-
1
-
-
0034743672
-
Creatine increase survival and delays motor symptoms in a transgenic animal model of Huntington's disease
-
Andreassen O.A., Dedeoglu A., Ferrante R.J., Jenkins B.G., Ferrante K.L., Thomas M., Friedlich A., Browne S.E., Schilling G., Borchelt D.R., Hersch S.M., Ross C.A., and Beal M.F. Creatine increase survival and delays motor symptoms in a transgenic animal model of Huntington's disease. Neurobiol. Dis. 8 (2001) 479-491
-
(2001)
Neurobiol. Dis.
, vol.8
, pp. 479-491
-
-
Andreassen, O.A.1
Dedeoglu, A.2
Ferrante, R.J.3
Jenkins, B.G.4
Ferrante, K.L.5
Thomas, M.6
Friedlich, A.7
Browne, S.E.8
Schilling, G.9
Borchelt, D.R.10
Hersch, S.M.11
Ross, C.A.12
Beal, M.F.13
-
2
-
-
0035968856
-
Lipoic acid improves survival in transgenic mouse models of Huntington's disease
-
Andreassen O.A., Ferrante R.J., Dedeoglu A., and Beal M.F. Lipoic acid improves survival in transgenic mouse models of Huntington's disease. NeuroReport 12 (2001) 3371-3373
-
(2001)
NeuroReport
, vol.12
, pp. 3371-3373
-
-
Andreassen, O.A.1
Ferrante, R.J.2
Dedeoglu, A.3
Beal, M.F.4
-
3
-
-
0034955984
-
Dichloroacetate exerts therapeutic effects in transgenic mouse models of Huntington's disease
-
Andreassen O.A., Ferrante R.J., Huang H.M., Dedeoglu A., Park L., Ferrante K.L., Kwon J., Borchelt D.R., Ross C.A., Gibson G.E., and Beal M.F. Dichloroacetate exerts therapeutic effects in transgenic mouse models of Huntington's disease. Ann. Neurol. 50 (2001) 112-117
-
(2001)
Ann. Neurol.
, vol.50
, pp. 112-117
-
-
Andreassen, O.A.1
Ferrante, R.J.2
Huang, H.M.3
Dedeoglu, A.4
Park, L.5
Ferrante, K.L.6
Kwon, J.7
Borchelt, D.R.8
Ross, C.A.9
Gibson, G.E.10
Beal, M.F.11
-
4
-
-
0037002444
-
Huntington's disease of the endocrine pancreas: insulin deficiency and diabetes mellitus due to impaired insulin gene expression
-
Andreassen O.A., Dedeoglu A., Stanojevic V., Hughes D.B., Browne S.E., Leech C.A., Ferrante R.J., Habener J.F., Beal M.F., and Thomas M.K. Huntington's disease of the endocrine pancreas: insulin deficiency and diabetes mellitus due to impaired insulin gene expression. Neurobiol. Dis. 11 (2002) 410-424
-
(2002)
Neurobiol. Dis.
, vol.11
, pp. 410-424
-
-
Andreassen, O.A.1
Dedeoglu, A.2
Stanojevic, V.3
Hughes, D.B.4
Browne, S.E.5
Leech, C.A.6
Ferrante, R.J.7
Habener, J.F.8
Beal, M.F.9
Thomas, M.K.10
-
5
-
-
49549088134
-
CEP-1347 reduces mutant huntingtin-associated neurotoxicity and restores BDNF levels in R6/2 mice
-
Apostol B.L., Simmons D.A., Zuccato C., Illes K., Pallos J., Casale M., Conforti P., Ramos C., Roarke M., Kathuria S., Cattaneo E., Marsh J.L., and Thompson L.M. CEP-1347 reduces mutant huntingtin-associated neurotoxicity and restores BDNF levels in R6/2 mice. Mol. Cell. Neurosci. 39 (2008) 8-20
-
(2008)
Mol. Cell. Neurosci.
, vol.39
, pp. 8-20
-
-
Apostol, B.L.1
Simmons, D.A.2
Zuccato, C.3
Illes, K.4
Pallos, J.5
Casale, M.6
Conforti, P.7
Ramos, C.8
Roarke, M.9
Kathuria, S.10
Cattaneo, E.11
Marsh, J.L.12
Thompson, L.M.13
-
6
-
-
0035216624
-
Effect of DL-alpha-lipoic acid on glutathione metabolic enzymes in aged rats
-
Arivazhagan P., Ramanathan K., and Panneerselvam C. Effect of DL-alpha-lipoic acid on glutathione metabolic enzymes in aged rats. Exp. Gerontol. 37 (2001) 81-87
-
(2001)
Exp. Gerontol.
