 0033535948 scopus 로고    scopus 로고
    • Declines in mitochondrial respiration during cardiac reperfusion: Age-dependent inactivation of alpha-ketoglutarate dehydrogenase
    • Lucas DT, Szweda LI. Declines in mitochondrial respiration during cardiac reperfusion: age-dependent inactivation of alpha-ketoglutarate dehydrogenase. Proc Natl Acad Sci USA 1999; 96:6689-9.
    • (1999) Proc. Natl. Acad. Sci. USA , vol.96 , pp. 6689-6699
    • Lucas, D.T.1    Szweda, L.I.2
  • 25
    • 0028010899 scopus 로고
    • Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies
    • Rustin P, Lebidois J, Chretien D, Bourgeron T, Piechaud JF, Rotig A, et al. Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies. J Pediatr 1994;124:224-8.
    • (1994) J. Pediatr. , vol.124 , pp. 224-228
    • Rustin, P.1    Lebidois, J.2    Chretien, D.3    Bourgeron, T.4    Piechaud, J.F.5    Rotig, A.6
  • 27
    • 0029361568 scopus 로고
    • Impaired mitochondrial function in idiopathic dilated cardiomyopathy: Biochemical and molecular analysis
    • Marín-García J, Goldenthal MJ, Pierpont ME, Ananthakrishnan R. Impaired mitochondrial function in idiopathic dilated cardiomyopathy: biochemical and molecular analysis. J Card Fail 1995;1:285-91.
    • (1995) J. Card. Fail. , vol.1 , pp. 285-291
    • Marín-García, J.1    Goldenthal, M.J.2    Pierpont, M.E.3    Ananthakrishnan, R.4
  • 32
    • 0029962873 scopus 로고    scopus 로고
    • Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA Lys gene (G8363)
    • Santorelli FM, Mak SC, El-Schahawi M, Casali C, Shanske S, Baram TZ, et al. Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA Lys gene (G8363). Am J Hum Genet 1996;58:933-9.
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 933-939
    • Santorelli, F.M.1    Mak, S.C.2    El-Schahawi, M.3    Casali, C.4    Shanske, S.5    Baram, T.Z.6
  • 33
    • 0028070162 scopus 로고
    • Maternally inherited cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA Gly gene
    • Merante F, Tein I, Benson L, Robinson BH. Maternally inherited cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA Gly gene. Am J Hum Genet 1994;55:437-46.
    • (1994) Am. J. Hum. Genet. , vol.55 , pp. 437-446
    • Merante, F.1    Tein, I.2    Benson, L.3    Robinson, B.H.4
  • 34
    • 0025807222 scopus 로고
    • Maternally inherited myopathy and cardiomyopathy: Association with mutation in mitochondrial DNA tRNA Leu
    • Zeviani M, Gellera C, Antozzi C, Rimoldi M, Morandi L, Villani F, et al. Maternally inherited myopathy and cardiomyopathy:association with mutation in mitochondrial DNA tRNA Leu. Lancet 1991;338:143-7.
    • (1991) Lancet , vol.338 , pp. 143-147
    • Zeviani, M.1    Gellera, C.2    Antozzi, C.3    Rimoldi, M.4    Morandi, L.5    Villani, F.6
  • 38
    • 0033366515 scopus 로고    scopus 로고
    • Maternally inherited cardiomyopathy: An atypical presentation of the mtDNA 12S rRNA gene A 1555G mutation
    • Santorelli FM, Tanji K, Manta P, Casali C, Krishna S, Hays AP, et al. Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A 1555G mutation. Am J Hum Genet 1999;64:295-300.
    • (1999) Am. J. Hum. Genet. , vol.64 , pp. 295-300
    • Santorelli, F.M.1    Tanji, K.2    Manta, P.3    Casali, C.4    Krishna, S.5    Hays, A.P.6
  • 39
    • 18244413442 scopus 로고    scopus 로고
    • Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy
    • Arbustini E, Diegoli M, Fasani R, Grasso M, Morbini P, Banchieri N, et al. Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy. Am J Pathol l998; 153:1501-10.
    • (1998) Am. J. Pathol. , vol.153 , pp. 1501-1510
    • Arbustini, E.1    Diegoli, M.2    Fasani, R.3    Grasso, M.4    Morbini, P.5    Banchieri, N.6
  • 40
    • 0031257633 scopus 로고    scopus 로고
    • Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy
    • Li YY, Maisch B, Rose ML, Hengstenberg C. Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy. J Mol Cell Cardiol 1997;29:2699-709.
    • (1997) J. Mol. Cell Cardiol. , vol.29 , pp. 2699-2709
    • Li, Y.Y.1    Maisch, B.2    Rose, M.L.3    Hengstenberg, C.4
  • 41
    • 0034519248 scopus 로고    scopus 로고
    • The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations
    • Marín-García J, Goldenthal MJ, Ananthakrishnan R, Pierpont ME. The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations. J Card Fail 2000;6:321-9.
    • (2000) J. Card. Fail. , vol.6 , pp. 321-329
    • Marín-García, J.1    Goldenthal, M.J.2    Ananthakrishnan, R.3    Pierpont, M.E.4
  • 42
    • 0026892973 scopus 로고
    • Heart disease and mitochondrial DNA mutations
    • Shoffner JM, Wallace DC. Heart disease and mitochondrial DNA mutations. Heart Dis Stroke 1992;1:235-41.
    • (1992) Heart Dis. Stroke , vol.1 , pp. 235-241
    • Shoffner, J.M.1    Wallace, D.C.2
  • 43
    • 0028355321 scopus 로고
    • Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial point mutation (T8993G)
    • Pastores GM, Santorelli FM, Shanske S, Gelb BD, Fyfe B, Wolfe D, et al. Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial point mutation (T8993G). Am J Med Genet 1994;50:265-71.
