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Volumn 6, Issue , 2015, Pages

Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; MUSCLEBLIND LIKE 1 PROTEIN; RNA BINDING PROTEIN; UNCLASSIFIED DRUG; APO-DYSTROPHIN 1; DMD PROTEIN, HUMAN; DYSTROPHIN PROTEIN, ZEBRAFISH; MBNL1 PROTEIN, HUMAN; MEMBRANE PROTEIN; MUSCLE PROTEIN; ZEBRAFISH PROTEIN;

EID: 84930669555     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms8205     Document Type: Article
Times cited : (72)

References (51)
  • 1
    • 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, J. D. 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 69, 385 (1992).
    • (1992) Cell , vol.69 , pp. 385
    • Brook, J.D.1
  • 2
    • 0026598119 scopus 로고
    • An unstable triplet repeat in a gene related to myotonic muscular dystrophy
    • Fu, Y. H. et al. An unstable triplet repeat in a gene related to myotonic muscular dystrophy. Science 255, 1256-1258 (1992).
    • (1992) Science , vol.255 , pp. 1256-1258
    • Fu, Y.H.1
  • 3
    • 0026603841 scopus 로고
    • Myotonic dystrophy mutation: An unstable CTG repeat in the 3' untranslated region of the gene
    • Mahadevan, M. et al. Myotonic dystrophy mutation: An unstable CTG repeat in the 3' untranslated region of the gene. Science 255, 1253-1255 (1992).
    • (1992) Science , vol.255 , pp. 1253-1255
    • Mahadevan, M.1
  • 4
    • 0346243804 scopus 로고    scopus 로고
    • A muscleblind knockout model for myotonic dystrophy
    • Kanadia, R. N. et al. A muscleblind knockout model for myotonic dystrophy. Science 302, 1978-1980 (2003).
    • (2003) Science , vol.302 , pp. 1978-1980
    • Kanadia, R.N.1
  • 5
    • 0042698594 scopus 로고    scopus 로고
    • Developmental expression of mouse muscleblind genes Mbnl1 Mbnl2 and Mbnl3
    • Kanadia, R. N. et al. Developmental expression of mouse muscleblind genes Mbnl1, Mbnl2 and Mbnl3. Gene Expr. Patterns 3, 459-462 (2003).
    • (2003) Gene Expr. Patterns , vol.3 , pp. 459-462
    • Kanadia, R.N.1
  • 6
    • 34948834723 scopus 로고    scopus 로고
    • Increased steady-state levels of CUGBP1 in myotonic dystrophy 1 are due to PKC-mediated hyperphosphorylation
    • Kuyumcu-Martinez, N. M., Wang, G. S. & Cooper, T. A. Increased steady-state levels of CUGBP1 in myotonic dystrophy 1 are due to PKC-mediated hyperphosphorylation. Mol. Cell 28, 68-78 (2007).
    • (2007) Mol. Cell , vol.28 , pp. 68-78
    • Kuyumcu-Martinez, N.M.1    Wang, G.S.2    Cooper, T.A.3
  • 7
    • 0034622926 scopus 로고    scopus 로고
    • Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat
    • Mankodi, A. et al. Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat. Science 289, 1769-1773 (2000).
    • (2000) Science , vol.289 , pp. 1769-1773
    • Mankodi, A.1
  • 8
    • 0034282958 scopus 로고    scopus 로고
    • Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy
    • Miller, J. W. et al. Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy. EMBO J. 19, 4439-4448 (2000).
    • (2000) EMBO J. , vol.19 , pp. 4439-4448
    • Miller, J.W.1
  • 9
    • 0032076126 scopus 로고    scopus 로고
    • Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy
    • Philips, A. V., Timchenko, L. T. & Cooper, T. A. Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy. Science 280, 737-741 (1998).
    • (1998) Science , vol.280 , pp. 737-741
    • Philips, A.V.1    Timchenko, L.T.2    Cooper, T.A.3
  • 10
    • 0034194141 scopus 로고    scopus 로고
    • Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability
    • Seznec, H. et al. Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability. Hum. Mol. Genet. 9, 1185-1194 (2000).
    • (2000) Hum. Mol. Genet. , vol.9 , pp. 1185-1194
    • Seznec, H.1
  • 11
    • 0036347927 scopus 로고    scopus 로고
    • Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing
    • Charlet, B. N. et al. Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing. Mol. Cell 10, 45-53 (2002).
    • (2002) Mol. Cell , vol.10 , pp. 45-53
    • Charlet, B.N.1
  • 12
    • 79958101846 scopus 로고    scopus 로고
    • Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
    • Fugier, C. et al. Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy. Nat. Med. 17, 720-725 (2011).
