-
1
-
-
0037097202
-
Striatal neurochemical changes in transgenic models of Huntington's disease
-
Ariano M.A., Aronin N., Difiglia M., Tagle D.A., Sibley D.R., Leavitt B.R., Hayden M.R., Levine M.S. Striatal neurochemical changes in transgenic models of Huntington's disease. J. Neurosci. Res. 68:2002;716-729.
-
(2002)
J. Neurosci. Res.
, vol.68
, pp. 716-729
-
-
Ariano, M.A.1
Aronin, N.2
Difiglia, M.3
Tagle, D.A.4
Sibley, D.R.5
Leavitt, B.R.6
Hayden, M.R.7
Levine, M.S.8
-
2
-
-
0034237719
-
Energetics in the pathogenesis of neurodegenerative diseases
-
Beal M.F. Energetics in the pathogenesis of neurodegenerative diseases. Trends Neurosci. 23:2000;298-304.
-
(2000)
Trends Neurosci.
, vol.23
, pp. 298-304
-
-
Beal, M.F.1
-
3
-
-
0027433553
-
Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid
-
Beal M.F., Brouillet E., Jenkins B.G., Ferrante R.J., Kowall N.W., Miller J.M., Storey E., Srivastava R., Rosen B.R., Hyman B.T. Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid. J. Neurosci. 13:1993;4181-4192.
-
(1993)
J. Neurosci.
, vol.13
, pp. 4181-4192
-
-
Beal, M.F.1
Brouillet, E.2
Jenkins, B.G.3
Ferrante, R.J.4
Kowall, N.W.5
Miller, J.M.6
Storey, E.7
Srivastava, R.8
Rosen, B.R.9
Hyman, B.T.10
-
4
-
-
0037775906
-
Calpain is a major cell death effector responsible for the selective striatal degeneration induced in vivo by 3-nitropropionate implications for Huntington's disease
-
Bizat N., Hermel J.M., Boyer F., Creminon C., Ouary S., Escartin C., Hantraye P., Krajewski S., Brouillet E. Calpain is a major cell death effector responsible for the selective striatal degeneration induced in vivo by 3-nitropropionate implications for Huntington's disease. J. Neurosci. 23:2003;5020-5030.
-
(2003)
J. Neurosci.
, vol.23
, pp. 5020-5030
-
-
Bizat, N.1
Hermel, J.M.2
Boyer, F.3
Creminon, C.4
Ouary, S.5
Escartin, C.6
Hantraye, P.7
Krajewski, S.8
Brouillet, E.9
-
5
-
-
0036405496
-
Striatal and cortical neurochemical changes induced by chronic metabolic compromise in the 3-nitropropionic model of Huntington's disease
-
Blum D., Galas M.C., Gall D., Cuvelier L., Schiffmann S.N. Striatal and cortical neurochemical changes induced by chronic metabolic compromise in the 3-nitropropionic model of Huntington's disease. Neurobiol. Dis. 10:2002;410-426.
-
(2002)
Neurobiol. Dis.
, vol.10
, pp. 410-426
-
-
Blum, D.1
Galas, M.C.2
Gall, D.3
Cuvelier, L.4
Schiffmann, S.N.5
-
6
-
-
0035854087
-
Topological analysis of striatal lesions induced by 3-nitropropionic acid in the Lewis rat
-
Blum D., Gall D., Cuvelier L., Schiffmann S.N. Topological analysis of striatal lesions induced by 3-nitropropionic acid in the Lewis rat. NeuroReport. 12:2001;1769-1772.
-
(2001)
NeuroReport
, vol.12
, pp. 1769-1772
-
-
Blum, D.1
Gall, D.2
Cuvelier, L.3
Schiffmann, S.N.4
-
7
-
-
0037107346
-
The adenosine A1 receptor agonist adenosine amine congener exerts a neuroprotective effect against the development of striatal lesions and motor impairments in the 3-nitropropionic acid model of neurotoxicity
-
Blum D., Gall D., Galas M.C., d'Alcantara P., Bantubungi K., Schiffmann S.N. The adenosine A1 receptor agonist adenosine amine congener exerts a neuroprotective effect against the development of striatal lesions and motor impairments in the 3-nitropropionic acid model of neurotoxicity. J. Neurosci. 22:2002;9122-9133.