    • (1994) Am. J. Med. Genet. , vol.50 , pp. 265-271
    • Pastores, G.M.1    Santorelli, F.M.2    Shanske, S.3    Gelb, B.D.4    Fyfe, B.5    Wolfe, D.6
  • 44
    • 0028918471 scopus 로고
    • Cardiac involvement in mitochondrial diseases: A study of 17 patients with mitochondrial DNA defects
    • Anan R, Nakagawa M, Miyata M, Higuchi I, Nakao S, Suehara M, et al. Cardiac involvement in mitochondrial diseases:a study of 17 patients with mitochondrial DNA defects. Circulation 1995;91:955-61.
    • (1995) Circulation , vol.91 , pp. 955-961
    • Anan, R.1    Nakagawa, M.2    Miyata, M.3    Higuchi, I.4    Nakao, S.5    Suehara, M.6
  • 49
    • 0023883150 scopus 로고
    • Deletions of mtDNA in patients with mitochondrial myopathies
    • Holt IJ, Harding AE, Morgan-Hughes JA. Deletions of mtDNA in patients with mitochondrial myopathies. Nature 1988;331: 717-9.
    • (1988) Nature , vol.331 , pp. 717-719
    • Holt, I.J.1    Harding, A.E.2    Morgan-Hughes, J.A.3
  • 51
    • 0345698798 scopus 로고    scopus 로고
    • The common 4977 base pair deletion of mitochondrial DNA preferentially accumulates in the cardiac conduction system of patients with Kearns-Sayre syndrome
    • Muller-Hocker J, Jacob U, Seibel P. The common 4977 base pair deletion of mitochondrial DNA preferentially accumulates in the cardiac conduction system of patients with Kearns-Sayre syndrome. Mod Pathol 1998;11:295-301.
    • (1998) Mod. Pathol. , vol.11 , pp. 295-301
    • Muller-Hocker, J.1    Jacob, U.2    Seibel, P.3
  • 52
    • 0029996721 scopus 로고    scopus 로고
    • Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy
    • Bohlega S, Tanji K, Santorelli FM, Hirano M, al-Jishi A, DiMauro S. Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy. Neurology 1996;46:1329-34.
    • (1996) Neurology , vol.46 , pp. 1329-1334
    • Bohlega, S.1    Tanji, K.2    Santorelli, F.M.3    Hirano, M.4    al-Jishi, A.5    DiMauro, S.6
  • 53
    • 0026463567 scopus 로고
    • Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA
    • Suomalainen A, Paetau A, Leinonen H, Majander A, Peltonen L, Somer H. Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA. Lancet 1992;340: 1319-20.
    • (1992) Lancet , vol.340 , pp. 1319-1320
    • Suomalainen, A.1    Paetau, A.2    Leinonen, H.3    Majander, A.4    Peltonen, L.5    Somer, H.6
  • 55
    • 0026471872 scopus 로고
    • Accumulation of deletions in human mitochondrial DNA during normal aging: Analysis by quantitative PCR
    • 1180
    • Simonetti S, Chen X, DiMauro S, Schon E. Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR. Biochim Biophys Acta 1992; 1180:113-22.
    • (1992) Biochim. Biophys. Acta , pp. 113-122
    • Simonetti, S.1    Chen, X.2    DiMauro, S.3    Schon, E.4
  • 57
    • 0028990381 scopus 로고
    • Mitochondrial toxicity of antiviral drugs
    • Lewis W, Dalakas MC. Mitochondrial toxicity of antiviral drugs. Nature Med 1995;1:417-22.
    • (1995) Nature Med. , vol.1 , pp. 417-422
    • Lewis, W.1    Dalakas, M.C.2
  • 58
    • 0026564682 scopus 로고
    • Cardiomyopathy associated with antiretroviral therapy in patients with HIV infection: A report of 6 cases
    • Herskowitz A, Willoughby SB, Baughman KL, Schulman SP, Bartlett JD. Cardiomyopathy associated with antiretroviral therapy in patients with HIV infection: a report of 6 cases. Ann Intern Med 1992;116:311-13.
    • (1992) Ann. Intern. Med. , vol.116 , pp. 311-313
    • Herskowitz, A.1    Willoughby, S.B.2    Baughman, K.L.3    Schulman, S.P.4    Bartlett, J.D.5
  • 59
    • 17344366560 scopus 로고    scopus 로고
    • Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient
    • Huizing M, Iacobazzi V, Ijlst L, Savelkoul P, Ruitenbeek W, van den Heuvel L, et al. Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient. Am J Hum Genet 1997;61:1239-45.
    • (1997) Am. J. Hum. Genet. , vol.61 , pp. 1239-1245
    • Huizing, M.1    Iacobazzi, V.2    Ijlst, L.3    Savelkoul, P.4    Ruitenbeek, W.5    van den Heuvel, L.6
  • 60
    • 13344270899 scopus 로고    scopus 로고
    • Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion
    • Campuzano V, Montermini L, Molto MD, Pianese L, Cossee M, Cavalcanti F, et al. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 1996;271:1423-7.
    • (1996) Science , vol.271 , pp. 1423-1427
    • Campuzano, V.1    Montermini, L.2    Molto, M.D.3    Pianese, L.4    Cossee, M.5    Cavalcanti, F.6
  • 61
    • 0032699506 scopus 로고    scopus 로고
    • Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
    • Papadopoulou LC, Sue CM, Davidson MM, Tanji K, Nishino I, Sadlock JE, et al. Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene. Nat Genet 1999;23:333-7.
    • (1999) Nat. Genet. , vol.23 , pp. 333-337
    • Papadopoulou, L.C.1    Sue, C.M.2    Davidson, M.M.3    Tanji, K.4    Nishino, I.5    Sadlock, J.E.6
  • 64
    • 0028817917 scopus 로고
    • Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency: Causing cardiomyopathy and sudden death in childhood
    • Strauss AW, Powell CK, Hale DE, Anderson MM, Ahuja A, Brackett JC, et al. Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency: causing cardiomyopathy and sudden death in childhood. Proc Natl Acad Sci USA 1995 92:10496-500.
