메뉴 건너뛰기




Volumn 18, Issue 10, 1996, Pages 789-797

Myelin mutants: Model systems for the study of normal and abnormal myelination

Author keywords

[No Author keywords available]

Indexed keywords

ANIMALIA; BOS TAURUS; BOVINAE; CANIS FAMILIARIS;

EID: 0030271561     PISSN: 02659247     EISSN: None     Source Type: Journal    
DOI: 10.1002/bies.950181005     Document Type: Review
Times cited : (65)

References (71)
  • 1
    • 0004214945 scopus 로고
    • Plenum Press, New York and London
    • Morell, P. (1984). Myelin, pp 147-195. Plenum Press, New York and London.
    • (1984) Myelin , pp. 147-195
    • Morell, P.1
  • 2
  • 4
    • 0024074053 scopus 로고
    • Unwrapping the genes of myelin
    • Lemke, G. (1988). Unwrapping the genes of myelin. Neuron 1, 535-543.
    • (1988) Neuron , vol.1 , pp. 535-543
    • Lemke, G.1
  • 5
    • 0028122616 scopus 로고
    • Neurological mouse mutants and the genes of myelin
    • Nave, K.-A. (1994). Neurological mouse mutants and the genes of myelin. J. Neurosci. Res 38, 607-612.
    • (1994) J. Neurosci. Res , vol.38 , pp. 607-612
    • Nave, K.-A.1
  • 7
    • 0027584197 scopus 로고
    • The molecular genetics of myelination: An update
    • Lemke, G. (1993). The molecular genetics of myelination: An update. Glia 7, 263-271.
    • (1993) Glia , vol.7 , pp. 263-271
    • Lemke, G.1
  • 8
    • 0022413538 scopus 로고
    • Chromosomal mapping of mouse myelin basic protein gene and structure and transcription of the partially deleted gene in shiverer mutant mice
    • Roach, A., Takahashi, N., Pravtcheva, D., Ruddle, F. and Hood, L. (1985). Chromosomal mapping of mouse myelin basic protein gene and structure and transcription of the partially deleted gene in shiverer mutant mice. Cell 42, 149-155.
    • (1985) Cell , vol.42 , pp. 149-155
    • Roach, A.1    Takahashi, N.2    Pravtcheva, D.3    Ruddle, F.4    Hood, L.5
  • 9
    • 0025138265 scopus 로고
    • Post-transcriptional events are responsible for low expression of myelin basic protein in myelin deficient mice: Role of antisense RNA
    • Tosic, M., Roach, A., de Rivaz, J., Dolivo, M. and Matthieu, J.-M. (1990) Post-transcriptional events are responsible for low expression of myelin basic protein in myelin deficient mice: role of antisense RNA. EMBO J. 9, 401-406.
    • (1990) EMBO J. , vol.9 , pp. 401-406
    • Tosic, M.1    Roach, A.2    De Rivaz, J.3    Dolivo, M.4    Matthieu, J.-M.5
  • 10
    • 0023613854 scopus 로고
    • Expression of a myelin basic protein gene in transgenic shiverer mice: Correction of the dysmyelinating phenotype
    • Readhead, C. et al. (1987). Expression of a myelin basic protein gene in transgenic shiverer mice: correction of the dysmyelinating phenotype. Cell 48, 703-712.
    • (1987) Cell , vol.48 , pp. 703-712
    • Readhead, C.1
  • 11
    • 0023623847 scopus 로고
    • Myelin deficient mice: Expression of myelin basic protein and generation of mice with varying levels of myelin
    • Popko, B. et al. (1987). Myelin deficient mice: expression of myelin basic protein and generation of mice with varying levels of myelin. Cell 48, 713-721.
    • (1987) Cell , vol.48 , pp. 713-721
    • Popko, B.1
  • 12
    • 0026615047 scopus 로고
    • 0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons
    • 0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons. Cell 71, 565-576.
