메뉴 건너뛰기




Volumn 49, Issue 2, 2014, Pages 984-990

Amyotrophic lateral sclerosis and skeletal muscle: An update

Author keywords

Amyotrophic lateral sclerosis; Mitochondria; Myogenic factors; Proteasome; Skeletal muscle fibres

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; MYOGENIC FACTOR; MYOSIN HEAVY CHAIN; MYOSIN LIGHT CHAIN; PROTEASOME; TAR DNA BINDING PROTEIN; TRANSCRIPTION FACTOR FKHRL1; TRANSCRIPTION FACTOR NFAT; UNCOUPLING PROTEIN 3;

EID: 84896543905     PISSN: 08937648     EISSN: 15591182     Source Type: Journal    
DOI: 10.1007/s12035-013-8578-4     Document Type: Article
Times cited : (57)

References (67)
  • 1
    • 0025653451 scopus 로고
    • Cellular and molecular diversities of mammalian skeletal muscle fibers
    • Pette D, Staron RS (1990) Cellular and molecular diversities of mammalian skeletal muscle fibers. Rev Physiol Biochem Pharmacol 116:1-76
    • (1990) Rev Physiol Biochem Pharmacol , vol.116 , pp. 1-76
    • Pette, D.1    Staron, R.S.2
  • 2
    • 0028048536 scopus 로고
    • Maximum shortening velocity and coexistence of myosin heavy chain isoforms in single skinned fast fibres of rat skeletal muscle
    • DOI 10.1007/BF00122115
    • Bottinelli R, Betto R, Schiaffino S, Reggiani C (1994) Maximum shortening velocity and coexistence of myosin heavy chain isoforms in single skinned fast fibres of rat skeletal muscle. J Muscle Res Cell Motil 15:413-419 (Pubitemid 24263449)
    • (1994) Journal of Muscle Research and Cell Motility , vol.15 , Issue.4 , pp. 413-419
    • Bottinelli, R.1    Betto, R.2    Schiaffino, S.3    Reggiani, C.4
  • 5
    • 33749056809 scopus 로고    scopus 로고
    • ALS: A Disease of Motor Neurons and Their Nonneuronal Neighbors
    • DOI 10.1016/j.neuron.2006.09.018, PII S0896627306007252
    • Boillée S, Velde CV, Cleveland DW (2006) ALS: a disease of motor neurons and their nonneuronal neighbors. Neuron 52:39-59 (Pubitemid 44466358)
    • (2006) Neuron , vol.52 , Issue.1 , pp. 39-59
    • Boillee, S.1    Vande, V.C.2    Cleveland, D.W.3
  • 6
    • 3943102116 scopus 로고    scopus 로고
    • Unraveling the mechanisms involved in motor neuron degeneration in ALS
    • DOI 10.1146/annurev.neuro.27.070203.144244
    • Bruijn L, Miller TM, Cleveland DW (2004) Unraveling the mechanisms involved in motor neuron degeneration in ALS. Annu Rev Neurosci 27:723-749 (Pubitemid 39050419)
    • (2004) Annual Review of Neuroscience , vol.27 , pp. 723-749
    • Bruijn, L.I.1    Miller, T.M.2    Cleveland, D.W.3
  • 7
    • 54849404282 scopus 로고    scopus 로고
    • Skeletal muscle is a primary target of SOD1G93A-mediated toxicity
    • Dobrowolny G, Aucello M, Rizzuto E et al (2008) Skeletal muscle is a primary target of SOD1G93A-mediated toxicity. Cell Metab 8:425-436
    • (2008) Cell Metab , vol.8 , pp. 425-436
    • Dobrowolny, G.1    Aucello, M.2    Rizzuto, E.3
  • 11
    • 34247473080 scopus 로고    scopus 로고
    • Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model
    • DOI 10.1038/nn1885, PII NN1885
    • Di Giorgio FP, Carrasco MA, Siao MC, Maniatis T, Eggan K (2007) Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model. Nat Neurosci 10:608-614 (Pubitemid 46652442)
    • (2007) Nature Neuroscience , vol.10 , Issue.5 , pp. 608-614
    • Di, G.F.P.1    Carrasco, M.A.2    Siao, M.C.3    Maniatis, T.4    Eggan, K.5
  • 12
    • 34247475338 scopus 로고    scopus 로고
    • Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons
    • DOI 10.1038/nn1876, PII NN1876
