메뉴 건너뛰기




Volumn 72, Issue 4, 1999, Pages 1773-1776

Brain neurotransmitter deficits in mice transgenic for the Huntington's disease mutation

Author keywords

5 Hydroxytryptamine; Catecholamines; GABA; Huntington's disease; Neurodegeneration; Transgenic mice

Indexed keywords

4 AMINOBUTYRIC ACID; CATECHOLAMINE; NEUROTRANSMITTER; SEROTONIN;

EID: 0033066942     PISSN: 00223042     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1471-4159.1999.721773.x     Document Type: Article
Times cited : (82)

References (23)
  • 2
    • 0022548849 scopus 로고
    • Reduced high-affinity glutamate uptake sites in the brains of patients with Huntington's disease
    • Cross A. J., Slater P., and Reynolds G. P. (1986) Reduced high-affinity glutamate uptake sites in the brains of patients with Huntington's disease. Neurosci. Lett. 67, 198-202.
    • (1986) Neurosci. Lett. , vol.67 , pp. 198-202
    • Cross, A.J.1    Slater, P.2    Reynolds, G.P.3
  • 4
    • 0032501740 scopus 로고    scopus 로고
    • Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?
    • Davies S. W., Beardsall K., Turmaine M., DiFiglia M., Aronin N., and Bates G. P. (1998) Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions? Lancet 351, 131-133.
    • (1998) Lancet , vol.351 , pp. 131-133
    • Davies, S.W.1    Beardsall, K.2    Turmaine, M.3    DiFiglia, M.4    Aronin, N.5    Bates, G.P.6
  • 5
    • 0030752709 scopus 로고    scopus 로고
    • Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neuntes in brain
    • DiFiglia M., Sapp E., Chase K. O., Davies S. W., Bates G. P., Vonsattel J. P., and Aronin N. (1997) Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neuntes in brain. Science 277, 1990-1993.
    • (1997) Science , vol.277 , pp. 1990-1993
    • DiFiglia, M.1    Sapp, E.2    Chase, K.O.3    Davies, S.W.4    Bates, G.P.5    Vonsattel, J.P.6    Aronin, N.7
  • 6
    • 0025718650 scopus 로고
    • Excitatory amino acid binding sites in the caudate nucleus and frontal cortex of Huntington's disease
    • Dure L. S., Young A. B., and Penney J. B. (1991) Excitatory amino acid binding sites in the caudate nucleus and frontal cortex of Huntington's disease. Ann. Neurol. 30, 785-793.
    • (1991) Ann. Neurol. , vol.30 , pp. 785-793
    • Dure, L.S.1    Young, A.B.2    Penney, J.B.3
  • 8
    • 0021330769 scopus 로고
    • Glutamate: A neurotransmitter in mammalian brain
    • Fonnum F. (1984) Glutamate: a neurotransmitter in mammalian brain. J. Neurochem. 42, 1-11.
    • (1984) J. Neurochem. , vol.42 , pp. 1-11
    • Fonnum, F.1
  • 9
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
    • Huntington's Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72, 971-983.
    • (1993) Cell , vol.72 , pp. 971-983
  • 10
    • 0021139033 scopus 로고
    • Reduced Purkinje cell density in Huntington's disease
    • Jeste D. V., Barban L., and Parisi J. (1984) Reduced Purkinje cell density in Huntington's disease. Exp. Neurol. 85, 78-86.
    • (1984) Exp. Neurol. , vol.85 , pp. 78-86
    • Jeste, D.V.1    Barban, L.2    Parisi, J.3
  • 12
    • 0030897669 scopus 로고    scopus 로고
    • Striatal dopamine nerve terminal markers but not nigral cellularity are reduced in spinocerebellar ataxia type 1
    • Kish S. J., Guttman M., Robitaille Y., El-Awar M., Chang L.-J., and Levey A. I. (1997) Striatal dopamine nerve terminal markers but not nigral cellularity are reduced in spinocerebellar ataxia type 1. Neurology 48, 1109-1111.
    • (1997) Neurology , vol.48 , pp. 1109-1111
    • Kish, S.J.1    Guttman, M.2    Robitaille, Y.3    El-Awar, M.4    Chang, L.-J.5    Levey, A.I.6
  • 15