    • (2011) Nat. Med. , vol.17 , pp. 720-725
    • Fugier, C.1
  • 13
    • 0034873099 scopus 로고    scopus 로고
    • Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy
    • Savkur, R. S., Philips, A. V. & Cooper, T. A. Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy. Nat. Genet. 29, 40-47 (2001).
    • (2001) Nat. Genet. , vol.29 , pp. 40-47
    • Savkur, R.S.1    Philips, A.V.2    Cooper, T.A.3
  • 14
    • 84857662317 scopus 로고    scopus 로고
    • Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of CaV1.1 calcium channel
    • Tang, Z. Z. et al. Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of CaV1.1 calcium channel. Hum. Mol. Genet. 21, 1312-1324 (2012).
    • (2012) Hum. Mol. Genet. , vol.21 , pp. 1312-1324
    • Tang, Z.Z.1
  • 15
    • 36849035575 scopus 로고    scopus 로고
    • Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy
    • Wheeler, T. M., Lueck, J. D., Swanson, M. S., Dirksen, R. T. & Thornton, C. A. Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy. J. Clin. Invest. 117, 3952-3957 (2007).
    • (2007) J. Clin. Invest. , vol.117 , pp. 3952-3957
    • Wheeler, T.M.1    Lueck, J.D.2    Swanson, M.S.3    Dirksen, R.T.4    Thornton, C.A.5
  • 16
    • 84882334678 scopus 로고    scopus 로고
    • Reexpression of pyruvate kinase M2 in type 1 myofibers correlates with altered glucose metabolism in myotonic dystrophy
    • Gao, Z. & Cooper, T. A. Reexpression of pyruvate kinase M2 in type 1 myofibers correlates with altered glucose metabolism in myotonic dystrophy. Proc. Natl. Acad. Sci. U. S. A. 110, 13570-13575 (2013).
    • (2013) Proc. Natl. Acad. Sci. U. S. A. , vol.110 , pp. 13570-13575
    • Gao, Z.1    Cooper, T.A.2
  • 18
    • 84888085706 scopus 로고    scopus 로고
    • Splicing biomarkers of disease severity in myotonic dystrophy
    • Nakamori, M. et al. Splicing biomarkers of disease severity in myotonic dystrophy. Ann. Neurol. 74, 862-872 (2013).
    • (2013) Ann. Neurol. , vol.74 , pp. 862-872
    • Nakamori, M.1
  • 19
    • 84855175087 scopus 로고    scopus 로고
    • The dystrophin-glycoprotein complex in the prevention of muscle damage
    • Gumerson, J. D. & Michele, D. E. The dystrophin-glycoprotein complex in the prevention of muscle damage. Biomed. Res. Int. 2011, 210797 (2011).
    • (2011) Biomed. Res. Int. , vol.2011 , pp. 210797
    • Gumerson, J.D.1    Michele, D.E.2
  • 20
    • 84881347420 scopus 로고    scopus 로고
    • Identification of new dystroglycan complexes in skeletal muscle
    • Johnson, E. K. et al. Identification of new dystroglycan complexes in skeletal muscle. PLoS ONE 8, e73224 (2013).
    • (2013) PLoS ONE , vol.8 , pp. e73224
    • Johnson, E.K.1
  • 21
    • 0023614188 scopus 로고
    • Dystrophin: The protein product of the duchenne muscular dystrophy locus
    • Hoffman, E. P., Brown, Jr. R. H. & Kunkel, L. M. Dystrophin: The protein product of the duchenne muscular dystrophy locus. Cell 51, 919-928 (1987).
    • (1987) Cell , vol.51 , pp. 919-928
    • Hoffman, E.P.1    Brown, R.H.2    Kunkel, L.M.3
  • 22
    • 0023614271 scopus 로고
    • Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
    • Koenig, M. et al. Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50, 509-517 (1987).
    • (1987) Cell , vol.50 , pp. 509-517
    • Koenig, M.1
  • 23
    • 0029086696 scopus 로고
    • Cloning and characterization of alternatively spliced isoforms of Dp71
    • Austin, R. C., Howard, P. L., D'Souza, V. N., Klamut, H. J. & Ray, P. N. Cloning and characterization of alternatively spliced isoforms of Dp71. Hum. Mol. Genet. 4, 1475-1483 (1995).
