메뉴 건너뛰기




Volumn 38, Issue 3, 2009, Pages 323-336

Dystrophic pathology in the intrinsic and extrinsic laryngeal muscles in the mdx mouse

Author keywords

Degeneration; Duchenne muscular dystrophy; Intrinsic laryngeal; mdx; Skeletal muscle

Indexed keywords

BETA DYSTROGLYCAN; CAVEOLIN 3; DYSTROPHIN; EVANS BLUE; UTROPHIN;

EID: 67049160572     PISSN: 19160216     EISSN: None     Source Type: Journal    
DOI: 10.2310/7070.2009.080102     Document Type: Article
Times cited : (8)

References (58)
  • 1
    • 0023614188 scopus 로고
    • Dystrophin: The protein product of the Duchenne muscular dystrophy locus
    • Hoffman EP, Brown RH, Kunkel LM. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 1987;51: 919-928
    • (1987) Cell , vol.51 , pp. 919-928
    • Hoffman, E.P.1    Brown, R.H.2    Kunkel, L.M.3
  • 2
    • 0027275643 scopus 로고
    • A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin
    • Ervasti JM, Campbell KP. A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. J Cell Biol 1993;122:809-823
    • (1993) J Cell Biol , vol.122 , pp. 809-823
    • Ervasti, J.M.1    Campbell, K.P.2
  • 3
    • 0034665276 scopus 로고    scopus 로고
    • Dystrophin associates with caveolae of rat cardiac myocytes
    • Doyle DD, Goings G, Upshaw-Earley J, et al. Dystrophin associates with caveolae of rat cardiac myocytes. Circ Res 2000;87:480-488
    • (2000) Circ Res , vol.87 , pp. 480-488
    • Doyle, D.D.1    Goings, G.2    Upshaw-Earley, J.3
  • 4
    • 0026782972 scopus 로고
    • Differential expression of muscular dystrophy in diaphragm versus hindlimb muscles of mdx mice
    • Dupont-Versteegden EE, McCarter RJ. Differential expression of muscular dystrophy in diaphragm versus hindlimb muscles of mdx mice. Muscle Nerve 1992;15:1105-1110
    • (1992) Muscle Nerve , vol.15 , pp. 1105-1110
    • Dupont-Versteegden, E.E.1    McCarter, R.J.2
  • 5
    • 0027729004 scopus 로고
    • Morphometric analysis of mdx diaphragm muscle fibres. Comparison with hindlimb muscles
    • Louboutin JP, Fichter-Gagnepain V, Thaon E, Fardeau M. Morphometric analysis of mdx diaphragm muscle fibres. Comparison with hindlimb muscles. Neuromuscul Disord 1993; 3:463-469
    • (1993) Neuromuscul Disord , vol.3 , pp. 463-469
    • Louboutin, J.P.1    Fichter-Gagnepain, V.2    Thaon, E.3    Fardeau, M.4
  • 6
    • 0033970498 scopus 로고    scopus 로고
    • Eye muscle sparing by the muscular dystrophies: Lessons to be learned?
    • Andrade FH, Porter JD, Kaminski HJ. Eye muscle sparing by the muscular dystrophies: lessons to be learned? Microsc Res Tech 2000;48:192-203.
