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Volumn 883, Issue , 1999, Pages

Introduction to the third international symposium on Charcot-Marie-Tooth disorders

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN PROTEIN; PMP22 PROTEIN, HUMAN;

EID: 0033554312     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1999.tb08559.x     Document Type: Conference Paper
Times cited : (5)

References (52)
  • 2
    • 0001046663 scopus 로고
    • Heriditary and sensory neuropathies
    • P.J. Dyck, P.K. Thomas, J.W. Griffin, P.A. Low & J.F. Poduslo, Eds.: WB Saunders. Philadelphia/London/Toronto/Montreal
    • DYCK, P.J., P. CHANCE R. LEBO & J.A. CARNEY. 1993. Heriditary and sensory neuropathies. In Peripheral Neuropathy. P.J. Dyck, P.K. Thomas, J.W. Griffin, P.A. Low & J.F. Poduslo, Eds.: 1094-1127. WB Saunders. Philadelphia/London/Toronto/Montreal.
    • (1993) Peripheral Neuropathy , pp. 1094-1127
    • Dyck, P.J.1    Chance, P.2    Lebo, R.3    Carney, J.A.4
  • 3
    • 0002896804 scopus 로고
    • Sur une forme particulaire d'atrophie musculaire progressive souvent familial debutant par les pieds et les jambes et atteingnant plus tard les mains
    • CHARCOT, J.M. & P. MARIE. 1886. Sur une forme particulaire d'atrophie musculaire progressive souvent familial debutant par les pieds et les jambes et atteingnant plus tard les mains. Rev. Med. 6: 97-138.
    • (1886) Rev. Med. , vol.6 , pp. 97-138
    • Charcot, J.M.1    Marie, P.2
  • 4
    • 0039900877 scopus 로고
    • Transplantation of nerve from patients with Charcot-Marie-Tooth (CMT) disease into immune-suppressed mice
    • AGUAYO, A.J., S. PERKINS, G. BRAY & I. DUNCAN. 1978. Transplantation of nerve from patients with Charcot-Marie-Tooth (CMT) disease into immune-suppressed mice. J. Neuropathol. Exp. Neurol. 37: 582.
    • (1978) J. Neuropathol. Exp. Neurol. , vol.37 , pp. 582
    • Aguayo, A.J.1    Perkins, S.2    Bray, G.3    Duncan, I.4
  • 6
    • 0026410609 scopus 로고
    • The duplication in Charcot-Marie-Tooth disease type 1A spans at least 1100 kb on chromosome 17p11.2
    • HOOGENDIJK, J.E., G.W. HENSELS, I. ZORN, L. VALENTIJN, et al. 1991. The duplication in Charcot-Marie-Tooth disease type 1A spans at least 1100 kb on chromosome 17p11.2. Hum. Genet. 88: 215-218.
    • (1991) Hum. Genet. , vol.88 , pp. 215-218
    • Hoogendijk, J.E.1    Hensels, G.W.2    Zorn, I.3    Valentijn, L.4
  • 7
    • 0025997898 scopus 로고
    • Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
    • The HMSN Collaborative Research Group
    • RAEYMAEKERS, P., V. TIMMERMAN, E. NELIS, J.P. DE, et al. 1991. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group. Neuromusc. Disord. 1: 93-97.
    • (1991) Neuromusc. Disord. , vol.1 , pp. 93-97
    • Raeymaekers, P.1    Timmerman, V.2    Nelis, E.3    De, J.P.4
  • 8
    • 0026879614 scopus 로고
    • The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A
    • PATEL, P.I., B.B. ROA, A.A. WELCHER, S.R. SCHOENER, et al. 1992. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. Nat. Genet. 1: 159-165.
    • (1992) Nat. Genet. , vol.1 , pp. 159-165
    • Patel, P.I.1    Roa, B.B.2    Welcher, A.A.3    Schoener, S.R.4
  • 9
    • 0026879838 scopus 로고
    • Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A
    • MATSUNAMI, N., B. SMITH, L. BALLARD, M.W. LENSCH, et al. 1992. Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A. Nat. Genet. 1: 176-179.
    • (1992) Nat. Genet. , vol.1 , pp. 176-179
    • Matsunami, N.1    Smith, B.2    Ballard, L.3    Lensch, M.W.4
  • 10
    • 0026879615 scopus 로고
    • The peripheral myelin protein gene PMP22 is contained within the Charcot-Marie-Tooth disease type 1A duplication
    • published erratum appears in Nat. Genet. 1992 Sept. 2(1): 84
    • TIMMERMAN, V., E. NELIS, H.W. VAN, B.W. NIEUWENHUIJSEN, et al. 1992. The peripheral myelin protein gene PMP22 is contained within the Charcot-Marie-Tooth disease type 1A duplication [published erratum appears in Nat. Genet. 1992 Sept. 2(1): 84]. Nat. Genet. 1: 171-175.
