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Volumn 71, Issue 3, 2008, Pages 434-438

Dystrophin: From non-ischemic cardiomyopathy to ischemic cardiomyopathy

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN;

EID: 47549086497     PISSN: 03069877     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mehy.2008.04.004     Document Type: Article
Times cited : (2)

References (26)
  • 1
    • 2342621479 scopus 로고    scopus 로고
    • The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma
    • Lapidos K.A., Kakkar R., and McNally E.M. The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma. Circ Res 94 (2004) 1023-1031
    • (2004) Circ Res , vol.94 , pp. 1023-1031
    • Lapidos, K.A.1    Kakkar, R.2    McNally, E.M.3
  • 2
    • 0034612267 scopus 로고    scopus 로고
    • Distinct patterns of dystrophin organization in myocyte sarcolemma and transverse tubules of normal and diseased human myocardium
    • Kaprielian R.R., Stevenson S., Rothery S.M., Cullen M.J., and Severs N.J. Distinct patterns of dystrophin organization in myocyte sarcolemma and transverse tubules of normal and diseased human myocardium. Circulation 101 (2000) 2586-2594
    • (2000) Circulation , vol.101 , pp. 2586-2594
    • Kaprielian, R.R.1    Stevenson, S.2    Rothery, S.M.3    Cullen, M.J.4    Severs, N.J.5
  • 3
    • 0024582731 scopus 로고
    • Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus
    • Feener C.A., Koenig M., and Kunkel L.M. Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus. Nature 338 (1989) 509-511
    • (1989) Nature , vol.338 , pp. 509-511
    • Feener, C.A.1    Koenig, M.2    Kunkel, L.M.3
  • 4
    • 0034997703 scopus 로고    scopus 로고
    • Dystrophin-deficient myocardium is vulnerable to pressure overload in vivo
    • Kamogawa Y., Biro S., Maeda M., et al. Dystrophin-deficient myocardium is vulnerable to pressure overload in vivo. Cardiovasc Res 50 (2001) 509-515
    • (2001) Cardiovasc Res , vol.50 , pp. 509-515
    • Kamogawa, Y.1    Biro, S.2    Maeda, M.3
  • 5
    • 0033165780 scopus 로고    scopus 로고
    • Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart muscle disease study group
    • Mestroni L., Rocco C., Gregori D., et al. Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart muscle disease study group. J Am Coll Cardiol 34 (1999) 181-190
    • (1999) J Am Coll Cardiol , vol.34 , pp. 181-190
    • Mestroni, L.1    Rocco, C.2    Gregori, D.3
  • 6
    • 0030066219 scopus 로고    scopus 로고
    • Dystrophin expression in muscles of mdx mice after adenovirus-mediated in vivo gene transfer
    • Acsadi G., Lochmuller H., Jani A., et al. Dystrophin expression in muscles of mdx mice after adenovirus-mediated in vivo gene transfer. Hum Gene Ther 7 (1996) 129-140
    • (1996) Hum Gene Ther , vol.7 , pp. 129-140
    • Acsadi, G.1    Lochmuller, H.2    Jani, A.3
  • 7
    • 27144512277 scopus 로고    scopus 로고
    • Cardiac involvement in muscular dystrophies: molecular mechanisms
    • Goodwin F.C., and Muntoni F. Cardiac involvement in muscular dystrophies: molecular mechanisms. Muscle Nerve 32 (2005) 577-588
    • (2005) Muscle Nerve , vol.32 , pp. 577-588
    • Goodwin, F.C.1    Muntoni, F.2
  • 8
    • 0034058436 scopus 로고    scopus 로고
    • Altered membrane proteins and permeability correlate with cardiac dysfunction in cardiomyopathic hamsters
    • Ikeda Y., Martone M., Gu Y., et al. Altered membrane proteins and permeability correlate with cardiac dysfunction in cardiomyopathic hamsters. Am J Physiol Heart Circ Physiol 278 (2000) H1362-H1370
    • (2000) Am J Physiol Heart Circ Physiol , vol.278
    • Ikeda, Y.1    Martone, M.2    Gu, Y.3
  • 9
    • 34547904662 scopus 로고    scopus 로고
    • Novel mutation in splicing donor of dystrophin gene first exon in a patient with dilated cardiomyopathy but no clinical signs of skeletal myopathy