    • (1992) Cell , vol.71 , pp. 565-576
    • Giese, K.P.1    Martini, R.2    Lemke, G.3    Soriano, P.4    Schachner, M.5
  • 13
    • 0029065654 scopus 로고
    • Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin
    • Martini, R., Mohajeri, M.H., Kasper, S., Giese, K.P. and Schachner, M. (1995). Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin. J. Neurosci. 15, 4488-4495.
    • (1995) J. Neurosci. , vol.15 , pp. 4488-4495
    • Martini, R.1    Mohajeri, M.H.2    Kasper, S.3    Giese, K.P.4    Schachner, M.5
  • 14
    • 0028902548 scopus 로고
    • Biology and genetics of hereditary motor and sensory neuropathies
    • Suter, U. and Snipes, G.J. (1995). Biology and genetics of hereditary motor and sensory neuropathies. Annu. Rev. Neurosci. 16, 45-75.
    • (1995) Annu. Rev. Neurosci. , vol.16 , pp. 45-75
    • Suter, U.1    Snipes, G.J.2
  • 15
    • 0029014126 scopus 로고
    • Molecular anatomy and genetics of myelin proteins in the peripheral nervous system
    • Snipes, G.J. and Suter, U. (1995). Molecular anatomy and genetics of myelin proteins in the peripheral nervous system. J. Anat. 186, 483-494.
    • (1995) J. Anat. , vol.186 , pp. 483-494
    • Snipes, G.J.1    Suter, U.2
  • 16
    • 0029093622 scopus 로고
    • Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models
    • Snipes, G.J. and Suter, U. (1995). Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models. Brain Pathol. 5, 233-247.
    • (1995) Brain Pathol. , vol.5 , pp. 233-247
    • Snipes, G.J.1    Suter, U.2
  • 17
    • 0028014579 scopus 로고
    • Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)
    • Fairweather, N. et al. (1994). Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1). Hum. Mol. Genet. 3, 29-34.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 29-34
    • Fairweather, N.1
  • 18
    • 0029054613 scopus 로고
    • New point mutations and deletions of the connexin 32 gene in X-linked Charcot-Marie-Tooth neuropathy
    • Ionasescu, V., Searby, C., Ionasescu, R. and Meschino, W. (1995). New point mutations and deletions of the connexin 32 gene in X-linked Charcot-Marie-Tooth neuropathy. Neuromusc. Disord. 5, 297-300.
    • (1995) Neuromusc. Disord. , vol.5 , pp. 297-300
    • Ionasescu, V.1    Searby, C.2    Ionasescu, R.3    Meschino, W.4
  • 19
    • 0029431669 scopus 로고
    • New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease
    • Bone, L.J. et al. (1995). New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease. Neurology 45, 1863-1866.
    • (1995) Neurology , vol.45 , pp. 1863-1866
    • Bone, L.J.1
  • 20
    • 0029563471 scopus 로고
    • Connexin32 is a myelin-related protein in the PNS and CNS
    • Scherer, S.S. et al. (1995). Connexin32 is a myelin-related protein in the PNS and CNS. J. Neurosci. 15, 8281-8294.
    • (1995) J. Neurosci. , vol.15 , pp. 8281-8294
    • Scherer, S.S.1
  • 21
    • 0028851362 scopus 로고
    • Peripheral myelin protein 22: Facts and hypotheses
    • Suter, U. and Snipes, G.J. (1995). Peripheral myelin protein 22: Facts and hypotheses. J. Neurosci. Res. 40, 145-151.
    • (1995) J. Neurosci. Res. , vol.40 , pp. 145-151
    • Suter, U.1    Snipes, G.J.2
  • 22
    • 0029588323 scopus 로고
    • Widespread expression of the peripheral myelin protein-22 gene (pmp22) in neural and non-neural tissues during murine development
    • Baechner, D. et al. (1995). Widespread expression of the peripheral myelin protein-22 gene (pmp22) in neural and non-neural tissues during murine development. J. Neurosci. Res. 42, 733-741.