    • (1992) Nat. Genet. , vol.1 , pp. 171-175
    • Timmerman, V.1    Nelis, E.2    Van, H.W.3    Nieuwenhuijsen, B.W.4
  • 11
    • 0026879648 scopus 로고
    • The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A
    • VALENTIJN, L.J., P.A. BOLHUIS, I. ZORN, J.E. HOOGENDIJK, et al. 1992. The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A. Nat. Genet. 1: 166-170.
    • (1992) Nat. Genet. , vol.1 , pp. 166-170
    • Valentijn, L.J.1    Bolhuis, P.A.2    Zorn, I.3    Hoogendijk, J.E.4
  • 12
    • 0026605507 scopus 로고
    • Trembler mouse carries a point mutation in a myelin gene
    • SUTER, U., A.A. WELCHER, T. OZCELIK, G.J. SNIPES, 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    Welcher, A.A.2    Ozcelik, T.3    Snipes, G.J.4
  • 13
    • 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., J.J. MOSKOW, A.A. WELCHER, G.J. SNIPES, et al. 1992. 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 89: 4382-4386.
    • (1992) Proc. Natl. Acad. Sci. USA , vol.89 , pp. 4382-4386
    • Suter, U.1    Moskow, J.J.2    Welcher, A.A.3    Snipes, G.J.4
  • 14
    • 0027031611 scopus 로고
    • Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A
    • VALENTIJN, L.J., F. BAAS, R.A. WOLTERMAN, J.E. HOOGENDIJK, et al. 1992. Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A. Nat. Genet. 2: 288-291.
    • (1992) Nat. Genet. , vol.2 , pp. 288-291
    • Valentijn, L.J.1    Baas, F.2    Wolterman, R.A.3    Hoogendijk, J.E.4
  • 15
    • 0027509953 scopus 로고
    • DNA deletion associated with hereditary neuropathy with liability to pressure palsies
    • CHANCE, P.F., M.K. ALDERSON, K.A. LEPPIG, M.W. LENSCH, et al. 1993. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell 72: 143-151.
    • (1993) Cell , vol.72 , pp. 143-151
    • Chance, P.F.1    Alderson, M.K.2    Leppig, K.A.3    Lensch, M.W.4
  • 17
    • 0031943222 scopus 로고    scopus 로고
    • Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathics
    • WARNER, L.E., P. MANCIAS, I.J. BUTLER, C.M. MCDONALD, et al. 1998. Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathics. Nat. Genet. 18: 382-384.
    • (1998) Nat. Genet. , vol.18 , pp. 382-384
    • Warner, L.E.1    Mancias, P.2    Butler, I.J.3    McDonald, C.M.4
  • 18
    • 0027772413 scopus 로고
    • Connexin mutations in X-linked Charcot-Marie-Tooth disease
    • BERGOFFEN, J., S.S. SCHERER, S. WANG, M. ORONZI-SCOTT, et al. 1993. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science 262: 3039-2042.
    • (1993) Science , vol.262 , pp. 3039-12042
    • Bergoffen, J.1    Scherer, S.S.2    Wang, S.3    Oronzi-Scott, M.4
  • 19
    • 0029894937 scopus 로고    scopus 로고
    • Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and xq13
    • TIMMERMAN, V., P. DEJONGHE, P. SPOELDERS, S. SIMOKOVIC, et al. 1996. Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and xq13. Neurology 46: 1311-1318.
    • (1996) Neurology , vol.46 , pp. 1311-1318
    • Timmerman, V.1    Dejonghe, P.2    Spoelders, P.3    Simokovic, S.4
  • 20
    • 0023864835 scopus 로고
    • Axons regulate Schwann cell expression of the major myelin and NGF receptor genes
    • LEMKE, G. & M. CHAO. 1988, Axons regulate Schwann cell expression of the major myelin and NGF receptor genes. Development 102: 499-504.
    • (1988) Development , vol.102 , pp. 499-504
    • Lemke, G.1    Chao, M.2
  • 21
    • 0028221758 scopus 로고
    • Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A
    • YOSHIKAWA, H., T. NISHIMURA, Y. NAKATSUJI, H. FUJIMURA, et al. 1994. Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A. Ann. Neurol. 35: 445-450.
