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Volumn 10, Issue 2, 2015, Pages

FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; C2C12 CELL LINE; CELL ACTIVATION; CELL COUNT; CELL DIFFERENTIATION; CONTROLLED STUDY; FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FHL1 GENE; FRG1 GENE; GENE EXPRESSION; GENE OVEREXPRESSION; IN VITRO STUDY; KYPHOSIS; MALE; MOUSE; MUSCLE CELL; MUSCLE FUNCTION; MUSCLE MASS; MYOBLAST; MYOFIBROSIS; NONHUMAN; QUADRICEPS FEMORIS MUSCLE; SATELLITE CELL; TRANSGENE; TRANSGENIC MOUSE; TRICEPS BRACHII MUSCLE; ANIMAL; CELL LINE; CYTOLOGY; FEMALE; FIBROSIS; GENETICS; HUMAN; METABOLISM; MUSCLE DEVELOPMENT; PATHOLOGY; PATHOPHYSIOLOGY; SKELETAL MUSCLE;

EID: 84923239746     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0117665     Document Type: Article
Times cited : (8)

References (91)
  • 1
    • 0032541318 scopus 로고    scopus 로고
    • FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates
    • PMID: 9714712
    • Grewal PK, Todd LC, van der Maarel S, Frants RR, Hewitt JE (1998) FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates. Gene 216: 13-19. PMID: 9714712
    • (1998) Gene , vol.216 , pp. 13-19
    • Grewal, P.K.1    Todd, L.C.2    Van Der Maarel, S.3    Frants, R.R.4    Hewitt, J.E.5
  • 2
    • 33644522383 scopus 로고    scopus 로고
    • Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1
    • PMID: 16341202
    • Gabellini D, D'Antona G, Moggio M, Prelle A, Zecca C, et al. (2006) Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1. Nature 439: 973-977. PMID: 16341202
    • (2006) Nature , vol.439 , pp. 973-977
    • Gabellini, D.1    D'Antona, G.2    Moggio, M.3    Prelle, A.4    Zecca, C.5
  • 4
    • 84873515320 scopus 로고    scopus 로고
    • Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD)
    • PMID: 23300487
    • Pistoni M, Shiue L, Cline MS, Bortolanza S, Neguembor MV, et al. (2013) Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD). Plos Genetics 9: e1003186. doi: 10.1371/journal.pgen.1003186 PMID: 23300487
    • (2013) Plos Genetics , vol.9 , pp. e1003186
    • Pistoni, M.1    Shiue, L.2    Cline, M.S.3    Bortolanza, S.4    Neguembor, M.V.5
  • 5
    • 79960737300 scopus 로고    scopus 로고
    • Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling protein
    • PMID: 21699900
    • Sun CY, van Koningsbruggen S, Long SW, Straasheijm K, Klooster R, et al. (2011) Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling protein. Journal of Molecular Biology 411: 397-416. doi: 10.1016/j.jmb.2011.06.014 PMID: 21699900
    • (2011) Journal of Molecular Biology , vol.411 , pp. 397-416
    • Sun, C.Y.1    Van Koningsbruggen, S.2    Long, S.W.3    Straasheijm, K.4    Klooster, R.5
  • 6
    • 77951145598 scopus 로고    scopus 로고
    • Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites
    • PMID: 20215405
    • Liu Q, Jones TI, Tang VW, Brieher WM, Jones PL (2010) Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites. Journal of Cell Science 123: 1116-1123. doi: 10.1242/jcs.058958 PMID: 20215405
    • (2010) Journal of Cell Science , vol.123 , pp. 1116-1123
    • Liu, Q.1    Jones, T.I.2    Tang, V.W.3    Brieher, W.M.4    Jones, P.L.5
  • 7
    • 66349093652 scopus 로고    scopus 로고
    • Muscular dystrophy candidate gene FRG1 is critical for muscle development
    • PMID: 19097195
    • Hanel ML, Wuebbles RD, Jones PL (2009) Muscular dystrophy candidate gene FRG1 is critical for muscle development. Dev Dyn 238: 1502-1512. doi: 10.1002/dvdy.21830 PMID: 19097195
    • (2009) Dev Dyn , vol.238 , pp. 1502-1512
    • Hanel, M.L.1    Wuebbles, R.D.2    Jones, P.L.3
  • 8
    • 84902517476 scopus 로고    scopus 로고
    • Facioscapulohumeral dystrophy: The path to consensus on pathophysiology
    • PMID: 24940479
    • Tawil R, van der Maarel SM, Tapscott SJ (2014) Facioscapulohumeral dystrophy: the path to consensus on pathophysiology. Skelet Muscle 4: 12. doi: 10.1186/2044-5040-4-12 PMID: 24940479
    • (2014) Skelet Muscle , vol.4 , pp. 12
    • Tawil, R.1    Van Der Maarel, S.M.2    Tapscott, S.J.3
  • 10
    • 0034882438 scopus 로고    scopus 로고
    • Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy
    • PMID: 11525880
    • Flanigan KM, Coffeen CM, Sexton L, Stauffer D, Brunner S, et al. (2001) Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy. Neuromuscul Disord 11: 525-529. PMID: 11525880
    • (2001) Neuromuscul Disord , vol.11 , pp. 525-529
    • Flanigan, K.M.1    Coffeen, C.M.2    Sexton, L.3    Stauffer, D.4    Brunner, S.5
  • 11
    • 66549122709 scopus 로고    scopus 로고
    • Facioscapulohumeral muscular dystrophy: Epidemiological and molecular study in a north-east Italian population sample
    • PMID: 19320656
    • Mostacciuolo ML, Pastorello E, Vazza G, Miorin M, Angelini C, et al. (2009) Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. Clin Genet 75: 550-555. doi: 10.1111/j.1399-0004.2009.01158.x PMID: 19320656
    • (2009) Clin Genet , vol.75 , pp. 550-555
    • Mostacciuolo, M.L.1    Pastorello, E.2    Vazza, G.3    Miorin, M.4    Angelini, C.5
  • 12
