메뉴 건너뛰기




Volumn 2012, Issue , 2012, Pages

Neural and molecular features on Charcot-Marie-Tooth disease plasticity and therapy

Author keywords

[No Author keywords available]

Indexed keywords

ANTIGESTAGEN; ASCORBIC ACID; CURCUMIN; HEAT SHOCK PROTEIN 22; HEAT SHOCK PROTEIN 27; HISTONE DEACETYLASE 6; HISTONE DEACETYLASE 6 INHIBITOR; HISTONE DEACETYLASE INHIBITOR; MYELIN; NEU DIFFERENTIATION FACTOR; NEUROTROPHIC FACTOR; ONAPRISTONE; UNCLASSIFIED DRUG;

EID: 84863752359     PISSN: 20905904     EISSN: 16875443     Source Type: Journal    
DOI: 10.1155/2012/171636     Document Type: Review
Times cited : (14)

References (113)
  • 1
    • 0016266593 scopus 로고
    • Genetic and clinical aspects of Charcot Marie Tooth's disease
    • Skre H., Genetic and clinical aspects of Charcot Marie Tooth's disease Clinical Genetics 1974 6 2 98 118
    • (1974) Clinical Genetics , vol.6 , Issue.2 , pp. 98-118
    • Skre, H.1
  • 2
  • 3
    • 0000907007 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth peripheral neuropathies and related disorders
    • Scriver C. R. Beaudet A. L. Sly W. S. Valle D. Childs B. Kinzler K. W. Vogelstein B. 8th New York, NY, USA McGraw-Hill
    • Lupski J. R., Garcia C. A., Scriver C. R., Beaudet A. L., Sly W. S., Valle D., Childs B., Kinzler K. W., Vogelstein B., Charcot-Marie-Tooth peripheral neuropathies and related disorders The Metabolic and Molecular Bases of Inherited Disease 2000 8th New York, NY, USA McGraw-Hill 5759 5788
    • (2000) The Metabolic and Molecular Bases of Inherited Disease , pp. 5759-5788
    • Lupski, J.R.1    Garcia, C.A.2
  • 4
    • 84863750923 scopus 로고    scopus 로고
    • Hereditary motor and sensory neuropathies
    • Rimoin R. L. Connor J. M. Pyeritz R. E. Korf B. R. 5th Philadelphia, Pa, USA Churchill Livingstone Elsevier
    • Szigeti K., Lupski J. R., Rimoin R. L., Connor J. M., Pyeritz R. E., Korf B. R., Hereditary motor and sensory neuropathies Emory and Rimoins Principles and Practice of Medical Genetics 2007 5th Philadelphia, Pa, USA Churchill Livingstone Elsevier 2946 2962
    • (2007) Emory and Rimoins Principles and Practice of Medical Genetics , pp. 2946-2962
    • Szigeti, K.1    Lupski, J.R.2
  • 7
    • 33745278558 scopus 로고    scopus 로고
    • Clinical and electrophysiological aspects of charcot-marie-tooth disease
    • Pareyson D., Scaioli V., Laur M., Clinical and electrophysiological aspects of charcot-marie-tooth disease NeuroMolecular Medicine 2006 8 1-2 3 22
    • (2006) NeuroMolecular Medicine , vol.8 , Issue.12 , pp. 3-22
    • Pareyson, D.1    Scaioli, V.2    Laur, M.3
  • 8
    • 60149083988 scopus 로고    scopus 로고
    • Molecular mechanisms of inherited demyelinating neuropathies
    • Scherer S. S., Wrabetz L., Molecular mechanisms of inherited demyelinating neuropathies Glia 2008 56 14 1578 1589
    • (2008) Glia , vol.56 , Issue.14 , pp. 1578-1589
    • Scherer, S.S.1    Wrabetz, L.2
  • 9
    • 0032896064 scopus 로고    scopus 로고
    • The neurobiology of Schwann cells
    • Mirsky R., Jessen K. R., The neurobiology of Schwann cells Brain Pathology 1999 9 2 293 311 (Pubitemid 29157717)
    • (1999) Brain Pathology , vol.9 , Issue.2 , pp. 293-311
    • Mirsky, R.1    Jessen, K.R.2
  • 10
    • 0000481399 scopus 로고
    • Development of peripheral nerve fibres
    • Dyck P. J. Thomas P. K. Griffin J. W. Low P. A. Poduslo J. F. 3th Philadelphia, Pa, USA WB Saunders
    • Webster H., De F., Dyck P. J., Thomas P. K., Griffin J. W., Low P. A., Poduslo J. F., Development of peripheral nerve fibres Peripheral Neuropathy 1993 3th Philadelphia, Pa, USA WB Saunders 243 266
    • (1993) Peripheral Neuropathy , pp. 243-266
    • Webster, H.1    De, F.2
  • 11
    • 7044272358 scopus 로고    scopus 로고
    • Mechanisms and roles of axon-Schwann cell interactions
    • DOI 10.1523/JNEUROSCI.3649-04.2004
    • Corfas G., Velardez M. O., Ko C. P., Ratner N., Peles E., Mechanisms and roles of axon-Schwann cell interactions Journal of Neuroscience 2004 24 42 9250 9260 (Pubitemid 39426161)
    • (2004) Journal of Neuroscience , vol.24 , Issue.42 , pp. 9250-9260
    • Corfas, G.1    Velardez, M.O.2    Ko, C.-P.3    Ratner, N.4    Peles, E.5
  • 12
    • 0028855446 scopus 로고
    • Differential expression of ARIA isoforms in the rat brain
    • Corfas G., Rosen K. M., Aratake H., Krauss R., Fischbach G. D., Differential expression of ARIA isoforms in the rat brain Neuron 1995 14 1 103 115
    • (1995) Neuron , vol.14 , Issue.1 , pp. 103-115
    • Corfas, G.1    Rosen, K.M.2    Aratake, H.3    Krauss, R.4    Fischbach, G.D.5