-
(2002)
J. Neurosci.
, vol.22
, pp. 9122-9133
-
-
Blum, D.1
Gall, D.2
Galas, M.C.3
D'Alcantara, P.4
Bantubungi, K.5
Schiffmann, S.N.6
-
8
-
-
0038231381
-
Adenosine receptors and Huntington's disease: Implications for pathogenesis and therapeutics
-
Blum D., Hourez R., Galas M.C., Popoli P., Schiffmann S.N. Adenosine receptors and Huntington's disease: implications for pathogenesis and therapeutics. Lancet Neurol. 2:2003;366-374.
-
(2003)
Lancet Neurol.
, vol.2
, pp. 366-374
-
-
Blum, D.1
Hourez, R.2
Galas, M.C.3
Popoli, P.4
Schiffmann, S.N.5
-
9
-
-
0034624921
-
Decreased striatal monoaminergic terminals in Huntington disease
-
Bohnen N.I., Koeppe R.A., Meyer P., Ficaro E., Wernette K., Kilbourn M.R., Kuhl D.E., Frey K.A., Albin R.L. Decreased striatal monoaminergic terminals in Huntington disease. Neurology. 54:2000;1753-1759.
-
(2000)
Neurology
, vol.54
, pp. 1753-1759
-
-
Bohnen, N.I.1
Koeppe, R.A.2
Meyer, P.3
Ficaro, E.4
Wernette, K.5
Kilbourn, M.R.6
Kuhl, D.E.7
Frey, K.A.8
Albin, R.L.9
-
10
-
-
0032815680
-
Replicating Huntington's disease phenotype in experimental animals
-
Brouillet E., Conde F., Beal M.F., Hantraye P. Replicating Huntington's disease phenotype in experimental animals. Prog. Neurobiol. 59:1999;427-468.
-
(1999)
Prog. Neurobiol.
, vol.59
, pp. 427-468
-
-
Brouillet, E.1
Conde, F.2
Beal, M.F.3
Hantraye, P.4
-
11
-
-
0031914584
-
Partial inhibition of brain succinate dehydrogenase by 3-nitropropionic acid is sufficient to initiate striatal degeneration in rat
-
Brouillet E., Guyot M.C., Mittoux V., Altairac S., Conde F., Palfi S., Hantraye P. Partial inhibition of brain succinate dehydrogenase by 3-nitropropionic acid is sufficient to initiate striatal degeneration in rat. J Neurochem. 70:1998;794-805.
-
(1998)
J Neurochem.
, vol.70
, pp. 794-805
-
-
Brouillet, E.1
Guyot, M.C.2
Mittoux, V.3
Altairac, S.4
Conde, F.5
Palfi, S.6
Hantraye, P.7
-
12
-
-
0029118136
-
Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates
-
Brouillet E., Hantraye P., Ferrante R.J., Dolan R., Leroy-Willig A., Kowall N.W., Beal M.F. Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates. Proc. Natl. Acad. Sci. USA. 92:1995;7105-7109.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 7105-7109
-
-
Brouillet, E.1
Hantraye, P.2
Ferrante, R.J.3
Dolan, R.4
Leroy-Willig, A.5
Kowall, N.W.6
Beal, M.F.7
-
13
-
-
0035211142
-
Perseverative behavior underlying attentional set-shifting deficits in rats chronically treated with the neurotoxin 3-nitropropionic acid
-
El Massioui N., Ouary S., Cheruel F., Hantraye P., Brouillet E. Perseverative behavior underlying attentional set-shifting deficits in rats chronically treated with the neurotoxin 3-nitropropionic acid. Exp. Neurol. 172:2001;172-181.
-
(2001)
Exp. Neurol.
, vol.172
, pp. 172-181
-
-
El Massioui, N.1
Ouary, S.2
Cheruel, F.3
Hantraye, P.4
Brouillet, E.5
-
14
-
-
0030897476
-
PET study of the pre- and post-synaptic dopaminergic markers for the neurodegenerative process in Huntington's disease
-
Ginovart N., Lundin A., Farde L., Halldin C., Backman L., Swahn C.G., Pauli S., Sedvall G. PET study of the pre- and post-synaptic dopaminergic markers for the neurodegenerative process in Huntington's disease. Brain. 120:(Pt 3):1997;503-514.