    • 84915829052 scopus 로고    scopus 로고
    • Population-based incidence and prevalence of facioscapulohumeral dystrophy
    • PMID: 25122204
    • Deenen JC, Arnts H, van der Maarel SM, Padberg GW, Verschuuren JJ, et al. (2014) Population-based incidence and prevalence of facioscapulohumeral dystrophy. Neurology 83: 1056-1059. doi: 10.1212/WNL.0000000000000797 PMID: 25122204
    • (2014) Neurology , vol.83 , pp. 1056-1059
    • Deenen, J.C.1    Arnts, H.2    Van Der Maarel, S.M.3    Padberg, G.W.4    Verschuuren, J.J.5
  • 13
    • 0026080958 scopus 로고
    • Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization
    • PMID: 2037288
    • Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, et al. (1991) Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization. Genomics 9: 570-575. PMID: 2037288
    • (1991) Genomics , vol.9 , pp. 570-575
    • Wijmenga, C.1    Padberg, G.W.2    Moerer, P.3    Wiegant, J.4    Liem, L.5
  • 14
    • 0344436078 scopus 로고    scopus 로고
    • Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
    • PMID: 10433963
    • Gabriels J, Beckers MC, Ding H, De Vriese A, Plaisance S, et al. (1999) Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element. Gene 236: 25-32. PMID: 10433963
    • (1999) Gene , vol.236 , pp. 25-32
    • Gabriels, J.1    Beckers, M.C.2    Ding, H.3    De Vriese, A.4    Plaisance, S.5
  • 15
    • 77957327192 scopus 로고    scopus 로고
    • A unifying genetic model for facioscapulohumeral muscular dystrophy
    • PMID: 20724583
    • Lemmers RJ, van der Vliet PJ, Klooster R, Sacconi S, Camano P, et al. (2010) A unifying genetic model for facioscapulohumeral muscular dystrophy. Science 329: 1650-1653. doi: 10.1126/science.1189044 PMID: 20724583
    • (2010) Science , vol.329 , pp. 1650-1653
    • Lemmers, R.J.1    Van Der Vliet, P.J.2    Klooster, R.3    Sacconi, S.4    Camano, P.5
  • 17
    • 84855956147 scopus 로고    scopus 로고
    • DUX4 Activates Germ line Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy
    • PMID: 22209328
    • Geng LN, Yao ZZ, Snider L, Fong AP, Cech JN, et al. (2012) DUX4 Activates Germ line Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy. Developmental Cell 22: 38-51. doi: 10.1016/j.devcel.2011.11.013 PMID: 22209328
    • (2012) Developmental Cell , vol.22 , pp. 38-51
    • Geng, L.N.1    Yao, Z.Z.2    Snider, L.3    Fong, A.P.4    Cech, J.N.5
  • 18
    • 84888236297 scopus 로고    scopus 로고
    • DUX4 binding to retroelements creates promoters that are active in FSHD muscle and testis
    • PMID: 24278031
    • Young JM, Whiddon JL, Yao Z, Kasinathan B, Snider L, et al. (2013) DUX4 binding to retroelements creates promoters that are active in FSHD muscle and testis. Plos Genetics 9: e1003947. doi: 10.1371/journal.pgen.1003947 PMID: 24278031
    • (2013) Plos Genetics , vol.9 , pp. e1003947
    • Young, J.M.1    Whiddon, J.L.2    Yao, Z.3    Kasinathan, B.4    Snider, L.5
  • 19
    • 84964817861 scopus 로고    scopus 로고
    • Conditional over-expression of PITX1 causes skeletal muscle dystrophy in mice
    • PMID: 23125914
    • Pandey SN, Cabotage J, Shi R, Dixit M, Sutherland M, et al. (2012) Conditional over-expression of PITX1 causes skeletal muscle dystrophy in mice. Biol Open 1: 629-639. PMID: 23125914
    • (2012) Biol Open , vol.1 , pp. 629-639
    • Pandey, S.N.1    Cabotage, J.2    Shi, R.3    Dixit, M.4    Sutherland, M.5
  • 20
    • 84872415036 scopus 로고    scopus 로고
    • Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy
    • PMID: 23108159
    • Mitsuhashi H, Mitsuhashi S, Lynn-Jones T, Kawahara G, Kunkel LM (2013) Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy. Human Molecular Genetics 22: 568-577. doi: 10.1093/hmg/dds467 PMID: 23108159
    • (2013) Human Molecular Genetics , vol.22 , pp. 568-577
    • Mitsuhashi, H.1    Mitsuhashi, S.2    Lynn-Jones, T.3    Kawahara, G.4    Kunkel, L.M.5
  • 21
    • 84876821220 scopus 로고    scopus 로고
    • Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD
    • PMID: 23593020
    • Krom YD, Thijssen PE, Young JM, den Hamer B, Balog J, et al. (2013) Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD. Plos Genetics 9: e1003415. doi: 10.1371/journal.pgen.1003415 PMID: 23593020
    • (2013) Plos Genetics , vol.9 , pp. e1003415
    • Krom, Y.D.1    Thijssen, P.E.2    Young, J.M.3    Den Hamer, B.4    Balog, J.5
  • 22
    • 84922547186 scopus 로고    scopus 로고
    • Dominant Lethal Pathologies in Male Mice Engineered to Contain an X-Linked DUX4 Transgene
    • PMID: 25176645
    • Dandapat A, Bosnakovski D, Hartweck LM, Arpke RW, Baltgalvis KA, et al. (2014) Dominant Lethal Pathologies in Male Mice Engineered to Contain an X-Linked DUX4 Transgene. Cell Reports 8: 1484-1496. doi: 10.1016/j.celrep.2014.07.056 PMID: 25176645
    • (2014) Cell Reports , vol.8 , pp. 1484-1496
    • Dandapat, A.1    Bosnakovski, D.2    Hartweck, L.M.3    Arpke, R.W.4    Baltgalvis, K.A.5
  • 23
  • 24
    • 0030009384 scopus 로고    scopus 로고
    • Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
    • PMID: 8733044