  • 13
    • 0028827104 scopus 로고
    • Multiple essential functions of neuregulin in development
    • Meyer D., Birchmeier C., Multiple essential functions of neuregulin in development Nature 1995 378 6555 386 390
    • (1995) Nature , vol.378 , Issue.6555 , pp. 386-390
    • Meyer, D.1    Birchmeier, C.2
  • 15
    • 0025438055 scopus 로고
    • Altered slow axonal transport and regeneration in a myelin-deficient mutant mouse: The trembler as an in vivo model for schwann cell-axon interactions
    • De Waegh S., Brady S. T., Altered slow axonal transport and regeneration in a myelin-deficient mutant mouse: the trembler as an in vivo model for schwann cell-axon interactions Journal of Neuroscience 1990 10 6 1855 1865
    • (1990) Journal of Neuroscience , vol.10 , Issue.6 , pp. 1855-1865
    • De Waegh, S.1    Brady, S.T.2
  • 17
    • 77950357531 scopus 로고    scopus 로고
    • Biology of peripheral inherited neuropathies: Schwann cell axonal interactions
    • Shy M. E., Biology of peripheral inherited neuropathies: schwann cell axonal interactions Advances in Experimental Medicine and Biology 2009 652 171 181
    • (2009) Advances in Experimental Medicine and Biology , vol.652 , pp. 171-181
    • Shy, M.E.1
  • 18
    • 33645276591 scopus 로고    scopus 로고
    • Mechanisms of disease: A molecular genetic update on hereditary axonal neuropathies
    • Zchner S., Vance J. M., Mechanisms of disease: a molecular genetic update on hereditary axonal neuropathies Nature Clinical Practice Neurology 2006 2 1 45 53
    • (2006) Nature Clinical Practice Neurology , vol.2 , Issue.1 , pp. 45-53
    • Zchner, S.1    Vance, J.M.2
  • 20
    • 67649390851 scopus 로고    scopus 로고
    • Diagnosis, natural history, and management of Charcot-Marie-Tooth disease
    • Pareyson D., Marchesi C., Diagnosis, natural history, and management of Charcot-Marie-Tooth disease The Lancet Neurology 2009 8 7 654 667
    • (2009) The Lancet Neurology , vol.8 , Issue.7 , pp. 654-667
    • Pareyson, D.1    Marchesi, C.2
  • 25
    • 0027972378 scopus 로고
    • Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
    • Chance P. F., Abbas N., Lensch M. W., Pentao L., Roa B. B., Patel P. I., Lupski J. R., Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17 Human Molecular Genetics 1994 3 2 223 228 (Pubitemid 24060934)
    • (1994) Human Molecular Genetics , vol.3 , Issue.2 , pp. 223-228
    • Chance, P.F.1    Abbas, N.2    Lensch, M.W.3    Pentao, L.4    Roa, B.B.5    Patel, P.I.6    Lupski, J.R.7
  • 27
    • 0030919434 scopus 로고    scopus 로고
    • Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies
    • DOI 10.1007/s004390050442
    • Bort S., Nelis E., Timmerman V., Sevilla T., Cruz-Martnez A., Martnez F., Milln J. M., Arpa J., Vlchez J. J., Prieto F., Van Broeckhoven C., Palau F., Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies Human Genetics 1997 99 6 746 754 (Pubitemid 27243752)
    • (1997) Human Genetics , vol.99 , Issue.6 , pp. 746-754
    • Bort, S.1    Nelis, E.2    Timmerman, V.3    Sevilla, T.4    Cruz-Martinez, A.5    Martinez, F.6    Millan, J.M.7    Arpa, J.8    Vilchez, J.J.9    Prieto, F.10    Van Broeckhoven, C.11    Palau, F.12
  • 28
    • 32044432488 scopus 로고    scopus 로고
    • Hereditary motor and sensory neuropathies involving altered dosage or mutation of PMP22: The CMT1A duplication and HNPP deletion
    • Dyck P. L. Thomas P. K. 4th Philadelphia, Pa, USA Elsevier Saunders
    • Lupski J. R., Chance P. F., Dyck P. L., Thomas P. K., Hereditary motor and sensory neuropathies involving altered dosage or mutation of PMP22: the CMT1A duplication and HNPP deletion Peripheral Neuropathy 2005 4th Philadelphia, Pa, USA Elsevier Saunders 1659 1680
    • (2005) Peripheral Neuropathy , pp. 1659-1680
    • Lupski, J.R.1    Chance, P.F.2
  • 30
    • 33645074670 scopus 로고    scopus 로고
    • Alterations in degradative pathways and protein aggregation in a neuropathy model based on PMP22 overexpression
    • Fortun J., Go J. C., Li J., Amici S. A., Dunn W. A. Jr., Notterpek L., Alterations in degradative pathways and protein aggregation in a neuropathy model based on PMP22 overexpression Neurobiology of Disease 2006 22 1 153 164
    • (2006) Neurobiology of Disease , vol.22 , Issue.1 , pp. 153-164
    • Fortun, J.1    Go, J.C.2    Li, J.3    Amici, S.A.4    Dunn Jr., W.A.5    Notterpek, L.6
  • 31
    • 0344874551 scopus 로고    scopus 로고
    • Emerging Role for Autophagy in the Removal of Aggresomes in Schwann Cells
