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Volumn 7, Issue 6, 2012, Pages

Homologous recombination mediates functional recovery of dysferlin deficiency following AAV5 gene transfer

Author keywords

[No Author keywords available]

Indexed keywords

ADENOVIRUS VECTOR; COMPLEMENTARY DNA; DYSFERLIN; MESSENGER RNA;

EID: 84862487885     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0039233     Document Type: Article
Times cited : (67)

References (48)
  • 1
    • 17344363640 scopus 로고    scopus 로고
    • A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
    • Bashir R, Britton S, Strachan T, Keers S, Vafiadaki E, et al. (1998) A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nat Genet 20: 37-42.
    • (1998) Nat Genet , vol.20 , pp. 37-42
    • Bashir, R.1    Britton, S.2    Strachan, T.3    Keers, S.4    Vafiadaki, E.5
  • 2
    • 17344365600 scopus 로고    scopus 로고
    • Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
    • Liu J, Aoki M, Illa I, Wu C, Fardeau M, et al. (1998) Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nat Genet 20: 31-36.
    • (1998) Nat Genet , vol.20 , pp. 31-36
    • Liu, J.1    Aoki, M.2    Illa, I.3    Wu, C.4    Fardeau, M.5
  • 3
    • 0035109410 scopus 로고    scopus 로고
    • Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype
    • Illa I, Serrano-Munuera C, Gallardo E, Lasa A, Rojas-Garcia R, et al. (2001) Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype. Ann Neurol 49: 130-134.
    • (2001) Ann Neurol , vol.49 , pp. 130-134
    • Illa, I.1    Serrano-Munuera, C.2    Gallardo, E.3    Lasa, A.4    Rojas-Garcia, R.5
  • 4
    • 39749105590 scopus 로고    scopus 로고
    • Complete fatty degeneration of lumbar erector spinae muscles caused by a primary dysferlinopathy
    • Seror P, Krahn M, Laforet P, Leturcq F, Maisonobe T, (2008) Complete fatty degeneration of lumbar erector spinae muscles caused by a primary dysferlinopathy. Muscle Nerve 37: 410-414.
    • (2008) Muscle Nerve , vol.37 , pp. 410-414
    • Seror, P.1    Krahn, M.2    Laforet, P.3    Leturcq, F.4    Maisonobe, T.5
  • 8
    • 84555223124 scopus 로고    scopus 로고
    • Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I
    • Rosales XQ, Moser SJ, Tran T, McCarthy B, Dunn N, et al. (2011) Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I. J Cardiovasc Magn Reson 13: 39.
    • (2011) J Cardiovasc Magn Reson , vol.13 , pp. 39
    • Rosales, X.Q.1    Moser, S.J.2    Tran, T.3    McCarthy, B.4    Dunn, N.5
  • 9
    • 36448994441 scopus 로고    scopus 로고
    • A translational approach for limb vascular delivery of the micro-dystrophin gene without high volume or high pressure for treatment of Duchenne muscular dystrophy
    • Rodino-Klapac LR, Janssen PM, Montgomery CL, Coley BD, Chicoine LG, et al. (2007) A translational approach for limb vascular delivery of the micro-dystrophin gene without high volume or high pressure for treatment of Duchenne muscular dystrophy. J Transl Med 5: 45.
    • (2007) J Transl Med , vol.5 , pp. 45
    • Rodino-Klapac, L.R.1    Janssen, P.M.2    Montgomery, C.L.3    Coley, B.D.4    Chicoine, L.G.5
  • 10
    • 74149085535 scopus 로고    scopus 로고
    • Persistent expression of FLAG-tagged micro dystrophin in nonhuman primates following intramuscular and vascular delivery
    • Rodino-Klapac LR, Montgomery CL, Bremer WG, Shontz KM, Malik V, et al. (2010) Persistent expression of FLAG-tagged micro dystrophin in nonhuman primates following intramuscular and vascular delivery. Mol Ther 18: 109-117.
    • (2010) Mol Ther , vol.18 , pp. 109-117
    • Rodino-Klapac, L.R.1    Montgomery, C.L.2    Bremer, W.G.3    Shontz, K.M.4    Malik, V.5
  • 11
    • 0035943022 scopus 로고    scopus 로고
    • Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy
    • Aoki M, Liu J, Richard I, Bashir R, Britton S, et al. (2001) Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy. Neurology 57: 271-278.