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 10496-10500
    • Strauss, A.W.1    Powell, C.K.2    Hale, D.E.3    Anderson, M.M.4    Ahuja, A.5    Brackett, J.C.6
  • 65
    • 0025242644 scopus 로고
    • Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: A cause of lethal myopathy and cardiomyopathy in early childhood
    • Rocchiccioli F, Wanders RJ, Aubourg P, Vianey-Liaud C, Ijlst L, Fabre M, et al. Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhood. Pediatr Res 1990;28:657-62.
    • (1990) Pediatr. Res. , vol.28 , pp. 657-662
    • Rocchiccioli, F.1    Wanders, R.J.2    Aubourg, P.3    Vianey-Liaud, C.4    Ijlst, L.5    Fabre, M.6
  • 66
    • 0033555567 scopus 로고    scopus 로고
    • Short-chain acyl-CoA dehydrogenase deficiency: A cause of ophthalmoplegia and multicore myopathy
    • Tein I, Haslam RH, Rhead WJ, Bennett MJ, Becker LE, Vockley J. Short-chain acyl-CoA dehydrogenase deficiency:a cause of ophthalmoplegia and multicore myopathy. Neurology 1999; 52:366-72.
    • (1999) Neurology , vol.52 , pp. 366-372
    • Tein, I.1    Haslam, R.H.2    Rhead, W.J.3    Bennett, M.J.4    Becker, L.E.5    Vockley, J.6
  • 67
    • 0025022129 scopus 로고
    • A genetic defect in carnitine transport causing primary carnitine deficiency
    • Stanley CA, Treem WR, Hale DE, Coates PM. A genetic defect in carnitine transport causing primary carnitine deficiency. Prog Clin Biol Res 1990;321:457-64.
    • (1990) Prog. Clin. Biol. Res. , vol.321 , pp. 457-464
    • Stanley, C.A.1    Treem, W.R.2    Hale, D.E.3    Coates, P.M.4
  • 69
    • 0032729717 scopus 로고    scopus 로고
    • Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children
    • Bonnet D, Martin D, de Lonlay P, Villain E, Jouvet P, Rabier D, et al. Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children. Circulation 1999;100:2248-53.
    • (1999) Circulation , vol.100 , pp. 2248-2253
    • Bonnet, D.1    Martin, D.2    de Lonlay, P.3    Villain, E.4    Jouvet, P.5    Rabier, D.6
  • 70
    • 0024551414 scopus 로고
    • Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation
    • Corr PB, Creer MH, Yamada KA, Saffitz JE, Sobel BE. Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation. J Clin Invest 1989;83:927-36.
    • (1989) J. Clin. Invest. , vol.83 , pp. 927-936
    • Corr, P.B.1    Creer, M.H.2    Yamada, K.A.3    Saffitz, J.E.4    Sobel, B.E.5
  • 71
    • 0024455648 scopus 로고
    • Developmental cardiac metabolism in health and disease
    • Tripp ME. Developmental cardiac metabolism in health and disease. Pediatr Cardiol 1989;10:150-8.
    • (1989) Pediatr. Cardiol. , vol.10 , pp. 150-158
    • Tripp, M.E.1
  • 73
    • 0036126877 scopus 로고    scopus 로고
    • Infantile dilated x-linked cardiomyopathy, g4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle
    • Bissler JJ, Tsoras M, Goring HH, Hug P, Chuck G, Tombragel E, et al. Infantile dilated x-linked cardiomyopathy, g4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle. Lab Invest 2002;82: 335-44.
    • (2002) Lab. Invest. , vol.82 , pp. 335-344
    • Bissler, J.J.1    Tsoras, M.2    Goring, H.H.3    Hug, P.4    Chuck, G.5    Tombragel, E.6
  • 75
    • 0027221634 scopus 로고
    • Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy
    • Fananapazir L, Dalakas MC, Cyran F, Cohn G, Epstein ND. Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy. Proc Natl Acad Sci USA 1993;90:3993-7.
    • (1993) Proc. Natl. Acad. Sci. USA , vol.90 , pp. 3993-3997
    • Fananapazir, L.1    Dalakas, M.C.2    Cyran, F.3    Cohn, G.4    Epstein, N.D.5
  • 77
    • 15644384508 scopus 로고    scopus 로고
    • Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure
    • Arbustini E, Fasani R, Morbini P, Diegoli M, Grasso M, Dal Bello B, et al. Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure. Heart 1998;80:548-58.
    • (1998) Heart , vol.80 , pp. 548-558
    • Arbustini, E.1    Fasani, R.2    Morbini, P.3    Diegoli, M.4    Grasso, M.5    Dal Bello, B.6
  • 78
    • 0034683573 scopus 로고    scopus 로고
    • Desmin cytoskeleton linked to muscle mitochondrial distribution and respiratory function
    • Milner DJ, Mavroidis M, Weisleder N, Capetanaki Y. Desmin cytoskeleton linked to muscle mitochondrial distribution and respiratory function. J Cell Biol 2000;150:1283-98.
    • (2000) J. Cell Biol. , vol.150 , pp. 1283-1298
    • Milner, D.J.1    Mavroidis, M.2    Weisleder, N.3    Capetanaki, Y.4
  • 79
    • 0034222631 scopus 로고    scopus 로고
    • Adaptive changes in response to acute hypoxia, ischemia and reperfusion in human cardiac cell
    • Corbucci GG. Adaptive changes in response to acute hypoxia, ischemia and reperfusion in human cardiac cell. Minerva Anestesiol 2000:66:523-30.
    • (2000) Minerva Anestesiol. , vol.66 , pp. 523-530
    • Corbucci, G.G.1
  • 81
    • 0026074885 scopus 로고
    • Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease
    • Corral-Debrinski M, Stepien G, Shoffner JM, Lott MT, Kanter K, Wallace DC. Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease. JAMA 1991;266:1812-6.
    • (1991) JAMA , vol.266 , pp. 1812-1816
    • Corral-Debrinski, M.1    Stepien, G.2    Shoffner, J.M.3    Lott, M.T.4    Kanter, K.5    Wallace, D.C.6
  • 82
    • 0032775546 scopus 로고    scopus 로고
    • Lipid peroxidation and alterations to oxidative metabolism in mitochondria isolated from rat heart subjected to ischemia and reperfusion
    • Paradies G, Petrosillo G, Pistolese M, Di Venosa N, Serena D, Ruggiero FM. Lipid peroxidation and alterations to oxidative metabolism in mitochondria isolated from rat heart subjected to ischemia and reperfusion. Free Radic Biol Med 1999;27:42-50.