    • Fortun J., Dunn W. A. Jr., Joy S., Li J., Notterpek L., Emerging Role for Autophagy in the Removal of Aggresomes in Schwann Cells Journal of Neuroscience 2003 23 33 10672 10680 (Pubitemid 37485281)
    • (2003) Journal of Neuroscience , vol.23 , Issue.33 , pp. 10672-10680
    • Fortun, J.1    Dunn Jr., W.A.2    Joy, S.3    Li, J.4    Notterpek, L.5
  • 32
    • 33846320884 scopus 로고    scopus 로고
    • The formation of peripheral myelin protein 22 aggregates is hindered by the enhancement of autophagy and expression of cytoplasmic chaperones
    • DOI 10.1016/j.nbd.2006.09.018, PII S096999610600235X
    • Fortun J., Verrier J. D., Go J. C., Madorsky I., Dunn W. A. Jr., Notterpek L., The formation of peripheral myelin protein 22 aggregates is hindered by the enhancement of autophagy and expression of cytoplasmic chaperones Neurobiology of Disease 2007 25 2 252 265 (Pubitemid 46124007)
    • (2007) Neurobiology of Disease , vol.25 , Issue.2 , pp. 252-265
    • Fortun, J.1    Verrier, J.D.2    Go, J.C.3    Madorsky, I.4    Dunn, W.A.5    Notterpek, L.6
  • 33
    • 0030883723 scopus 로고    scopus 로고
    • Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain-of-function allele
    • DOI 10.1002/(SICI)1097-4547(19970915)49:6<671::AID-JNR2>3.0.CO;2-4
    • Aldkofer K., Naef R., Suter U., Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain-of-function allele Journal of Neuroscience Research 1997 49 671 680 (Pubitemid 27430167)
    • (1997) Journal of Neuroscience Research , vol.49 , Issue.6 , pp. 671-680
    • Adlkofer, K.1    Naef, R.2    Suter, U.3
  • 34
    • 0018305362 scopus 로고
    • Proposed nomenclature for PNS myelin proteins
    • DOI 10.1007/BF00964152
    • Eylar E. H., Uyemura K., Brostoff S. W., Proposed nomenclature for PNS myelin proteins Neurochemical Research 1979 4 2 289 293 (Pubitemid 9244371)
    • (1979) Neurochemical Research , vol.4 , Issue.2 , pp. 289-293
    • Eylar, E.H.1    Uyemura, K.2    Brostoff, S.W.3
  • 37
    • 34547631080 scopus 로고    scopus 로고
    • Mechanisms of disease: Inherited demyelinating neuropathies - From basic to clinical research
    • DOI 10.1038/ncpneuro0583, PII NCPNEURO0583
    • Nave K. A., Sereda M. W., Ehrenreich H., Mechanisms of disease: inherited demyelinating neuropathiesFrom basic to clinical research Nature Clinical Practice Neurology 2007 3 8 453 464 (Pubitemid 47202502)
    • (2007) Nature Clinical Practice Neurology , vol.3 , Issue.8 , pp. 453-464
    • Nave, K.-A.1    Sereda, M.W.2    Ehrenreich, H.3
  • 38
    • 38749104284 scopus 로고    scopus 로고
    • Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice
    • DOI 10.1016/j.neuron.2007.12.021, PII S0896627307010343
    • Pennuto M., Tinelli E., Malaguti M., Del Carro U., D'Antonio M., Ron D., Quattrini A., Feltri M. L., Wrabetz L., Ablation of the UPR-Mediator CHOP Restores MotorFunction and Reduces Demyelination inCharcot-Marie-Tooth 1B Mice Neuron 2008 57 3 393 405 (Pubitemid 351179164)
    • (2008) Neuron , vol.57 , Issue.3 , pp. 393-405
    • Pennuto, M.1    Tinelli, E.2    Malaguti, M.3    Del Carro, U.4    D'Antonio, M.5    Ron, D.6    Quattrini, A.7    Feltri, M.L.8    Wrabetz, L.9
  • 39
    • 84856177824 scopus 로고    scopus 로고
    • Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth disease
    • Maeda M. H., Mitsui J., Soong B. W., Takahashi Y., Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth disease Annals of Neurology 2012 71 84 92
    • (2012) Annals of Neurology , vol.71 , pp. 84-92
    • Maeda, M.H.1    Mitsui, J.2    Soong, B.W.3    Takahashi, Y.4
  • 40
    • 34248583157 scopus 로고    scopus 로고
    • Axonal Charcot-Marie-Tooth disease: The fog is only slowly lifting
    • DOI 10.1212/01.wnl.0000266399.43823.af, PII 0000611420070515000002
    • Pareyson D., Axonal Charcot-Marie-Tooth disease: the fog is only slowly lifting Neurology 2007 68 20 1649 1650 (Pubitemid 46763250)
    • (2007) Neurology , vol.68 , Issue.20 , pp. 1649-1650
    • Pareyson, D.1
  • 42
    • 33750452725 scopus 로고    scopus 로고
    • Dissecting Mitochondrial Fusion
    • DOI 10.1016/j.devcel.2006.10.009, PII S1534580706004618
    • Chan D. C., Dissecting mitochondrial fusion Developmental Cell 2006 11 5 592 594 (Pubitemid 44644971)
    • (2006) Developmental Cell , vol.11 , Issue.5 , pp. 592-594
    • Chan, D.C.1
  • 43
    • 27544466847 scopus 로고    scopus 로고
    • Mitochondrial morphology and dynamics in yeast and multicellular eukaryotes
    • DOI 10.1146/annurev.genet.38.072902.093019
    • Okamoto K., Shaw J. M., Mitochondrial morphology and dynamics in yeast and multicellular eukaryotes Annual Review of Genetics 2005 39 503 536 (Pubitemid 43011125)
