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Volumn 57, Issue 2, 2013, Pages 86-92

Muscleblind-like1 undergoes Ectopic relocation in the nuclei of skeletal muscles in myotonic dystrophy and sarcopenia

Author keywords

Cell nucleus; MBNL1; Myotonic dystrophy; Sarcopenia; Skeletal muscle

Indexed keywords

MUS;

EID: 84892635431     PISSN: 1121760X     EISSN: None     Source Type: Journal    
DOI: 10.4081/ejh.2013.e15     Document Type: Article
Times cited : (16)

References (72)
  • 2
    • 33644858553 scopus 로고    scopus 로고
    • The Muscleblind family of proteins: An emerging class of regulators of developmentally programmed alternative splicing
    • Pascual M, Vicente M, Monferrer L, Artero R. The Muscleblind family of proteins: an emerging class of regulators of developmentally programmed alternative splicing. Differentiation 2006;74:65-80.
    • (2006) Differentiation , vol.74 , pp. 65-80
    • Pascual, M.1    Vicente, M.2    Monferrer, L.3    Artero, R.4
  • 4
    • 15544387787 scopus 로고    scopus 로고
    • Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to Drosophila
    • Houseley JM, Wang Z, Brock GJ, Soloway J, Artero R, Perez-Alonso M, et al. Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to Drosophila. Hum Mol Genet 2005;14:873-883.
    • (2005) Hum Mol Genet , vol.14 , pp. 873-883
    • Houseley, J.M.1    Wang, Z.2    Brock, G.J.3    Soloway, J.4    Artero, R.5    Perez-Alonso, M.6
  • 6
    • 0013394889 scopus 로고    scopus 로고
    • Mechanisms of alternative pre-messenger RNA splicing
    • Black DL. Mechanisms of alternative pre-messenger RNA splicing. Annu Rev Biochem 2003;72:291-336.
    • (2003) Annu Rev Biochem , vol.72 , pp. 291-336
    • Black, D.L.1
  • 7
    • 80054003119 scopus 로고    scopus 로고
    • Alternative splicing regulation by Muscleblind proteins: From development to disease
    • Fernandez-Costa JM, Llamusi MB, Garcia-Lopez A, Artero R. Alternative splicing regulation by Muscleblind proteins: from development to disease. Biol Rev 2011;86: 947-958.
    • (2011) Biol Rev , vol.86 , pp. 947-958
    • Fernandez-Costa, J.M.1    Llamusi, M.B.2    Garcia-Lopez, A.3    Artero, R.4
  • 8
    • 10744219570 scopus 로고    scopus 로고
    • Histopa -thological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2
    • Vihola A, Bassez G, Meola G, Zhang S, Haapasalo H, Paetau A, et al. Histopa -thological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2. Neurology 2003;60:1854-1857.
    • (2003) Neurology , vol.60 , pp. 1854-1857
    • Vihola, A.1    Bassez, G.2    Meola, G.3    Zhang, S.4    Haapasalo, H.5    Paetau, A.6
  • 9
    • 0142027590 scopus 로고    scopus 로고
    • Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myoton-ic dystrophy of different European origins: A single shared haplotype indicates an ancestral founder effect
    • Bachinski LL, Udd B, Meola G, Sansone V, Bassez G, Eymard B, et al. Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myoton-ic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect. Am J Hum Gen 2003;73:835-848.
    • (2003) Am J Hum Gen , vol.73 , pp. 835-848
    • Bachinski, L.L.1    Udd, B.2    Meola, G.3    Sansone, V.4    Bassez, G.5    Eymard, B.6
  • 10
    • 8744295714 scopus 로고    scopus 로고
    • Myotonic dystrophy type 2 and related myotonic disorders
    • rd. Myotonic dystrophy type 2 and related myotonic disorders. J Neurol 2004;251:1173-1182.