    • Nagai M, Re DB, Nagata T, Chalazonitis A, Jessell TM, Wichterle H, Przedborski S (2007) Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons. Nat Neurosci 10:615-622 (Pubitemid 46652435)
    • (2007) Nature Neuroscience , vol.10 , Issue.5 , pp. 615-622
    • Nagai, M.1    Re, D.B.2    Nagata, T.3    Chalazonitis, A.4    Jessell, T.M.5    Wichterle, H.6    Przedborski, S.7
  • 14
    • 42949166848 scopus 로고    scopus 로고
    • Mitochondrial dysfunction in SOD1G93A-bearing astrocytes promotes motor neuron degeneration: Prevention by mitochondrial-targeted antioxidants
    • Cassina P, Cassina A, Pehar M et al (2008) Mitochondrial dysfunction in SOD1G93A-bearing astrocytes promotes motor neuron degeneration: prevention by mitochondrial-targeted antioxidants. J Neurosci 28:4115-4122
    • (2008) J Neurosci , vol.28 , pp. 4115-4122
    • Cassina, P.1    Cassina, A.2    Pehar, M.3
  • 16
    • 56549096129 scopus 로고    scopus 로고
    • Human embryonic stem cell-derived motor neurons are sensitive to the toxic effect of glial cells carrying an ALS-causing mutation
    • Di Giorgio FP, Boulting GL, Bobrowicz S, Eggan KC (2008) Human embryonic stem cell-derived motor neurons are sensitive to the toxic effect of glial cells carrying an ALS-causing mutation. Cell Stem Cell 3:637-648
    • (2008) Cell Stem Cell , vol.3 , pp. 637-648
    • Di Giorgio, F.P.1    Boulting, G.L.2    Bobrowicz, S.3    Eggan, K.C.4
  • 17
    • 56549115885 scopus 로고    scopus 로고
    • Non-cell-autonomous effect of human SOD1 G37R astrocytes on motor neurons derived from human embryonic stem cells
    • Marchetto MC, Muotri AR, Mu Y, Smith AM, Cezar GG, Gage FH (2008) Non-cell-autonomous effect of human SOD1 G37R astrocytes on motor neurons derived from human embryonic stem cells. Cell Stem Cell 3:649-657
    • (2008) Cell Stem Cell , vol.3 , pp. 649-657
    • Marchetto, M.C.1    Muotri, A.R.2    Mu, Y.3    Smith, A.M.4    Cezar, G.G.5    Gage, F.H.6
  • 19
    • 80052783545 scopus 로고    scopus 로고
    • Astrocytes from familial and sporadic ALS patients are toxic to motor neurons
    • Haidet-Phillips AM, Hester ME, Miranda CJ et al (2011) Astrocytes from familial and sporadic ALS patients are toxic to motor neurons. Nat Biotechnol 29:824-828
    • (2011) Nat Biotechnol , vol.29 , pp. 824-828
    • Haidet-Phillips, A.M.1    Hester, M.E.2    Miranda, C.J.3
  • 20
    • 80055074312 scopus 로고    scopus 로고
    • Astrocytes carrying the superoxide dismutase 1 (SOD1G93A) mutation induce wild-type motor neuron degeneration in vivo
    • Papadeas ST, Kraig SE, O'Banion C, Lepore AC, Maragakis NJ (2011) Astrocytes carrying the superoxide dismutase 1 (SOD1G93A) mutation induce wild-type motor neuron degeneration in vivo. Proc Natl Acad Sci U S A 108:17803-17808
    • (2011) Proc Natl Acad Sci U S A , vol.108 , pp. 17803-17808
    • Papadeas, S.T.1    Kraig, S.E.2    O'Banion, C.3    Lepore, A.C.4    Maragakis, N.J.5
  • 21
    • 78650550891 scopus 로고    scopus 로고
    • Astrocyte loss of mutant SOD1 delays ALS disease onset and progression in G85R transgenic mice
    • Wang L, Gutmann DH, Roos RP (2011) Astrocyte loss of mutant SOD1 delays ALS disease onset and progression in G85R transgenic mice. Hum Mol Genet 20:286-293
    • (2011) Hum Mol Genet , vol.20 , pp. 286-293
    • Wang, L.1    Gutmann, D.H.2    Roos, R.P.3
  • 23
    • 33746320200 scopus 로고    scopus 로고
    • Modified expression of Bcl-2 and SOD1 proteins in lymphocytes from sporadic ALS patients
    • DOI 10.1016/j.neulet.2006.01.057, PII S0304394006001066