    • Tupler R, Berardinelli A, Barbierato L, Frants R, Hewitt JE, et al. (1996) Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy. J Med Genet 33: 366-370. PMID: 8733044
    • (1996) J Med Genet , vol.33 , pp. 366-370
    • Tupler, R.1    Berardinelli, A.2    Barbierato, L.3    Frants, R.4    Hewitt, J.E.5
  • 26
    • 84860885909 scopus 로고    scopus 로고
    • A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy
    • PMID: 22541069
    • Cabianca DS, Casa V, Bodega B, Xynos A, Ginelli E, et al. (2012) A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy. Cell 149: 819-831. doi: 10.1016/j.cell.2012.03.035 PMID: 22541069
    • (2012) Cell , vol.149 , pp. 819-831
    • Cabianca, D.S.1    Casa, V.2    Bodega, B.3    Xynos, A.4    Ginelli, E.5
  • 27
    • 0037047439 scopus 로고    scopus 로고
    • Inappropriate gene activation in FSHD: A repressor complex binds a chromosomal repeat deleted in dystrophic muscle
    • PMID: 12176321
    • Gabellini D, Green MR, Tupler R (2002) Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle. Cell 110: 339-348. PMID: 12176321
    • (2002) Cell , vol.110 , pp. 339-348
    • Gabellini, D.1    Green, M.R.2    Tupler, R.3
  • 28
    • 33847234593 scopus 로고    scopus 로고
    • Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
    • PMID: 17151338
    • Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R (2007) Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Neurology 68: 569-577. PMID: 17151338
    • (2007) Neurology , vol.68 , pp. 569-577
    • Osborne, R.J.1    Welle, S.2    Venance, S.L.3    Thornton, C.A.4    Tawil, R.5
  • 29
    • 70450275779 scopus 로고    scopus 로고
    • Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level
    • PMID: 19809486
    • Klooster R, Straasheijm K, Shah B, Sowden J, Frants R, et al. (2009) Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level. European Journal of Human Genetics 17: 1615-1624. doi: 10.1038/ejhg.2009.62 PMID: 19809486
    • (2009) European Journal of Human Genetics , vol.17 , pp. 1615-1624
    • Klooster, R.1    Straasheijm, K.2    Shah, B.3    Sowden, J.4    Frants, R.5
  • 30
    • 0344875044 scopus 로고    scopus 로고
    • Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation
    • PMID: 14519683
    • Winokur ST, Chen YW, Masny PS, Martin JH, Ehmsen JT, et al. (2003) Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation. Human Molecular Genetics 12: 2895-2907. PMID: 14519683
    • (2003) Human Molecular Genetics , vol.12 , pp. 2895-2907
    • Winokur, S.T.1    Chen, Y.W.2    Masny, P.S.3    Martin, J.H.4    Ehmsen, J.T.5
  • 31
    • 0345227304 scopus 로고    scopus 로고
    • Testing the position-effectvariegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q
    • PMID: 14506132
    • Jiang G, Yang F, van Overveld PG, Vedanarayanan V, van der Maarel S, et al. (2003) Testing the position-effectvariegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q. Human Molecular Genetics 12: 2909-2921. PMID: 14506132
    • (2003) Human Molecular Genetics , vol.12 , pp. 2909-2921
    • Jiang, G.1    Yang, F.2    Van Overveld, P.G.3    Vedanarayanan, V.4    Van Der Maarel, S.5
  • 32
    • 77949656794 scopus 로고    scopus 로고
    • Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei
    • PMID: 19888305
    • Masny PS, Chan OYA, de Greef JC, Bengtsson U, Ehrlich M, et al. (2010) Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei. European Journal of Human Genetics 18: 448-456. doi: 10.1038/ejhg.2009.183 PMID: 19888305
    • (2010) European Journal of Human Genetics , vol.18 , pp. 448-456
    • Masny, P.S.1    Chan, O.Y.A.2    De Greef, J.C.3    Bengtsson, U.4    Ehrlich, M.5
  • 33
    • 84879856340 scopus 로고    scopus 로고
    • Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells
    • PMID: 23525014
    • Xynos A, Neguembor MV, Caccia R, Licastro D, Nonis A, et al. (2013) Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells. Journal of Cell Science 126: 2236-2245. doi: 10.1242/jcs.121533 PMID: 23525014
    • (2013) Journal of Cell Science , vol.126 , pp. 2236-2245
    • Xynos, A.1    Neguembor, M.V.2    Caccia, R.3    Licastro, D.4    Nonis, A.5
  • 34
    • 67650314502 scopus 로고    scopus 로고
    • FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy
    • PMID: 25608223
    • Wuebbles RD, Hanel ML, Jones PL (2009) FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy. Disease Models &Mechanisms 2: 267-274. doi: 10.1111/jvh.12392 PMID: 25608223
    • (2009) Disease Models &Mechanisms , vol.2 , pp. 267-274
    • Wuebbles, R.D.1    Hanel, M.L.2    Jones, P.L.3
  • 35
    • 84885342118 scopus 로고    scopus 로고
    • FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis
    • PMID: 23720823
    • Neguembor MV, Xynos A, Onorati MC, Caccia R, Bortolanza S, et al. (2013) FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis. Journal of Molecular Cell Biology 5: 294-307. doi: 10.1093/jmcb/mjt018 PMID: 23720823
    • (2013) Journal of Molecular Cell Biology , vol.5 , pp. 294-307
    • Neguembor, M.V.1    Xynos, A.2    Onorati, M.C.3    Caccia, R.4    Bortolanza, S.5
  • 36