    • (2004) J Neurol , vol.251 , pp. 1173-1182
    • Meola, G.1    Moxley, R.T.2
  • 11
    • 0034873099 scopus 로고    scopus 로고
    • Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy
    • Savkur RS, Philips AV, Cooper TA. Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy. Nat Genet 2001;29: 40-47.
    • (2001) Nat Genet , vol.29 , pp. 40-47
    • Savkur, R.S.1    Philips, A.V.2    Cooper, T.A.3
  • 14
    • 0027122152 scopus 로고
    • Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member
    • Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, et al. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member. Cell 1992; 69:385-387.
    • (1992) Cell , vol.69 , pp. 385-387
    • Brook, J.D.1    McCurrach, M.E.2    Harley, H.G.3    Buckler, A.J.4    Church, D.5    Aburatani, H.6
  • 15
  • 16
    • 0026603841 scopus 로고
    • Myotonic dystrophy mutation: An unstable CTG repeat in the 3' untranslated region of the gene
    • Mahadevan M, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jansen G, et al. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene. Science 1992;255:1253-1255.
    • (1992) Science , vol.255 , pp. 1253-1255
    • Mahadevan, M.1    Tsilfidis, C.2    Sabourin, L.3    Shutler, G.4    Amemiya, C.5    Jansen, G.6
  • 17
    • 0028947317 scopus 로고
    • Foci of trinu-cleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues
    • Taneja KL, McCurrach M, Schalling M, Housman D, Singer RH. Foci of trinu-cleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues. J Cell Biol 1995;128:995-1002.
    • (1995) J Cell Biol , vol.128 , pp. 995-1002
    • Taneja, K.L.1    McCurrach, M.2    Schalling, M.3    Housman, D.4    Singer, R.H.5
  • 20
    • 0036537492 scopus 로고    scopus 로고
    • Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells
    • Fardaei M, Rogers MT, Thorpe HM, Larkin K, Hamshere MG, Harper PS, et al. Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells. Hum Mol Genet 2002;11:805-814.
    • (2002) Hum Mol Genet , vol.11 , pp. 805-814
    • Fardaei, M.1    Rogers, M.T.2    Thorpe, H.M.3    Larkin, K.4    Hamshere, M.G.5    Harper, P.S.6
  • 21
    • 0034783271 scopus 로고    scopus 로고
    • Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2
    • Mankodi A, Urbinati CR, Yuan QP, Moxley RT, Sansone V, Krym M, et al. Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2. Hum Mol Genet 2001;10:2165-21670.
    • (2001) Hum Mol Genet , vol.10 , pp. 2165-21670
    • Mankodi, A.1    Urbinati, C.R.2    Yuan, Q.P.3    Moxley, R.T.4    Sansone, V.5    Krym, M.6
  • 22
    • 0034282958 scopus 로고    scopus 로고
    • Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy
    • Miller JW, Urbinati CR, Teng-Umnuay P, Stenberg MG, Byrne BJ, Thornton CA, et al. Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy. EMBO J 2000;19:4439-4448.
    • (2000) EMBO J , vol.19 , pp. 4439-4448
    • Miller, J.W.1    Urbinati, C.R.2    Teng-Umnuay, P.3    Stenberg, M.G.4    Byrne, B.J.5    Thornton, C.A.6
  • 24
    • 33745248133 scopus 로고    scopus 로고
    • Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy
    • Lin X, Miller JW, Mankodi A, Kanadia RN, Yuan Y, Moxley RT, et al. Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy. Hum Mol Genet 2006;15:2087-2097.
