메뉴 건너뛰기




Volumn 24, Issue 2, 1998, Pages 87-90

Myelin disorders

Author keywords

[No Author keywords available]

Indexed keywords

MUTANT PROTEIN; MYELIN;

EID: 0031900475     PISSN: 03051846     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2990.1998.00033.x     Document Type: Conference Paper
Times cited : (3)

References (30)
  • 1
    • 0028784820 scopus 로고
    • Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
    • Adlkofer K, Martini R, Aguzzi A, Zielasek J, Toyka KV, Suter U. Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice. Nat Genet 1995; 11: 274-80
    • (1995) Nat Genet , vol.11 , pp. 274-280
    • Adlkofer, K.1    Martini, R.2    Aguzzi, A.3    Zielasek, J.4    Toyka, K.V.5    Suter, U.6
  • 2
    • 0027772413 scopus 로고
    • Connexin mutations in X-linked Charcot-Marie-Tooth disease
    • Bergoffen J, Scherer SS, Wang S et al. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science 1993; 262: 2039-42
    • (1993) Science , vol.262 , pp. 2039-2042
    • Bergoffen, J.1    Scherer, S.S.2    Wang, S.3
  • 3
    • 0027986675 scopus 로고
    • Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice
    • Boison D, Stoffel W. Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice. Proc Natl Acad Sci USA 1994; 91: 11709-13
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 11709-11713
    • Boison, D.1    Stoffel, W.2
  • 4
    • 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, Zoidl G, Wilms S, Gillen CP, Kuhn HG, Muller HW. Differential expression of two mRNA species indicates a dual function of peripheral myelin protein PMP22 in cell growth and myelination. J Neurosci Res 1994; 37: 529-37
    • (1994) J Neurosci Res , vol.37 , pp. 529-537
    • Bosse, F.1    Zoidl, G.2    Wilms, S.3    Gillen, C.P.4    Kuhn, H.G.5    Muller, H.W.6
  • 5
    • 0028240173 scopus 로고
    • Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease
    • Ellis D, Malcolm S. Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease. Nature Genet 1994; 6: 333-4
    • (1994) Nature Genet , vol.6 , pp. 333-334
    • Ellis, D.1    Malcolm, S.2
  • 6
    • 0029159803 scopus 로고
    • Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: Its relation to the demyelinating peripheral neuropathy CMT1A
    • Fabbreti E, Edomi P, Brancolini C, Schneider C. Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: its relation to the demyelinating peripheral neuropathy CMT1A. Genes Dev 1995; 9: 1846-56
    • (1995) Genes Dev , vol.9 , pp. 1846-1856
    • Fabbreti, E.1    Edomi, P.2    Brancolini, C.3    Schneider, C.4
  • 7
    • 0030036917 scopus 로고    scopus 로고
    • A cellular mechanism governing the severity of Peliaeus-Merzbacher disease
    • Gow A, Lazzarini RA. A cellular mechanism governing the severity of Peliaeus-Merzbacher disease. Nature Genet 1996; 13: 422-8
    • (1996) Nature Genet , vol.13 , pp. 422-428
    • Gow, A.1    Lazzarini, R.A.2
  • 8
    • 0028112375 scopus 로고
    • Mammalian artificial chromosomes: A new tool for gene therapy
    • Huxley C. Mammalian artificial chromosomes: a new tool for gene therapy. Generapy 1994; 1: 7-12
    • (1994) Generapy , vol.1 , pp. 7-12
    • Huxley, C.1
  • 9
    • 0029877942 scopus 로고    scopus 로고
    • Construction of a mouse model of Charcot-Marie-Tooth disease type 1a by pronuclear injection of human YAC DNA
    • Huxley C, Passage E, Manson A et al. Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA. Hum Mol Genet 1996; 5: 563-9
    • (1996) Hum Mol Genet , vol.5 , pp. 563-569
    • Huxley, C.1    Passage, E.2    Manson, A.3
  • 10
    • 0028788494 scopus 로고
    • Dejerine-Sottas disease with de novo dominant point mutation of PMP22 gene