    • (2001) Neurology , vol.57 , pp. 271-278
    • Aoki, M.1    Liu, J.2    Richard, I.3    Bashir, R.4    Britton, S.5
  • 12
    • 10744219571 scopus 로고    scopus 로고
    • Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype
    • Takahashi T, Aoki M, Tateyama M, Kondo E, Mizuno T, et al. (2003) Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype. Neurology 60: 1799-1804.
    • (2003) Neurology , vol.60 , pp. 1799-1804
    • Takahashi, T.1    Aoki, M.2    Tateyama, M.3    Kondo, E.4    Mizuno, T.5
  • 13
    • 17444449419 scopus 로고    scopus 로고
    • Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13
    • Liu J, Wu C, Bossie K, Bejaoui K, Hosler BA, et al. (1998) Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13. Genomics 49: 23-29.
    • (1998) Genomics , vol.49 , pp. 23-29
    • Liu, J.1    Wu, C.2    Bossie, K.3    Bejaoui, K.4    Hosler, B.A.5
  • 14
    • 33750502406 scopus 로고    scopus 로고
    • Mutation impact on dysferlin inferred from database analysis and computer-based structural predictions
    • Therrien C, Dodig D, Karpati G, Sinnreich M, (2006) Mutation impact on dysferlin inferred from database analysis and computer-based structural predictions. J Neurol Sci 250: 71-78.
    • (2006) J Neurol Sci , vol.250 , pp. 71-78
    • Therrien, C.1    Dodig, D.2    Karpati, G.3    Sinnreich, M.4
  • 15
    • 0037738510 scopus 로고    scopus 로고
    • Defective membrane repair in dysferlin-deficient muscular dystrophy
    • Bansal D, Miyake K, Vogel SS, Groh S, Chen CC, et al. (2003) Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature 423: 168-172.
    • (2003) Nature , vol.423 , pp. 168-172
    • Bansal, D.1    Miyake, K.2    Vogel, S.S.3    Groh, S.4    Chen, C.C.5
  • 16
    • 0347379869 scopus 로고    scopus 로고
    • Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing
    • Lennon NJ, Kho A, Bacskai BJ, Perlmutter SL, Hyman BT, et al. (2003) Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing. J Biol Chem 278: 50466-50473.
    • (2003) J Biol Chem , vol.278 , pp. 50466-50473
    • Lennon, N.J.1    Kho, A.2    Bacskai, B.J.3    Perlmutter, S.L.4    Hyman, B.T.5
  • 17
    • 34548009359 scopus 로고    scopus 로고
    • Dysferlin and muscle membrane repair
    • Han R, Campbell KP, (2007) Dysferlin and muscle membrane repair. Curr Opin Cell Biol 19: 409-416.
    • (2007) Curr Opin Cell Biol , vol.19 , pp. 409-416
    • Han, R.1    Campbell, K.P.2
  • 18
    • 0033673056 scopus 로고    scopus 로고
    • Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb-girdle muscular dystrophies
    • Piccolo F, Moore SA, Ford GC, Campbell KP, (2000) Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb-girdle muscular dystrophies. Ann Neurol 48: 902-912.
    • (2000) Ann Neurol , vol.48 , pp. 902-912
    • Piccolo, F.1    Moore, S.A.2    Ford, G.C.3    Campbell, K.P.4
  • 19
    • 13244284886 scopus 로고    scopus 로고
    • Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism
    • Cenacchi G, Fanin M, De Giorgi LB, Angelini C, (2005) Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism. J Clin Pathol 58: 190-195.
    • (2005) J Clin Pathol , vol.58 , pp. 190-195
    • Cenacchi, G.1    Fanin, M.2    de Giorgi, L.B.3    Angelini, C.4
  • 20
    • 0029849257 scopus 로고    scopus 로고
    • Quantitative analysis of the packaging capacity of recombinant adeno-associated virus
    • Dong JY, Fan PD, Frizzell RA, (1996) Quantitative analysis of the packaging capacity of recombinant adeno-associated virus. Hum Gene Ther 7: 2101-2112.
    • (1996) Hum Gene Ther , vol.7 , pp. 2101-2112
    • Dong, J.Y.1    Fan, P.D.2    Frizzell, R.A.3
  • 22
    • 0031582213 scopus 로고    scopus 로고
    • The packaging capacity of adeno-associated virus (AAV) and the potential for wild-type-plus AAV gene therapy vectors
    • Hermonat PL, Quirk JG, Bishop BM, Han L, (1997) The packaging capacity of adeno-associated virus (AAV) and the potential for wild-type-plus AAV gene therapy vectors. FEBS Lett 407: 78-84.