    • (2006) Hum Mol Genet , vol.15 , pp. 2087-2097
    • Lin, X.1    Miller, J.W.2    Mankodi, A.3    Kanadia, R.N.4    Yuan, Y.5    Moxley, R.T.6
  • 25
    • 58149492467 scopus 로고    scopus 로고
    • A postnatal switch of CELF and MBNL proteins repro-grams alternative splicing in the developing heart
    • Kalsotra A, Xiao X, Ward AJ, Castle JC, Johnson JM, Burge CB, et al. A postnatal switch of CELF and MBNL proteins repro-grams alternative splicing in the developing heart. Proc Natl Acad Sci USA 2008;105:20333-20338.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 20333-20338
    • Kalsotra, A.1    Xiao, X.2    Ward, A.J.3    Castle, J.C.4    Johnson, J.M.5    Burge, C.B.6
  • 26
    • 85011940615 scopus 로고    scopus 로고
    • Conserved developmental alternative splicing of muscleblind-like (MBNL) transcripts regulates MBNL localization and activity
    • Terenzi F, Ladd AN. Conserved developmental alternative splicing of muscleblind-like (MBNL) transcripts regulates MBNL localization and activity. RNA Biol 2010; 7:43-55.
    • (2010) RNA Biol , vol.7 , pp. 43-55
    • Terenzi, F.1    Ladd, A.N.2
  • 27
    • 33748373580 scopus 로고    scopus 로고
    • RNA-mediated neu-romuscular disorders
    • Ranum LP, Cooper TA. RNA-mediated neu-romuscular disorders. Annu Rev Neurosci 2006;29:259-277.
    • (2006) Annu Rev Neurosci , vol.29 , pp. 259-277
    • Ranum, L.P.1    Cooper, T.A.2
  • 28
    • 67249165478 scopus 로고    scopus 로고
    • The protein factors MBNL1 and U2AF65 bind alternative RNA structures to regulate splicing
    • Warf MB, Diegel JV, von Hippel PH, Berglund JA. The protein factors MBNL1 and U2AF65 bind alternative RNA structures to regulate splicing. PNAS 2009; 106:9203-9208.
    • (2009) PNAS , vol.106 , pp. 9203-9208
    • Warf, M.B.1    Diegel, J.V.2    von Hippel, P.H.3    Berglund, J.A.4
  • 29
    • 80052272221 scopus 로고    scopus 로고
    • Alternative splicing of myomesin 1 gene is aberrantly regulated in myotonic dystrophy type 1
    • Koebis M, Ohsawa N, Kino Y, Sasagawa N, Nishino I, Ishiura S. Alternative splicing of myomesin 1 gene is aberrantly regulated in myotonic dystrophy type 1. Genes Cells 2011;16:961-972.
    • (2011) Genes Cells , vol.16 , pp. 961-972
    • Koebis, M.1    Ohsawa, N.2    Kino, Y.3    Sasagawa, N.4    Nishino, I.5    Ishiura, S.6
  • 30
    • 81955167967 scopus 로고    scopus 로고
    • Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues
    • Rinaldi F, Terracciano C, Pisani V, Massa R, Loro E, Vergani L, et al. Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues. Neurobiol Dis 2012;45: 264-271.
    • (2012) Neurobiol Dis , vol.45 , pp. 264-271
    • Rinaldi, F.1    Terracciano, C.2    Pisani, V.3    Massa, R.4    Loro, E.5    Vergani, L.6
  • 31
    • 79958101846 scopus 로고    scopus 로고
    • Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
    • Fugier C, Klein AF, Hammer C, Vassilopoulos S, Ivarsson Y, Toussaint A, et al. Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy. Nature Med 2011;17:720-726.
    • (2011) Nature Med , vol.17 , pp. 720-726
    • Fugier, C.1    Klein, A.F.2    Hammer, C.3    Vassilopoulos, S.4    Ivarsson, Y.5    Toussaint, A.6
  • 32
    • 0036347927 scopus 로고    scopus 로고
    • Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing
    • Charlet BN, Savkur RS, Singh G, Philips AV, Grice EA, Cooper TA. Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing. Mol Cell 2002;10:45-53.
    • (2002) Mol Cell , vol.10 , pp. 45-53
    • Charlet, B.N.1    Savkur, R.S.2    Singh, G.3    Philips, A.V.4    Grice, E.A.5    Cooper, T.A.6
  • 33
    • 84857662317 scopus 로고    scopus 로고
    • Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of Ca(V)1.1 calcium channel
    • Tang ZZ, Yarotskyy V, Wei L, Sobczak K, Nakamori M, Eichinger K, et al. Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of Ca(V)1.1 calcium channel. Hum Mol Genet 2012;21:1312-1324.