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 1475-1483
    • Austin, R.C.1    Howard, P.L.2    D'Souza, V.N.3    Klamut, H.J.4    Ray, P.N.5
  • 24
    • 0034162942 scopus 로고    scopus 로고
    • Expression and synthesis of alternatively spliced variants of Dp71 in adult human brain
    • Austin, R. C., Morris, G. E., Howard, P. L., Klamut, H. J. & Ray, P. N. Expression and synthesis of alternatively spliced variants of Dp71 in adult human brain. Neuromuscul. Disord. 10, 187-193 (2000).
    • (2000) Neuromuscul. Disord. , vol.10 , pp. 187-193
    • Austin, R.C.1    Morris, G.E.2    Howard, P.L.3    Klamut, H.J.4    Ray, P.N.5
  • 25
    • 0024582731 scopus 로고
    • Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus
    • Feener, C. A., Koenig, M. & Kunkel, L. M. Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus. Nature 338, 509-511 (1989).
    • (1989) Nature , vol.338 , pp. 509-511
    • Feener, C.A.1    Koenig, M.2    Kunkel, L.M.3
  • 26
    • 0034683567 scopus 로고    scopus 로고
    • Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain
    • Crawford, G. E. et al. Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain. J. Cell Biol. 150, 1399-1410 (2000).
    • (2000) J. Cell Biol. , vol.150 , pp. 1399-1410
    • Crawford, G.E.1
  • 27
    • 0026519484 scopus 로고
    • Human and murine dystrophin mRNA transcripts are differentially expressed during skeletal muscle, heart, and brain development
    • Bies, R. D. et al. Human and murine dystrophin mRNA transcripts are differentially expressed during skeletal muscle, heart, and brain development. Nucleic Acids Res. 20, 1725-1731 (1992).
    • (1992) Nucleic Acids Res. , vol.20 , pp. 1725-1731
    • Bies, R.D.1
  • 28
    • 0036045421 scopus 로고    scopus 로고
    • The 3'-untranslated region of the dystrophin gene-conservation and consequences of loss
    • Greener, M. J., Sewry, C. A., Muntoni, F. & Roberts, R. G. The 3'-untranslated region of the dystrophin gene-conservation and consequences of loss. Eur. J. Hum. Genet. 10, 413-420 (2002).
    • (2002) Eur. J. Hum. Genet. , vol.10 , pp. 413-420
    • Greener, M.J.1    Sewry, C.A.2    Muntoni, F.3    Roberts, R.G.4
  • 29
    • 84860179725 scopus 로고    scopus 로고
    • New function for the RNA helicase p68/DDX5 as a modifier of MBNL1 activity on expanded CUG repeats
    • Laurent, F.-X. et al. New function for the RNA helicase p68/DDX5 as a modifier of MBNL1 activity on expanded CUG repeats. Nucleic Acids Res. 40, 3159-3171 (2012).
    • (2012) Nucleic Acids Res. , vol.40 , pp. 3159-3171
    • Laurent, F.-X.1
  • 30
    • 84896959065 scopus 로고    scopus 로고
    • Compound loss of muscleblind-like function in myotonic dystrophy
    • Lee, K.-Y. et al. Compound loss of muscleblind-like function in myotonic dystrophy. EMBO Mol. Med. 5, 1887-1900 (2013).
    • (2013) EMBO Mol. Med. , vol.5 , pp. 1887-1900
    • Lee, K.-Y.1
  • 31
    • 77956108781 scopus 로고    scopus 로고
    • CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1
    • Ward, A. J., Rimer, M., Killian, J. M., Dowling, J. J. & Cooper, T. A. CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1. Hum. Mol. Genet. 19, 3614-3622 (2010).
    • (2010) Hum. Mol. Genet. , vol.19 , pp. 3614-3622
    • Ward, A.J.1    Rimer, M.2    Killian, J.M.3    Dowling, J.J.4    Cooper, T.A.5
  • 32
    • 33846991596 scopus 로고    scopus 로고
    • The dystrotelin, dystrophin and dystrobrevin superfamily: New paralogues and old isoforms
    • Jin, H. et al. The dystrotelin, dystrophin and dystrobrevin superfamily: New paralogues and old isoforms. BMC Genomics 8, 19 (2007).
    • (2007) BMC Genomics , vol.8 , pp. 19
    • Jin, H.1
  • 33
    • 0141886430 scopus 로고    scopus 로고
    • Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo
    • Bassett, D. I. et al. Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo. Dev. Camb. Engl. 130, 5851-5860 (2003).