    • Cova E, Cereda C, Galli A, Curti D, Finotti C, Di Poto C, Corato M, Mazzini G, Ceroni M (2006) Modified expression of Bcl-2 and SOD1 proteins in lymphocytes from sporadic ALS patients. Neurosci Lett 399:186-190 (Pubitemid 44308127)
    • (2006) Neuroscience Letters , vol.399 , Issue.3 , pp. 186-190
    • Cova, E.1    Cereda, C.2    Galli, A.3    Curti, D.4    Finotti, C.5    Di, P.C.6    Corato, M.7    Mazzini, G.8    Ceroni, M.9
  • 24
    • 75149155060 scopus 로고    scopus 로고
    • Oxidative stress in ALS: Key role in motor neuron injury and therapeutic target
    • Barber SC, Shaw PJ (2010) Oxidative stress in ALS: key role in motor neuron injury and therapeutic target. Free Rad Biol Med 48:629-641
    • (2010) Free Rad Biol Med , vol.48 , pp. 629-641
    • Barber, S.C.1    Shaw, P.J.2
  • 25
    • 33751003518 scopus 로고    scopus 로고
    • Oxidative stress in ALS: A mechanism of neurodegeneration and a therapeutic target
    • DOI 10.1016/j.bbadis.2006.03.008, PII S0925443906000524
    • Barber SC, Mead RJ, Shaw PJ (2006) Oxidative stress in ALS: a mechanism of neurodegeneration and a therapeutic target. Biochim Biophys Acta 1762:1051-1067 (Pubitemid 44750575)
    • (2006) Biochimica et Biophysica Acta - Molecular Basis of Disease , vol.1762 , Issue.11-12 , pp. 1051-1067
    • Barber, S.C.1    Mead, R.J.2    Shaw, P.J.3
  • 27
    • 61349156118 scopus 로고    scopus 로고
    • Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
    • Kwiatkowski TJ Jr, Bosco DA, Leclerc AL et al (2009) Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323:1205-1208
    • (2009) Science , vol.323 , pp. 1205-1208
    • Kwiatkowski Jr., T.J.1    Bosco, D.A.2    Leclerc, A.L.3
  • 29
    • 80052580969 scopus 로고    scopus 로고
    • Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ASL and ALS/dementia
    • Deng HX, Chen W, Hong ST et al (2011) Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ASL and ALS/dementia. Nature 477:211-215
    • (2011) Nature , vol.477 , pp. 211-215
    • Deng, H.X.1    Chen, W.2    Hong, S.T.3
  • 30
    • 80054837386 scopus 로고    scopus 로고
    • A hexanucleotide repeat expansion in the C9ORF72 is the cause of the chromosome 9p21-linked ALS-FTD
    • Renton AE, Majounie E, Waite A et al (2011) A hexanucleotide repeat expansion in the C9ORF72 is the cause of the chromosome 9p21-linked ALS-FTD. Neuron 72:257-268
    • (2011) Neuron , vol.72 , pp. 257-268
    • Renton, A.E.1    Majounie, E.2    Waite, A.3
  • 31
    • 80054832080 scopus 로고    scopus 로고
    • Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
    • DeJesus-Hernandez M, Mackenzie IR, Boeve BF et al (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72:245-256
    • (2011) Neuron , vol.72 , pp. 245-256
    • DeJesus-Hernandez, M.1    Mackenzie, I.R.2    Boeve, B.F.3
  • 32
    • 77953530958 scopus 로고    scopus 로고
    • Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice
    • Wong M, Martin LJ (2010) Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice. Hum Mol Genet 19:2284-2302
    • (2010) Hum Mol Genet , vol.19 , pp. 2284-2302
    • Wong, M.1    Martin, L.J.2
  • 33
    • 84860458565 scopus 로고    scopus 로고
    • Elevated PGC-1α activity sustains mitochondrial biogenesis and muscle function without extending survival in a mouse model of inherited ALS
    • Da Cruz S, Parone PA, Lopes VS et al (2012) Elevated PGC-1α activity sustains mitochondrial biogenesis and muscle function without extending survival in a mouse model of inherited ALS. Cell Metab 15:778-786
    • (2012) Cell Metab , vol.15 , pp. 778-786
    • Da Cruz, S.1    Parone, P.A.2    Lopes, V.S.3