    • (2005) Annual Review of Genetics , vol.39 , pp. 503-536
    • Okamoto, K.1    Shaw, J.M.2
  • 44
    • 57349100367 scopus 로고    scopus 로고
    • Mitofusin 2 tethers endoplasmic reticulum to mitochondria
    • De Brito O. M., Scorrano L., Mitofusin 2 tethers endoplasmic reticulum to mitochondria Nature 2008 456 7222 605 610
    • (2008) Nature , vol.456 , Issue.7222 , pp. 605-610
    • De Brito, O.M.1    Scorrano, L.2
  • 47
    • 34547601410 scopus 로고    scopus 로고
    • Mitochondrial Fusion Protects against Neurodegeneration in the Cerebellum
    • DOI 10.1016/j.cell.2007.06.026, PII S0092867407007933
    • Chen H., McCaffery J. M., Chan D. C., Mitochondrial fusion protects against neurodegeneration in the cerebellum Cell 2007 130 3 548 562 (Pubitemid 47198302)
    • (2007) Cell , vol.130 , Issue.3 , pp. 548-562
    • Chen, H.1    McCaffery, J.M.2    Chan, D.C.3
  • 48
    • 35448960851 scopus 로고    scopus 로고
    • Functions and dysfunctions of mitochondrial dynamics
    • DOI 10.1038/nrm2275, PII NRM2275
    • Detmer S. A., Chan D. C., Functions and dysfunctions of mitochondrial dynamics Nature Reviews Molecular Cell Biology 2007 8 11 870 879 (Pubitemid 47622562)
    • (2007) Nature Reviews Molecular Cell Biology , vol.8 , Issue.11 , pp. 870-879
    • Detmer, S.A.1    Chan, D.C.2
  • 49
    • 38349185051 scopus 로고    scopus 로고
    • Hindlimb gait defects due to motor axon loss and reduced distal muscles in a transgenic mouse model of Charcot-Marie-Tooth type 2A
    • Detmer S. A., Velde C. V., Cleveland D. W., Chan D. C., Hindlimb gait defects due to motor axon loss and reduced distal muscles in a transgenic mouse model of Charcot-Marie-Tooth type 2A Human Molecular Genetics 2008 17 3 367 375
    • (2008) Human Molecular Genetics , vol.17 , Issue.3 , pp. 367-375
    • Detmer, S.A.1    Velde, C.V.2    Cleveland, D.W.3    Chan, D.C.4
  • 50
    • 77951896551 scopus 로고    scopus 로고
    • Expression of mitofusin 2R94Q in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A
    • Cartoni R., Arnaud E., Médard J. J., Poirot O., Courvoisier D. S., Chrast R., Martinou J. C., Expression of mitofusin 2R94Q in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A Brain 2010 133 5 1460 1469
    • (2010) Brain , vol.133 , Issue.5 , pp. 1460-1469
    • Cartoni, R.1    Arnaud, E.2    Médard, J.J.3    Poirot, O.4    Courvoisier, D.S.5    Chrast, R.6    Martinou, J.C.7
  • 51
    • 77949801029 scopus 로고    scopus 로고
    • Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex
    • Misko A., Jiang S., Wegorzewska I., Milbrandt J., Baloh R. H., Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex Journal of Neuroscience 2010 30 12 4232 4240
    • (2010) Journal of Neuroscience , vol.30 , Issue.12 , pp. 4232-4240
    • Misko, A.1    Jiang, S.2    Wegorzewska, I.3    Milbrandt, J.4    Baloh, R.H.5
  • 52
    • 0033925726 scopus 로고    scopus 로고
    • Axonal Charcot-Marie-Tooth disease and the neurofilament light gene (NF- L)
    • DOI 10.1086/302986
    • Lupski J. R., Axonal Charcot-Marie-Tooth disease and the neurofilament light gene (NF- L) American Journal of Human Genetics 2000 67 1 8 10 (Pubitemid 30481538)
    • (2000) American Journal of Human Genetics , vol.67 , Issue.1 , pp. 8-10
    • Lupski, J.R.1
  • 53
    • 84857708526 scopus 로고    scopus 로고
    • Normal role of the low-molecular-weight neurofilament protein in mitochondrial dynamics and disruption in Charcot-Marie-Tooth disease
    • Gentil B. J., Minotti S., Beange M., Baloh R. H., Julien J. P., Durham H. D., Normal role of the low-molecular-weight neurofilament protein in mitochondrial dynamics and disruption in Charcot-Marie-Tooth disease The FASEB Journal 2011 26 3 1194 1203
    • (2011) The FASEB Journal , vol.26 , Issue.3 , pp. 1194-1203
    • Gentil, B.J.1    Minotti, S.2    Beange, M.3    Baloh, R.H.4    Julien, J.P.5    Durham, H.D.6
  • 54
    • 77954162482 scopus 로고    scopus 로고
    • Reversal of neuropathy phenotypes in conditional mouse model of Charcot-Marie-Tooth disease type 2E
    • Dequen F., Filali M., Larivire R. C., Perrot R., Hisanaga S. I., Julien J. P., Reversal of neuropathy phenotypes in conditional mouse model of Charcot-Marie-Tooth disease type 2E Human Molecular Genetics 2010 19 13 2616 2629
    • (2010) Human Molecular Genetics , vol.19 , Issue.13 , pp. 2616-2629
    • Dequen, F.1    Filali, M.2    Larivire, R.C.3    Perrot, R.4    Hisanaga, S.I.5    Julien, J.P.6
  • 55
    • 0025085880 scopus 로고