    • 33749605124 scopus 로고    scopus 로고
    • Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes
    • PMID: 17013991
    • Celegato B, Capitanio D, Pescatori M, Romualdi C, Pacchioni B, et al. (2006) Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes. Proteomics 6: 5303-5321. PMID: 17013991
    • (2006) Proteomics , vol.6 , pp. 5303-5321
    • Celegato, B.1    Capitanio, D.2    Pescatori, M.3    Romualdi, C.4    Pacchioni, B.5
  • 37
    • 79958759071 scopus 로고    scopus 로고
    • Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns
    • PMID: 21695143
    • Cheli S, Francois S, Bodega B, Ferrari F, Tenedini E, et al. (2011) Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns. Plos One 6: e20966. doi: 10.1371/journal.pone.0020966 PMID: 21695143
    • (2011) Plos One , vol.6 , pp. e20966
    • Cheli, S.1    Francois, S.2    Bodega, B.3    Ferrari, F.4    Tenedini, E.5
  • 38
    • 84871296824 scopus 로고    scopus 로고
    • FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes
    • PMID: 23272181
    • Tassin A, Leroy B, Laoudj-Chenivesse D, Wauters A, Vanderplanck C, et al. (2012) FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes. Plos One 7: e51865. doi: 10.1371/journal.pone.0051865 PMID: 23272181
    • (2012) Plos One , vol.7 , pp. e51865
    • Tassin, A.1    Leroy, B.2    Laoudj-Chenivesse, D.3    Wauters, A.4    Vanderplanck, C.5
  • 40
    • 0034815139 scopus 로고    scopus 로고
    • Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts
    • PMID: 11595515
    • Furling D, Lemieux D, Taneja K, Puymirat J (2001) Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts. Neuromuscular Disorders 11: 728-735. PMID: 11595515
    • (2001) Neuromuscular Disorders , vol.11 , pp. 728-735
    • Furling, D.1    Lemieux, D.2    Taneja, K.3    Puymirat, J.4
  • 42
    • 12144288743 scopus 로고    scopus 로고
    • Inhibition of myogenesis in transgenic mice expressing the human DMPK 3 '-UTR
    • PMID: 14734627
    • Storbeck CJ, Drmanic S, Daniel K, Waring JD, Jirik FR, et al. (2004) Inhibition of myogenesis in transgenic mice expressing the human DMPK 3 '-UTR. Human Molecular Genetics 13: 589-600. PMID: 14734627
    • (2004) Human Molecular Genetics , vol.13 , pp. 589-600
    • Storbeck, C.J.1    Drmanic, S.2    Daniel, K.3    Waring, J.D.4    Jirik, F.R.5
  • 43
    • 0033578613 scopus 로고    scopus 로고
    • Characterization of two isoforms of the skeletal muscle LIM protein 1, SLIM1. Localization of SLIM1 at focal adhesions and the isoform slimmer in the nucleus of myoblasts and cytoplasm of myotubes suggests distinct roles in the cytoskeleton and in nuclear-cytoplasmic communication
    • PMID: 10480922
    • Brown S, McGrath MJ, Ooms LM, Gurung R, Maimone MM, et al. (1999) Characterization of two isoforms of the skeletal muscle LIM protein 1, SLIM1. Localization of SLIM1 at focal adhesions and the isoform slimmer in the nucleus of myoblasts and cytoplasm of myotubes suggests distinct roles in the cytoskeleton and in nuclear-cytoplasmic communication. Journal of Biological Chemistry 274: 27083-27091. PMID: 10480922
    • (1999) Journal of Biological Chemistry , vol.274 , pp. 27083-27091
    • Brown, S.1    McGrath, M.J.2    Ooms, L.M.3    Gurung, R.4    Maimone, M.M.5
  • 44
    • 40549108276 scopus 로고    scopus 로고
    • Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy
    • PMID: 18274675
    • Schessl J, Zou Y, McGrath MJ, Cowling BS, Maiti B, et al. (2008) Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy. Journal of Clinical Investigation 118: 904-912. doi: 10.1172/JCI34450 PMID: 18274675
    • (2008) Journal of Clinical Investigation , vol.118 , pp. 904-912
    • Schessl, J.1    Zou, Y.2    McGrath, M.J.3    Cowling, B.S.4    Maiti, B.5
  • 45
    • 38749136299 scopus 로고    scopus 로고
    • X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1
    • PMID: 18179901
    • Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, et al. (2008) X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1. American Journal of Human Genetics 82: 208-213. doi: 10.1016/j.ajhg.2007.09.013 PMID: 18179901
    • (2008) American Journal of Human Genetics , vol.82 , pp. 208-213
    • Quinzii, C.M.1    Vu, T.H.2    Min, K.C.3    Tanji, K.4    Barral, S.5
  • 46
    • 38749121773 scopus 로고    scopus 로고
    • An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1
    • PMID: 18179888
    • Windpassinger C, Schoser B, Straub V, Hochmeister S, Noor A, et al. (2008) An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1. American Journal of Human Genetics 82: 88-99. doi: 10.1016/j.ajhg.2007.09.004 PMID: 18179888
    • (2008) American Journal of Human Genetics , vol.82 , pp. 88-99
    • Windpassinger, C.1    Schoser, B.2    Straub, V.3    Hochmeister, S.4    Noor, A.5
  • 48
    • 58249091742 scopus 로고    scopus 로고
    • Identification of FHL1 as a regulator of skeletal muscle mass: Implications for human myopathy
    • PMID: 19075112
    • Cowling BS, McGrath MJ, Nguyen MA, Cottle DL, Kee AJ, et al. (2008) Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy. Journal of Cell Biology 183: 1033-1048. doi: 10.1083/jcb.200804077 PMID: 19075112