  • 34
    • 0036843064 scopus 로고    scopus 로고
    • Skeletal muscle fiber function and rate of disease progression in amyotrophic lateral sclerosis
    • DOI 10.1002/mus.10257
    • Krivickas LS, Yang JI, Kim SK, Frontera WR (2002) Skeletal muscle fibre function and rate of disease progression in amyotrophic lateral sclerosis. Muscle Nerve 26:636-643 (Pubitemid 35266087)
    • (2002) Muscle and Nerve , vol.26 , Issue.5 , pp. 636-643
    • Krivickas, L.S.1    Yang, J.-I.2    Kim, S.-K.3    Frontera, W.R.4
  • 35
    • 48949120504 scopus 로고    scopus 로고
    • Preferential motor unit loss in the SOD1 G93A transgenic mouse model of amyotrophic lateral sclerosis
    • DOI 10.1113/jphysiol.2007.149286
    • Hegedus J, Putman CT, Tyreman N, Gordon T (2008) Preferential motor unit loss in the SOD1G93A transgenic mouse model of amyotrophic lateral sclerosis. J Physiol 586(14):3337-3351 (Pubitemid 352003870)
    • (2008) Journal of Physiology , vol.586 , Issue.14 , pp. 3337-3351
    • Hegedus, J.1    Putman, C.T.2    Tyreman, N.3    Gordon, T.4
  • 36
    • 35349025311 scopus 로고    scopus 로고
    • G93A mouse model of amyotrophic lateral sclerosis
    • DOI 10.1016/j.nbd.2007.07.003, PII S0969996107001416
    • Hegedus J, Putman CT, Gordon T (2007) Time course of preferential motor unit loss in the SOD1G93A mouse model of amyotrophic lateral sclerosis. Neurobiol Dis 28:154-164 (Pubitemid 47615455)
    • (2007) Neurobiology of Disease , vol.28 , Issue.2 , pp. 154-164
    • Hegedus, J.1    Putman, C.T.2    Gordon, T.3
  • 37
    • 0034175513 scopus 로고    scopus 로고
    • Early and selective loss of neuromuscular synapse subtypes with low sprouting competence in motoneuron diseases
    • Frey D, Schneider C, Xu L, Borg J, Spooren W, Caroni P (2000) Early and selective loss of neuromuscular synapse subtypes with low sprouting competence in motoneuron diseases. J Neurosci 20:2534-2542 (Pubitemid 30220340)
    • (2000) Journal of Neuroscience , vol.20 , Issue.7 , pp. 2534-2542
    • Frey, D.1    Schneider, C.2    Xu, L.3    Borg, J.4    Spooren, W.5    Caroni, P.6
  • 38
    • 23744445580 scopus 로고    scopus 로고
    • A compensatory subpopulation of motor neurons in a mouse model of amyotrophic lateral sclerosis
    • DOI 10.1002/cne.20620
    • Schaefer AM, Sanes JR, Lichtman JW (2005) A compensatory subpopulation of motor neurons in a mouse model of amyotrophic lateral sclerosis. J Comp Neurol 490:209-219 (Pubitemid 41140989)
    • (2005) Journal of Comparative Neurology , vol.490 , Issue.3 , pp. 209-219
    • Schaefer, A.M.1    Sanes, J.R.2    Lichtman, J.W.3
  • 39
    • 0043095290 scopus 로고    scopus 로고
    • Skeletal muscle properties in a transgenic mouse model for amyotrophic lateral sclerosis: Effects of creatine treatment
    • DOI 10.1016/S0969-9961(03)00041-X
    • Derave W, Van Den Bosch L, Lemmens G, Eijnde BO, Robberecht W, Hespel P (2003) Skeletal muscle properties in a transgenic mouse model for amyotrophic lateral sclerosis: effects of creatine treatment. Neurobiol Dis 13:264-272 (Pubitemid 36937208)
    • (2003) Neurobiology of Disease , vol.13 , Issue.3 , pp. 264-272
    • Derave, W.1    Van Den, B.L.2    Lemmens, G.3    Eijnde, B.O.4    Robberecht, W.5    Hespel, P.6
  • 40
    • 17044391881 scopus 로고    scopus 로고
    • Properties of slow- and fast-twitch muscle fibres in a mouse model of amyotrophic lateral sclerosis
    • Atkin JD, Scott RL, West JM, Lopes E, Quah AK, Cheema SS (2005) Properties of slow- and fast-twitch muscle fibres in a mouse model of amyotrophic lateral sclerosis. Neuromuscul Disord 15:377-388