    • Kimura S., Ikezawa M., Ozasa S., et al. Novel mutation in splicing donor of dystrophin gene first exon in a patient with dilated cardiomyopathy but no clinical signs of skeletal myopathy. J Child Neurol 22 (2007) 901-906
    • (2007) J Child Neurol , vol.22 , pp. 901-906
    • Kimura, S.1    Ikezawa, M.2    Ozasa, S.3
  • 10
    • 0035403114 scopus 로고    scopus 로고
    • Dystrophin-deficient cardiomyocytes are abnormally vulnerable to mechanical stress-induced contractile failure and injury
    • Danialou G., Comtois A.S., Dudley R., et al. Dystrophin-deficient cardiomyocytes are abnormally vulnerable to mechanical stress-induced contractile failure and injury. FASEB J 15 (2001) 1655-1657
    • (2001) FASEB J , vol.15 , pp. 1655-1657
    • Danialou, G.1    Comtois, A.S.2    Dudley, R.3
  • 12
    • 0028964364 scopus 로고
    • Myoblast transfer and gene therapy in muscular dystrophies
    • Pagel C.N., and Morgan J.E. Myoblast transfer and gene therapy in muscular dystrophies. Microsc Res Tech 30 (1995) 469-479
    • (1995) Microsc Res Tech , vol.30 , pp. 469-479
    • Pagel, C.N.1    Morgan, J.E.2
  • 13
    • 13944271703 scopus 로고    scopus 로고
    • Transfer of the full-length dystrophin-coding sequence into muscle cells by a dual high-capacity hybrid viral vector with site-specific integration ability
    • Goncalves M.A., van Nierop G.P., Tijssen M.R., et al. Transfer of the full-length dystrophin-coding sequence into muscle cells by a dual high-capacity hybrid viral vector with site-specific integration ability. J Virol 79 (2005) 3146-3162
    • (2005) J Virol , vol.79 , pp. 3146-3162
    • Goncalves, M.A.1    van Nierop, G.P.2    Tijssen, M.R.3
  • 14
    • 5444275698 scopus 로고    scopus 로고
    • Recombinant adeno-associated viral (rAAV) vectors as therapeutic tools for Duchenne muscular dystrophy (DMD)
    • Athanasopoulos T., Graham I.R., Foster H., and Dickson G. Recombinant adeno-associated viral (rAAV) vectors as therapeutic tools for Duchenne muscular dystrophy (DMD). Gene Ther 11 Suppl. 1 (2004) S109-S121
    • (2004) Gene Ther , vol.11 , Issue.SUPPL. 1
    • Athanasopoulos, T.1    Graham, I.R.2    Foster, H.3    Dickson, G.4
  • 15
    • 34249337407 scopus 로고    scopus 로고
    • Systemic administration of micro-dystrophin restores cardiac geometry and prevents dobutamine-induced cardiac pump failure
    • Townsend D., Blankinship M.J., Allen J.M., Gregorevic P., Chamberlain J.S., and Metzger J.M. Systemic administration of micro-dystrophin restores cardiac geometry and prevents dobutamine-induced cardiac pump failure. Mol Ther 15 (2007) 1086-1092
    • (2007) Mol Ther , vol.15 , pp. 1086-1092
    • Townsend, D.1    Blankinship, M.J.2    Allen, J.M.3    Gregorevic, P.4    Chamberlain, J.S.5    Metzger, J.M.6
  • 16
    • 0141841602 scopus 로고    scopus 로고
    • Microdystrophin gene therapy of cardiomyopathy restores dystrophin-glycoprotein complex and improves sarcolemma integrity in the mdx mouse heart
    • Yue Y., Li Z., Harper S.Q., Davisson R.L., Chamberlain J.S., and Duan D. Microdystrophin gene therapy of cardiomyopathy restores dystrophin-glycoprotein complex and improves sarcolemma integrity in the mdx mouse heart. Circulation 108 (2003) 1626-1632
    • (2003) Circulation , vol.108 , pp. 1626-1632
    • Yue, Y.1    Li, Z.2    Harper, S.Q.3    Davisson, R.L.4    Chamberlain, J.S.5    Duan, D.6
  • 17
    • 0033758449 scopus 로고    scopus 로고
    • Animal models for muscular dystrophy: valuable tools for the development of therapies
    • Allamand V., and Campbell K.P. Animal models for muscular dystrophy: valuable tools for the development of therapies. Hum Mol Genet 9 (2000) 2459-2467
    • (2000) Hum Mol Genet , vol.9 , pp. 2459-2467
    • Allamand, V.1    Campbell, K.P.2
  • 18
    • 0034665285 scopus 로고    scopus 로고
    • Dissociation of sarcoglycans and the dystrophin carboxyl terminus from the sarcolemma in enteroviral cardiomyopathy