    • (2012) Hum Mol Genet , vol.21 , pp. 1312-1324
    • Tang, Z.Z.1    Yarotskyy, V.2    Wei, L.3    Sobczak, K.4    Nakamori, M.5    Eichinger, K.6
  • 34
    • 33748919081 scopus 로고    scopus 로고
    • Interaction of musleblind, CUG-BP1 and hnRNP H proteins in DM1-associated aberrant IR splicing
    • Paul S, Dansithong W, Kim D, Rossi J, Webster NJG, Comai L, et al. Interaction of musleblind, CUG-BP1 and hnRNP H proteins in DM1-associated aberrant IR splicing. EMBO J 2006;25:4271-4283.
    • (2006) EMBO J , vol.25 , pp. 4271-4283
    • Paul, S.1    Dansithong, W.2    Kim, D.3    Rossi, J.4    Webster, N.J.G.5    Comai, L.6
  • 35
    • 70849130776 scopus 로고    scopus 로고
    • RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: An immunocy-tochemical study
    • Perdoni F, Malatesta M, Cardani R, Giagnacovo M, Mancinelli E, Meola G, et al. RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocy-tochemical study. Eur J Histochem 2009; 53:151-158.
    • (2009) Eur J Histochem , vol.53 , pp. 151-158
    • Perdoni, F.1    Malatesta, M.2    Cardani, R.3    Giagnacovo, M.4    Mancinelli, E.5    Meola, G.6
  • 36
    • 1942488260 scopus 로고    scopus 로고
    • Ultrastructural cytochemical analyses of nuclear functional architecture
    • Fakan S. Ultrastructural cytochemical analyses of nuclear functional architecture. Eur J Histochem 2004;48:5-14.
    • (2004) Eur J Histochem , vol.48 , pp. 5-14
    • Fakan, S.1
  • 37
    • 79956224888 scopus 로고    scopus 로고
    • RNA processing is altered in skeletal muscle nuclei of patients affected by myotonic dystrophy
    • Malatesta M, Giagnacovo M, Cardani R, Meola G, Pellicciari C. RNA processing is altered in skeletal muscle nuclei of patients affected by myotonic dystrophy. Histochem Cell Biol 2011;135:419-425.
    • (2011) Histochem Cell Biol , vol.135 , pp. 419-425
    • Malatesta, M.1    Giagnacovo, M.2    Cardani, R.3    Meola, G.4    Pellicciari, C.5
  • 39
    • 70349245041 scopus 로고    scopus 로고
    • Nuclei of aged myofibres undergo structural and func-tional changes suggesting impairment in RNA processing
    • Malatesta M, Perdoni F, Muller S, Zancanaro C, Pellicciari C. Nuclei of aged myofibres undergo structural and func-tional changes suggesting impairment in RNA processing. Eur J Histochem 2009; 53:97-106.
    • (2009) Eur J Histochem , vol.53 , pp. 97-106
    • Malatesta, M.1    Perdoni, F.2    Muller, S.3    Zancanaro, C.4    Pellicciari, C.5
  • 41
    • 80054977782 scopus 로고    scopus 로고
    • Physical training modulates structural and functional features of cell nuclei in type II myofibers of old mice
    • Malatesta M, Fattoretti P, Giagnacovo M, Pellicciari C, Zancanaro C. Physical training modulates structural and functional features of cell nuclei in type II myofibers of old mice. Rejuvenation Res 2011;14:543-552.