    • (2005) Neuromuscul Disord , vol.15 , pp. 377-388
    • Atkin, J.D.1    Scott, R.L.2    West, J.M.3    Lopes, E.4    Quah, A.K.5    Cheema, S.S.6
  • 42
    • 37249070405 scopus 로고    scopus 로고
    • Satellite and stem cells in muscle growth and repair
    • DOI 10.1242/dev.005934
    • Le Grand F, Rudnicki M (2007) Satellite and stem cells in muscle growth and repair. Development 134:3953-3957 (Pubitemid 350269412)
    • (2007) Development , vol.134 , Issue.22 , pp. 3953-3957
    • Le, G.F.1    Rudnicki, M.2
  • 43
    • 34447287334 scopus 로고    scopus 로고
    • Skeletal muscle progenitor cells and the role of Pax genes
    • Buckingham M (2007) Skeletal muscle progenitor cells and the role of Pax genes. C R Biol 330:530-533
    • (2007) C R Biol , vol.330 , pp. 530-533
    • Buckingham, M.1
  • 44
    • 0035495925 scopus 로고    scopus 로고
    • Muscle satellite cells are multipotential stem cells that exhibit myogenic, osteogenic, and adipogenic differentiation
    • Asakura A, Komaki M, Rudnicki M (2001) Muscle satellite cells are multipotential stem cells that exhibit myogenic, osteogenic, and adipogenic differentiation. Differentiation 68:245-253 (Pubitemid 33754997)
    • (2001) Differentiation , vol.68 , Issue.4-5 , pp. 245-253
    • Asakura, A.1    Komaki, M.2    Rudnicki, M.A.3
  • 45
    • 0034651562 scopus 로고    scopus 로고
    • A new look at the origin, function, and 'stem-cell' status of muscle satellite cells
    • DOI 10.1006/dbio.1999.9565
    • Seale P, Rudnicki MA (2000) A new look at the origin, function, and 'stem-cell' status of muscle satellite cells. Dev Biol 218:115-124 (Pubitemid 30101962)
    • (2000) Developmental Biology , vol.218 , Issue.2 , pp. 115-124
    • Seale, P.1    Rudnicki, M.A.2
  • 50
    • 1542374572 scopus 로고    scopus 로고
    • Mécanismes moléculaires de la sclérose latérale amyotrophique: Apports récents de l'analyse de modeles animaux
    • Dupuis L, Muller A, Meininger V, Loeffler JP (2004) Molecular mechanisms of amyotrophic lateral sclerosis: recent contributions from studies in animal models (in French). Rev Neurol (Paris) 160:35-43 (Pubitemid 38315598)
    • (2004) Revue Neurologique , vol.160 , Issue.1 , pp. 35-43
    • Dupuis, L.1    Muller, A.2    Meininger, V.3    Loeffler, J.P.4
  • 51
    • 0035516124 scopus 로고    scopus 로고
    • From Charcot to Lou Gehrig: Deciphering selective motor neuron death in ALS
    • DOI 10.1038/35097565
    • Cleveland DW, Rothstein JD (2001) From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS. Nat Rev Neurosci 2:806-819 (Pubitemid 33674062)
    • (2001) Nature Reviews Neuroscience , vol.2 , Issue.11 , pp. 806-819
    • Cleveland, D.W.1    Rothstein, J.D.2
  • 52
    • 0013911740 scopus 로고
    • Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis
    • Afifi AK, Aleu FP, Goodgold J, MacKay B (1966) Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis. Neurology 16:475-481
    • (1966) Neurology , vol.16 , pp. 475-481
    • Afifi, A.K.1    Aleu, F.P.2    Goodgold, J.3    MacKay, B.4
  • 53
    • 0030019414 scopus 로고    scopus 로고
    • Ultrastructural study of synapses in the anterior horn neurons of patients with amyotrophic lateral sclerosis
    • DOI 10.1016/0304-3940(96)12314-4
    • Sasaki S, Iwata M (1996) Ultrastructural study of synapses in the anterior horn neurons of patients with amyotrophic lateral sclerosis. Neurosci Lett 204:53-56 (Pubitemid 26053674)
    • (1996) Neuroscience Letters , vol.204 , Issue.1-2 , pp. 53-56