    • (2003) Dev. Camb. Engl. , vol.130 , pp. 5851-5860
    • Bassett, D.I.1
  • 34
    • 78650170393 scopus 로고    scopus 로고
    • Dystrophindeficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology
    • Berger, J., Berger, S., Hall, T. E., Lieschke, G. J. & Currie, P. D. Dystrophindeficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology. Neuromuscul. Disord. 20, 826-832 (2010).
    • (2010) Neuromuscul. Disord. , vol.20 , pp. 826-832
    • Berger, J.1    Berger, S.2    Hall, T.E.3    Lieschke, G.J.4    Currie, P.D.5
  • 35
    • 5444275698 scopus 로고    scopus 로고
    • Recombinant adeno-associated viral (rAAV) vectors as therapeutic tools for Duchenne muscular dystrophy (DMD
    • Athanasopoulos, T., Graham, I. R., Foster, H. & Dickson, G. Recombinant adeno-associated viral (rAAV) vectors as therapeutic tools for Duchenne muscular dystrophy (DMD). Gene Ther. 11(Suppl 1): S109-S121 (2004).
    • (2004) Gene Ther. , vol.11 , pp. 109-121
    • Athanasopoulos, T.1    Graham, I.R.2    Foster, H.3    Dickson, G.4
  • 36
    • 79960073531 scopus 로고    scopus 로고
    • Codon optimization of the microdystrophin gene for Duchene muscular dystrophy gene therapy
    • Athanasopoulos, T., Foster, H., Foster, K. & Dickson, G. Codon optimization of the microdystrophin gene for Duchene muscular dystrophy gene therapy. Methods Mol. Biol. 709, 21-37 (2011).
    • (2011) Methods Mol. Biol. , vol.709 , pp. 21-37
    • Athanasopoulos, T.1    Foster, H.2    Foster, K.3    Dickson, G.4
  • 37
    • 54949097323 scopus 로고    scopus 로고
    • Codon and mRNA sequence optimization of microdystrophin transgenes improves expression and physiological outcome in dystrophic mdx mice following AAV2/8 gene transfer
    • Foster, H. et al. Codon and mRNA sequence optimization of microdystrophin transgenes improves expression and physiological outcome in dystrophic mdx mice following AAV2/8 gene transfer. Mol. Ther. J. Am. Soc. Gene Ther. 16, 1825-1832 (2008).
    • (2008) Mol. Ther. J. Am. Soc. Gene Ther. , vol.16 , pp. 1825-1832
    • Foster, H.1
  • 38
    • 33745894322 scopus 로고    scopus 로고
    • RAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice
    • Gregorevic, P. et al. rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice. Nat. Med. 12, 787-789 (2006).
    • (2006) Nat. Med. , vol.12 , pp. 787-789
    • Gregorevic, P.1
  • 39
    • 81855224742 scopus 로고    scopus 로고
    • Delivery of AAV2/9-microdystrophin genes incorporating helix 1 of the coiled-coil motif in the C-terminal domain of dystrophin improves muscle pathology and restores the level of a1-syntrophin and a-dystrobrevin in skeletal muscles of mdx mice
    • Koo, T. et al. Delivery of AAV2/9-microdystrophin genes incorporating helix 1 of the coiled-coil motif in the C-terminal domain of dystrophin improves muscle pathology and restores the level of a1-syntrophin and a-dystrobrevin in skeletal muscles of mdx mice. Hum. Gene Ther. 22, 1379-1388 (2011).
    • (2011) Hum. Gene Ther. , vol.22 , pp. 1379-1388
    • Koo, T.1
  • 40
    • 80053399347 scopus 로고    scopus 로고
    • Long-term functional adeno-associated virus-microdystrophin expression in the dystrophic CXMDj dog
    • Koo, T. et al. Long-term functional adeno-associated virus-microdystrophin expression in the dystrophic CXMDj dog. J. Gene Med. 13, 497-506 (2011).
    • (2011) J. Gene Med. , vol.13 , pp. 497-506
    • Koo, T.1
  • 41
    • 65649111197 scopus 로고    scopus 로고
    • Dystrophins carrying spectrin-like repeats 16 and 17 anchor nNOS to the sarcolemma and enhance exercise performance in a mouse model of muscular dystrophy
    • Lai, Y. et al. Dystrophins carrying spectrin-like repeats 16 and 17 anchor nNOS to the sarcolemma and enhance exercise performance in a mouse model of muscular dystrophy. J. Clin. Invest. 119, 624-635 (2009).