    • (2008) Journal of Cell Biology , vol.183 , pp. 1033-1048
    • Cowling, B.S.1    McGrath, M.J.2    Nguyen, M.A.3    Cottle, D.L.4    Kee, A.J.5
  • 49
    • 0017759258 scopus 로고
    • Serial Passing and Differentiation of Myogenic Cells Isolated from Dystrophic Mouse Muscle
    • PMID: 563524
    • Yaffe D, Saxel O (1977) Serial Passing and Differentiation of Myogenic Cells Isolated from Dystrophic Mouse Muscle. Nature 270: 725-727. PMID: 563524
    • (1977) Nature , vol.270 , pp. 725-727
    • Yaffe, D.1    Saxel, O.2
  • 50
    • 36348958434 scopus 로고    scopus 로고
    • Transgenic overexpression of ADAM12 suppresses muscle regeneration and aggravates dystrophy in aged mdx mice
    • PMID: 17982130
    • Jorgensen LH, Jensen CH, Wewer UM, Schroder HD (2007) Transgenic overexpression of ADAM12 suppresses muscle regeneration and aggravates dystrophy in aged mdx mice. American Journal of Pathology 171: 1599-1607. PMID: 17982130
    • (2007) American Journal of Pathology , vol.171 , pp. 1599-1607
    • Jorgensen, L.H.1    Jensen, C.H.2    Wewer, U.M.3    Schroder, H.D.4
  • 51
    • 44949231424 scopus 로고    scopus 로고
    • Analyzing real-time PCR data by the comparative C(T) method
    • PMID: 18546601
    • Schmittgen TD, Livak KJ (2008) Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc 3: 1101-1108. PMID: 18546601
    • (2008) Nat Protoc , vol.3 , pp. 1101-1108
    • Schmittgen, T.D.1    Livak, K.J.2
  • 53
    • 84880617578 scopus 로고    scopus 로고
    • Elucidation of target muscle and detailed development of dorsal motor neurons in chick embryo spinal cord
    • PMID: 23504940
    • Kobayashi N, Homma S, Okada T, Masuda T, Sato N, et al. (2013) Elucidation of target muscle and detailed development of dorsal motor neurons in chick embryo spinal cord. J Comp Neurol 521: 2987-3002. doi: 10.1002/cne.23326 PMID: 23504940
    • (2013) J Comp Neurol , vol.521 , pp. 2987-3002
    • Kobayashi, N.1    Homma, S.2    Okada, T.3    Masuda, T.4    Sato, N.5
  • 54
    • 0037764082 scopus 로고    scopus 로고
    • Class III beta-tubulin in human development and cancer
    • PMID: 12740870
    • Katsetos CD, Herman MM, Mork SJ (2003) Class III beta-tubulin in human development and cancer. Cell Motil Cytoskeleton 55: 77-96. PMID: 12740870
    • (2003) Cell Motil Cytoskeleton , vol.55 , pp. 77-96
    • Katsetos, C.D.1    Herman, M.M.2    Mork, S.J.3
  • 56
    • 84892454097 scopus 로고    scopus 로고
    • Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy
    • PMID: 24087791
    • D'Arcy CE, Feeney SJ, McLean CA, Gehrig SM, Lynch GS, et al. (2014) Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy. Human Molecular Genetics 23: 618-636. doi: 10. 1093/hmg/ddt449 PMID: 24087791
    • (2014) Human Molecular Genetics , vol.23 , pp. 618-636
    • D'Arcy, C.E.1    Feeney, S.J.2    McLean, C.A.3    Gehrig, S.M.4    Lynch, G.S.5
  • 57
    • 21844436541 scopus 로고    scopus 로고
    • EID3 is a novel EID family member and an inhibitor of CBP-dependent co-activation
    • PMID: 15987788
    • Bavner A, Matthews J, Sanyal S, Gustafsson JA, Treuter E (2005) EID3 is a novel EID family member and an inhibitor of CBP-dependent co-activation. Nucleic Acids Research 33: 3561-3569. PMID: 15987788
    • (2005) Nucleic Acids Research , vol.33 , pp. 3561-3569
    • Bavner, A.1    Matthews, J.2    Sanyal, S.3    Gustafsson, J.A.4    Treuter, E.5
  • 58
    • 4444305799 scopus 로고    scopus 로고
    • Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse
    • PMID: 15351425
    • Briguet A, Courdier-Fruh I, Foster M, Meier T, Magyar JP (2004) Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse. Neuromuscul Disord 14: 675-682. PMID: 15351425
    • (2004) Neuromuscul Disord , vol.14 , pp. 675-682
    • Briguet, A.1    Courdier-Fruh, I.2    Foster, M.3    Meier, T.4    Magyar, J.P.5
  • 59
    • 84885346693 scopus 로고    scopus 로고
    • Spatiotemporal patterns of Pax3, Pax6, and Pax7 expression in the developing brain of a urodele amphibian, Pleurodeles waltl
    • PMID: 23784810
    • Joven A, Morona R, Gonzalez A, Moreno N (2013) Spatiotemporal patterns of Pax3, Pax6, and Pax7 expression in the developing brain of a urodele amphibian, Pleurodeles waltl. J Comp Neurol 521: 3913-3953. doi: 10.1002/cne.23385 PMID: 23784810
    • (2013) J Comp Neurol , vol.521 , pp. 3913-3953
    • Joven, A.1    Morona, R.2    Gonzalez, A.3    Moreno, N.4
  • 60
    • 41849143809 scopus 로고    scopus 로고
    • In vivo time-lapse microscopy reveals no loss of murine myonuclei during weeks of muscle atrophy
    • PMID: 18317591
    • Bruusgaard JC, Gundersen K (2008) In vivo time-lapse microscopy reveals no loss of murine myonuclei during weeks of muscle atrophy. Journal of Clinical Investigation 118: 1450-1457. doi: 10.1172/JCI34022 PMID: 18317591
    • (2008) Journal of Clinical Investigation , vol.118 , pp. 1450-1457
    • Bruusgaard, J.C.1    Gundersen, K.2
  • 61
    • 77957921360 scopus 로고    scopus 로고