-
(1997)
Brain
, vol.120
, Issue.PT 3
, pp. 503-514
-
-
Ginovart, N.1
Lundin, A.2
Farde, L.3
Halldin, C.4
Backman, L.5
Swahn, C.G.6
Pauli, S.7
Sedvall, G.8
-
15
-
-
0033119123
-
Nuclear and neuropil aggregates in Huntington's disease: Relationship to neuropathology
-
Gutekunst C.A., Li S.H., Yi H., Mulroy J.S., Kuemmerle S., Jones R., Rye D., Ferrante R.J., Hersch S.M., Li X.J. Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology. J. Neurosci. 19:1999;2522-2534.
-
(1999)
J. Neurosci.
, vol.19
, pp. 2522-2534
-
-
Gutekunst, C.A.1
Li, S.H.2
Yi, H.3
Mulroy, J.S.4
Kuemmerle, S.5
Jones, R.6
Rye, D.7
Ferrante, R.J.8
Hersch, S.M.9
Li, X.J.10
-
16
-
-
0034212341
-
Neuronal cell death in Huntington's disease: A potential role for dopamine
-
Jakel R.J., Maragos W.F. Neuronal cell death in Huntington's disease: a potential role for dopamine. Trends Neurosci. 23:2000;239-245.
-
(2000)
Trends Neurosci.
, vol.23
, pp. 239-245
-
-
Jakel, R.J.1
Maragos, W.F.2
-
17
-
-
0036591536
-
3-Nitropropionic acid-induced changes in bilayer fluidity in synaptosomal membranes: Implications for Huntington's disease
-
LaFontaine M.A., Geddes J.W., Butterfield D.A. 3-Nitropropionic acid-induced changes in bilayer fluidity in synaptosomal membranes: implications for Huntington's disease. Neurochem. Res. 27:2002;507-511.
-
(2002)
Neurochem. Res.
, vol.27
, pp. 507-511
-
-
Lafontaine, M.A.1
Geddes, J.W.2
Butterfield, D.A.3
-
18
-
-
0027000762
-
Effect of striatal lesion with quinolinate on the development of substantia nigra dopaminergic neurons: A quantitative morphological analysis
-
Macaya A., Burke R.E. Effect of striatal lesion with quinolinate on the development of substantia nigra dopaminergic neurons: a quantitative morphological analysis. Dev. Neurosci. 14:1992;362-368.
-
(1992)
Dev. Neurosci
, vol.14
, pp. 362-368
-
-
MacAya, A.1
Burke, R.E.2
-
19
-
-
0037090963
-
Mitochondrial toxin inhibition of [(3)H]dopamine uptake into rat striatal synaptosomes
-
Maragos W.F., Zhu J., Chesnut M.D., Dwoskin L.P. Mitochondrial toxin inhibition of [(3)H]dopamine uptake into rat striatal synaptosomes. Biochem. Pharmacol. 63:2002;1499-1505.
-
(2002)
Biochem. Pharmacol.
, vol.63
, pp. 1499-1505
-
-
Maragos, W.F.1
Zhu, J.2
Chesnut, M.D.3
Dwoskin, L.P.4
-
20
-
-
0030580581
-
Effects of a-phenyl-tert-butyl nitrone on neuronal survival and motor function following intrastriatal injections of quinolinate or 3-nitropropionic acid
-
Nakao N., Brundin P. Effects of a-phenyl-tert-butyl nitrone on neuronal survival and motor function following intrastriatal injections of quinolinate or 3-nitropropionic acid. Neuroscience. 76:1997;749-761.
-
(1997)
Neuroscience
, vol.76
, pp. 749-761
-
-
Nakao, N.1
Brundin, P.2
-
21
-
-
0034127284
-
Major strain differences in response to chronic systemic administration of the mitochondrial toxin 3-nitropropionic acid in rats: Implications for neuroprotection studies
-
Ouary S., Bizat N., Altairac S., Menetrat H., Mittoux V., Conde F., Hantraye P., Brouillet E. Major strain differences in response to chronic systemic administration of the mitochondrial toxin 3-nitropropionic acid in rats: implications for neuroprotection studies. Neuroscience. 97:2000;521-530.