    • (1995) J. Neurosci. Res. , vol.42 , pp. 733-741
    • Baechner, D.1
  • 24
    • 0028268350 scopus 로고
    • Differential expression of two mRNA species indicates a dual function of peripheral myelin protein PMP22 in cell growth and myelination
    • Bosse, F., Zoldl, G., Wilms, S., Gillen, C.P., Kuhn, H.G. and Müller, H.W. (1994). Differential expression of two mRNA species indicates a dual function of peripheral myelin protein PMP22 in cell growth and myelination. J. Neurosci. Res. 37, 529-537.
    • (1994) J. Neurosci. Res. , vol.37 , pp. 529-537
    • Bosse, F.1    Zoldl, G.2    Wilms, S.3    Gillen, C.P.4    Kuhn, H.G.5    Müller, H.W.6
  • 25
    • 0028610199 scopus 로고
    • Molecular genetics of Charcot-Marie-Tooth neuropathy
    • Roa, B.B. and Lupski, J.R. (1994). Molecular genetics of Charcot-Marie-Tooth neuropathy. Adv. Hum. Genet. 22, 117-152.
    • (1994) Adv. Hum. Genet. , vol.22 , pp. 117-152
    • Roa, B.B.1    Lupski, J.R.2
  • 26
    • 0027981751 scopus 로고
    • Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies
    • Chance, P.F. and Fischbeck, K.H. (1994). Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies. Hum. Mol. Genet. 3, 1503-1507.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1503-1507
    • Chance, P.F.1    Fischbeck, K.H.2
  • 27
    • 0026605507 scopus 로고
    • Trembler mouse carries a point mutation in a myelin gene
    • Suter, U. et al. (1992). Trembler mouse carries a point mutation in a myelin gene. Nature 356, 241-244.
    • (1992) Nature , vol.356 , pp. 241-244
    • Suter, U.1
  • 28
    • 15844393894 scopus 로고    scopus 로고
    • A transgenic rat model of Charcot-Marie-Tooth disease
    • Sereda, M. et al. (1996). A transgenic rat model of Charcot-Marie-Tooth disease. Neuron 16, 1049-1060.
    • (1996) Neuron , vol.16 , pp. 1049-1060
    • Sereda, M.1
  • 29
    • 0028784820 scopus 로고
    • Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
    • Adlkofer, K., Martini, R., Aguzzi, A., Zlelasek, J., Toyka, K.V. and Suter, U. (1995). Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice. Nature Genet. 11, 274-280.
    • (1995) Nature Genet. , vol.11 , pp. 274-280
    • Adlkofer, K.1    Martini, R.2    Aguzzi, A.3    Zlelasek, J.4    Toyka, K.V.5    Suter, U.6
  • 30
    • 0002478352 scopus 로고    scopus 로고
    • The Schwann cell lineage: Embryonic and early postnatal development
    • (ed. K. R. Jessen and W. D. Richardson), Bios, Oxford
    • Stewart, H.J.S., Mirsky, R. and Jessen, K.R. (1996). The Schwann cell lineage: embryonic and early postnatal development. In Glial Cell Development. Basic Principles and Clinical Relevance (ed. K. R. Jessen and W. D. Richardson), pp 1-30. Bios, Oxford.
    • (1996) Glial Cell Development. Basic Principles and Clinical Relevance , pp. 1-30
    • Stewart, H.J.S.1    Mirsky, R.2    Jessen, K.R.3
  • 32
    • 0028824925 scopus 로고
    • Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies
    • Martini, R., Zielasek, J., Toyka, K.V., Giese, K.P. and Schachner, M. (1995). Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies. Nature Genet. 11, 281-286.
    • (1995) Nature Genet. , vol.11 , pp. 281-286
    • Martini, R.1    Zielasek, J.2    Toyka, K.V.3    Giese, K.P.4    Schachner, M.5
  • 33
    • 0027759985 scopus 로고    scopus 로고
    • Genetics of Pelizaeus-Merzbacher disease
    • 19S3
    • Hodes, M.E., Pratt, V.M. and Dlouhy, S.R. (19S3). Genetics of Pelizaeus-Merzbacher disease. Dev. Neurosci. 15, 383-394.