    • 0026094729 scopus 로고
    • Electrochemical detection of human brain transmitter amino acids by high-performance liquid chromatograpny of stable o-phthalaldehyde-sulphite derivatives
    • Pearson S., Czudek C., Mercer K., and Reynolds G. P. (1991) Electrochemical detection of human brain transmitter amino acids by high-performance liquid chromatograpny of stable o-phthalaldehyde-sulphite derivatives. J. Neural Transm. Gen. Sect. 86, 151-157.
    • (1991) J. Neural Transm. Gen. Sect. , vol.86 , pp. 151-157
    • Pearson, S.1    Czudek, C.2    Mercer, K.3    Reynolds, G.P.4
  • 16
    • 0015790444 scopus 로고
    • Huntington's chorea: Deficiency of gamma-aminobutyric acid in brain
    • Perry T. L., Hansen S., and Kloster M. (1973) Huntington's chorea: deficiency of gamma-aminobutyric acid in brain. N. Engl. J. Med. 288, 337-342.
    • (1973) N. Engl. J. Med. , vol.288 , pp. 337-342
    • Perry, T.L.1    Hansen, S.2    Kloster, M.3
  • 17
    • 0031802550 scopus 로고    scopus 로고
    • Transgenic models and subcellular pathology - Do they tell us what goes wrong in Huntington's disease?
    • Reynolds G. P. and Dalton C. F. (1998) Transgenic models and subcellular pathology - do they tell us what goes wrong in Huntington's disease? Mol. Psychiatry 3, 192-195.
    • (1998) Mol. Psychiatry , vol.3 , pp. 192-195
    • Reynolds, G.P.1    Dalton, C.F.2
  • 18
    • 0022568877 scopus 로고
    • Striatal dopamine and homovanillic acid in Huntington's disease
    • Reynolds G. P. and Garrett N. J. (1986) Striatal dopamine and homovanillic acid in Huntington's disease. J. Neural Transm. 65, 151-155.
    • (1986) J. Neural Transm. , vol.65 , pp. 151-155
    • Reynolds, G.P.1    Garrett, N.J.2
  • 19
    • 0023258197 scopus 로고
    • Decreased glutamic acid and increased 5-hydroxytryptamine in Huntington's disease brain
    • Reynolds G. P. and Pearson S. J. (1987) Decreased glutamic acid and increased 5-hydroxytryptamine in Huntington's disease brain. Neurosci. Lett. 78, 233-238.
    • (1987) Neurosci. Lett. , vol.78 , pp. 233-238
    • Reynolds, G.P.1    Pearson, S.J.2
  • 20
    • 0025033490 scopus 로고
    • Brain GABA levels in asymptomatic Huntington's disease
    • Reynolds G. P. and Pearson S. J. (1990) Brain GABA levels in asymptomatic Huntington's disease. N. Engl. J. Med. 323, 682.
    • (1990) N. Engl. J. Med. , vol.323 , pp. 682
    • Reynolds, G.P.1    Pearson, S.J.2
  • 21
    • 0028170323 scopus 로고
    • 3H]L-689,560 binding to the glycine site of the glutamate/NMDA receptor in the brain in Huntington's disease
    • 3H]L-689,560 binding to the glycine site of the glutamate/NMDA receptor in the brain in Huntington's disease. J. Neurol. Sci. 125, 46-49.
    • (1994) J. Neurol. Sci. , vol.125 , pp. 46-49
    • Reynolds, G.P.1    Pearson, S.J.2    Hutson, P.H.3
  • 22
    • 0028832215 scopus 로고
    • Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype
    • Robitaille Y., Schut L., and Kish S. J. (1995) Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype. Acta Neuropathol. (Berl.) 90, 572-581.
    • (1995) Acta Neuropathol. (Berl.) , vol.90 , pp. 572-581
    • Robitaille, Y.1    Schut, L.2    Kish, S.J.3
  • 23
    • 0029895292 scopus 로고    scopus 로고
    • Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease
    • Weeks R. A., Piccini P., Harding A. E., and Brooks D. J. (1996) Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease. Ann. Neurol. 40, 49-54.
    • (1996) Ann. Neurol. , vol.40 , pp. 49-54
    • Weeks, R.A.1    Piccini, P.2    Harding, A.E.3    Brooks, D.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.