    • (1999) Free Radic. Biol. Med. , vol.27 , pp. 42-50
    • Paradies, G.1    Petrosillo, G.2    Pistolese, M.3    Di Venosa, N.4    Serena, D.5    Ruggiero, F.M.6
  • 85
    • 0033962709 scopus 로고    scopus 로고
    • Evidence for mitochondrial K ATP channels as effectors of human myocardial preconditioning
    • Ghosh S, Standen NB, Galinanes M. Evidence for mitochondrial K ATP channels as effectors of human myocardial preconditioning. Cardiovasc Res 2000;45:934-40.
    • (2000) Cardiovasc. Res. , vol.45 , pp. 934-940
    • Ghosh, S.1    Standen, N.B.2    Galinanes, M.3
  • 86
    • 0032550363 scopus 로고    scopus 로고
    • The permeability transition pore complex: A target for apoptosis regulation by caspases and Bcl-2 related proteins
    • Marzo I, Brenner C, Zamzami N, Susin SA, Beutner G, Brdiczka D, et al. The permeability transition pore complex: a target for apoptosis regulation by caspases and Bcl-2 related proteins. J Exp Med 1998;187:1261-71.
    • (1998) J. Exp. Med. , vol.187 , pp. 1261-1271
    • Marzo, I.1    Brenner, C.2    Zamzami, N.3    Susin, S.A.4    Beutner, G.5    Brdiczka, D.6
  • 87
    • 0032566649 scopus 로고    scopus 로고
    • Bax and adenine nucleotide translocator cooperate in the mitochondrial control of apoptosis
    • Marzo I, Brenner C, Zamzami N, Jurgensmeier JM, Susin SA, Vieira HL, et al. Bax and adenine nucleotide translocator cooperate in the mitochondrial control of apoptosis. Science 1998;281:2027-31.
    • (1998) Science , vol.281 , pp. 2027-2031
    • Marzo, I.1    Brenner, C.2    Zamzami, N.3    Jurgensmeier, J.M.4    Susin, S.A.5    Vieira, H.L.6
  • 88
    • 0032504568 scopus 로고    scopus 로고
    • The mitochondrial permeability transition in cell death: A common mechanism in necrosis, apoptosis and autophagy
    • Lemasters JJ, Nieminen AL, Qian T, Trost LC, Elmore SP, Nishimura Y, et al. The mitochondrial permeability transition in cell death: a common mechanism in necrosis, apoptosis and autophagy. Biochim Biophys Acta 1998;1366:177-96.
    • (1998) Biochim. Biophys. Acta , vol.1366 , pp. 177-196
    • Lemasters, J.J.1    Nieminen, A.L.2    Qian, T.3    Trost, L.C.4    Elmore, S.P.5    Nishimura, Y.6
  • 89
    • 0029810095 scopus 로고    scopus 로고
    • Mitochondrial dysfunction is a primary event in glutamate neurotoxicity
    • Schinder AF, Olson EC, Spitzer NC, Montal M. Mitochondrial dysfunction is a primary event in glutamate neurotoxicity. J NeuroSci 1996;16:6125-33.
    • (1996) J. NeuroSci. , vol.16 , pp. 6125-6133
    • Schinder, A.F.1    Olson, E.C.2    Spitzer, N.C.3    Montal, M.4
  • 90
    • 0036194529 scopus 로고    scopus 로고
    • Mitochondria as a pharmacological target
    • Szewczyk A, Wojtczak L. Mitochondria as a pharmacological target. Pharmacol Rev 2002;54:101-27.
    • (2002) Pharmacol. Rev. , vol.54 , pp. 101-127
    • Szewczyk, A.1    Wojtczak, L.2
  • 93
    • 0032961434 scopus 로고    scopus 로고
    • Cardioselective and cumulative oxidation of mitochondrial DNA following subchronic doxorubicin administration
    • Serrano J, Palmeira CM, Kuehl DW, Wallace KB. Cardioselective and cumulative oxidation of mitochondrial DNA following subchronic doxorubicin administration. Biochim Biophys Acta 1999;1411:201-5.
    • (1999) Biochim. Biophys. Acta , vol.1411 , pp. 201-205
    • Serrano, J.1    Palmeira, C.M.2    Kuehl, D.W.3    Wallace, K.B.4
  • 94
    • 0035881024 scopus 로고    scopus 로고
    • Interference with calcium-dependent mitochondrial bioenergetics in cardiac myocytes isolated from doxorubicin-treated rats
    • Zhou S, Heller LJ, Wallace KB. Interference with calcium-dependent mitochondrial bioenergetics in cardiac myocytes isolated from doxorubicin-treated rats. Toxicol Appl Pharmacol 2001;175:60-7.
    • (2001) Toxicol. Appl. Pharmacol. , vol.175 , pp. 60-67
    • Zhou, S.1    Heller, L.J.2    Wallace, K.B.3
  • 95
    • 0028130476 scopus 로고
    • Disruption of mitochondrial calcium homeostasis following chronic doxorubicin administration
    • Solem LE, Henry TR, Wallace KB. Disruption of mitochondrial calcium homeostasis following chronic doxorubicin administration. Toxicol Appl Pharmacol 1994;129:214-22.
    • (1994) Toxicol. Appl. Pharmacol. , vol.129 , pp. 214-222
    • Solem, L.E.1    Henry, T.R.2    Wallace, K.B.3
  • 97
    • 0029781555 scopus 로고    scopus 로고
    • The protective role of manganese superoxide dismutase against adriamycin-induced acute cardiac toxicity in transgenic mice
    • Yen HC, Oberley TD, Vichitbandha S, Ho YS, St Clair DK. The protective role of manganese superoxide dismutase against adriamycin-induced acute cardiac toxicity in transgenic mice. J Clin Invest 1996;98:1253-60.