    • Dev. Neurosci. , vol.15 , pp. 383-394
    • Hodes, M.E.1    Pratt, V.M.2    Dlouhy, S.R.3
  • 34
    • 0028142316 scopus 로고
    • Genetic homogeneity of Pelizaeus-Merzbacher disease: Tight linkage to the proteolipoprotein locus in 16 affected families
    • Boespflug-Tanguy, O. et al. (1994). Genetic homogeneity of Pelizaeus-Merzbacher disease: Tight linkage to the proteolipoprotein locus in 16 affected families. Am. J. Hum. Genet. 55, 461-467.
    • (1994) Am. J. Hum. Genet. , vol.55 , pp. 461-467
    • Boespflug-Tanguy, O.1
  • 35
    • 0028239867 scopus 로고
    • X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus
    • Saugier-Veber, P. et al. (1994). X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus. Nature Genet. 6, 257-262.
    • (1994) Nature Genet. , vol.6 , pp. 257-262
    • Saugier-Veber, P.1
  • 36
    • 0026767888 scopus 로고
    • Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene
    • Schneider, A. et al. (1992). Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene. Nature 358, 758-761.
    • (1992) Nature , vol.358 , pp. 758-761
    • Schneider, A.1
  • 37
    • 0029145584 scopus 로고
    • Neuropathology and genetics of Pelizaeus-Merzbacher disease
    • Seitelberger, F. (1995). Neuropathology and genetics of Pelizaeus-Merzbacher disease. Brain Pathol. 5, 267-273.
    • (1995) Brain Pathol. , vol.5 , pp. 267-273
    • Seitelberger, F.1
  • 38
    • 0022540450 scopus 로고
    • Oligodendroglial cell death in jimpy mice: An explanation for the myelin deficit
    • Knapp, P.E., Skoff, R.P. and Redstone, D.W. (1986). Oligodendroglial cell death in jimpy mice: an explanation for the myelin deficit. J. Neurosci. 6, 2813-2822.
    • (1986) J. Neurosci. , vol.6 , pp. 2813-2822
    • Knapp, P.E.1    Skoff, R.P.2    Redstone, D.W.3
  • 39
    • 0025687842 scopus 로고
    • Dissection of the phenotype and genotype of the X-linked myelin mutants
    • Duncan, I.D. (1990). Dissection of the phenotype and genotype of the X-linked myelin mutants. Ann. N. Y. Acad. Sci. 605, 110-121.
    • (1990) Ann. N. Y. Acad. Sci. , vol.605 , pp. 110-121
    • Duncan, I.D.1
  • 40
    • 0028903559 scopus 로고
    • A case of Pelizaeus-Merzbacher disease showing increased dosage of the proteolipid protein gene
    • Harding, B., Ellis, D. and Malcolm, S. (1995). A case of Pelizaeus-Merzbacher disease showing increased dosage of the proteolipid protein gene. Neuropathol. Appl. Neurobiol. 21, 111-115.
    • (1995) Neuropathol. Appl. Neurobiol. , vol.21 , pp. 111-115
    • Harding, B.1    Ellis, D.2    Malcolm, S.3
  • 41
    • 0028325902 scopus 로고
    • Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage
    • Readhead, C., Schneider, A., Griffiths, I.R. and Nave, K. (1994). Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage. Neuron 12, 583-595.
    • (1994) Neuron , vol.12 , pp. 583-595
    • Readhead, C.1    Schneider, A.2    Griffiths, I.R.3    Nave, K.4
  • 42
    • 0028133486 scopus 로고
    • Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene
    • Kagawa, T. et al. (1994). Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene. Neuron 13, 427-442.
    • (1994) Neuron , vol.13 , pp. 427-442
    • Kagawa, T.1
  • 43
    • 0028893387 scopus 로고
    • Over-expression of the DM-20 myelin proteolipid causes central nervous system demyelination in transgenic mice
    • Johnson, R.S., Roder, J.C. and Riordan, J.R. (1995). Over-expression of the DM-20 myelin proteolipid causes central nervous system demyelination in transgenic mice. J. Neurochem. 64, 967-976.