    • (1997) FEBS Lett , vol.407 , pp. 78-84
    • Hermonat, P.L.1    Quirk, J.G.2    Bishop, B.M.3    Han, L.4
  • 23
    • 0036127393 scopus 로고    scopus 로고
    • Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy
    • Harper SQ, Hauser MA, DelloRusso C, Duan D, Crawford RW, et al. (2002) Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy. Nat Med 8: 253-261.
    • (2002) Nat Med , vol.8 , pp. 253-261
    • Harper, S.Q.1    Hauser, M.A.2    DelloRusso, C.3    Duan, D.4    Crawford, R.W.5
  • 24
    • 0029122522 scopus 로고
    • Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy
    • Wells DJ, Wells KE, Asante EA, Turner G, Sunada Y, et al. (1995) Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. Hum Mol Genet 4: 1245-1250.
    • (1995) Hum Mol Genet , vol.4 , pp. 1245-1250
    • Wells, D.J.1    Wells, K.E.2    Asante, E.A.3    Turner, G.4    Sunada, Y.5
  • 25
    • 0034121397 scopus 로고    scopus 로고
    • A new dual-vector approach to enhance recombinant adeno-associated virus-mediated gene expression through intermolecular cis activation
    • Duan D, Yue Y, Yan Z, Engelhardt JF, (2000) A new dual-vector approach to enhance recombinant adeno-associated virus-mediated gene expression through intermolecular cis activation. Nat Med 6: 595-598.
    • (2000) Nat Med , vol.6 , pp. 595-598
    • Duan, D.1    Yue, Y.2    Yan, Z.3    Engelhardt, J.F.4
  • 26
    • 33947247444 scopus 로고    scopus 로고
    • Efficient whole-body transduction with trans-splicing adeno-associated viral vectors
    • Ghosh A, Yue Y, Long C, Bostick B, Duan D, (2007) Efficient whole-body transduction with trans-splicing adeno-associated viral vectors. Mol Ther 15: 750-755.
    • (2007) Mol Ther , vol.15 , pp. 750-755
    • Ghosh, A.1    Yue, Y.2    Long, C.3    Bostick, B.4    Duan, D.5
  • 27
    • 77952502008 scopus 로고    scopus 로고
    • Efficient recovery of dysferlin deficiency by dual adeno-associated vector-mediated gene transfer
    • Lostal W, Bartoli M, Bourg N, Roudaut C, Bentaib A, et al. (2010) Efficient recovery of dysferlin deficiency by dual adeno-associated vector-mediated gene transfer. Hum Mol Genet 19: 1897-1907.
    • (2010) Hum Mol Genet , vol.19 , pp. 1897-1907
    • Lostal, W.1    Bartoli, M.2    Bourg, N.3    Roudaut, C.4    Bentaib, A.5
  • 28
    • 77958065739 scopus 로고    scopus 로고
    • A naturally occurring human minidysferlin protein repairs sarcolemmal lesions in a mouse model of dysferlinopathy
    • Krahn M, Wein N, Bartoli M, Lostal W, Courrier S, et al. (2010) A naturally occurring human minidysferlin protein repairs sarcolemmal lesions in a mouse model of dysferlinopathy. Sci Transl Med 2: 50ra69.
    • (2010) Sci Transl Med , vol.2
    • Krahn, M.1    Wein, N.2    Bartoli, M.3    Lostal, W.4    Courrier, S.5
  • 29
    • 74149093851 scopus 로고    scopus 로고
    • Evidence for the failure of adeno-associated virus serotype 5 to package a viral genome & or = 8.2 kb
    • Lai Y, Yue Y, Duan D, (2010) Evidence for the failure of adeno-associated virus serotype 5 to package a viral genome & or = 8.2 kb. Mol Ther 18: 75-79.
    • (2010) Mol Ther , vol.18 , pp. 75-79
    • Lai, Y.1    Yue, Y.2    Duan, D.3
  • 30
    • 43049119982 scopus 로고    scopus 로고
    • Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice
    • Allocca M, Doria M, Petrillo M, Colella P, Garcia-Hoyos M, et al. (2008) Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice. J Clin Invest 118: 1955-1964.
    • (2008) J Clin Invest , vol.118 , pp. 1955-1964
    • Allocca, M.1    Doria, M.2    Petrillo, M.3    Colella, P.4    Garcia-Hoyos, M.5
  • 31
    • 74049092844 scopus 로고    scopus 로고
    • Characterization of genome integrity for oversized recombinant AAV vector
    • Dong B, Nakai H, Xiao W, (2010) Characterization of genome integrity for oversized recombinant AAV vector. Mol Ther 18: 87-92.