    • (1996) J. Clin. Invest. , vol.98 , pp. 1253-1260
    • Yen, H.C.1    Oberley, T.D.2    Vichitbandha, S.3    Ho, Y.S.4    St Clair, D.K.5
  • 98
    • 0034948867 scopus 로고    scopus 로고
    • Activation of A (3) adenosine receptor protects against doxorubicin-induced cardiotoxicity
    • Shneyvays V, Mamedova L, Zinman T, Jacobson K, Shainberg A. Activation of A (3) adenosine receptor protects against doxorubicin-induced cardiotoxicity. J Mol Cell Cardiol 2001;33: 1249-61.
    • (2001) J. Mol. Cell Cardiol. , vol.33 , pp. 1249-1261
    • Shneyvays, V.1    Mamedova, L.2    Zinman, T.3    Jacobson, K.4    Shainberg, A.5
  • 100
    • 0034913884 scopus 로고    scopus 로고
    • Metallothionein inhibits doxorubicin-induced mitochondrial cytochrome c release and caspase-3 activation in cardiomyocytes
    • Wang GW, Klein JB, Kang YJ. Metallothionein inhibits doxorubicin-induced mitochondrial cytochrome c release and caspase-3 activation in cardiomyocytes. J Pharmacol Exp Ther 2001;298: 461-8.
    • (2001) J. Pharmacol. Exp. Ther. , vol.298 , pp. 461-468
    • Wang, G.W.1    Klein, J.B.2    Kang, Y.J.3
  • 101
    • 0029550220 scopus 로고
    • The role of the ADP/ATP carrier in the pathogenesis of viral heart disease
    • Schulze K, Schultheiss HP. The role of the ADP/ATP carrier in the pathogenesis of viral heart disease. Eur Heart J 1995;16 (Suppl O):64-7.
    • (1995) Eur. Heart J. , vol.16 , Issue.SUPPL. O , pp. 64-67
    • Schulze, K.1    Schultheiss, H.P.2
  • 104
    • 0027305393 scopus 로고
    • Synthesis of ventricular mitochondrial proteins in vivo: Effect of acute ethanol toxicity
    • Siddiq T, Salisbury JR, Richardson PJ, Preedy VR. Synthesis of ventricular mitochondrial proteins in vivo: effect of acute ethanol toxicity. Alcohol Clin Exp Res 1993;17:894-9.
    • (1993) Alcohol Clin. Exp. Res. , vol.17 , pp. 894-899
    • Siddiq, T.1    Salisbury, J.R.2    Richardson, P.J.3    Preedy, V.R.4
  • 105
    • 0032212902 scopus 로고    scopus 로고
    • Fatty acid ethyl esters: Potentially toxic products of myocardial ethanol metabolism
    • Beckemeier ME, Bora PS. Fatty acid ethyl esters: potentially toxic products of myocardial ethanol metabolism. J Mol Cell Cardiol 1998;30:2487-94.
    • (1998) J. Mol. Cell Cardiol. , vol.30 , pp. 2487-2494
    • Beckemeier, M.E.1    Bora, P.S.2
  • 106
    • 0034843897 scopus 로고    scopus 로고
    • Alcohol and the heart
    • Schoppet M, Maisch B. Alcohol and the heart. Herz 2001;26: 345-52.
    • (2001) Herz , vol.26 , pp. 345-352
    • Schoppet, M.1    Maisch, B.2
  • 107
    • 0031011211 scopus 로고    scopus 로고
    • A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator
    • Graham BH, Waymire KG, Cottrell B, Trounce IA, MacGregor GR, Wallace DC. A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator. Nat Genet 1997;16:226-34.
    • (1997) Nat. Genet. , vol.16 , pp. 226-234
    • Graham, B.H.1    Waymire, K.G.2    Cottrell, B.3    Trounce, I.A.4    MacGregor, G.R.5    Wallace, D.C.6
  • 108
    • 0029838063 scopus 로고    scopus 로고
    • Neurodegeneration, myocardial injury, and perinatal death in mitochondrial superoxide dismutase-deficient mice
    • Lebovitz RM, Zhang H, Vogel H, Cartwright Jr, Dionne L, Lu N, et al. Neurodegeneration, myocardial injury, and perinatal death in mitochondrial superoxide dismutase-deficient mice. Proc Natl Acad Sci USA 1996;93:9782-7.
    • (1996) Proc. Natl. Acad. Sci. USA , vol.93 , pp. 9782-9787
    • Lebovitz, R.M.1    Zhang, H.2    Vogel, H.3    Cartwright A., Jr.4    Dionne, L.5    Lu, N.6
  • 109
    • 0028827252 scopus 로고
    • Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase
    • Li Y, Huang TT, Carlson EJ, Melov S, Ursell PC, Olson JL, et al. Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase. Nat Genet 1995;11:376-81.
    • (1995) Nat. Genet. , vol.11 , pp. 376-381
    • Li, Y.1    Huang, T.T.2    Carlson, E.J.3    Melov, S.4    Ursell, P.C.5    Olson, J.L.6
  • 111
    • 0034987233 scopus 로고    scopus 로고
    • Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death
    • Ibdah JA, Paul H, Zhao Y, Binford S, Salleng K, Cline M, et al. Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death. J Clin Invest 2001;107: 1403-9.
    • (2001) J. Clin. Invest. , vol.107 , pp. 1403-1409
    • Ibdah, J.A.1    Paul, H.2    Zhao, Y.3    Binford, S.4    Salleng, K.5    Cline, M.6
  • 112
    • 0032924872 scopus 로고    scopus 로고
    • Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression
    • Wang J, Wilhelmsson H, Graff C, Li H, Oldfors A, Rustin P, et al. Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression. Nat Genet 1999;21:133-7.