    • (2000) Microsc Res Tech , vol.48 , pp. 192-203
    • Andrade, F.H.1    Porter, J.D.2    Kaminski, H.J.3
  • 7
    • 0026795393 scopus 로고
    • Extraocular muscles are spared in advanced Duchenne dystrophy
    • Kaminski HJ, al-Hakim M, Leigh RJ, et al. Extraocular muscles are spared in advanced Duchenne dystrophy. Ann Neurol 1992;32: 586-588
    • (1992) Ann Neurol , vol.32 , pp. 586-588
    • Kaminski, H.J.1    Al-Hakim, M.2    Leigh, R.J.3
  • 8
    • 0029143830 scopus 로고
    • Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: Role for calcium homeostasis in extraocular muscle sparing
    • Khurana TS, Prendergast RA, Alameddine HS, et al. Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing. J Exp Med 1995;182:467-475
    • (1995) J Exp Med , vol.182 , pp. 467-475
    • Khurana, T.S.1    Prendergast, R.A.2    Alameddine, H.S.3
  • 9
    • 0038661155 scopus 로고    scopus 로고
    • Constitutive properties, not molecular adaptations, mediate extraocular muscle sparing in dystrophic mdx mice
    • Porter JD, Merriam AP, Khanna S, et al. Constitutive properties, not molecular adaptations, mediate extraocular muscle sparing in dystrophic mdx mice. FASEB J 2003;17:893-895
    • (2003) FASEB J , vol.17 , pp. 893-895
    • Porter, J.D.1    Merriam, A.P.2    Khanna, S.3
  • 10
    • 0019429034 scopus 로고
    • Histological and ultrastructural findings in the vocal muscles of patients suffering from muscular dystrophies
    • Manolides L, Baloyannis S. Histological and ultrastructural findings in the vocal muscles of patients suffering from muscular dystrophies. Arch Otorhinolaryngol 1981;230:181-188
    • (1981) Arch Otorhinolaryngol , vol.230 , pp. 181-188
    • Manolides, L.1    Baloyannis, S.2
  • 11
    • 33847684752 scopus 로고    scopus 로고
    • Intrinsic laryngeal muscles are spared from myonecrosis in the mdx mouse model of Duchenne muscular dystrophy
    • Marques MJ, Ferretti R, Vomero VU, et al. Intrinsic laryngeal muscles are spared from myonecrosis in the mdx mouse model of Duchenne muscular dystrophy. Muscle Nerve 2007;35:349-353
    • (2007) Muscle Nerve , vol.35 , pp. 349-353
    • Marques, M.J.1    Ferretti, R.2    Vomero, V.U.3
  • 12
    • 0031974681 scopus 로고    scopus 로고
    • Reading ability and processing in Duchenne muscular dystrophy and spinal muscular atrophy
    • Billard C, Gillet P, Barthez M, et al. Reading ability and processing in Duchenne muscular dystrophy and spinal muscular atrophy. Dev Med Child Neurol 1998;40:12-20.
    • (1998) Dev Med Child Neurol , vol.40 , pp. 12-20
    • Billard, C.1    Gillet, P.2    Barthez, M.3
  • 14
    • 2442699165 scopus 로고    scopus 로고
    • Developmental progress in Duchenne muscular dystrophy: Lessons for earlier detection
    • Parsons EP, Clarke AJ, Bradley DM. Developmental progress in Duchenne muscular dystrophy: lessons for earlier detection. Eur J Paediatr Neurol 2004;8:145-153
    • (2004) Eur J Paediatr Neurol , vol.8 , pp. 145-153
    • Parsons, E.P.1    Clarke, A.J.2    Bradley, D.M.3
  • 15
    • 1342282774 scopus 로고    scopus 로고
    • Specific cognitive deficits are common in children with Duchenne muscular dystrophy
    • Wicksell RK, Kihlgren M, Melin L, Eeg-Olofsson O. Specific cognitive deficits are common in children with Duchenne muscular dystrophy. Dev Med Child Neurol 2004;46:154-159
    • (2004) Dev Med Child Neurol , vol.46 , pp. 154-159
    • Wicksell, R.K.1    Kihlgren, M.2    Melin, L.3    Eeg-Olofsson, O.4
  • 16
    • 0033910264 scopus 로고    scopus 로고
    • Severe mechanical dysfunction in pharyngeal muscle from adult mdx mice
    • Attal P, Lambert F, Marchand-Adam S, et al. Severe mechanical dysfunction in pharyngeal muscle from adult mdx mice. Am J Respir Crit Care Med 2000;162:78-281.