    • (2010) Mol Ther , vol.18 , pp. 87-92
    • Dong, B.1    Nakai, H.2    Xiao, W.3
  • 32
    • 74049085498 scopus 로고    scopus 로고
    • Effect of genome size on AAV vector packaging
    • Wu Z, Yang H, Colosi P, (2010) Effect of genome size on AAV vector packaging. Mol Ther 18: 80-86.
    • (2010) Mol Ther , vol.18 , pp. 80-86
    • Wu, Z.1    Yang, H.2    Colosi, P.3
  • 33
    • 33846300685 scopus 로고    scopus 로고
    • Design of tissue-specific regulatory cassettes for high-level rAAV-mediated expression in skeletal and cardiac muscle
    • Salva MZ, Himeda CL, Tai PW, Nishiuchi E, Gregorevic P, et al. (2007) Design of tissue-specific regulatory cassettes for high-level rAAV-mediated expression in skeletal and cardiac muscle. Mol Ther 15: 320-329.
    • (2007) Mol Ther , vol.15 , pp. 320-329
    • Salva, M.Z.1    Himeda, C.L.2    Tai, P.W.3    Nishiuchi, E.4    Gregorevic, P.5
  • 34
    • 0032850960 scopus 로고    scopus 로고
    • Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B
    • Bittner RE, Anderson LV, Burkhardt E, Bashir R, Vafiadaki E, et al. (1999) Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B. Nat Genet 23: 141-142.
    • (1999) Nat Genet , vol.23 , pp. 141-142
    • Bittner, R.E.1    Anderson, L.V.2    Burkhardt, E.3    Bashir, R.4    Vafiadaki, E.5
  • 35
    • 5744230326 scopus 로고    scopus 로고
    • Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency
    • Ho M, Post CM, Donahue LR, Lidov HG, Bronson RT, et al. (2004) Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency. Hum Mol Genet 13: 1999-2010.
    • (2004) Hum Mol Genet , vol.13 , pp. 1999-2010
    • Ho, M.1    Post, C.M.2    Donahue, L.R.3    Lidov, H.G.4    Bronson, R.T.5
  • 36
    • 84555203376 scopus 로고    scopus 로고
    • Unmasking potential intracellular roles for dysferlin through improved immunolabeling methods
    • Roche JA, Ru LW, O'Neill AM, Resneck WG, Lovering RM, et al. (2011) Unmasking potential intracellular roles for dysferlin through improved immunolabeling methods. J Histochem Cytochem 59: 964-975.
    • (2011) J Histochem Cytochem , vol.59 , pp. 964-975
    • Roche, J.A.1    Ru, L.W.2    O'Neill, A.M.3    Resneck, W.G.4    Lovering, R.M.5
  • 37
    • 3142731311 scopus 로고    scopus 로고
    • LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies
    • Barresi R, Michele DE, Kanagawa M, Harper HA, Dovico SA, et al. (2004) LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. Nat Med 10: 696-703.
    • (2004) Nat Med , vol.10 , pp. 696-703
    • Barresi, R.1    Michele, D.E.2    Kanagawa, M.3    Harper, H.A.4    Dovico, S.A.5
  • 38
    • 0037211475 scopus 로고    scopus 로고
    • The 105th ENMC sponsored workshop: pathogenesis in the non-sarcoglycan limb-girdle muscular dystrophies, Naarden, April 12-14, 2002
    • Bushby KM, Beckmann JS, (2003) The 105th ENMC sponsored workshop: pathogenesis in the non-sarcoglycan limb-girdle muscular dystrophies, Naarden, April 12-14, 2002. Neuromuscul Disord 13: 80-90.
    • (2003) Neuromuscul Disord , vol.13 , pp. 80-90
    • Bushby, K.M.1    Beckmann, J.S.2
  • 39
    • 10744226857 scopus 로고    scopus 로고
    • Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan
    • Longman C, Brockington M, Torelli S, Jimenez-Mallebrera C, Kennedy C, et al. (2003) Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan. Hum Mol Genet 12: 2853-2861.