    • (2011) Rejuvenation Res , vol.14 , pp. 543-552
    • Malatesta, M.1    Fattoretti, P.2    Giagnacovo, M.3    Pellicciari, C.4    Zancanaro, C.5
  • 42
    • 77953870112 scopus 로고    scopus 로고
    • Sarcopenia: European consensus on definition and diagnosis: Report of the European Working Group on Sarcopenia in Older People
    • European Working Group on Sarcopenia in Older People
    • Cruz-Jentoft AJ, Baeyens J P, Bauer JM, Boirie Y, Cederholm T, Landi F, et al.; European Working Group on Sarcopenia in Older People. Sarcopenia: European consensus on definition and diagnosis: Report of the European Working Group on Sarcopenia in Older People. Age Ageing 2010;39:412-423.
    • (2010) Age Ageing , vol.39 , pp. 412-423
    • Cruz-Jentoft, A.J.1    Baeyens, J.P.2    Bauer, J.M.3    Boirie, Y.4    Cederholm, T.5    Landi, F.6
  • 44
    • 78249287818 scopus 로고    scopus 로고
    • Structural and functional alterations of the cell nucleus in skeletal muscle wasting: The evidence in situ
    • Malatesta M, Meola G. Structural and functional alterations of the cell nucleus in skeletal muscle wasting: the evidence in situ. Eur J Histochem 2010;54:e44.
    • (2010) Eur J Histochem , vol.54
    • Malatesta, M.1    Meola, G.2
  • 45
  • 46
    • 84876709377 scopus 로고    scopus 로고
    • Skeletal muscle features in myotonic dystrophy and sarcopenia: Do similar nuclear mechanisms lead to skeletal muscle wasting?
    • Malatesta M. Skeletal muscle features in myotonic dystrophy and sarcopenia: do similar nuclear mechanisms lead to skeletal muscle wasting? Eur J Histochem 2012; 56:e36.
    • (2012) Eur J Histochem , vol.56
    • Malatesta, M.1
  • 47
    • 79956101359 scopus 로고    scopus 로고
    • Myotonic dystrophy type 2 (DM2) and related disorders report of the 180th INMC workshop including guidelines on diagnostics and management 3-5 December 2010, Naarden, The Netherlands
    • Udd B, Meola G, Krahe R, Wansink DG, Bassez G, Kress W, et al. Myotonic dystrophy type 2 (DM2) and related disorders report of the 180th INMC workshop including guidelines on diagnostics and management 3-5 December 2010, Naarden, The Netherlands. Neuromuscl Disord 2011;21:443-450.
    • (2011) Neuromuscl Disord , vol.21 , pp. 443-450
    • Udd, B.1    Meola, G.2    Krahe, R.3    Wansink, D.G.4    Bassez, G.5    Kress, W.6
  • 48
    • 0028863055 scopus 로고
    • Human aging, muscle mass, and fibre type composition
    • Lexell J. Human aging, muscle mass, and fibre type composition. J Gerontol A Biol Sci Med Sci 1995;50:11-16.
    • (1995) J Gerontol a Biol Sci Med Sci , vol.50 , pp. 11-16
    • Lexell, J.1
  • 49
    • 0014510120 scopus 로고
    • A new staining procedure for electron microscopical cytology
    • Bernhard W. A new staining procedure for electron microscopical cytology. J Ultrastruct Res 1969;27:250-265.
    • (1969) J Ultrastruct Res , vol.27 , pp. 250-265
    • Bernhard, W.1
  • 52
    • 34948864433 scopus 로고    scopus 로고
    • Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2
    • Cardani R, Mancinelli E, Rotondo G, Sansone V, Meola G. Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2. Eur J Histochem 2006;50:177-182.
    • (2006) Eur J Histochem , vol.50 , pp. 177-182
    • Cardani, R.1    Mancinelli, E.2    Rotondo, G.3    Sansone, V.4    Meola, G.5
  • 53
    • 0021334795 scopus 로고
    • Ultrastructural distribution of nuclear ribonu-cleoproteins as visualized by immunocyto-chemistry on thin sections
    • Fakan S, Leser G, Martin TE. Ultrastructural distribution of nuclear ribonu-cleoproteins as visualized by immunocyto-chemistry on thin sections. J Cell Biol 1984;98:358-363.