    • (1994) Ann. Neurol. , vol.35 , pp. 445-450
    • Yoshikawa, H.1    Nishimura, T.2    Nakatsuji, Y.3    Fujimura, H.4
  • 22
    • 0028230766 scopus 로고
    • Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1A sural nerve biopsies
    • HANEMANN, C.O., G. STOLL, D. DURSO, W. FRICKE, et al. 1994. Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1A sural nerve biopsies. J. Neurosci. Res. 37: 654-659.
    • (1994) J. Neurosci. Res. , vol.37 , pp. 654-659
    • Hanemann, C.O.1    Stoll, G.2    Durso, D.3    Fricke, W.4
  • 23
    • 0029931697 scopus 로고    scopus 로고
    • Ultrastructural PMP22 expression in inherited demyelinating neuropathies
    • VALLAT, J.M., P. SINDOU, P.M. PREUX, F. TABARAUD, et al. 1996. Ultrastructural PMP22 expression in inherited demyelinating neuropathies. Ann. Neurol. 39; 813-817.
    • (1996) Ann. Neurol. , vol.39 , pp. 813-817
    • Vallat, J.M.1    Sindou, P.2    Preux, P.M.3    Tabaraud, F.4
  • 24
    • 0028325902 scopus 로고
    • Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage
    • READHEAD, C., A. SCHNEIDER, I. GRIFFITHS & K. A. NAVE. 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.3    Nave, K.A.4
  • 25
    • 0028133486 scopus 로고
    • Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene
    • KAGAWA, T., K. IKENAKA, Y. INOUE, S. KURIYAMA, 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    Ikenaka, K.2    Inoue, Y.3    Kuriyama, S.4
  • 26
    • 15844393894 scopus 로고    scopus 로고
    • A transgeneic rat model of Charcot-Marie-Tooth disease
    • SEREDA, M., I. GRIFFITHS, A. PUHLHOFER, et al. 1996. A transgeneic rat model of Charcot-Marie-Tooth disease. Neuron 16: 1049-1060.
    • (1996) Neuron , vol.16 , pp. 1049-1060
    • Sereda, M.1    Griffiths, I.2    Puhlhofer, A.3
  • 27
    • 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., E. PASSAGE, A. MANSON, G. PUTZU, et al. 1996. Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA. Hum. Mol. Genet. 5: 563-569.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 563-569
    • Huxley, C.1    Passage, E.2    Manson, A.3    Putzu, G.4
  • 28
    • 16044362374 scopus 로고    scopus 로고
    • Clinical phenotypes of different MPZ (P-0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination
    • WARNER, L.E., M.J. HILZ, S.H. APPEL, J.M. KILLIAN, et al. 1996. Clinical phenotypes of different MPZ (P-0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination. Neuron 17: 451-460.
    • (1996) Neuron , vol.17 , pp. 451-460
    • Warner, L.E.1    Hilz, M.J.2    Appel, S.H.3    Killian, J.M.4
  • 30
    • 0028902548 scopus 로고
    • Biology and genetics of hereditary motor and sensory neuropathies
    • SUTER, U. & J. SNIPES. 1995. Biology and genetics of hereditary motor and sensory neuropathies. Annu. Rev. Neurosci. 18: 45-75.
    • (1995) Annu. Rev. Neurosci. , vol.18 , pp. 45-75
    • Suter, U.1    Snipes, J.2
  • 31
    • 0030246987 scopus 로고    scopus 로고
    • Crystal structure of the extracellular domain from P-0, the major structural protein of peripheral nerve myelin
    • SHAPIRO, L., J.P. DOYLE, P. HENSLEY, D.R. COLMAN, et al. 1996. Crystal structure of the extracellular domain from P-0, the major structural protein of peripheral nerve myelin. Neuron 17: 435-449.
    • (1996) Neuron , vol.17 , pp. 435-449
    • Shapiro, L.1    Doyle, J.P.2    Hensley, P.3    Colman, D.R.4
  • 32
    • 0030611992 scopus 로고    scopus 로고
    • 0 knockout mice develop a peripheral neruopathy that resembles chronic inflammatory demyelinating polyneuropthy (CIDP)
    • 0 knockout mice develop a peripheral neruopathy that resembles chronic inflammatory demyelinating polyneuropthy (CIDP). J. Neuropathol. Exp. Neurol. 56(7): 811-821.
    • (1997) J. Neuropathol. Exp. Neurol. , vol.56 , Issue.7 , pp. 811-821
    • Shy, M.E.1    Arroyo, E.2    Sladky, J.3    Menichella, D.4
  • 34
    • 0028824925 scopus 로고
    • 0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited hyman neuropathies
    • 0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited hyman neuropathies. Nat. Genet. 11: 281-285.