    • (2003) Hum Mol Genet , vol.12 , pp. 2853-2861
    • Longman, C.1    Brockington, M.2    Torelli, S.3    Jimenez-Mallebrera, C.4    Kennedy, C.5
  • 42
    • 78249253608 scopus 로고    scopus 로고
    • Sustained alpha-sarcoglycan gene expression after gene transfer in limb-girdle muscular dystrophy, type 2D
    • Mendell JR, Rodino-Klapac LR, Rosales XQ, Coley BD, Galloway G, et al. (2010) Sustained alpha-sarcoglycan gene expression after gene transfer in limb-girdle muscular dystrophy, type 2D. Ann Neurol 68: 629-638.
    • (2010) Ann Neurol , vol.68 , pp. 629-638
    • Mendell, J.R.1    Rodino-Klapac, L.R.2    Rosales, X.Q.3    Coley, B.D.4    Galloway, G.5
  • 43
    • 70350067897 scopus 로고    scopus 로고
    • Limb-girdle muscular dystrophy type 2D gene therapy restores alpha-sarcoglycan and associated proteins
    • Mendell JR, Rodino-Klapac LR, Rosales-Quintero X, Kota J, Coley BD, et al. (2009) Limb-girdle muscular dystrophy type 2D gene therapy restores alpha-sarcoglycan and associated proteins. Ann Neurol 66: 290-297.
    • (2009) Ann Neurol , vol.66 , pp. 290-297
    • Mendell, J.R.1    Rodino-Klapac, L.R.2    Rosales-Quintero, X.3    Kota, J.4    Coley, B.D.5
  • 44
    • 0033541640 scopus 로고    scopus 로고
    • Highly purified recombinant adeno-associated virus vectors are biologically active and free of detectable helper and wild-type viruses
    • Clark KR, Liu X, McGrath JP, Johnson PR, (1999) Highly purified recombinant adeno-associated virus vectors are biologically active and free of detectable helper and wild-type viruses. Hum Gene Ther 10: 1031-1039.
    • (1999) Hum Gene Ther , vol.10 , pp. 1031-1039
    • Clark, K.R.1    Liu, X.2    McGrath, J.P.3    Johnson, P.R.4
  • 45
    • 27744584507 scopus 로고    scopus 로고
    • Characterization of adeno-associated virus genomes isolated from human tissues
    • Schnepp BC, Jensen RL, Chen CL, Johnson PR, Clark KR, (2005) Characterization of adeno-associated virus genomes isolated from human tissues. J Virol 79: 14793-14803.
    • (2005) J Virol , vol.79 , pp. 14793-14803
    • Schnepp, B.C.1    Jensen, R.L.2    Chen, C.L.3    Johnson, P.R.4    Clark, K.R.5
  • 46
    • 65249180738 scopus 로고    scopus 로고
    • Overexpression of Galgt2 in skeletal muscle prevents injury resulting from eccentric contractions in both mdx and wild-type mice
    • Martin PT, Xu R, Rodino-Klapac LR, Oglesbay E, Camboni M, et al. (2009) Overexpression of Galgt2 in skeletal muscle prevents injury resulting from eccentric contractions in both mdx and wild-type mice. Am J Physiol Cell Physiol 296: C476-488.
    • (2009) Am J Physiol Cell Physiol , vol.296
    • Martin, P.T.1    Xu, R.2    Rodino-Klapac, L.R.3    Oglesbay, E.4    Camboni, M.5
  • 47
    • 80051552743 scopus 로고    scopus 로고
    • Early treatment with lisinopril and spironolactone preserves cardiac and skeletal muscle in Duchenne muscular dystrophy mice
    • Rafael-Fortney JA, Chimanji NS, Schill KE, Martin CD, Murray JD, et al. (2011) Early treatment with lisinopril and spironolactone preserves cardiac and skeletal muscle in Duchenne muscular dystrophy mice. Circulation 124: 582-588.
    • (2011) Circulation , vol.124 , pp. 582-588
    • Rafael-Fortney, J.A.1    Chimanji, N.S.2    Schill, K.E.3    Martin, C.D.4    Murray, J.D.5
  • 48
    • 80055024624 scopus 로고    scopus 로고
    • mdx(cv) mice manifest more severe muscle dysfunction and diaphragm force deficits than do mdx Mice
    • Beastrom N, Lu H, Macke A, Canan BD, Johnson EK, et al. (2011) mdx(cv) mice manifest more severe muscle dysfunction and diaphragm force deficits than do mdx Mice. Am J Pathol 179: 2464-2474.
    • (2011) Am J Pathol , vol.179 , pp. 2464-2474
    • Beastrom, N.1    Lu, H.2    Macke, A.3    Canan, B.D.4    Johnson, E.K.5


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