    • (2009) J. Clin. Invest. , vol.119 , pp. 624-635
    • Lai, Y.1
  • 42
    • 0028985719 scopus 로고
    • Mammalian alpha 1-and beta 1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus
    • Suzuki, A., Yoshida, M. & Ozawa, E. Mammalian alpha 1-and beta 1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus. J. Cell Biol. 128, 373-381 (1995).
    • (1995) J. Cell Biol. , vol.128 , pp. 373-381
    • Suzuki, A.1    Yoshida, M.2    Ozawa, E.3
  • 43
    • 0030775377 scopus 로고    scopus 로고
    • Dystrobrevin and dystrophin: An interaction through coiled-coil motifs
    • Sadoulet-Puccio, H. M., Rajala, M. & Kunkel, L. M. Dystrobrevin and dystrophin: An interaction through coiled-coil motifs. Proc. Natl Acad. Sci. USA 94, 12413-12418 (1997).
    • (1997) Proc. Natl Acad. Sci. USA , vol.94 , pp. 12413-12418
    • Sadoulet-Puccio, H.M.1    Rajala, M.2    Kunkel, L.M.3
  • 44
    • 0031947501 scopus 로고    scopus 로고
    • Dystrophins in vertebrates and invertebrates
    • Roberts, R. G. & Bobrow, M. Dystrophins in vertebrates and invertebrates. Hum. Mol. Genet. 7, 589-595 (1998).
    • (1998) Hum. Mol. Genet. , vol.7 , pp. 589-595
    • Roberts, R.G.1    Bobrow, M.2
  • 45
    • 0014518682 scopus 로고
    • The histographic analysis of human muscle biopsies with regard to fiber types. 3. Myotonias myasthenia gravis and hypokalemic periodic paralysis
    • Brooke, M. H. & Engel, W. K. The histographic analysis of human muscle biopsies with regard to fiber types. 3. Myotonias, myasthenia gravis, and hypokalemic periodic paralysis. Neurology 19, 469-477 (1969).
    • (1969) Neurology , vol.19 , pp. 469-477
    • Brooke, M.H.1    Engel, W.K.2
  • 47
    • 0014406348 scopus 로고
    • The ultrastructural morphology of the muscle fiber in myotonic dystrophy
    • Schroder, J. M. & Adams, R. D. The ultrastructural morphology of the muscle fiber in myotonic dystrophy. Acta Neuropathol. 10, 218-241 (1968).
    • (1968) Acta Neuropathol. , vol.10 , pp. 218-241
    • Schroder, J.M.1    Adams, R.D.2
  • 48
    • 84864452901 scopus 로고    scopus 로고
    • PEP-FOLD: An updated de novo structure prediction server for both linear and disulfide bonded cyclic peptides
    • Thévenet, P. et al. PEP-FOLD: An updated De novo structure prediction server for both linear and disulfide bonded cyclic peptides. Nucleic Acids Res. 40, W288-W293 (2012).
    • (2012) Nucleic Acids Res. , vol.40 , pp. 288-293
    • Thévenet, P.1
  • 49
    • 0035964342 scopus 로고    scopus 로고
    • Electrostatics of nanosystems: Application to microtubules and the ribosome
    • Baker, N. A., Sept, D., Joseph, S., Holst, M. J. & McCammon, J. A. Electrostatics of nanosystems: Application to microtubules and the ribosome. Proc. Natl Acad. Sci. USA 98, 10037-10041 (2001).
    • (2001) Proc. Natl Acad. Sci. USA , vol.98 , pp. 10037-10041
    • Baker, N.A.1    Sept, D.2    Joseph, S.3    Holst, M.J.4    McCammon, J.A.5
  • 50
    • 65449186590 scopus 로고    scopus 로고
    • PLATINUM: A web tool for analysis of hydrophobic/hydrophilic organization of biomolecular complexes
    • Pyrkov, T. V., Chugunov, A. O., Krylov, N. A., Nolde, D. E. & Efremov, R. G. PLATINUM: A web tool for analysis of hydrophobic/hydrophilic organization of biomolecular complexes. Bioinformatics 25, 1201-1202 (2009).
    • (2009) Bioinformatics , vol.25 , pp. 1201-1202
    • Pyrkov, T.V.1    Chugunov, A.O.2    Krylov, N.A.3    Nolde, D.E.4    Efremov, R.G.5
  • 51
    • 0034782974 scopus 로고    scopus 로고
    • Defective satellite cells in congenital myotonic dystrophy
    • Furling, D. et al. Defective satellite cells in congenital myotonic dystrophy. Hum. Mol. Genet. 10, 2079-2087 (2001).
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 2079-2087
    • Furling, D.1


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