    • (1995) J. Neurochem. , vol.64 , pp. 967-976
    • Johnson, R.S.1    Roder, J.C.2    Riordan, J.R.3
  • 44
    • 0027986675 scopus 로고
    • Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice
    • Boison, D. and Stoffel, W. (1994). Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice. Proc. Natl Acad. Sci. USA 91, 11709-11713.
    • (1994) Proc. Natl Acad. Sci. USA , vol.91 , pp. 11709-11713
    • Boison, D.1    Stoffel, W.2
  • 45
    • 0029127508 scopus 로고
    • Adhesive properties of proteolipid protein are responsible for the compaction of CNS myelin sheaths
    • Boison, D., Büssow, H., D'Urso, D., Müller, H.-W. and Stoffel, W. (1995). Adhesive properties of proteolipid protein are responsible for the compaction of CNS myelin sheaths. J. Neurosci. 15, 5502-5513.
    • (1995) J. Neurosci. , vol.15 , pp. 5502-5513
    • Boison, D.1    Büssow, H.2    D'Urso, D.3    Müller, H.-W.4    Stoffel, W.5
  • 46
    • 0026348463 scopus 로고
    • Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease
    • Raskind, W.H., Williams, C.A., Hudson, L.D. and Bird, T.D. (1991). Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease. Am. J. Hum. Genet. 49, 1355-1360.
    • (1991) Am. J. Hum. Genet. , vol.49 , pp. 1355-1360
    • Raskind, W.H.1    Williams, C.A.2    Hudson, L.D.3    Bird, T.D.4
  • 47
    • 0029079396 scopus 로고
    • Dominant-negative action of the jimpy mutation in mice complemented with an autosomal transgene for myelin proteolipid protein
    • Schneider, A., Griffiths, I.R., Readhead, C. and Nave, K.-A. (1995). Dominant-negative action of the jimpy mutation in mice complemented with an autosomal transgene for myelin proteolipid protein. Proc. Natl Acad. Sci. USA 92, 4447-4451.
    • (1995) Proc. Natl Acad. Sci. USA , vol.92 , pp. 4447-4451
    • Schneider, A.1    Griffiths, I.R.2    Readhead, C.3    Nave, K.-A.4
  • 48
    • 0028017717 scopus 로고
    • A combination of PLP and DM20 transgenes promotes partial myelination in the jimpy mouse
    • Nadon, N.L., Arnheiter, H. and Hudson, L.D. (1994) A combination of PLP and DM20 transgenes promotes partial myelination in the jimpy mouse. J. Neurochem. 63, 822-833.
    • (1994) J. Neurochem. , vol.63 , pp. 822-833
    • Nadon, N.L.1    Arnheiter, H.2    Hudson, L.D.3
  • 49
    • 0028226949 scopus 로고
    • Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport
    • Gow, A., Friedrich, V.L., Jr. and Lazzarini, R.A. (1994). Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport. J. Neurosci. Res. 37, 574-583.
    • (1994) J. Neurosci. Res. , vol.37 , pp. 574-583
    • Gow, A.1    Friedrich Jr., V.L.2    Lazzarini, R.A.3
  • 51
    • 0029146122 scopus 로고
    • Glial transplants: An in vivo analysis of extrinsic and intrinsic determinants of dysmyelination in genetic variants
    • Lachapelle, F. (1995). Glial transplants: An in vivo analysis of extrinsic and intrinsic determinants of dysmyelination in genetic variants. Brain Pathol. 5, 289-299.
    • (1995) Brain Pathol. , vol.5 , pp. 289-299
    • Lachapelle, F.1
  • 52
    • 0028963118 scopus 로고
    • Expression of the proteolipid protein gene in glial cells of the post natal peripheral nervous system of rodents
    • Griffiths, I.R., Dickinson, P. and Montague, P. (1995). Expression of the proteolipid protein gene in glial cells of the post natal peripheral nervous system of rodents. Neuropath. Appl. Neurobiol. 21, 97-110.