    • (1984) J Cell Biol , vol.98 , pp. 358-363
    • Fakan, S.1    Leser, G.2    Martin, T.E.3
  • 54
    • 0032917782 scopus 로고    scopus 로고
    • Ultrastructural analysis of transcription and splicing in the cell nucleus after bromo-UTP microinjection
    • Cmarko D, Verschure PJ, Martin TE, Dahmus ME, Krause S, Fu XD, et al. Ultrastructural analysis of transcription and splicing in the cell nucleus after bromo-UTP microinjection. Mol Biol Cell 1999;10:211-223.
    • (1999) Mol Biol Cell , vol.10 , pp. 211-223
    • Cmarko, D.1    Verschure, P.J.2    Martin, T.E.3    Dahmus, M.E.4    Krause, S.5    Fu, X.D.6
  • 55
    • 0025936626 scopus 로고
    • Associations between distinct pre-mRNA splicing components and the cell nucleus
    • Spector DL, Fu X-D, Maniatis T. Associations between distinct pre-mRNA splicing components and the cell nucleus. EMBO J 1991;10:3467-3481.
    • (1991) EMBO J , vol.10 , pp. 3467-3481
    • Spector, D.L.1    Fu, X.-D.2    Maniatis, T.3
  • 56
    • 0029931320 scopus 로고    scopus 로고
    • The RNA 3' cleavage factors CstF 64 kDa and CPSF 100 kDa are concentrated in nuclear domains closely associated with coiled bodies and newly synthesized RNA
    • Schul W, Groenhout B, Koberna K, Takagaki Y, Jenny A, Manders EM, et al. The RNA 3' cleavage factors CstF 64 kDa and CPSF 100 kDa are concentrated in nuclear domains closely associated with coiled bodies and newly synthesized RNA. EMBO J 1996;15:2883-2892.
    • (1996) EMBO J , vol.15 , pp. 2883-2892
    • Schul, W.1    Groenhout, B.2    Koberna, K.3    Takagaki, Y.4    Jenny, A.5    Manders, E.M.6
  • 58
    • 0030589683 scopus 로고    scopus 로고
    • Ultrastructure of the nucleus in relation to transcription and splicing: Roles of perichromatinfibrils and interchromatin granules
    • Puvion E, Puvion-Dutilleul F. Ultrastructure of the nucleus in relation to transcription and splicing: roles of perichromatinfibrils and interchromatin granules. Exp Cell Res 1996;229:217-225.
    • (1996) Exp Cell Res , vol.229 , pp. 217-225
    • Puvion, E.1    Puvion-Dutilleul, F.2
  • 59
    • 65449177319 scopus 로고    scopus 로고
    • Universal nuclear domains of somatic and germ cells: Some lessons from oocyte interchromatin granule cluster and Cajal body structure and molecular composition
    • Bogolyubov D, Stepanova I, Parfenov V. Universal nuclear domains of somatic and germ cells: some lessons from oocyte interchromatin granule cluster and Cajal body structure and molecular composition. Bioessays 2009;31:400-409.
    • (2009) Bioessays , vol.31 , pp. 400-409
    • Bogolyubov, D.1    Stepanova, I.2    Parfenov, V.3
  • 61
    • 34548842522 scopus 로고    scopus 로고
    • Defining early steps in mRNA transport: Mutant mRNA in myoton-ic dystrophy type I is blocked at entry into SC-35 domains
    • Smith K P, Byron M, Johnson C, Xing Y, Lawrence JB. Defining early steps in mRNA transport: mutant mRNA in myoton-ic dystrophy type I is blocked at entry into SC-35 domains. J Cell Biol 2007;178:951-964.