    • (2000) Am J Respir Crit Care Med , vol.162 , pp. 78-281
    • Attal, P.1    Lambert, F.2    Marchand-Adam, S.3
  • 18
    • 13444271582 scopus 로고    scopus 로고
    • Laryngeal muscle fibre types
    • Hoh JFY. Laryngeal muscle fibre types. Acta Physiol Scand 2005; 183:133-149
    • (2005) Acta Physiol Scand , vol.183 , pp. 133-149
    • Hoh, J.F.Y.1
  • 19
    • 33144464298 scopus 로고    scopus 로고
    • Effect of recurrent laryngeal nerve section on the laryngeal muscles of adult rabbits
    • Shinners MJ, Goding GS, McLoon LK. Effect of recurrent laryngeal nerve section on the laryngeal muscles of adult rabbits. Otolaryngol Head Neck Surg 2006;134:413-418
    • (2006) Otolaryngol Head Neck Surg , vol.134 , pp. 413-418
    • Shinners, M.J.1    Goding, G.S.2    McLoon, L.K.3
  • 20
    • 0029562175 scopus 로고
    • Diagnosis and treatment of unilateral cricothyroid muscle paralysis with a modified Isshiki type 4 thyroplasty
    • Shaw GY, Searle JP, Hoover LA. Diagnosis and treatment of unilateral cricothyroid muscle paralysis with a modified Isshiki type 4 thyroplasty. Otolaryngol Head Neck Surg 1995;113:679-688
    • (1995) Otolaryngol Head Neck Surg , vol.113 , pp. 679-688
    • Shaw, G.Y.1    Searle, J.P.2    Hoover, L.A.3
  • 21
  • 22
    • 0024499349 scopus 로고
    • Respiratory functions of the larynx
    • Bartlett D. Respiratory functions of the larynx. Physiol Rev 1989; 69:33-57.
    • (1989) Physiol Rev , vol.69 , pp. 33-57
    • Bartlett, D.1
  • 23
    • 0025828693 scopus 로고
    • Respiratory-related activity of cricothyroid muscle in awake normal humans
    • Wheatley JR, Brancatisano A, Engel LA. Respiratory-related activity of cricothyroid muscle in awake normal humans. J Appl Physiol 1991;70:2226-2232
    • (1991) J Appl Physiol , vol.70 , pp. 2226-2232
    • Wheatley, J.R.1    Brancatisano, A.2    Engel, L.A.3
  • 24
    • 0034035867 scopus 로고    scopus 로고
    • Current concepts of respiratory complications of neuromuscular disease in children
    • Schramm CM. Current concepts of respiratory complications of neuromuscular disease in children. Curr Opin Pediatr 2000;12: 203-207
    • (2000) Curr Opin Pediatr , vol.12 , pp. 203-207
    • Schramm, C.M.1
  • 25
    • 33751320375 scopus 로고    scopus 로고
    • Feeding problems and weight gain in Duchenne muscular dystrophy
    • Pane M, Vasta I, Messina S, et al. Feeding problems and weight gain in Duchenne muscular dystrophy. Eur J Paediatr Neurol 2006; 10:231-236
    • (2006) Eur J Paediatr Neurol , vol.10 , pp. 231-236
    • Pane, M.1    Vasta, I.2    Messina, S.3
  • 26
    • 0028431769 scopus 로고
    • Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathies
    • Sahashi K, Ibi T, Suoh H, et al. Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathies. Intern Med 1994;33:277-283
    • (1994) Intern Med , vol.33 , pp. 277-283
    • Sahashi, K.1    Ibi, T.2    Suoh, H.3
  • 27
    • 0028910144 scopus 로고
    • Characterization of revertant muscle fibers in Duchenne muscular dystrophy, using exon-specific monoclonal antibodies against dystrophin
    • Thanh LT, Nguyen TM, Helliwell TR, Morris GE. Characterization of revertant muscle fibers in Duchenne muscular dystrophy, using exon-specific monoclonal antibodies against dystrophin. Am J Hum Genet 1995;56:725-731
    • (1995) Am J Hum Genet , vol.56 , pp. 725-731
    • Thanh, L.T.1    Nguyen, T.M.2    Helliwell, T.R.3    Morris, G.E.4
  • 28
    • 0030767225 scopus 로고    scopus 로고
    • Revertant fibres: A possible genetic therapy for Duchenne muscular dystrophy?