    • (1999) Nat. Genet. , vol.21 , pp. 133-137
    • Wang, J.1    Wilhelmsson, H.2    Graff, C.3    Li, H.4    Oldfors, A.5    Rustin, P.6
  • 113
    • 0035138072 scopus 로고    scopus 로고
    • Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits
    • Puccio H, Simon D, Cossee M, Criqui-Filipe P, Tiziano F, Melki J, et al. Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits. Nat Genet 2001;27: 181-6.
    • (2001) Nat. Genet. , vol.27 , pp. 181-186
    • Puccio, H.1    Simon, D.2    Cossee, M.3    Criqui-Filipe, P.4    Tiziano, F.5    Melki, J.6
  • 114
    • 0034724327 scopus 로고    scopus 로고
    • Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy
    • Li H, Wilhelmsson H, Hanson A, Thoren P, Duffy J, Rustin P, et al. Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy. Proc Natl Acad Sci USA 2000;97:3467-72.
    • (2000) Proc. Natl. Acad. Sci. USA , vol.97 , pp. 3467-3472
    • Li, H.1    Wilhelmsson, H.2    Hanson, A.3    Thoren, P.4    Duffy, J.5    Rustin, P.6
  • 116
    • 0033772263 scopus 로고    scopus 로고
    • Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes
    • Inoue K, Nakada K, Ogura A, Isobe K, Goto Y, Nonaka I, et al. Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes. Nat Genet 2000;26:176-81.
    • (2000) Nat. Genet. , vol.26 , pp. 176-181
    • Inoue, K.1    Nakada, K.2    Ogura, A.3    Isobe, K.4    Goto, Y.5    Nonaka, I.6
  • 117
    • 0035834582 scopus 로고    scopus 로고
    • Correlation of functional and ultrastructural abnormalities of mitochondria in mouse heart carrying a pathogenic mutant mtDNA with a 4696-bp deletion
    • Nakada K, Inoue K, Chen CS, Nonaka I, Goto Y, Ogura A, et al. Correlation of functional and ultrastructural abnormalities of mitochondria in mouse heart carrying a pathogenic mutant mtDNA with a 4696-bp deletion. Biochem Biophys Res Commun 2001;288:901-7.
    • (2001) Biochem. Biophys. Res. Commun. , vol.288 , pp. 901-907
    • Nakada, K.1    Inoue, K.2    Chen, C.S.3    Nonaka, I.4    Goto, Y.5    Ogura, A.6
  • 118
    • 0034881326 scopus 로고    scopus 로고
    • Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA
    • Nakada K, Inoue K, Ono T, Isobe K, Ogura A, Goto YI, et al. Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA. Nat Med 2001;7:934-40.
    • (2001) Nat. Med. , vol.7 , pp. 934-940
    • Nakada, K.1    Inoue, K.2    Ono, T.3    Isobe, K.4    Ogura, A.5    Goto, Y.I.6
  • 119
    • 0036143320 scopus 로고    scopus 로고
    • The cardiac phenotype induced by PPARalpha overexpression mimics that caused by diabetes mellitus
    • Finck BN, Lehman JJ, Leone TC, Welch MJ, Bennett MJ, Kovacs A, et al. The cardiac phenotype induced by PPARalpha overexpression mimics that caused by diabetes mellitus. J Clin Invest 2002;109:121-30.
    • (2002) J. Clin. Invest. , vol.109 , pp. 121-130
    • Finck, B.N.1    Lehman, J.J.2    Leone, T.C.3    Welch, M.J.4    Bennett, M.J.5    Kovacs, A.6
  • 120
    • 0033803048 scopus 로고    scopus 로고
    • Peroxisome proliferator-activated receptor gamma coactivator-1 promotes cardiac mitochondrial biogenesis
    • Lehman JJ, Barger PM, Kovacs A, Saffitz JE, Medeiros DM, Kelly DP. Peroxisome proliferator-activated receptor gamma coactivator-1 promotes cardiac mitochondrial biogenesis. J Clin Invest 2000;106:847-56.
    • (2000) J. Clin. Invest. , vol.106 , pp. 847-856
    • Lehman, J.J.1    Barger, P.M.2    Kovacs, A.3    Saffitz, J.E.4    Medeiros, D.M.5    Kelly, D.P.6
  • 121
    • 0031940986 scopus 로고    scopus 로고
    • A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase
    • Melov S, Schneider JA, Day BJ, Hinerfeld D, Coskun P, Mirra SS, et al. A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase. Nat Genet 1998;18:159-63.
    • (1998) Nat. Genet. , vol.18 , pp. 159-163
    • Melov, S.1    Schneider, J.A.2    Day, B.J.3    Hinerfeld, D.4    Coskun, P.5    Mirra, S.S.6
  • 123
    • 0025968499 scopus 로고
    • In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy patient mitochondria
    • Chomyn A, Meola G, Bresolin N, Lai ST, Scarlato G, Attardi G. In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy patient mitochondria. Mol Cell Biol 1991;11:2236-44.
    • (1991) Mol. Cell Biol. , vol.11 , pp. 2236-2244
    • Chomyn, A.1    Meola, G.2    Bresolin, N.3    Lai, S.T.4    Scarlato, G.5    Attardi, G.6
  • 125
    • 0028037791 scopus 로고
    • Oxidative phosphorylation diseases and mito-chondrial DNA mutations: Diagnosis and treatment
    • Shoffner JM, Wallace DC. Oxidative phosphorylation diseases and mito-chondrial DNA mutations: diagnosis and treatment. Annu Rev Nutr 1994;14:535-68.
    • (1994) Annu. Rev. Nutr. , vol.14 , pp. 535-568
    • Shoffner, J.M.1    Wallace, D.C.2
  • 126
    • 2542530560 scopus 로고
    • Response of patients in classes III and IV of cardiomyopathy to therapy in a blind and cross-over trial with coenzyme Q10
    • Langsjuen P, Vadhanavikit S, Folkers K. Response of patients in classes III and IV of cardiomyopathy to therapy in a blind and cross-over trial with coenzyme Q10. Proc Natl Acad Sci USA 1985;82:4240-4.