    • Astroglial loss and edema formation in the rat piriform cortex and hippocampus following pilocarpine-induced status epilepticus
    • PMID: 20886625
    • Kim JE, Yeo SI, Ryu HJ, Kim MJ, Kim DS, et al. (2010) Astroglial loss and edema formation in the rat piriform cortex and hippocampus following pilocarpine-induced status epilepticus. J Comp Neurol 518: 4612-4628. doi: 10.1002/cne.22482 PMID: 20886625
    • (2010) J Comp Neurol , vol.518 , pp. 4612-4628
    • Kim, J.E.1    Yeo, S.I.2    Ryu, H.J.3    Kim, M.J.4    Kim, D.S.5
  • 62
    • 77649309210 scopus 로고    scopus 로고
    • Dynamics of muscle fibre growth during postnatal mouse development
    • PMID: 20175910
    • White RB, Bierinx AS, Gnocchi VF, Zammit PS (2010) Dynamics of muscle fibre growth during postnatal mouse development. Bmc Developmental Biology 10: 21. doi: 10.1186/1471-213X-10-21 PMID: 20175910
    • (2010) Bmc Developmental Biology , vol.10 , pp. 21
    • White, R.B.1    Bierinx, A.S.2    Gnocchi, V.F.3    Zammit, P.S.4
  • 63
    • 84859910158 scopus 로고    scopus 로고
    • Hsp72 preserves muscle function and slows progression of severe muscular dystrophy
    • PMID: 22495301
    • Gehrig SM, van der Poel C, Sayer TA, Schertzer JD, Henstridge DC, et al. (2012) Hsp72 preserves muscle function and slows progression of severe muscular dystrophy. Nature 484: 394-398. doi: 10.1038/nature10980 PMID: 22495301
    • (2012) Nature , vol.484 , pp. 394-398
    • Gehrig, S.M.1    Van Der Poel, C.2    Sayer, T.A.3    Schertzer, J.D.4    Henstridge, D.C.5
  • 64
    • 84858800356 scopus 로고    scopus 로고
    • Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy
    • PMID: 22153988
    • Wang CH, Leung M, Liang WC, Hsieh TJ, Chen TH, et al. (2012) Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy. Neuromuscul Disord 22: 331-338. doi: 10.1016/j.nmd.2011.10.018 PMID: 22153988
    • (2012) Neuromuscul Disord , vol.22 , pp. 331-338
    • Wang, C.H.1    Leung, M.2    Liang, W.C.3    Hsieh, T.J.4    Chen, T.H.5
  • 65
    • 67149122523 scopus 로고    scopus 로고
    • Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies
    • PMID: 18808326
    • Wallace GQ, McNally EM (2009) Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies. Annu Rev Physiol 71: 37-57. doi: 10.1146/annurev.physiol.010908.163216 PMID: 18808326
    • (2009) Annu Rev Physiol , vol.71 , pp. 37-57
    • Wallace, G.Q.1    McNally, E.M.2
  • 66
    • 79956137778 scopus 로고    scopus 로고
    • Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1
    • PMID: 21603621
    • Chen SC, Frett E, Marx J, Bosnakovski D, Reed X, et al. (2011) Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1. Plos One 6: e19780. doi: 10.1371/journal.pone.0019780 PMID: 21603621
    • (2011) Plos One , vol.6 , pp. e19780
    • Chen, S.C.1    Frett, E.2    Marx, J.3    Bosnakovski, D.4    Reed, X.5
  • 67
    • 0027476102 scopus 로고
    • Quantitative analysis of the human alpha-skeletal actin gene in transgenic mice
    • PMID: 7678010
    • Brennan KJ, Hardeman EC (1993) Quantitative analysis of the human alpha-skeletal actin gene in transgenic mice. Journal of Biological Chemistry 268: 719-725. PMID: 7678010
    • (1993) Journal of Biological Chemistry , vol.268 , pp. 719-725
    • Brennan, K.J.1    Hardeman, E.C.2
  • 69
    • 84876274371 scopus 로고    scopus 로고
    • Type 2 Innate Signals Stimulate Fibro/Adipogenic Progenitors to Facilitate Muscle Regeneration
    • PMID: 23582327
    • Heredia JE, Mukundan L, Chen FM, Mueller AA, Deo RC, et al. (2013) Type 2 Innate Signals Stimulate Fibro/Adipogenic Progenitors to Facilitate Muscle Regeneration. Cell 153: 376-388. doi: 10.1016/j.cell.2013.02.053 PMID: 23582327
    • (2013) Cell , vol.153 , pp. 376-388
    • Heredia, J.E.1    Mukundan, L.2    Chen, F.M.3    Mueller, A.A.4    Deo, R.C.5
  • 70
    • 0037726553 scopus 로고    scopus 로고
    • IL-4 acts as a myoblast recruitment factor during mammalian muscle growth
    • PMID: 12757709
    • Horsley V, Jansen KM, Mills ST, Pavlath GK (2003) IL-4 acts as a myoblast recruitment factor during mammalian muscle growth. Cell 113: 483-494. PMID: 12757709
    • (2003) Cell , vol.113 , pp. 483-494
    • Horsley, V.1    Jansen, K.M.2    Mills, S.T.3    Pavlath, G.K.4
  • 71
    • 77951700255 scopus 로고    scopus 로고
    • Regulatory interactions between muscle and the immune system during muscle regeneration
    • PMID: 20219869
    • Tidball JG, Villalta SA (2010) Regulatory interactions between muscle and the immune system during muscle regeneration. Am J Physiol Regul Integr Comp Physiol 298: R1173-1187. doi: 10.1152/ajpregu.00735.2009 PMID: 20219869
    • (2010) Am J Physiol Regul Integr Comp Physiol , vol.298 , pp. R1173-R1187
    • Tidball, J.G.1    Villalta, S.A.2
  • 72
    • 84861014560 scopus 로고    scopus 로고
    • Sphingosine-1-phosphate enhances satellite cell activation in dystrophic muscles through a S1PR2/STAT3 signaling pathway
    • PMID: 22606352
    • Loh KC, Leong WI, Carlson ME, Oskouian B, Kumar A, et al. (2012) Sphingosine-1-phosphate enhances satellite cell activation in dystrophic muscles through a S1PR2/STAT3 signaling pathway. Plos One 7: e37218. doi: 10.1371/journal.pone.0037218 PMID: 22606352