    • Wilton SD, Dye DE, Blechynden LM, Laing NG. Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy? Neuromuscul Disord 1997;7:329-335
    • (1997) Neuromuscul Disord , vol.7 , pp. 329-335
    • Wilton, S.D.1    Dye, D.E.2    Blechynden, L.M.3    Laing, N.G.4
  • 29
    • 0027176661 scopus 로고
    • Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin
    • Matsumura K, Tome FMS, Ionasescu V, et al. Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin. J Clin Invest 1993;92:866-871
    • (1993) J Clin Invest , vol.92 , pp. 866-871
    • Matsumura, K.1    Tome, F.M.S.2    Ionasescu, V.3
  • 30
    • 0027481238 scopus 로고
    • Duchenne muscular dystrophy: Deficiency of dystrophin-associated proteins in the sarcolemma
    • Ohlendieck K, Matsumura K, Ionasescu VV, et al. Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma. Neurology 1993;43:795-800.
    • (1993) Neurology , vol.43 , pp. 795-800
    • Ohlendieck, K.1    Matsumura, K.2    Ionasescu, V.V.3
  • 31
    • 0036188005 scopus 로고    scopus 로고
    • Distal mdx muscle groups exhibiting up-regulation of utrophin and rescue of dystrophin-associated glycoproteins exemplify a protected phenotype in muscular dystrophy
    • Dowling P, Culligan K, Ohlendieck K. Distal mdx muscle groups exhibiting up-regulation of utrophin and rescue of dystrophin-associated glycoproteins exemplify a protected phenotype in muscular dystrophy. Naturwissenschaften 2002;89:75-78
    • (2002) Naturwissenschaften , vol.89 , pp. 75-78
    • Dowling, P.1    Culligan, K.2    Ohlendieck, K.3
  • 32
    • 0038823857 scopus 로고    scopus 로고
    • Comparative analysis of Dp427-deficient mdx tissues shows that the milder dystrophic phenotype of extraocular and toe muscle fibres is associated with a persistent expression of β-dystroglycan
    • Dowling P, Lohan J, Ohlendieck K. Comparative analysis of Dp427-deficient mdx tissues shows that the milder dystrophic phenotype of extraocular and toe muscle fibres is associated with a persistent expression of β-dystroglycan. Eur J Cell Biol 2003;82: 222-230
    • (2003) Eur J Cell Biol , vol.82 , pp. 222-230
    • Dowling, P.1    Lohan, J.2    Ohlendieck, K.3
  • 33
    • 0028264218 scopus 로고
    • Talin, vinculin and DRP (utrophin) concentrations are increased at mdx myotendinous junctions following onset of necrosis
    • Law DJ, Allen DL, Tidball JG. Talin, vinculin and DRP (utrophin) concentrations are increased at mdx myotendinous junctions following onset of necrosis. J Cell Sci 1994;107:1477-1483
    • (1994) J Cell Sci , vol.107 , pp. 1477-1483
    • Law, D.J.1    Allen, D.L.2    Tidball, J.G.3
  • 34
    • 0026621608 scopus 로고
    • Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle
    • Matsumura K, Ervasti JM, Ohlendieck K, et al. Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle. Nature 1992;360:588-591
    • (1992) Nature , vol.360 , pp. 588-591
    • Matsumura, K.1    Ervasti, J.M.2    Ohlendieck, K.3
  • 35
    • 0026355180 scopus 로고
    • Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: Presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines
    • Nguyen M, Ellis JM, Love DR, et al. Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines. J Cell Biol 1991;115:1695-1700
    • (1991) J Cell Biol , vol.115 , pp. 1695-1700
    • Nguyen, M.1    Ellis, J.M.2    Love, D.R.3
  • 36
    • 0031824850 scopus 로고    scopus 로고