    • Ionasescu VV, Ionasescu R, Searby C, Neahring R. Dejerine-Sottas disease with de novo dominant point mutation of PMP22 gene. Neurology 1995; 45: 1766-7
    • (1995) Neurology , vol.45 , pp. 1766-1767
    • Ionasescu, V.V.1    Ionasescu, R.2    Searby, C.3    Neahring, R.4
  • 11
    • 0028133486 scopus 로고
    • Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene
    • Kagawa T, Ikenaka K, Inoue Y et al. Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene. Neuron 1994; 13: 427-42
    • (1994) Neuron , vol.13 , pp. 427-442
    • Kagawa, T.1    Ikenaka, K.2    Inoue, Y.3
  • 12
    • 0028276189 scopus 로고
    • Myelination in the absence of myelin-associated glycoprotein
    • Li C, Tropak MB, Gerlai R et al. Myelination in the absence of myelin-associated glycoprotein. Nature 1994; 369: 747-50
    • (1994) Nature , vol.369 , pp. 747-750
    • Li, C.1    Tropak, M.B.2    Gerlai, R.3
  • 13
    • 0029843863 scopus 로고    scopus 로고
    • Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage
    • Magyar JP, Martini R, Ruelicke T et al. Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage. J Neurosci 1996; 16: 5351-60
    • (1996) J Neurosci , vol.16 , pp. 5351-5360
    • Magyar, J.P.1    Martini, R.2    Ruelicke, T.3
  • 14
    • 0028824925 scopus 로고
    • Protein zero (Po) -deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies
    • Martini R, Zielasek J, Toyka KV, Giese KP, Schachne M. Protein zero (Po) -deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies. Nature Genet 1995; 11: 281-6
    • (1995) Nature Genet , vol.11 , pp. 281-286
    • Martini, R.1    Zielasek, J.2    Toyka, K.V.3    Giese, K.P.4    Schachne, M.5
  • 15
    • 0027958869 scopus 로고
    • Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin
    • Montag D, Giese KP, Bartsch U et al. Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin. Neuron 1994; 13: 229-46
    • (1994) Neuron , vol.13 , pp. 229-246
    • Montag, D.1    Giese, K.P.2    Bartsch, U.3
  • 16
    • 0343687249 scopus 로고    scopus 로고
    • Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice
    • Nelles E, Butzler C, Jung D et al. Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice. Proc Natl Acad Sci USA 1996; 93: 9565-70
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 9565-9570
    • Nelles, E.1    Butzler, C.2    Jung, D.3
  • 17
    • 0028339044 scopus 로고
    • A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies
    • Nicholson GA, Valentijn LJ, Cherryson AK et al. A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies. Nature Genet 1994; 6: 263-6
    • (1994) Nature Genet , vol.6 , pp. 263-266
    • Nicholson, G.A.1    Valentijn, L.J.2    Cherryson, A.K.3
  • 18
    • 0028231331 scopus 로고
    • Charcot-Marie-Tooth disease: A new paradigm for the mechanism of inherited disease
    • Patel PI, Lupski JR. Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease. Trends in Genet 1994; 10: 128-33
    • (1994) Trends in Genet , vol.10 , pp. 128-133
    • Patel, P.I.1    Lupski, J.R.2
  • 19
    • 0028325902 scopus 로고
    • Premature arrest of myelin formation in transgenic mice with increased proteolipid gene dosage
    • Readhead C, Schneider A, Griffiths I, Nave K-A. Premature arrest of myelin formation in transgenic mice with increased proteolipid gene dosage. Neuron 1994; 12: 583-95
    • (1994) Neuron , vol.12 , pp. 583-595
    • Readhead, C.1    Schneider, A.2    Griffiths, I.3    Nave, K.-A.4
  • 20
    • 0027486810 scopus 로고
    • Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene
    • Roa BB, Dyck PJ, Marks HG, Chance PF, Lupski JR. Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene. Nature Genet 1993; 5: 269-73