    • (1985) Proc. Natl. Acad. Sci. USA , vol.82 , pp. 4240-4244
    • Langsjuen, P.1    Vadhanavikit, S.2    Folkers, K.3
  • 131
    • 0033954046 scopus 로고    scopus 로고
    • Familial carnitine transporter defect: A treatable cause of cardiomyopathy in children
    • Pierpont ME, Breningstall GN, Stanley CA, Singh A. Familial carnitine transporter defect: a treatable cause of cardiomyopathy in children. Am Heart J 2000;139:S96-S106.
    • (2000) Am. Heart J. , vol.139
    • Pierpont, M.E.1    Breningstall, G.N.2    Stanley, C.A.3    Singh, A.4
  • 132
    • 0032922822 scopus 로고    scopus 로고
    • PUFA and aging modulate cardiac mitochondrial membrane lipid composition and Ca2+ activation of PDH
    • Pepe S, Tsuchiya N, Lakatta EG, Hansford RG. PUFA and aging modulate cardiac mitochondrial membrane lipid composition and Ca2+ activation of PDH. Am J Physiol 1999; 276:H149-58.
    • (1999) Am. J. Physiol. , vol.276
    • Pepe, S.1    Tsuchiya, N.2    Lakatta, E.G.3    Hansford, R.G.4
  • 133
    • 0029085021 scopus 로고
    • Disorders of mitochondrial long-chain fatty acid oxidation
    • Pollitt RJ. Disorders of mitochondrial long-chain fatty acid oxidation. J Inherit Metab Dis 1995;18:473-90.
    • (1995) J. Inherit. Metab. Dis. , vol.18 , pp. 473-490
    • Pollitt, R.J.1
  • 134
    • 0035933194 scopus 로고    scopus 로고
    • Myocardial free fatty acid and glucose use after carvedilol treatment in patients with congestive heart failure
    • Wallhaus TR, Taylor M, DeGrado TR, Russell DC, Stanko P, Nickles RJ, et al. Myocardial free fatty acid and glucose use after carvedilol treatment in patients with congestive heart failure. Circulation 2001;103:2441-6.
    • (2001) Circulation , vol.103 , pp. 2441-2446
    • Wallhaus, T.R.1    Taylor, M.2    DeGrado, T.R.3    Russell, D.C.4    Stanko, P.5    Nickles, R.J.6
  • 135
    • 0027384129 scopus 로고
    • Embryonic stem cell model systems for vascular morphogenesis and cardiac disorders
    • Doetschman T, Shull M, Kier A, Coffin JD. Embryonic stem cell model systems for vascular morphogenesis and cardiac disorders. Hypertension 1993;22:618-29.
    • (1993) Hypertension , vol.22 , pp. 618-629
    • Doetschman, T.1    Shull, M.2    Kier, A.3    Coffin, J.D.4
  • 137
    • 0031172872 scopus 로고    scopus 로고
    • Retinoic acid accelerates embryonic stem cell-derived cardiac differentiation and enhances development of ventricular cardiomyocytes
    • Wobus AM, Kaomei G, Shan J, Wellner MC, Rohwedel J, Ji G, et al. Retinoic acid accelerates embryonic stem cell-derived cardiac differentiation and enhances development of ventricular cardiomyocytes. J Mol Cell Cardiol 1997;29:1525-39.
    • (1997) J. Mol. Cell Cardiol. , vol.29 , pp. 1525-1539
    • Wobus, A.M.1    Kaomei, G.2    Shan, J.3    Wellner, M.C.4    Rohwedel, J.5    Ji, G.6
  • 140
    • 0034781151 scopus 로고    scopus 로고
    • Gene therapy of mitochondrial DNA mutations: A brief, biased history of allotopic expression in mammalian cells
    • Zullo SJ. Gene therapy of mitochondrial DNA mutations: a brief, biased history of allotopic expression in mammalian cells. Semin Neurol 2001;21:327-35.
    • (2001) Semin. Neurol. , vol.21 , pp. 327-335
    • Zullo, S.J.1
  • 141
    • 0034959104 scopus 로고    scopus 로고
    • Mitochondria transfection by oligonucleotides containing a signal peptide and vectorized by cationic liposomes
    • Geromel V, Cao A, Briane D, Vassy J, Rotig A, Rustin P, et al. Mitochondria transfection by oligonucleotides containing a signal peptide and vectorized by cationic liposomes. Antisense Nucleic Acid Drug Dev 2001;11:175-80.
    • (2001) Antisense Nucleic Acid Drug Dev. , vol.11 , pp. 175-180
    • Geromel, V.1    Cao, A.2    Briane, D.3    Vassy, J.4    Rotig, A.5    Rustin, P.6
  • 143
    • 0034989736 scopus 로고    scopus 로고
    • Towards mitochondrial gene therapy: DQAsomes as a strategy
    • Weissig V, Torchilin VP. Towards mitochondrial gene therapy: DQAsomes as a strategy. J Drug Target 2001;9:1-13.
    • (2001) J. Drug Target , vol.9 , pp. 1-13
    • Weissig, V.1    Torchilin, V.P.2
  • 144
    • 0036544631 scopus 로고    scopus 로고
    • Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus
    • Manfredi G, Fu J, Ojaimi J, Sadlock JE, Kwong JQ, Guy J, et al. Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus. Nat Genet 2002;30:394-9.
    • (2002) Nat. Genet. , vol.30 , pp. 394-399
    • Manfredi, G.1    Fu, J.2    Ojaimi, J.3    Sadlock, J.E.4    Kwong, J.Q.5    Guy, J.6
  • 145
    • 0030799693 scopus 로고    scopus 로고
    • A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA (Leu) (UUR) 3254C-to-G
    • Kawarai T, Kawakami H, Kozuka K, Izumi Y, Matsuyama Z, Watanabe C, et al. A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA (Leu) (UUR) 3254C-to-G. Neurology 1997;49:598-600.