    • The sparing of extraocular muscle in dystrophinopathy is lost in mice lacking utrophin and dystrophin
    • Porter JD, Rafael JA, Ragusa RJ, et al. The sparing of extraocular muscle in dystrophinopathy is lost in mice lacking utrophin and dystrophin. J Cell Sci 1998;111:1801-1811
    • (1998) J Cell Sci , vol.111 , pp. 1801-1811
    • Porter, J.D.1    Rafael, J.A.2    Ragusa, R.J.3
  • 37
    • 0029906168 scopus 로고    scopus 로고
    • Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
    • Tinsley JM, Potter AC, Phelps SR, et al. Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene. Nature 1996;384:349-353
    • (1996) Nature , vol.384 , pp. 349-353
    • Tinsley, J.M.1    Potter, A.C.2    Phelps, S.R.3
  • 38
    • 0031727771 scopus 로고    scopus 로고
    • Expression of full-length utrophin prevents muscular dystrophy in mdx mice
    • Tinsley J, Deconcinck N, Fisher R, et al. Expression of full-length utrophin prevents muscular dystrophy in mdx mice. Nat Med 1998;4:1441-1444
    • (1998) Nat Med , vol.4 , pp. 1441-1444
    • Tinsley, J.1    Deconcinck, N.2    Fisher, R.3
  • 39
    • 0029160868 scopus 로고
    • Absence of correlation between utrophin localization and quantity and clinical severity in Duchenne/Becker dystrophies
    • Vainzof M, Passos-Bueno MR, Man N, Zatz M. Absence of correlation between utrophin localization and quantity and clinical severity in Duchenne/Becker dystrophies. Am J Med Genet 1995; 58:305-309
    • (1995) Am J Med Genet , vol.58 , pp. 305-309
    • Vainzof, M.1    Passos-Bueno, M.R.2    Man, N.3    Zatz, M.4
  • 40
    • 21144432458 scopus 로고    scopus 로고
    • Satellite cells and utrophin are not directly correlated with the degree of muscle damage in mdx mice
    • Yamane A, Akutsu S, Diekwisch TGH, Matsuda R. Satellite cells and utrophin are not directly correlated with the degree of muscle damage in mdx mice. Am J Physiol 2005;289:C42-8.
    • (2005) Am J Physiol , vol.289
    • Yamane, A.1    Akutsu, S.2    Diekwisch, T.G.H.3    Matsuda, R.4
  • 41
    • 0032496393 scopus 로고    scopus 로고
    • Caveolin-3 is not an integral component of the dystrophin glycoprotein complex
    • Crosbie RH, Yamada H, Venzke DP, et al. Caveolin-3 is not an integral component of the dystrophin glycoprotein complex. FEBS Lett 1998;427:279-282
    • (1998) FEBS Lett , vol.427 , pp. 279-282
    • Crosbie, R.H.1    Yamada, H.2    Venzke, D.P.3
  • 42
    • 0034532164 scopus 로고    scopus 로고
    • Caveolin-3 directly interacts with the C-terminal tail of beta-dystroglycan. Identification of a central WW-like domain within caveolin family members
    • Sotgia F, Lee JK, Das K, et al. Caveolin-3 directly interacts with the C-terminal tail of beta-dystroglycan. Identification of a central WW-like domain within caveolin family members. J Biol Chem 2000;275:38048-38058
    • (2000) J Biol Chem , vol.275 , pp. 38048-38058
    • Sotgia, F.1    Lee, J.K.2    Das, K.3
  • 43
    • 0039397709 scopus 로고    scopus 로고
    • Dissecting the interaction between nitric oxide synthase (NOS) and caveolin
    • Garcia-Cardena G, Martasek P, Masters BS, et al. Dissecting the interaction between nitric oxide synthase (NOS) and caveolin. J Biol Chem 1997;272:25437-25440
    • (1997) J Biol Chem , vol.272 , pp. 25437-25440
    • Garcia-Cardena, G.1    Martasek, P.2    Masters, B.S.3
  • 44
    • 0037124116 scopus 로고    scopus 로고