    • (1995) Neuropath. Appl. Neurobiol. , vol.21 , pp. 97-110
    • Griffiths, I.R.1    Dickinson, P.2    Montague, P.3
  • 54
    • 0029944722 scopus 로고    scopus 로고
    • The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins
    • Ebersole, T.A., Chen, Q., Justice, M.J. and Artzt, K. (1996). The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins. Nature Genet. 12, 260-265.
    • (1996) Nature Genet. , vol.12 , pp. 260-265
    • Ebersole, T.A.1    Chen, Q.2    Justice, M.J.3    Artzt, K.4
  • 55
    • 0027984497 scopus 로고
    • Krox-20 controls myelination in the peripheral nervous system
    • Topilko, P. et al. (1994). Krox-20 controls myelination in the peripheral nervous system. Nature 371, 796-799.
    • (1994) Nature , vol.371 , pp. 796-799
    • Topilko, P.1
  • 56
    • 0029149372 scopus 로고
    • Premature Schwann cell differentiation and hypermyelination in mice expressing a targeted antagonist of the POU transcription factor SCIP
    • Weinstein, D.E., Burrola, P.G. and Lemke, G. (1995). Premature Schwann cell differentiation and hypermyelination in mice expressing a targeted antagonist of the POU transcription factor SCIP. Mol. Cell. Neurosci. 6, 212-229.
    • (1995) Mol. Cell. Neurosci. , vol.6 , pp. 212-229
    • Weinstein, D.E.1    Burrola, P.G.2    Lemke, G.3
  • 57
    • 0019484568 scopus 로고
    • Interactions between axons and their sheath cells
    • Bray, G.M., Rasminsky, M. and Aguayo, A.J. (1981). Interactions between axons and their sheath cells. Ann. Rev. Neurosci. 4, 127-162.
    • (1981) Ann. Rev. Neurosci. , vol.4 , pp. 127-162
    • Bray, G.M.1    Rasminsky, M.2    Aguayo, A.J.3
  • 58
    • 0018336468 scopus 로고
    • Axon-Schwann cell relationships in neuropathies of mutant mice
    • Aguayo, A.J., Bray, G.M. and Perkins, S.C. (1979). Axon-Schwann cell relationships in neuropathies of mutant mice. Ann. N. Y. Acad. Sci. 317, 512-531.
    • (1979) Ann. N. Y. Acad. Sci. , vol.317 , pp. 512-531
    • Aguayo, A.J.1    Bray, G.M.2    Perkins, S.C.3
  • 59
    • 0017593352 scopus 로고
    • Abnormal myelination in transplanted Trembler mouse Schwann cells
    • Aguayo, A.J., Attiwell, M., Trecarten, J., Perkins, S.C. and Bray, G.M. (1977). Abnormal myelination in transplanted Trembler mouse Schwann cells. Nature 265, 73-75.
    • (1977) Nature , vol.265 , pp. 73-75
    • Aguayo, A.J.1    Attiwell, M.2    Trecarten, J.3    Perkins, S.C.4    Bray, G.M.5
  • 60
    • 0026580004 scopus 로고
    • Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells
    • De Waegh, S.M., Lee, V.M.-Y. and Brady, S.T. (1992). Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells. Cell 68, 451-463.
    • (1992) Cell , vol.68 , pp. 451-463
    • De Waegh, S.M.1    Lee, V.M.-Y.2    Brady, S.T.3
  • 61
    • 0025949638 scopus 로고
    • Local control of axonal properties by Schwann cells: Neurofilaments and axonal transport in homologous and heterologous nerve grafts
    • De Waegh, S.M. and Brady, S.T. (1991). Local control of axonal properties by Schwann cells: Neurofilaments and axonal transport in homologous and heterologous nerve grafts. J. Neurosci. Res. 30, 201-212.