    • X-linked dominant hereditary motor and sensory neuropathy
    • Hahn A. F., Brown W. F., Koopman W. J., Feasby T. E., X-linked dominant hereditary motor and sensory neuropathy Brain 1990 113 5 1511 1525 (Pubitemid 20385928)
    • (1990) Brain , vol.113 , Issue.5 , pp. 1511-1525
    • Hahn, A.F.1    Brown, W.F.2    Koopman, W.J.3    Feasby, T.E.4
  • 58
    • 0030979840 scopus 로고    scopus 로고
    • Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32
    • Anzini P., Neuberg D. H.-H., Schachner M., Nelles E., Willecke K., Zielasek J., Toyka K. V., Suter U., Martini R., Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32 Journal of Neuroscience 1997 17 12 4545 4551 (Pubitemid 27246912)
    • (1997) Journal of Neuroscience , vol.17 , Issue.12 , pp. 4545-4551
    • Anzini, P.1    Neuberg, D.H.-H.2    Schachner, M.3    Nelles, E.4    Willecke, K.5    Zielasek, J.6    Toyka, K.V.7    Suter, U.8    Martini, R.9
  • 62
    • 1242306935 scopus 로고    scopus 로고
    • Evolutionary and Structural Analyses of GDAP1, Involved in Charcot-Marie-Tooth Disease, Characterize a Novel Class of Glutathione Transferase-Related Genes
    • DOI 10.1093/molbev/msh013
    • Marco A., Cuesta A., Pedrola L., Palau F., Marn I., Evolutionary and structural analyses of GDAP1, involved in Charcot-Marie-Tooth disease, characterize a novel class of glutathione transferase-related genes Molecular Biology and Evolution 2004 21 1 176 187 (Pubitemid 38233531)
    • (2004) Molecular Biology and Evolution , vol.21 , Issue.1 , pp. 176-187
    • Marco, A.1    Cuesta, A.2    Pedrola, L.3    Palau, F.4    Marin, I.5
  • 63
    • 17744376804 scopus 로고    scopus 로고
    • GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria
    • DOI 10.1093/hmg/ddi121
    • Pedrola L., Espert A., Wu X., Claramunt R., Shy M. E., Palau F., GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria Human Molecular Genetics 2005 14 8 1087 1094 (Pubitemid 40575884)
    • (2005) Human Molecular Genetics , vol.14 , Issue.8 , pp. 1087-1094
    • Pedrola, L.1    Espert, A.2    Wu, X.3    Claramunt, R.4    Shy, M.E.5    Palau, F.6
  • 65
    • 25444514731 scopus 로고    scopus 로고
    • Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: New implications for Charcot-Marie-Tooth disease
    • DOI 10.1083/jcb.200507087
    • Niemann A., Ruegg M., La Padula V., Schenone A., Suter U., Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease Journal of Cell Biology 2005 170 7 1067 1078 (Pubitemid 41362639)
    • (2005) Journal of Cell Biology , vol.170 , Issue.7 , pp. 1067-1078
    • Niemann, A.1    Ruegg, M.2    La Padula, V.3    Schenone, A.4    Suter, U.5
  • 67
    • 70350348361 scopus 로고    scopus 로고
    • GDAP1 mutations differ in their effects on mitochondrial dynamics and apoptosis depending on the mode of inheritance
    • Niemann A., Wagner K. M., Ruegg M., Suter U., GDAP1 mutations differ in their effects on mitochondrial dynamics and apoptosis depending on the mode of inheritance Neurobiology of Disease 2009 36 3 509 520
    • (2009) Neurobiology of Disease , vol.36 , Issue.3 , pp. 509-520
    • Niemann, A.1    Wagner, K.M.2    Ruegg, M.3    Suter, U.4
  • 68
    • 80054702542 scopus 로고    scopus 로고
    • The Charcot-Marie-Tooth related gene GDAP1 complements cell cycle delay at G2/M in S. cerevisiae fis1 defective cells
    • Estela A., Pla-Martn D., Snchez-Piris M., Sesaki H., Palau F., The Charcot-Marie-Tooth related gene GDAP1 complements cell cycle delay at G2/M in S. cerevisiae fis1 defective cells Journal of Biological Chemistry 2011 286 36777 36786
    • (2011) Journal of Biological Chemistry , vol.286 , pp. 36777-36786
    • Estela, A.1    Pla-Martn, D.2    Snchez-Piris, M.3    Sesaki, H.4    Palau, F.5
  • 71
    • 34247571924 scopus 로고    scopus 로고
    • The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4
    • DOI 10.1111/j.1399-0004.2007.00774.x
    • Claramunt R., Sevilla T., Lupo V., Cuesta A., Milln J. M., Vlchez J. J., Palau F., Espins C., The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4 Clinical Genetics 2007 71 4 343 349 (Pubitemid 46680799)
    • (2007) Clinical Genetics , vol.71 , Issue.4 , pp. 343-349
    • Claramunt, R.1    Sevilla, T.2    Lupo, V.3    Cuesta, A.4    Millan, J.M.5    Vilchez, J.J.6    Palau, F.7    Espinos, C.8
  • 73
    • 70449356628 scopus 로고    scopus 로고
    • Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway
    • Lupo V., Galindo M. I., Martnez-Rubio D., Sevilla T., Vlchez J. J., Palau F., Espins C., Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway Human Molecular Genetics 2009 18 23 4603 4614