    • Inhibition of lipid raft-dependent signaling by a dystrophy-associated mutant of caveolin- 3
    • Carozzi AJ, Roy S, Morrow IC, et al. Inhibition of lipid raft-dependent signaling by a dystrophy-associated mutant of caveolin- 3. J Biol Chem 2002;277:17944-17949
    • (2002) J Biol Chem , vol.277 , pp. 17944-17949
    • Carozzi, A.J.1    Roy, S.2    Morrow, I.C.3
  • 45
    • 0033569755 scopus 로고    scopus 로고
    • Targeted downregulation of caveolin-3 is sufficient to inhibit myotube formation in differentiating C2C12 myoblasts
    • Galbiati F, Volonte D, Engelman JA, et al. Targeted downregulation of caveolin-3 is sufficient to inhibit myotube formation in differentiating C2C12 myoblasts. J Biol Chem 1999;274:30315-30321
    • (1999) J Biol Chem , vol.274 , pp. 30315-30321
    • Galbiati, F.1    Volonte, D.2    Engelman, J.A.3
  • 46
    • 22244467369 scopus 로고    scopus 로고
    • Modulation of the caveolin-3 and Akt status in caveolae by insulin resistance in H9c2 cardiomyoblasts
    • Ha H, Pak Y. Modulation of the caveolin-3 and Akt status in caveolae by insulin resistance in H9c2 cardiomyoblasts. Exp Mol Med 2005;37:169-178
    • (2005) Exp Mol Med , vol.37 , pp. 169-178
    • Ha, H.1    Pak, Y.2
  • 47
    • 0034603998 scopus 로고    scopus 로고
    • Receptor-activated phospholipase D is present in caveolin-3-enriched light membranes of C2C12 myotubes
    • Meacci E, Donati C, Cencetti F, et al. Receptor-activated phospholipase D is present in caveolin-3-enriched light membranes of C2C12 myotubes. FEBS Lett 2000;473:10-14
    • (2000) FEBS Lett , vol.473 , pp. 10-14
    • Meacci, E.1    Donati, C.2    Cencetti, F.3
  • 48
    • 0030760305 scopus 로고    scopus 로고
    • Association of phosphofructokinase-M with caveolin-3 in differentiated skeletal myotubes
    • Scherer PE, Lisanti MP. Association of phosphofructokinase-M with caveolin-3 in differentiated skeletal myotubes. J Biol Chem 1997;272:20698-20705
    • (1997) J Biol Chem , vol.272 , pp. 20698-20705
    • Scherer, P.E.1    Lisanti, M.P.2
  • 49
    • 0346121432 scopus 로고    scopus 로고
    • A caveolin-3 mutant that causes limb girdle muscular dystrophy type 1C disrupts Src localization and activity and induces apoptosis in skeletal myotubes
    • Smythe GM, Eby JC, Disatnik MH, Rando TA. A caveolin-3 mutant that causes limb girdle muscular dystrophy type 1C disrupts Src localization and activity and induces apoptosis in skeletal myotubes. J Cell Sci 2003;116:4739-4749
    • (2003) J Cell Sci , vol.116 , pp. 4739-4749
    • Smythe, G.M.1    Eby, J.C.2    Disatnik, M.H.3    Rando, T.A.4
  • 50
    • 33747362294 scopus 로고    scopus 로고
    • Altered caveolin-3 expression disrupts PI(3) kinase signaling leading to death of cultured muscle cells
    • Smythe GM, Rando TA. Altered caveolin-3 expression disrupts PI(3) kinase signaling leading to death of cultured muscle cells. Exp Cell Res 2006;312:2816-2825
    • (2006) Exp Cell Res , vol.312 , pp. 2816-2825
    • Smythe, G.M.1    Rando, T.A.2
  • 51
    • 0036096748 scopus 로고    scopus 로고
    • Intracellular retention of glycosylphosphatidyl inositol-linked proteins in caveolin-deficient cells
    • Sotgia F, Razani B, Bonuccelli G, et al. Intracellular retention of glycosylphosphatidyl inositol-linked proteins in caveolin-deficient cells. Mol Cell Biol 2002;22:3905-3926
    • (2002) Mol Cell Biol , vol.22 , pp. 3905-3926