    • Lee G.H., Badorff C., and Knowlton K.U. Dissociation of sarcoglycans and the dystrophin carboxyl terminus from the sarcolemma in enteroviral cardiomyopathy. Circ Res 87 (2000) 489-495
    • (2000) Circ Res , vol.87 , pp. 489-495
    • Lee, G.H.1    Badorff, C.2    Knowlton, K.U.3
  • 19
    • 0033017374 scopus 로고    scopus 로고
    • Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy
    • Badorff C., Lee G.H., Lamphear B.J., et al. Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy. Nat Med 5 (1999) 320-326
    • (1999) Nat Med , vol.5 , pp. 320-326
    • Badorff, C.1    Lee, G.H.2    Lamphear, B.J.3
  • 20
    • 0036872209 scopus 로고    scopus 로고
    • Enteroviruses prefer the dystrophin-deficient heart
    • Chopra V. Enteroviruses prefer the dystrophin-deficient heart. Clin Genet 62 (2002) 370-372
    • (2002) Clin Genet , vol.62 , pp. 370-372
    • Chopra, V.1
  • 21
    • 0037232204 scopus 로고    scopus 로고
    • Left ventricular systolic dysfunction and ischemic cardiomyopathy
    • Henry L.B. Left ventricular systolic dysfunction and ischemic cardiomyopathy. Crit Care Nurs Q 26 (2003) 16-21
    • (2003) Crit Care Nurs Q , vol.26 , pp. 16-21
    • Henry, L.B.1
  • 22
    • 0842282918 scopus 로고    scopus 로고
    • Why do patients with ischemic cardiomyopathy and a substantial amount of viable myocardium not always recover in function after revascularization?
    • Schinkel A.F., Poldermans D., Rizzello V., et al. Why do patients with ischemic cardiomyopathy and a substantial amount of viable myocardium not always recover in function after revascularization?. J Thorac Cardiovasc Surg 127 (2004) 385-390
    • (2004) J Thorac Cardiovasc Surg , vol.127 , pp. 385-390
    • Schinkel, A.F.1    Poldermans, D.2    Rizzello, V.3
  • 23
    • 33646069690 scopus 로고    scopus 로고
    • Dystrophin is a possible end-target of ischemic preconditioning against cardiomyocyte oncosis during the early phase of reperfusion
    • Kyoi S., Otani H., Hamano A., et al. Dystrophin is a possible end-target of ischemic preconditioning against cardiomyocyte oncosis during the early phase of reperfusion. Cardiovasc Res 70 (2006) 354-363
    • (2006) Cardiovasc Res , vol.70 , pp. 354-363
    • Kyoi, S.1    Otani, H.2    Hamano, A.3
  • 24
    • 17844363973 scopus 로고    scopus 로고
    • Ischemia depletes dystrophin and inhibits protein synthesis in the canine heart: mechanisms of myocardial ischemic injury
    • Rodriguez M., Cai W.J., Kostin S., Lucchesi B.R., and Schaper J. Ischemia depletes dystrophin and inhibits protein synthesis in the canine heart: mechanisms of myocardial ischemic injury. J Mol Cell Cardiol 38 (2005) 723-733
    • (2005) J Mol Cell Cardiol , vol.38 , pp. 723-733
    • Rodriguez, M.1    Cai, W.J.2    Kostin, S.3    Lucchesi, B.R.4    Schaper, J.5
  • 25
    • 0034955468 scopus 로고    scopus 로고
    • Ischemic loss of sarcolemmal dystrophin and spectrin: correlation with myocardial injury
    • Armstrong S.C., Latham C.A., Shivell C.L., and Ganote C.E. Ischemic loss of sarcolemmal dystrophin and spectrin: correlation with myocardial injury. J Mol Cell Cardiol 33 (2001) 1165-1179
    • (2001) J Mol Cell Cardiol , vol.33 , pp. 1165-1179
    • Armstrong, S.C.1    Latham, C.A.2    Shivell, C.L.3    Ganote, C.E.4
  • 26
    • 3042672852 scopus 로고    scopus 로고
    • Ischemic preconditioning-mediated restoration of membrane dystrophin during reperfusion correlates with protection against contraction-induced myocardial injury
    • Kido M., Otani H., Kyoi S., et al. Ischemic preconditioning-mediated restoration of membrane dystrophin during reperfusion correlates with protection against contraction-induced myocardial injury. Am J Physiol Heart Circ Physiol 287 (2004) H81-H90
    • (2004) Am J Physiol Heart Circ Physiol , vol.287
    • Kido, M.1    Otani, H.2    Kyoi, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.