    • (2009) Human Molecular Genetics , vol.18 , Issue.23 , pp. 4603-4614
    • Lupo, V.1    Galindo, M.I.2    Martnez-Rubio, D.3    Sevilla, T.4    Vlchez, J.J.5    Palau, F.6    Espins, C.7
  • 76
    • 37749043369 scopus 로고    scopus 로고
    • Mitochondrial dynamics and peripheral neuropathy
    • Baloh R. H., Mitochondrial dynamics and peripheral neuropathy Neuroscientist 2008 14 1 12 18
    • (2008) Neuroscientist , vol.14 , Issue.1 , pp. 12-18
    • Baloh, R.H.1
  • 77
    • 33751160114 scopus 로고    scopus 로고
    • Neurotrophins and peripheral neuropathies
    • Sahenk Z., Neurotrophins and peripheral neuropathies Brain Pathology 2006 16 4 311 319
    • (2006) Brain Pathology , vol.16 , Issue.4 , pp. 311-319
    • Sahenk, Z.1
  • 78
    • 0019287251 scopus 로고
    • Axonal transport of the cytoskeleton in regenerating motor neurons: Constancy and change
    • DOI 10.1016/0006-8993(80)90144-4
    • Hoffman P. N., Lasek R. J., Axonal transport of the cytoskeleton in regenerating motor neurons: constancy and change Brain Research 1980 202 2 317 333 (Pubitemid 11130317)
    • (1980) Brain Research , vol.202 , Issue.2 , pp. 317-333
    • Hoffman, P.N.1    Lasek, R.J.2
  • 79
    • 0024549399 scopus 로고
    • Transport of cytoskeletal elements from parent axons into regenerating daughter axons
    • McQuarrie I. G., Lasek R. J., Transport of cytoskeletal elements from parent axons into regenerating daughter axons Journal of Neuroscience 1989 9 2 436 446 (Pubitemid 19069487)
    • (1989) Journal of Neuroscience , vol.9 , Issue.2 , pp. 436-446
    • McQuarrie, I.G.1    Lasek, R.J.2
  • 80
    • 12144254738 scopus 로고    scopus 로고
    • Axonal protein synthesis and degradation are necessary for efficient growth cone regeneration
    • DOI 10.1523/JNEUROSCI.3073-04.2005
    • Verma P., Chierzi S., Codd A. M., Campbell D. S., Meyer R. L., Holt C. E., Fawcett J. W., Axonal protein synthesis and degradation are necessary for efficient growth cone regeneration Journal of Neuroscience 2005 25 2 331 342 (Pubitemid 40105603)
    • (2005) Journal of Neuroscience , vol.25 , Issue.2 , pp. 331-342
    • Verma, P.1    Chierzi, S.2    Codd, A.M.3    Campbell, D.S.4    Meyer, R.L.5    Holt, C.E.6    Fawcett, J.W.7
  • 81
    • 32344443093 scopus 로고    scopus 로고
    • The evolving roles of axonally synthesized proteins in regeneration
    • DOI 10.1016/j.conb.2006.01.002, PII S0959438806000031, Development
    • Willis D. E., Twiss J. L., The evolving roles of axonally synthesized proteins in regeneration Current Opinion in Neurobiology 2006 16 1 111 118 (Pubitemid 43221861)
    • (2006) Current Opinion in Neurobiology , vol.16 , Issue.1 , pp. 111-118
    • Willis, D.E.1    Twiss, J.L.2
  • 82
    • 34447635901 scopus 로고    scopus 로고
    • Neural plasticity after peripheral nerve injury and regeneration
    • DOI 10.1016/j.pneurobio.2007.06.005, PII S0301008207001098
    • Navarro X., Viv M., Valero-Cabré A., Neural plasticity after peripheral nerve injury and regeneration Progress in Neurobiology 2007 82 4 163 201 (Pubitemid 47088051)
    • (2007) Progress in Neurobiology , vol.82 , Issue.4 , pp. 163-201
    • Navarro, X.1    Vivo, M.2    Valero-Cabre, A.3
  • 85
    • 33947219362 scopus 로고    scopus 로고
    • Ascorbic acid inhibits PMP22 expression by reducing cAMP levels
    • DOI 10.1016/j.nmd.2006.12.008, PII S0960896606006365
    • Kaya F., Belin S., Bourgeois P., Micaleff J., Blin O., Fontés M., Ascorbic acid inhibits PMP22 expression by reducing cAMP levels Neuromuscular Disorders 2007 17 3 248 253 (Pubitemid 46420772)
    • (2007) Neuromuscular Disorders , vol.17 , Issue.3 , pp. 248-253
    • Kaya, F.1    Belin, S.2    Bourgeois, P.3    Micaleff, J.4    Blin, O.5    Fontes, M.6
  • 87
    • 0344666404 scopus 로고    scopus 로고
    • Progesterone stimulates the activity of the promoters of peripheral myelin protein-22 and protein zero genes in Schwann cells
    • Désarnaud F., Do Thi A. N., Brown A. M., Lemke G., Suter U., Baulieu E. E., Schumacher M., Progesterone stimulates the activity of the promoters of peripheral myelin protein-22 and protein zero genes in Schwann cells Journal of Neurochemistry 1998 71 4 1765 1768 (Pubitemid 28443052)
    • (1998) Journal of Neurochemistry , vol.71 , Issue.4 , pp. 1765-1768
    • Desarnaud, F.1    Do Thi, A.N.2    Brown, A.M.3    Lemke, G.4    Suter, U.5    Baulieu, E.-E.6    Schumacher, M.7
  • 88
    • 0347185347 scopus 로고    scopus 로고
    • Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A)