    • (2012) Plos One , vol.7 , pp. e37218
    • Loh, K.C.1    Leong, W.I.2    Carlson, M.E.3    Oskouian, B.4    Kumar, A.5
  • 74
    • 84880397926 scopus 로고    scopus 로고
    • Myomaker is a membrane activator of myoblast fusion and muscle formation
    • PMID: 23868259
    • Millay DP, O'Rourke JR, Sutherland LB, Bezprozvannaya S, Shelton JM, et al. (2013) Myomaker is a membrane activator of myoblast fusion and muscle formation. Nature 499: 301-305. doi: 10.1038/nature12343 PMID: 23868259
    • (2013) Nature , vol.499 , pp. 301-305
    • Millay, D.P.1    O'Rourke, J.R.2    Sutherland, L.B.3    Bezprozvannaya, S.4    Shelton, J.M.5
  • 75
    • 84893019463 scopus 로고    scopus 로고
    • Galphai2 signaling is required for skeletal muscle growth, regeneration, and satellite cell proliferation and differentiation
    • PMID: 24298018
    • Minetti GC, Feige JN, Bombard F, Heier A, Morvan F, et al. (2014) Galphai2 signaling is required for skeletal muscle growth, regeneration, and satellite cell proliferation and differentiation. Molecular and Cellular Biology 34: 619-630. doi: 10.1128/MCB.00957-13 PMID: 24298018
    • (2014) Molecular and Cellular Biology , vol.34 , pp. 619-630
    • Minetti, G.C.1    Feige, J.N.2    Bombard, F.3    Heier, A.4    Morvan, F.5
  • 76
    • 84903469617 scopus 로고    scopus 로고
    • Primary cilia control hedgehog signaling during muscle differentiation and are deregulated in rhabdomyosarcoma
    • PMID: 24927541
    • Fu W, Asp P, Canter B, Dynlacht BD (2014) Primary cilia control hedgehog signaling during muscle differentiation and are deregulated in rhabdomyosarcoma. Proc Natl Acad Sci U S A 111: 9151-9156. doi: 10.1073/pnas.1323265111 PMID: 24927541
    • (2014) Proc Natl Acad Sci U S A , vol.111 , pp. 9151-9156
    • Fu, W.1    Asp, P.2    Canter, B.3    Dynlacht, B.D.4
  • 77
    • 84879864816 scopus 로고    scopus 로고
    • Brain and muscle Arnt-like 1 is a key regulator of myogenesis
    • PMID: 23525013
    • Chatterjee S, Nam D, Guo B, Kim JM, Winnier GE, et al. (2013) Brain and muscle Arnt-like 1 is a key regulator of myogenesis. Journal of Cell Science 126: 2213-2224. doi: 10.1242/jcs.120519 PMID: 23525013
    • (2013) Journal of Cell Science , vol.126 , pp. 2213-2224
    • Chatterjee, S.1    Nam, D.2    Guo, B.3    Kim, J.M.4    Winnier, G.E.5
  • 78
    • 85027917443 scopus 로고    scopus 로고
    • Smad3 signaling is required for satellite cell function and myogenic differentiation of myoblasts
    • PMID: 21502976
    • Ge X, McFarlane C, Vajjala A, Lokireddy S, Ng ZH, et al. (2011) Smad3 signaling is required for satellite cell function and myogenic differentiation of myoblasts. Cell Res 21: 1591-1604. doi: 10.1038/cr.2011.72 PMID: 21502976
    • (2011) Cell Res , vol.21 , pp. 1591-1604
    • Ge, X.1    McFarlane, C.2    Vajjala, A.3    Lokireddy, S.4    Ng, Z.H.5
  • 79
    • 0038273864 scopus 로고    scopus 로고
    • Intact satellite cells lead to remarkable protection against Smn gene defect in differentiated skeletal muscle
    • PMID: 12743106
    • Nicole S, Desforges B, Millet G, Lesbordes J, Cifuentes-Diaz C, et al. (2003) Intact satellite cells lead to remarkable protection against Smn gene defect in differentiated skeletal muscle. Journal of Cell Biology 161: 571-582. PMID: 12743106
    • (2003) Journal of Cell Biology , vol.161 , pp. 571-582
    • Nicole, S.1    Desforges, B.2    Millet, G.3    Lesbordes, J.4    Cifuentes-Diaz, C.5
  • 80
    • 37149022054 scopus 로고    scopus 로고
    • Muscle-specific overexpression of the type 1 IGF receptor results in myoblast-independent muscle hypertrophy via PI3K, and not calcineurin, signaling
    • PMID: 17940216
    • Quinn LS, Anderson BG, Plymate SR (2007) Muscle-specific overexpression of the type 1 IGF receptor results in myoblast-independent muscle hypertrophy via PI3K, and not calcineurin, signaling. Am J Physiol Endocrinol Metab 293: E1538-1551. PMID: 17940216
    • (2007) Am J Physiol Endocrinol Metab , vol.293 , pp. E1538-E1551
    • Quinn, L.S.1    Anderson, B.G.2    Plymate, S.R.3
  • 81
    • 84855306505 scopus 로고    scopus 로고
    • Down-Regulation of Myogenin Can Reverse Terminal Muscle Cell Differentiation
    • PMID: 23349657
    • Mastroyiannopoulos NP, Nicolaou P, Anayasa M, Uney JB, Phylactou LA (2012) Down-Regulation of Myogenin Can Reverse Terminal Muscle Cell Differentiation. Plos One 7. doi: 10.1371/journal.pone.0051204 PMID: 23349657
    • (2012) Plos One , vol.7
    • Mastroyiannopoulos, N.P.1    Nicolaou, P.2    Anayasa, M.3    Uney, J.B.4    Phylactou, L.A.5
  • 82
    • 0038236734 scopus 로고    scopus 로고
    • Calcineurin is a potent regulator for skeletal muscle regeneration by association with NFATc1 and GATA-2
    • PMID: 12557015
    • Sakuma K, Nishikawa J, Nakao R, Watanabe K, Totsuka T, et al. (2003) Calcineurin is a potent regulator for skeletal muscle regeneration by association with NFATc1 and GATA-2. Acta Neuropathologica 105: 271-280. PMID: 12557015