    • (1995) Nat. Genet. , vol.11 , pp. 281-285
    • Martini, R.1    Zielasek, J.2    Toyka, K.3    Giese, K.4
  • 35
    • 0029784279 scopus 로고    scopus 로고
    • Molecular specializations at nodes and paranodes in peripheral nerve
    • SCHERER, S.S. 1996. Molecular specializations at nodes and paranodes in peripheral nerve. Microsc. Res. Tech. 34: 452-461.
    • (1996) Microsc. Res. Tech. , vol.34 , pp. 452-461
    • Scherer, S.S.1
  • 36
    • 0024554331 scopus 로고
    • The application of nerve conduction and clinical studies to genetic counseliling in hereditary and sensory neuropathy type I
    • BERCIANO, J., O. COMBARROS, J. CALLEJA, J.M. POLO, et al. 1989. The application of nerve conduction and clinical studies to genetic counseliling in hereditary and sensory neuropathy type I. Muscle Nerve 12: 302-306.
    • (1989) Muscle Nerve , vol.12 , pp. 302-306
    • Berciano, J.1    Combarros, O.2    Calleja, J.3    Polo, J.M.4
  • 37
    • 0021061363 scopus 로고
    • Peroneal muscular atrophy. Part 1, Clinical and electrophysiological study
    • BOUCHE, P., R. GHERARDI, H.P. CATHALA, J. LHERMITE, et al. 1983. Peroneal muscular atrophy. Part 1, Clinical and electrophysiological study. J. Neurol. Sci. 61: 389-399.
    • (1983) J. Neurol. Sci. , vol.61 , pp. 389-399
    • Bouche, P.1    Gherardi, R.2    Cathala, H.P.3    Lhermite, J.4
  • 38
    • 0023113382 scopus 로고
    • Prevalence of hereditary motor and sensory neuropathy in Cantabria
    • COMBARROS, O., J. CALLEJA & J.M. POLO. 1989. Prevalence of hereditary motor and sensory neuropathy in Cantabria. Acta Neurol. Scand. 75: 9-12.
    • (1989) Acta Neurol. Scand. , vol.75 , pp. 9-12
    • Combarros, O.1    Calleja, J.2    Polo, J.M.3
  • 39
    • 0018222952 scopus 로고
    • The peroneal muscular atrophy syndrome. Clinical, genetic, electrophysiological and nerve biopsy studies I. Clinical, genetic and electrophysiological findings and classification
    • DAVIS, C.J.F., W.G. BRADLEY & R. MADRID. 1978. The peroneal muscular atrophy syndrome. Clinical, genetic, electrophysiological and nerve biopsy studies I. Clinical, genetic and electrophysiological findings and classification. J. Genet, Hum. 26: 311-349.
    • (1978) J. Genet, Hum. , vol.26 , pp. 311-349
    • Davis, C.J.F.1    Bradley, W.G.2    Madrid, R.3
  • 40
    • 0014301249 scopus 로고
    • Lower motor and primary sensory neuron diseases with peroneal muscular atrophy I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies
    • DYCK, P.J. & E.H. LAMBERT. 1968. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. Arch. Neurol. 18: 603-618.
    • (1968) Arch. Neurol. , vol.18 , pp. 603-618
    • Dyck, P.J.1    Lambert, E.H.2
  • 41
    • 0001195801 scopus 로고
    • Inherited neuronal degeneration and atrophy affecting peripheral motor, sensory, and autonomic neurons
    • P.J. Dyck, P.K. Thomas, E.H. Lambert & R.E. Bunge, Eds.: W.B. Saunders. Philadelphia
    • DYCK, P.J. 1984. Inherited neuronal degeneration and atrophy affecting peripheral motor, sensory, and autonomic neurons. In Peripheral Neuropathy. P.J. Dyck, P.K. Thomas, E.H. Lambert & R.E. Bunge, Eds.: 1600-1642. W.B. Saunders. Philadelphia.
    • (1984) Peripheral Neuropathy , pp. 1600-1642
    • Dyck, P.J.1
  • 42
    • 0018942439 scopus 로고
    • The clinical features of hereditary motor and sensory neuropathy types I and II
    • HARDING, A.E. & P.K. THOMAS. 1980. The clinical features of hereditary motor and sensory neuropathy types I and II. Brain 103: 259-280.
    • (1980) Brain , vol.103 , pp. 259-280
    • Harding, A.E.1    Thomas, P.K.2
  • 43
    • 0020078781 scopus 로고
    • The electrodiagnostic distinctions between chronic familial and acquired demyelinating neuropathies
    • LEWIS, R.A. & A.J. SUMNER. 1982. The electrodiagnostic distinctions between chronic familial and acquired demyelinating neuropathies. Neurology 32: 592-596.