    • DOI 10.1038/nm957
    • Sereda M. W., Meyer zu Hrste G., Suter U., Uzma N., Nave K. A., Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A) Nature Medicine 2003 9 12 1533 1537 (Pubitemid 38004782)
    • (2003) Nature Medicine , vol.9 , Issue.12 , pp. 1533-1537
    • Sereda, M.W.1    Meyer Zu Horste, G.2    Suter, U.3    Uzma, N.4    Nave, K.-A.5
  • 89
    • 33846798265 scopus 로고    scopus 로고
    • Antiprogesterone therapy uncouples axonal loss from demyelination in a transgenic rat model of CMT1A neuropathy
    • DOI 10.1002/ana.21026
    • zu Horste G. M., Prukop T., Liebetanz D., Mobius W., Nave K. A., Sereda M. W., Antiprogesterone therapy uncouples axonal loss from demyelination in a transgenic rat model of CMT1A neuropathy Annals of Neurology 2007 61 1 61 72 (Pubitemid 46214245)
    • (2007) Annals of Neurology , vol.61 , Issue.1 , pp. 61-72
    • Zu Horste, G.M.1    Prukop, T.2    Liebetanz, D.3    Mobius, W.4    Nave, K.-A.5    Sereda, M.W.6
  • 90
    • 34548219064 scopus 로고    scopus 로고
    • Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: A potential therapy for inherited neuropathy
    • DOI 10.1086/519926
    • Khajavi M., Shiga K., Wiszniewski W., He F., Shaw C. A., Yan J., Wensel T. G., Snipes G. J., Lupski J. R., Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy American Journal of Human Genetics 2007 81 3 438 453 (Pubitemid 47330204)
    • (2007) American Journal of Human Genetics , vol.81 , Issue.3 , pp. 438-453
    • Khajavi, M.1    Shiga, K.2    Wiszniewski, W.3    He, F.4    Shaw, C.A.5    Yan, J.6    Wensel, T.G.7    Snipes, G.J.8    Lupski, J.R.9
  • 92
    • 80054735825 scopus 로고    scopus 로고
    • Evaluation of histone deacetylase inhibitors as therapeutics for neurodegenerative diseases Methods
    • Soragni E., Xu C., Cooper A., Plasterer H. L., Rusche J. R., Gottesfeld J. M., Evaluation of histone deacetylase inhibitors as therapeutics for neurodegenerative diseases Methods Molecular Biology 2011 793 495 508
    • (2011) Molecular Biology , vol.793 , pp. 495-508
    • Soragni, E.1    Xu, C.2    Cooper, A.3    Plasterer, H.L.4    Rusche, J.R.5    Gottesfeld, J.M.6
  • 93
    • 0002526365 scopus 로고    scopus 로고
    • The role of Schwann cell in nerve regeneration
    • Castellano B. Gonzlez B. Nieto Sampedro M. Boston, Mass, USA Kluwer Academic
    • Verd E., Navarro X., Castellano B., Gonzlez B., Nieto Sampedro M., The role of Schwann cell in nerve regeneration Understanding Glial Cells 1998 Boston, Mass, USA Kluwer Academic 319 359
    • (1998) Understanding Glial Cells , pp. 319-359
    • Verd, E.1    Navarro, X.2
  • 94
    • 0032191969 scopus 로고    scopus 로고
    • Recombinant human glial growth factor 2 (rhGGF 2) improves functional recovery of crushed peripheral nerve (a double-blind study)
    • DOI 10.1016/S0197-0186(98)00037-0, PII S0197018698000370
    • Chen L. E., Liu K., Seaber A. V., Katragadda S., Kirk C., Urbaniak J. R., Recombinant human Glial growth factor 2 (rhGGF 2) improves functional recovery of crushed peripheral nerve (a double-blind study) Neurochemistry International 1998 33 4 341 351 (Pubitemid 28529512)
    • (1998) Neurochemistry International , vol.33 , Issue.4 , pp. 341-351
    • Chen, L.-E.1    Liu, K.2    Seaber, A.V.3    Katragadda, S.4    Kirk, C.5    Urbaniak, J.R.6
  • 95
    • 61549136754 scopus 로고    scopus 로고
    • Neuregulin-1, a key axonal signal that drives Schwann cell growth and differentiation
    • Birchmeier C., Nave K. A., Neuregulin-1, a key axonal signal that drives Schwann cell growth and differentiation Glia 2008 56 14 1491 1497
    • (2008) Glia , vol.56 , Issue.14 , pp. 1491-1497
    • Birchmeier, C.1    Nave, K.A.2
  • 96
    • 78449298649 scopus 로고    scopus 로고
    • Nrg1/ErbB signaling networks in Schwann cell development and myelination
    • Newbern J., Birchmeier C., Nrg1/ErbB signaling networks in Schwann cell development and myelination Seminars in Cell and Developmental Biology 2010 21 9 922 928
    • (2010) Seminars in Cell and Developmental Biology , vol.21 , Issue.9 , pp. 922-928
    • Newbern, J.1    Birchmeier, C.2
  • 97
    • 24644446342 scopus 로고    scopus 로고
    • NT-3 promotes nerve regeneration and sensory improvement in CMT1A mouse models and in patients
    • DOI 10.1212/01.WNL.0000171978.70849.c5
    • Sahenk Z., Nagaraja H. N., McCracken B. S., King W. M., Freimer M. L., Cedarbaum J. M., Mendell J. R., NT-3 promotes nerve regeneration and sensory improvement in CMT1A mouse models and in patients Neurology 2005 65 5 681 689 (Pubitemid 41285845)