-
(2000)
Neuroscience
, vol.97
, pp. 521-530
-
-
Ouary, S.1
Bizat, N.2
Altairac, S.3
Menetrat, H.4
Mittoux, V.5
Conde, F.6
Hantraye, P.7
Brouillet, E.8
-
22
-
-
0024353643
-
A quantitative investigation of the substantia nigra in Huntington's disease
-
Oyanagi K., Takeda S., Takahashi H., Ohama E., Ikuta F. A quantitative investigation of the substantia nigra in Huntington's disease. Ann. Neurol. 26:1989;13-19.
-
(1989)
Ann. Neurol.
, vol.26
, pp. 13-19
-
-
Oyanagi, K.1
Takeda, S.2
Takahashi, H.3
Ohama, E.4
Ikuta, F.5
-
23
-
-
0036327065
-
Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines
-
Panov A.V., Gutekunst C.A., Leavitt B.R., Hayden M.R., Burke J.R., Strittmatter W.J., Greenamyre J.T. Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines. Nat. Neurosci. 5:2002;731-736.
-
(2002)
Nat. Neurosci.
, vol.5
, pp. 731-736
-
-
Panov, A.V.1
Gutekunst, C.A.2
Leavitt, B.R.3
Hayden, M.R.4
Burke, J.R.5
Strittmatter, W.J.6
Greenamyre, J.T.7
-
24
-
-
0036453663
-
Evidence for dysfunction of the nigrostriatal pathway in the R6/1 line of transgenic Huntington's disease mice
-
Petersen A., Puschban Z., Lotharius J., NicNiocaill B., Wiekop P., O'Connor W.T., Brundin P. Evidence for dysfunction of the nigrostriatal pathway in the R6/1 line of transgenic Huntington's disease mice. Neurobiol. Dis. 11:2002;134-146.
-
(2002)
Neurobiol. Dis.
, vol.11
, pp. 134-146
-
-
Petersen, A.1
Puschban, Z.2
Lotharius, J.3
Nicniocaill, B.4
Wiekop, P.5
O'Connor, W.T.6
Brundin, P.7
-
25
-
-
0033066942
-
Brain neurotransmitter deficits in mice transgenic for Huntington's disease mutation
-
Reynolds G.P., Dalton C., Tillery C.L., Mangiarini L., Davies S.W., Bates G. Brain neurotransmitter deficits in mice transgenic for Huntington's disease mutation. J. Neurochem. 72:1999;1773-1776.
-
(1999)
J. Neurochem.
, vol.72
, pp. 1773-1776
-
-
Reynolds, G.P.1
Dalton, C.2
Tillery, C.L.3
Mangiarini, L.4
Davies, S.W.5
Bates, G.6
-
26
-
-
0032851595
-
Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization
-
Sawa A., Wiegand G.W., Cooper J., Margolis R.L., Sharp A.H., Lawler J.F. Jr, Greenamyre J.T., Snyder S.H., Ross C.A. Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization. Nat. Med. 5:1999;1194-1198.
-
(1999)
Nat. Med.
, vol.5
, pp. 1194-1198
-
-
Sawa, A.1
Wiegand, G.W.2
Cooper, J.3
Margolis, R.L.4
Sharp, A.H.5
Lawler Jr., J.F.6
Greenamyre, J.T.7
Snyder, S.H.8
Ross, C.A.9
-
27
-
-
0030726727
-
Inhibition of striatal energy metabolism produces cell loss in the ispilateral substantia nigra
-
Sonsalla P.K., Manzino L., Sinton C.M., Liang C.L., German D.C., Zeevalk G.D. Inhibition of striatal energy metabolism produces cell loss in the ispilateral substantia nigra. Br. Res. 773:1997;223-226.
-
(1997)
Br. Res.
, vol.773
, pp. 223-226
-
-
Sonsalla, P.K.1
Manzino, L.2
Sinton, C.M.3
Liang, C.L.4
German, D.C.5
Zeevalk, G.D.6
-
28
-
-
0031565270
-
In vivo vulnerability of dopamine neurons to inhibition of energy metabolism
-
Zeevalk G.D., Manzino L., Hoppe J., Sonsalla P.K. In vivo vulnerability of dopamine neurons to inhibition of energy metabolism. Eur. J. Pharmacol. 320:1997;111-119.
-
(1997)
Eur. J. Pharmacol
, vol.320
, pp. 111-119
-
-
Zeevalk, G.D.1
Manzino, L.2
Hoppe, J.3
Sonsalla, P.K.4
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