    • (1982) Neurology , vol.32 , pp. 592-596
    • Lewis, R.A.1    Sumner, A.J.2
  • 44
    • 0027753971 scopus 로고
    • Uniform slowing of conduction velocities in Charcot-Marie-Tooth disease polyneuropathy type 1
    • KAKU, D.A., G.J. PARRY, R. MALAMUT, J.R. LUPSKI, et al. 1993. Uniform slowing of conduction velocities in Charcot-Marie-Tooth disease polyneuropathy type 1. Neurology 434: 2664-2667.
    • (1993) Neurology , vol.434 , pp. 2664-2667
    • Kaku, D.A.1    Parry, G.J.2    Malamut, R.3    Lupski, J.R.4
  • 46
    • 0029120917 scopus 로고
    • An adenoviral vector can transfer lacZ expression into Schwann cells in culture and in sciatic nerve
    • SHY, M.E., M. TANI, Y.J. SHI, S.A. WHYATT, et al. 1995. An adenoviral vector can transfer lacZ expression into Schwann cells in culture and in sciatic nerve. Ann. Neurol. 38: 429-436.
    • (1995) Ann. Neurol. , vol.38 , pp. 429-436
    • Shy, M.E.1    Tani, M.2    Shi, Y.J.3    Whyatt, S.A.4
  • 47
    • 0029741231 scopus 로고    scopus 로고
    • Transient immunosuppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice
    • LOCHMULLER, H., B.J. PETROF, G. PARI, N. LAROCHELLE, et al. 1996. Transient immunosuppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice. Gene. Ther. 3: 706-716.
    • (1996) Gene. Ther. , vol.3 , pp. 706-716
    • Lochmuller, H.1    Petrof, B.J.2    Pari, G.3    Larochelle, N.4
  • 48
    • 0028898039 scopus 로고
    • Adenovirus-mediated gene transfer into striated muscles
    • ACSADI, G., B. MASSIE & A. JANI. 1995. Adenovirus-mediated gene transfer into striated muscles. J. Mol. Med. 73: 165-180.
    • (1995) J. Mol. Med. , vol.73 , pp. 165-180
    • Acsadi, G.1    Massie, B.2    Jani, A.3
  • 49
    • 0008587777 scopus 로고    scopus 로고
    • Prevention of motoneuron death by adenovirus-mediated neurotiophic factors
    • GIMENEZ Y RIBOITA, M., F. REVAH, L. PRADIER, I. LOQUET, et al. 1997, Prevention of motoneuron death by adenovirus-mediated neurotiophic factors. J. Neurosci. Res. 48: 281-285.
    • (1997) J. Neurosci. Res. , vol.48 , pp. 281-285
    • Gimenez Y Riboita, M.1    Revah, F.2    Pradier, L.3    Loquet, I.4
  • 50
    • 0030953519 scopus 로고    scopus 로고
    • Gene therapy of murine motor neuron disease using adenoviral vectors for neurotrophic factors
    • HAASE, G., P. KENNEL, B. PETTMAN, E. VIGNE, et al. 1997. Gene therapy of murine motor neuron disease using adenoviral vectors for neurotrophic factors. Nat. Med. 3: 429-436.
    • (1997) Nat. Med. , vol.3 , pp. 429-436
    • Haase, G.1    Kennel, P.2    Pettman, B.3    Vigne, E.4
  • 51
    • 0028866451 scopus 로고
    • Gene transfer through the blood-nerve barrier: NGF-engineered neuritogenic T lymphocytes attenuate experimental autoimmune neuritis
    • KRAMER, R., Y. ZHANG, J. GEHRMANN, R. GOLD, et al. 1995. Gene transfer through the blood-nerve barrier: NGF-engineered neuritogenic T lymphocytes attenuate experimental autoimmune neuritis, Nat. Med. 11: 1162-1166.
    • (1995) Nat. Med. , vol.11 , pp. 1162-1166
    • Kramer, R.1    Zhang, Y.2    Gehrmann, J.3    Gold, R.4
  • 52
    • 0028898039 scopus 로고
    • Adenovirus-mediated gene transfer into striated muscles
    • ACSADI, G., B. MASSIE & A. JANI. 1995. Adenovirus-mediated gene transfer into striated muscles. J. Mol. Med. 73: 165-180.
    • (1995) J. Mol. Med. , vol.73 , pp. 165-180
    • Acsadi, G.1    Massie, B.2    Jani, A.3


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