    • (2005) Neurology , vol.65 , Issue.5 , pp. 681-689
    • Sahenk, Z.1    Nagaraja, H.N.2    McCracken, B.S.3    King, W.M.4    Freimer, M.L.5    Cedarbaum, J.M.6    Mendell, J.R.7
  • 98
    • 0033635904 scopus 로고    scopus 로고
    • Neurotrophins: Key regulators of cell fate and cell shape in the vertebrate nervous system
    • Bibel M., Barde Y. A., Neurotrophins: key regulators of cell fate and cell shape in the vertebrate nervous system Genes and Development 2000 14 23 2919 2937
    • (2000) Genes and Development , vol.14 , Issue.23 , pp. 2919-2937
    • Bibel, M.1    Barde, Y.A.2
  • 100
    • 34250192241 scopus 로고    scopus 로고
    • Gene therapy in peripheral nerve reconstruction approaches
    • DOI 10.2174/156652307780859035
    • Haastert K., Grothe C., Gene therapy in peripheral nerve reconstruction approaches Current Gene Therapy 2007 7 3 221 228 (Pubitemid 46902204)
    • (2007) Current Gene Therapy , vol.7 , Issue.3 , pp. 221-228
    • Haastert, K.1    Grothe, C.2
  • 102
    • 79958263554 scopus 로고    scopus 로고
    • Schwann cell targeting via intrasciatic injection of AAV8 as gene therapy strategy for peripheral nerve regeneration
    • Homs J., Ariza L., Pags G., Udina E., Navarro X., Chilln M., Bosch A., Schwann cell targeting via intrasciatic injection of AAV8 as gene therapy strategy for peripheral nerve regeneration Gene Therapy 2011 18 6 622 630
    • (2011) Gene Therapy , vol.18 , Issue.6 , pp. 622-630
    • Homs, J.1    Ariza, L.2    Pags, G.3    Udina, E.4    Navarro, X.5    Chilln, M.6    Bosch, A.7
  • 105
    • 26844567115 scopus 로고    scopus 로고
    • The potential of adipose-derived adult stem cells as a source of neuronal progenitor cells
    • DOI 10.1097/01.prs.0000182570.62814.e3
    • Kokai L. E., Rubin J. P., Marra K. G., The potential of adipose-derived adult stem cells as a source of neuronal progenitor cells Plastic and Reconstructive Surgery 2005 116 5 1453 1460 (Pubitemid 41456527)
    • (2005) Plastic and Reconstructive Surgery , vol.116 , Issue.5 , pp. 1453-1460
    • Kokai, L.E.1    Rubin, J.P.2    Marra, K.G.3
  • 106
    • 33750555590 scopus 로고    scopus 로고
    • Phenotypic and functional characteristics of mesenchymal stem cells differentiated along a Schwann cell lineage
    • DOI 10.1002/glia.20421
    • Caddick J., Kingham P. J., Gardiner N. J., Wiberg M., Terenghi G., Phenotypic and functional characteristics of mesenchymal stem cells differentiated along a Schwann cell lineage Glia 2006 54 8 840 849 (Pubitemid 44671989)
    • (2006) GLIA , vol.54 , Issue.8 , pp. 840-849
    • Caddick, J.1    Kingham, P.J.2    Gardiner, N.J.3    Wiberg, M.4    Terenghi, G.5
  • 107
    • 2442425936 scopus 로고    scopus 로고
    • Rat bone marrow mesenchymal stem cells express glial markers and stimulate nerve regeneration
    • DOI 10.1016/j.neulet.2004.03.077, PII S0304394004002861
    • Tohill M., Mantovani C., Wiberg M., Terenghi G., Rat bone marrow mesenchymal stem cells express Glial markers and stimulate nerve regeneration Neuroscience Letters 2004 362 3 200 203 (Pubitemid 38648941)
    • (2004) Neuroscience Letters , vol.362 , Issue.3 , pp. 200-203
    • Tohill, M.1    Mantovani, C.2    Wiberg, M.3    Terenghi, G.4
  • 108
    • 30344440721 scopus 로고    scopus 로고
    • Transdifferentiation of mesenchymal stem cells into Schwann cell-like myelinating cells
    • DOI 10.1016/j.ejcb.2005.09.021, PII S0171933505001676
    • Keilhoff G., Goihl A., Langnse K., Fansa H., Wolf G., Transdifferentiation of mesenchymal stem cells into Schwann cell-like myelinating cells European Journal of Cell Biology 2006 85 1 11 24 (Pubitemid 43055554)
    • (2006) European Journal of Cell Biology , vol.85 , Issue.1 , pp. 11-24
    • Keilhoff, G.1    Goihl, A.2    Langnase, K.3    Fansa, H.4    Wolf, G.5
  • 111
    • 34548737059 scopus 로고    scopus 로고
    • Adipose-derived stem cells differentiate into a Schwann cell phenotype and promote neurite outgrowth in vitro
    • DOI 10.1016/j.expneurol.2007.06.029, PII S0014488607002579
    • Kingham P. J., Kalbermatten D. F., Mahay D., Armstrong S. J., Wiberg M., Terenghi G., Adipose-derived stem cells differentiate into a Schwann cell phenotype and promote neurite outgrowth in vitro Experimental Neurology 2007 207 2 267 274 (Pubitemid 47432883)
    • (2007) Experimental Neurology , vol.207 , Issue.2 , pp. 267-274
    • Kingham, P.J.1    Kalbermatten, D.F.2    Mahay, D.3    Armstrong, S.J.4    Wiberg, M.5    Terenghi, G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.