    • (2003) Acta Neuropathologica , vol.105 , pp. 271-280
    • Sakuma, K.1    Nishikawa, J.2    Nakao, R.3    Watanabe, K.4    Totsuka, T.5
  • 83
    • 78650972892 scopus 로고    scopus 로고
    • Calcineurin-NFAT signaling critically regulates early lineage specification in mouse embryonic stem cells and embryos
    • PMID: 21211781
    • Li X, Zhu L, Yang A, Lin J, Tang F, et al. (2011) Calcineurin-NFAT signaling critically regulates early lineage specification in mouse embryonic stem cells and embryos. Cell Stem Cell 8: 46-58. doi: 10.1016/j.stem.2010.11.027 PMID: 21211781
    • (2011) Cell Stem Cell , vol.8 , pp. 46-58
    • Li, X.1    Zhu, L.2    Yang, A.3    Lin, J.4    Tang, F.5
  • 84
    • 0037073786 scopus 로고    scopus 로고
    • Requirement of nuclear factor of activated T-cells in calcineurin-mediated cardiomyocyte hypertrophy
    • PMID: 12226086
    • van Rooij E, Doevendans PA, de Theije CC, Babiker FA, Molkentin JD, et al. (2002) Requirement of nuclear factor of activated T-cells in calcineurin-mediated cardiomyocyte hypertrophy. Journal of Biological Chemistry 277: 48617-48626. PMID: 12226086
    • (2002) Journal of Biological Chemistry , vol.277 , pp. 48617-48626
    • Van Rooij, E.1    Doevendans, P.A.2    De Theije, C.C.3    Babiker, F.A.4    Molkentin, J.D.5
  • 85
    • 0035897418 scopus 로고    scopus 로고
    • Regulation of the growth of multinucleated muscle cells by an NFATC2-dependent pathway
    • PMID: 11309414
    • Horsley V, Friday BB, Matteson S, Kegley KM, Gephart J, et al. (2001) Regulation of the growth of multinucleated muscle cells by an NFATC2-dependent pathway. Journal of Cell Biology 153: 329-338. PMID: 11309414
    • (2001) Journal of Cell Biology , vol.153 , pp. 329-338
    • Horsley, V.1    Friday, B.B.2    Matteson, S.3    Kegley, K.M.4    Gephart, J.5
  • 86
    • 2342640319 scopus 로고    scopus 로고
    • Cell fusion in skeletal muscle - Central role of NFATC2 in regulating muscle cell size
    • PMID: 12963831
    • Pavlath GK, Horsley V (2003) Cell fusion in skeletal muscle - central role of NFATC2 in regulating muscle cell size. Cell Cycle 2: 420-423. PMID: 12963831
    • (2003) Cell Cycle , vol.2 , pp. 420-423
    • Pavlath, G.K.1    Horsley, V.2
  • 87
    • 84877775057 scopus 로고    scopus 로고
    • Phosphatidylserine receptor BAI1 and apoptotic cells as new promoters of myoblast fusion
    • PMID: 23615608
    • Hochreiter-Hufford AE, Lee CS, Kinchen JM, Sokolowski JD, Arandjelovic S, et al. (2013) Phosphatidylserine receptor BAI1 and apoptotic cells as new promoters of myoblast fusion. Nature 497: 263-267. doi: 10.1038/nature12135 PMID: 23615608
    • (2013) Nature , vol.497 , pp. 263-267
    • Hochreiter-Hufford, A.E.1    Lee, C.S.2    Kinchen, J.M.3    Sokolowski, J.D.4    Arandjelovic, S.5
  • 88
    • 79551686645 scopus 로고    scopus 로고
    • Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein
    • PMID: 20970242
    • Hanel ML, Sun CYJ, Jones TI, Long SW, Zanotti S, et al. (2011) Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein. Differentiation 81: 107-118. doi: 10.1016/j.diff.2010.09.185 PMID: 20970242
    • (2011) Differentiation , vol.81 , pp. 107-118
    • Hanel, M.L.1    Sun, C.Y.J.2    Jones, T.I.3    Long, S.W.4    Zanotti, S.5
  • 89
    • 84892576144 scopus 로고    scopus 로고
    • Altered Tnnt3 characterizes selective weakness of fast fibers in mice overexpressing FSHD region gene 1 (FRG1)
    • PMID: 24305066
    • Sancisi V, Germinario E, Esposito A, Morini E, Peron S, et al. (2014) Altered Tnnt3 characterizes selective weakness of fast fibers in mice overexpressing FSHD region gene 1 (FRG1). Am J Physiol Regul Integr Comp Physiol 306: R124-137. doi: 10.1152/ajpregu.00379.2013 PMID: 24305066
    • (2014) Am J Physiol Regul Integr Comp Physiol , vol.306 , pp. R124-R137
    • Sancisi, V.1    Germinario, E.2    Esposito, A.3    Morini, E.4    Peron, S.5
  • 90
    • 84862212313 scopus 로고    scopus 로고
    • Myogenesis in dysferlin-deficient myoblasts is inhibited by an intrinsic inflammatory response
    • PMID: 22560623
    • Cohen TV, Cohen JE, Partridge TA (2012) Myogenesis in dysferlin-deficient myoblasts is inhibited by an intrinsic inflammatory response. Neuromuscular Disorders 22: 648-658. doi: 10.1016/j.nmd.2012.03.002 PMID: 22560623
    • (2012) Neuromuscular Disorders , vol.22 , pp. 648-658
    • Cohen, T.V.1    Cohen, J.E.2    Partridge, T.A.3
  • 91
    • 84900796161 scopus 로고    scopus 로고
    • FHL1 mutants that cause clinically distinct human myopathies form protein aggregates and impair myoblast differentiation
    • PMID: 24634512
    • Wilding BR, McGrath MJ, Bonne G, Mitchell CA (2014) FHL1 mutants that cause clinically distinct human myopathies form protein aggregates and impair myoblast differentiation. Journal of Cell Science 127: 2269-2281. doi: 10.1242/jcs.140905 PMID: 24634512
    • (2014) Journal of Cell Science , vol.127 , pp. 2269-2281
    • Wilding, B.R.1    McGrath, M.J.2    Bonne, G.3    Mitchell, C.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.