    • (1991) J. Neurosci. Res. , vol.30 , pp. 201-212
    • De Waegh, S.M.1    Brady, S.T.2
  • 62
    • 0028923245 scopus 로고
    • Crucial role for the myelin-associated glycoprotein in the maintenance of axon-myelin integrity
    • Fruttiger, M., Montag, D., Schachner, M. and Martini, R. (1995). Crucial role for the myelin-associated glycoprotein in the maintenance of axon-myelin integrity. Eur. J. Neurosci. 7, 511-515.
    • (1995) Eur. J. Neurosci. , vol.7 , pp. 511-515
    • Fruttiger, M.1    Montag, D.2    Schachner, M.3    Martini, R.4
  • 63
    • 0016822082 scopus 로고
    • Development of onion bulb neuropathy in the trembler mouse. Comparison with normal nerve maturation
    • Ayers, M.M. and Anderson, R.M. (1975). Development of onion bulb neuropathy in the trembler mouse. Comparison with normal nerve maturation. Ada Neuropath. (Berl.) 32, 43-59.
    • (1975) Ada Neuropath. (Berl.) , vol.32 , pp. 43-59
    • Ayers, M.M.1    Anderson, R.M.2
  • 64
    • 0028264534 scopus 로고
    • Over-expression of MBP and PLP messenger RNA in 8-day-old trembler brain
    • Bascles, L., Bonnet, J. and Garbay, B. (1994). Over-expression of MBP and PLP messenger RNA in 8-day-old trembler brain. Neuroreport 5, 1221-1223.
    • (1994) Neuroreport , vol.5 , pp. 1221-1223
    • Bascles, L.1    Bonnet, J.2    Garbay, B.3
  • 65
    • 0029075810 scopus 로고
    • Peripheral myelin protein-22 is expressed in rat and mouse brain and spinal cord motoneurons
    • Parmantier, E., Cabon, F., Braun, C., D'Urso, D., Müller, H.W. and Zalc, B. (1995). Peripheral myelin protein-22 is expressed in rat and mouse brain and spinal cord motoneurons. Eur. J. Neurosci. 7, 1080-1088.
    • (1995) Eur. J. Neurosci. , vol.7 , pp. 1080-1088
    • Parmantier, E.1    Cabon, F.2    Braun, C.3    D'Urso, D.4    Müller, H.W.5    Zalc, B.6
  • 66
    • 0028848475 scopus 로고
    • Oligodendrocyte survival and function in the long-lived strain of the myelin deficient rat
    • Duncan, I.D., Nadon, N.L., Hoffman, R.L., Lunn, K.F., Csiza, C. and Wells, M.R. (1995). Oligodendrocyte survival and function in the long-lived strain of the myelin deficient rat. J. Neurocytol. 24, 745-762.
    • (1995) J. Neurocytol. , vol.24 , pp. 745-762
    • Duncan, I.D.1    Nadon, N.L.2    Hoffman, R.L.3    Lunn, K.F.4    Csiza, C.5    Wells, M.R.6
  • 67
  • 70
    • 0015499783 scopus 로고
    • Progressive ataxia of Charolais cattle associated with a myelin disorder
    • Palmer, A.C., Blakemore, W.F., Barlow, R.M., Fraser, J.A. and Ogden, A.L. (1972). Progressive ataxia of Charolais cattle associated with a myelin disorder. Vet. Rec. 91, 592-594.
    • (1972) Vet. Rec. , vol.91 , pp. 592-594
    • Palmer, A.C.1    Blakemore, W.F.2    Barlow, R.M.3    Fraser, J.A.4    Ogden, A.L.5
  • 71
    • 0016316603 scopus 로고
    • Progressive ataxia of Charolais cattle associated with disordered myelin
    • Blakemore, W.F., Palmer, A.C. and Barlow, R.M. (1974). Progressive ataxia of Charolais cattle associated with disordered myelin. Acta Neuropath. (Berl.) 29, 127-139.
    • (1974) Acta Neuropath. (Berl.) , vol.29 , pp. 127-139
    • Blakemore, W.F.1    Palmer, A.C.2    Barlow, R.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.