    • Sotgia, F.1    Razani, B.2    Bonuccelli, G.3
  • 52
    • 0344412990 scopus 로고    scopus 로고
    • Phosphofructokinase muscle-specific isoform requires caveolin-3 expression for plasma membrane recruitment and caveolar targeting: Implications for the pathogenesis of caveolin-related muscle diseases
    • Sotgia F, Bonuccelli G, Minetti C, et al. Phosphofructokinase muscle-specific isoform requires caveolin-3 expression for plasma membrane recruitment and caveolar targeting: implications for the pathogenesis of caveolin-related muscle diseases. Am J Pathol 2003; 163:2619-2634
    • (2003) Am J Pathol , vol.163 , pp. 2619-2634
    • Sotgia, F.1    Bonuccelli, G.2    Minetti, C.3
  • 53
    • 0030662249 scopus 로고    scopus 로고
    • Interaction of neuronal nitric-oxide synthase with caveolin-3 in skeletal muscle. Identification of a novel caveolin scaffolding/inhibitory domain
    • Venema VJ, Ju H, Zou R, Venema RC. Interaction of neuronal nitric-oxide synthase with caveolin-3 in skeletal muscle. Identification of a novel caveolin scaffolding/inhibitory domain. J Biol Chem 1997;272:28187-28190
    • (1997) J Biol Chem , vol.272 , pp. 28187-28190
    • Venema, V.J.1    Ju, H.2    Zou, R.3    Venema, R.C.4
  • 54
    • 0141429991 scopus 로고    scopus 로고
    • Modulation of myoblast fusion by caveolin-3 in dystrophic skeletal muscle cells: Implications for Duchenne muscular dystrophy and limb-girdle muscular dystrophy- 1C
    • Volonte D, Peoples AJ, Galbiati F. Modulation of myoblast fusion by caveolin-3 in dystrophic skeletal muscle cells: implications for Duchenne muscular dystrophy and limb-girdle muscular dystrophy- 1C. Mol Biol Cell 2003;14:4075-4088
    • (2003) Mol Biol Cell , vol.14 , pp. 4075-4088
    • Volonte, D.1    Peoples, A.J.2    Galbiati, F.3
  • 55
    • 0032504045 scopus 로고    scopus 로고
    • Increased caveolin-3 levels in mdx mouse muscles
    • Vaghy PL, Fang J, Wu W, Vaghy LP. Increased caveolin-3 levels in mdx mouse muscles. FEBS Lett 1998;431:125-127
    • (1998) FEBS Lett , vol.431 , pp. 125-127
    • Vaghy, P.L.1    Fang, J.2    Wu, W.3    Vaghy, L.P.4
  • 56
    • 0033546753 scopus 로고    scopus 로고
    • Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy
    • Repetto S, Bado M, Broda P, et al. Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy. Biochem Biophys Res Commun 1999;261:547-550
    • (1999) Biochem Biophys Res Commun , vol.261 , pp. 547-550
    • Repetto, S.1    Bado, M.2    Broda, P.3
  • 57
    • 12944317278 scopus 로고    scopus 로고
    • Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-likemuscular dystrophy phenotype
    • Galbiati F, Volonte D, Chu JB, et al. Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-likemuscular dystrophy phenotype. Proc Natl Acad Sci U S A 2000;97:9689-9694
    • (2000) Proc Natl Acad Sci U S A , vol.97 , pp. 9689-9694
    • Galbiati, F.1    Volonte, D.2    Chu, J.B.3
  • 58
    • 33745856252 scopus 로고    scopus 로고
    • Hypertrophic response of Duchenne and limb-girdle muscular dystrophies is associated with activation of Akt pathway
    • Peter AK, Crosbie RH. Hypertrophic response of Duchenne and limb-girdle muscular dystrophies is associated with activation of Akt pathway. Exp Cell Res 2006;312:2580-2591
    • (2006) Exp Cell Res , vol.312 , pp. 2580-2591
    • Peter, A.K.1    Crosbie, R.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.