    • (1993) Nature Genet , vol.5 , pp. 269-273
    • Roa, B.B.1    Dyck, P.J.2    Marks, H.G.3    Chance, P.F.4    Lupski, J.R.5
  • 21
    • 0027314668 scopus 로고
    • Charcot-Marie-Tooth disease type 1a association with a spontaneous point mutation in the PMP22 gene
    • Roa BB, Garcia CA, Suter U et al. Charcot-Marie-Tooth disease type 1A association with a spontaneous point mutation in the PMP22 gene. New Eng J Med 1993; 329: 96-101
    • (1993) New Eng J Med , vol.329 , pp. 96-101
    • Roa, B.B.1    Garcia, C.A.2    Suter, U.3
  • 22
    • 0029079396 scopus 로고
    • Dominant-negative action of the jimpy mutation in mice complemented with an autosomal transgene for myelin proteolipid protein
    • Schneider A, Griffiths IR, Readhead C, Nave K-A. Dominant-negative action of the jimpy mutation in mice complemented with an autosomal transgene for myelin proteolipid protein. Proc Natl Acad Sci USA 1995; 92: 4447-51
    • (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
  • 23
    • 15844393894 scopus 로고    scopus 로고
    • A transgenic rat model of Charcot-Marie-Tooth Disease
    • Sereda M, Griffiths I, Pühlhofer A et al. A transgenic rat model of Charcot-Marie-Tooth Disease. Neuron 1996; 16: 1049-60
    • (1996) Neuron , vol.16 , pp. 1049-1060
    • Sereda, M.1    Griffiths, I.2    Pühlhofer, A.3
  • 24
    • 0029014126 scopus 로고
    • Molecular anatomy and genetics of myelin proteins in the peripheral nervous system
    • Snipes GJ, Suter U. Molecular anatomy and genetics of myelin proteins in the peripheral nervous system. J Anat 1995; 186: 483-94
    • (1995) J Anat , vol.186 , pp. 483-494
    • Snipes, G.J.1    Suter, U.2
  • 25
    • 0026554289 scopus 로고
    • A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse
    • Suter U, Moskow JJ, Welcher AA et al. A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse. Proc Natl Acad Sci USA 1992; 89: 4382-6
    • (1992) Proc Natl Acad Sci USA , vol.89 , pp. 4382-4386
    • Suter, U.1    Moskow, J.J.2    Welcher, A.A.3
  • 26
    • 0026605507 scopus 로고
    • Trembler mouse carries a point mutation in a myelin gene
    • Suter U, Welcher AA, Ozcelik T et al. Trembler mouse carries a point mutation in a myelin gene. Nature 1992; 356: 241-4
    • (1992) Nature , vol.356 , pp. 241-244
    • Suter, U.1    Welcher, A.A.2    Ozcelik, T.3
  • 27
    • 0027031611 scopus 로고
    • Identical point mutations of PMP-22 in trembler-J mouse and Charcot-Marie-Tooth disease type 1A
    • Valentijn LJ, Baas F, Wolterman RA et al. Identical point mutations of PMP-22 in trembler-J mouse and Charcot-Marie-Tooth disease type 1A. Nat Genet 1992; 2: 288-90
    • (1992) Nat Genet , vol.2 , pp. 288-290
    • Valentijn, L.J.1    Baas, F.2    Wolterman, R.A.3
  • 29
    • 16044362374 scopus 로고    scopus 로고
    • Clinical phenotypes of different MPZ (Po) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination
    • Warner LE, Hilz MJ, Appel SH et al. Clinical phenotypes of different MPZ (Po) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination. Neuron 1996; 17: 451-60
    • (1996) Neuron , vol.17 , pp. 451-460
    • Warner, L.E.1    Hilz, M.J.2    Appel, S.H.3
  • 30
    • 0028950408 scopus 로고
    • Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: Modulation of cell growth
    • Zoidl G, Blass-Kampmann S, D'Urso D, Schmalenbach C, Müller HW. Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: modulation of cell growth. EMBO J 1995; 14: 1122-8
    • (1995) EMBO J , vol.14 , pp. 1122-1128
    • Zoidl, G.1    Blass-Kampmann, S.2    D'Urso, D.3    Schmalenbach, C.4    Müller, H.W.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.