    • (2007) J Cell Biol , vol.178 , pp. 951-964
    • Smith, K.P.1    Byron, M.2    Johnson, C.3    Xing, Y.4    Lawrence, J.B.5
  • 62
    • 9444254707 scopus 로고    scopus 로고
    • Rearrangement of nuclear ribonucleopro-tein (RNP)-containing structures during apoptosis and transcriptional arrest
    • Biggiogera M, Bottone MG, Scovassi AI, Soldani C, Vecchio L, Pellicciari C. Rearrangement of nuclear ribonucleopro-tein (RNP)-containing structures during apoptosis and transcriptional arrest. Biol Cell 2004;96:603-615.
    • (2004) Biol Cell , vol.96 , pp. 603-615
    • Biggiogera, M.1    Bottone, M.G.2    Scovassi, A.I.3    Soldani, C.4    Vecchio, L.5    Pellicciari, C.6
  • 65
    • 84867336680 scopus 로고    scopus 로고
    • Nuclear ribonucleo-protein-containing foci increase in size innon-dividing cells from patients with myotonic dystrophy type 2
    • Giagnacovo M, Malatesta M, Cardani R, Meola G, Pellicciari C. Nuclear ribonucleo-protein-containing foci increase in size innon-dividing cells from patients with myotonic dystrophy type 2. Histochem Cell Biol 2012;138:699-707.
    • (2012) Histochem Cell Biol , vol.138 , pp. 699-707
    • Giagnacovo, M.1    Malatesta, M.2    Cardani, R.3    Meola, G.4    Pellicciari, C.5
  • 68
    • 67650751240 scopus 로고    scopus 로고
    • Expression of RNA CCUG repeats dysregu-lates translation and degradation of proteins in myotonic dystrophy 2 patients
    • Salisbury E, Schoser B, Schneider-Gold C, Wang GL, Huichalaf C, Jin B, et al. Expression of RNA CCUG repeats dysregu-lates translation and degradation of proteins in myotonic dystrophy 2 patients. Am J Pathol 2009;175:748-762.
    • (2009) Am J Pathol , vol.175 , pp. 748-762
    • Salisbury, E.1    Schoser, B.2    Schneider-Gold, C.3    Wang, G.L.4    Huichalaf, C.5    Jin, B.6
  • 69
    • 77957845571 scopus 로고    scopus 로고
    • Expansion of CUG RNA repeats causes stress and inhibition of translation in myotonic dystrophy 1 (DM1) cells
    • Huichalaf C, Sakai K, Jin B, Jones K, Wang GL, Schoser B, et al. Expansion of CUG RNA repeats causes stress and inhibition of translation in myotonic dystrophy 1 (DM1) cells. FASEB J 2010;24:3706-3719.
    • (2010) FASEB J , vol.24 , pp. 3706-3719
    • Huichalaf, C.1    Sakai, K.2    Jin, B.3    Jones, K.4    Wang, G.L.5    Schoser, B.6
  • 70
    • 66149092830 scopus 로고    scopus 로고
    • Aging, exercise and muscle protein metabolism
    • Koopman R, van Loon LJC. Aging, exercise and muscle protein metabolism. J Appl Physiol 2009;106:2040-2048.
    • (2009) J Appl Physiol , vol.106 , pp. 2040-2048
    • Koopman, R.1    van Loon, L.J.C.2
  • 71
    • 84857706630 scopus 로고    scopus 로고
    • Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features: Ultrastructural evidence
    • Malatesta M, Giagnacovo M, Renna LV, Cardani R, Meola G, Pellicciari C. Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features: ultrastructural evidence. Eur J Histochem 2011;55:e26.
    • (2011) Eur J Histochem , vol.55
    • Malatesta, M.1    Giagnacovo, M.2    Renna, L.V.3    Cardani, R.4    Meola, G.5    Pellicciari, C.6
  • 72
    • 2342461060 scopus 로고    scopus 로고
    • Myotonic dystrophy: RNA pathogenesis comes into focus
    • Ranum L P, Day JW. Myotonic dystrophy: RNA pathogenesis comes into focus. Am J Hum Genet 2004;74:793-804.
    • (2004) Am J Hum Genet , vol.74 , pp. 793-804
    • Ranum, L.P.1    Day, J.W.2


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