    • Sasaki, S.1    Iwata, M.2
  • 54
    • 0036261301 scopus 로고    scopus 로고
    • Ultrastructural changes of mitochondria in the skeletal muscle of patients with amyotrophic lateral sclerosis
    • Chung MJ, Suh YL (2002) Ultrastructural changes of mitochondria in the skeletal muscle of patients with amyotrophic lateral sclerosis. Ultrastruct Pathol 26:3-7
    • (2002) Ultrastruct Pathol , vol.26 , pp. 3-7
    • Chung, M.J.1    Suh, Y.L.2
  • 56
    • 0345426778 scopus 로고    scopus 로고
    • Up-regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosis
    • Dupuis L, di Scala F, Rene F, de Tapia M, Oudart H, Pradat PF, Meininger V, Loeffler JP (2003) Up-regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosis. FASAB J 17:2091-2093
    • (2003) FASAB J , vol.17 , pp. 2091-2093
    • Dupuis, L.1    Di Scala, F.2    Rene, F.3    De Tapia, M.4    Oudart, H.5    Pradat, P.F.6    Meininger, V.7    Loeffler, J.P.8
  • 58
    • 0033934734 scopus 로고    scopus 로고
    • Mitochondria and the pathogenesis of ALS
    • Beal MF (2000) Mitochondria and the pathogenesis of ALS. Brain 123:1291-1292
    • (2000) Brain , vol.123 , pp. 1291-1292
    • Beal, M.F.1
  • 61
    • 0042827316 scopus 로고    scopus 로고
    • Neuromuscular accumulation of mutant superoxide dismutase 1 aggregates in a transgenic mouse model of familial amyotrophic lateral sclerosis
    • DOI 10.1016/S0304-3940(03)00893-0
    • Turner BJ, Lopes EC, Cheema SS (2003) Neuromuscular accumulation of mutant superoxide dismutase 1 aggregates in a transgenic mouse of familial amyotrophic lateral sclerosis. Neurosci Lett 350:132-136 (Pubitemid 37101429)
    • (2003) Neuroscience Letters , vol.350 , Issue.2 , pp. 132-136
    • Turner, B.J.1    Lopes, E.C.2    Cheema, S.S.3
  • 62
    • 84863035837 scopus 로고    scopus 로고
    • Proteinmisfolding,mitochondrial dysfunction and muscle loss are not directly dependent on soluble and aggregation state of mSOD1 protein in skeletal muscle of ALS
    • Wei R, Bhattacharya A, Chintalaramulu N, Jernigan AL, Liu Y, Van Remmen H, Chaudhuri AR (2012) Proteinmisfolding,mitochondrial dysfunction and muscle loss are not directly dependent on soluble and aggregation state of mSOD1 protein in skeletal muscle of ALS. Biochem Biophys Res Commun 417:1275-1279
    • (2012) Biochem Biophys Res Commun , vol.417 , pp. 1275-1279
    • Wei, R.1    Bhattacharya, A.2    Chintalaramulu, N.3    Jernigan, A.L.4    Liu, Y.5    Van Remmen, H.6    Chaudhuri, A.R.7
  • 63
    • 79959982281 scopus 로고    scopus 로고
    • Muscle cells and motoneurons differentially remove mutant SOD1 causing familial amyotrophic lateral sclerosis
    • Onesto E, Rusmini P, Crippa V, Ferri N, Zito A, Galbiati M, Poletti A (2011) Muscle cells and motoneurons differentially remove mutant SOD1 causing familial amyotrophic lateral sclerosis. J Neurochem 118:266-280
    • (2011) J Neurochem , vol.118 , pp. 266-280
    • Onesto, E.1    Rusmini, P.2    Crippa, V.3    Ferri, N.4    Zito, A.5    Galbiati, M.6    Poletti, A.7
  • 67
    • 80855136462 scopus 로고    scopus 로고
    • Abnormal TDP-43 and FUS proteins inmuscles of sporadic IBM: Similarities in a TARDBP-linked ALS patient
    • Hernandez Lain A, Millecamps S, Dubourg O et al (2011) Abnormal TDP-43 and FUS proteins inmuscles of sporadic IBM: similarities in a TARDBP-linked ALS patient. J Neurol Neurosurg Psychiatry 82:1414-1416
    • (2011) J Neurol Neurosurg Psychiatry , vol.82 , pp. 1414-1416
    • Hernandez Lain, A.1    Millecamps, S.2    Dubourg, O.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.