    • (1997) Neurology , vol.49 , pp. 598-600
    • Kawarai, T.1    Kawakami, H.2    Kozuka, K.3    Izumi, Y.4    Matsuyama, Z.5    Watanabe, C.6
  • 146
    • 0035058912 scopus 로고    scopus 로고
    • The mitochondrial DNA mutation T12297C affects a highly conserved nucleotide of tRNA (Len (CUN)) and is associated with dilated cardiomyopathy
    • Grasso M, Diegoli M, Brega A, Campana C, Tavazzi L, Arbustini E. The mitochondrial DNA mutation T12297C affects a highly conserved nucleotide of tRNA (Len (CUN)) and is associated with dilated cardiomyopathy. Eur J Hum Genet 2001;9: 311-5.
    • (2001) Eur. J. Hum. Genet. , vol.9 , pp. 311-315
    • Grasso, M.1    Diegoli, M.2    Brega, A.3    Campana, C.4    Tavazzi, L.5    Arbustini, E.6
  • 147
    • 0025260002 scopus 로고
    • Mitochondrial mutation in fatal infantile cardiomyopathy
    • Tanaka M, Ino H, Ohno K, Hattori K, Sato W, Ozawa T, et al. Mitochondrial mutation in fatal infantile cardiomyopathy. Lancet 1990;336:1452.
    • (1990) Lancet , vol.336 , pp. 1452
    • Tanaka, M.1    Ino, H.2    Ohno, K.3    Hattori, K.4    Sato, W.5    Ozawa, T.6
  • 148
    • 0029835998 scopus 로고    scopus 로고
    • An additional mitochondrial tRNA (Ile)point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy
    • Merante F, Myint T, Tein I, Benson L, Robinson BH. An additional mitochondrial tRNA (Ile)point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy. Hum Mutat 1996;8:216-22.
    • (1996) Hum. Mutat. , vol.8 , pp. 216-222
    • Merante, F.1    Myint, T.2    Tein, I.3    Benson, L.4    Robinson, B.H.5
  • 149
    • 0036135162 scopus 로고    scopus 로고
    • Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentations
    • Corona P, Lamantea E, Greco M, Carrara F, Agostino A, Guidetti D, et al. Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentations. Ann Neurol 2002;51: 118-22.
    • (2002) Ann. Neurol. , vol.51 , pp. 118-122
    • Corona, P.1    Lamantea, E.2    Greco, M.3    Carrara, F.4    Agostino, A.5    Guidetti, D.6
  • 150
    • 0034164636 scopus 로고    scopus 로고
    • Fatal hypertrophic cardiomyopathy associated with an A8296G mutation in the mitochondrial tRNA(Lys)gene
    • Akita Y, Koga Y, Iwanaga R, Wada N, Tsubone J, Fukuda S, et al. Fatal hypertrophic cardiomyopathy associated with an A8296G mutation in the mitochondrial tRNA(Lys)gene. Hum Mutat 2000;15:382.
    • (2000) Hum. Mutat. , vol.15 , pp. 382
    • Akita, Y.1    Koga, Y.2    Iwanaga, R.3    Wada, N.4    Tsubone, J.5    Fukuda, S.6
  • 151
    • 0034939410 scopus 로고    scopus 로고
    • A case of cardiomyopathy showing progression from the hypertrophic to the dilated form: Association of Mt 8348A- >G mutation in the mitochondrial tRNA (Lys) gene with severe ultrastructural alterations of mitochondria in cardiomyocytes
    • Terasaki F, Tanaka M, Kawamura K, Kanzaki Y, Okabe M, Hayashi T, et al. A case of cardiomyopathy showing progression from the hypertrophic to the dilated form: association of Mt 8348A- >G mutation in the mitochondrial tRNA (Lys) gene with severe ultrastructural alterations of mitochondria in cardiomyocytes. Jpn Circ J 2001;65:691-4.
    • (2001) Jpn. Circ. J. , vol.65 , pp. 691-694
    • Terasaki, F.1    Tanaka, M.2    Kawamura, K.3    Kanzaki, Y.4    Okabe, M.5    Hayashi, T.6
  • 152
    • 0034910767 scopus 로고    scopus 로고
    • A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathy
    • Karadimas C, Tanji K, Geremek M, Chronopoulou P, Vu T, Krishna S, et al. A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathy. J Child Neurol 2001;16:531-3.
    • (2001) J. Child Neurol. , vol.16 , pp. 531-533
    • Karadimas, C.1    Tanji, K.2    Geremek, M.3    Chronopoulou, P.4    Vu, T.5    Krishna, S.6
  • 153
    • 0034926430 scopus 로고    scopus 로고
    • A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy
    • Hsieh RH, Li JY, Pang CY, Wei YH. A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy. J Biomed Sci 2001;8:328-35.
    • (2001) J. Biomed. Sci. , vol.8 , pp. 328-335
    • Hsieh, R.H.1    Li, J.Y.2    Pang, C.Y.3    Wei, Y.H.4
  • 154
    • 0026468520 scopus 로고
    • Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy
    • Obayashi T, Hattori K, Sugiyama S, Tanaka M, Tanaka T, Itoyama S, et al. Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy. Am Heart J 1992;124:1263-9.
    • (1992) Am. Heart J. , vol.124 , pp. 1263-1269
    • Obayashi, T.1    Hattori, K.2    Sugiyama, S.3    Tanaka, M.4    Tanaka, T.5    Itoyama, S.6
  • 156
    • 0033888963 scopus 로고    scopus 로고
    • A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy
    • Andreu AL, Checcarelli N, Iwata S, Shanske S, DiMauro S. A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy. Pediatr Res 2000;48:311-4.
    • (2000) Pediatr. Res. , vol.48 , pp. 311-314
    • Andreu, A.L.1    Checcarelli, N.2    Iwata, S.3    Shanske, S.4    DiMauro, S.5
  • 157
    • 0032807973 scopus 로고    scopus 로고
    • A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase deficiency
    • Valnot I, Kassis J, Chretien D, de Lonlay P, Parfait B, Munnich A, et al. A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase deficiency. Hum Genet 1999;104:460-6.
    • (1999) Hum. Genet. , vol.104 , pp. 460-466
    • Valnot, I.1    Kassis, J.2    Chretien, D.3    de Lonlay, P.4    Parfait, B.5    Munnich, A.6


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