, vol.37
, pp. 81-87
-
-
Arivazhagan, P.1
Ramanathan, K.2
Panneerselvam, C.3
-
7
-
-
21544450545
-
p53 mediates cellular dysfunction and behavioral abnormalities in Huntington's disease
-
Bae B.I., Xu H., Igarashi S., Fujimuro M., Agrawal N., Taya Y., Hayward S.D., Moran T.H., Montell C., Ross C.A., Snyder S.H., and Sawa A. p53 mediates cellular dysfunction and behavioral abnormalities in Huntington's disease. Neuron 47 (2005) 29-41
-
(2005)
Neuron
, vol.47
, pp. 29-41
-
-
Bae, B.I.1
Xu, H.2
Igarashi, S.3
Fujimuro, M.4
Agrawal, N.5
Taya, Y.6
Hayward, S.D.7
Moran, T.H.8
Montell, C.9
Ross, C.A.10
Snyder, S.H.11
Sawa, A.12
-
8
-
-
33745392939
-
Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin
-
Benchoua A., Trioulier Y., Zala D., Gaillard M.C., Lefort N., Dufour N., Saudou F., Elalouf J.M., Hirsch E., Hantraye P., Déglon N., and Brouillet E. Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin. Mol. Biol. Cell 17 (2006) 1652-1663
-
(2006)
Mol. Biol. Cell
, vol.17
, pp. 1652-1663
-
-
Benchoua, A.1
Trioulier, Y.2
Zala, D.3
Gaillard, M.C.4
Lefort, N.5
Dufour, N.6
Saudou, F.7
Elalouf, J.M.8
Hirsch, E.9
Hantraye, P.10
Déglon, N.11
Brouillet, E.12
-
9
-
-
0035448951
-
Adenoviral brain-derived neurotrophic factor induces both neostriatal and olfactory neuronal recruitment from endogenous progenitor cells in the adult forebrain
-
Benraiss A., Chmielnicki E., Lerner K., Roh D., and Goldman S.A. Adenoviral brain-derived neurotrophic factor induces both neostriatal and olfactory neuronal recruitment from endogenous progenitor cells in the adult forebrain. J. Neurosci. 21 (2001) 6718-6731
-
(2001)
J. Neurosci.
, vol.21
, pp. 6718-6731
-
-
Benraiss, A.1
Chmielnicki, E.2
Lerner, K.3
Roh, D.4
Goldman, S.A.5
-
10
-
-
8844281519
-
The tolerability of riluzole in the treatment of patients with amyotrophic lateral sclerosis
-
Bensimon G., and Doble A. The tolerability of riluzole in the treatment of patients with amyotrophic lateral sclerosis. Expert Opin. Drug Saf. 3 (2004) 525-534
-
(2004)
Expert Opin. Drug Saf.
, vol.3
, pp. 525-534
-
-
Bensimon, G.1
Doble, A.2
-
11
-
-
20044392282
-
The R6/2 transgenic mouse model of Huntington's disease develops diabetes due to deficient β-cell mass
-
Björkqvist M., Fex M., Wierup N., Petersén Å., Gil J., Bacos K., Popovic N., Li J.Y., Sundler F., Brundin P., and Mulder H. The R6/2 transgenic mouse model of Huntington's disease develops diabetes due to deficient β-cell mass. Hum. Mol. Genet. 14 (2005) 565-574
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 565-574
-
-
Björkqvist, M.1
Fex, M.2
Wierup, N.3
Petersén, Å.4
Gil, J.5
Bacos, K.6
Popovic, N.7
Li, J.Y.8
Sundler, F.9
Brundin, P.10
Mulder, H.11
-
12
-
-
33745210300
-
Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease
-
Björkqvist M., Petersén Å., Bacos K., Isaacs J., Norlén P., Gil J., Popovic N., Sundler F., Bates G.P., Tabrizi S.J., Brundin P., and Mulder H. Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease. Hum. Mol. Genet. 15 (2006) 1713-1721
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 1713-1721
-
-
Björkqvist, M.1
Petersén, Å.2
Bacos, K.3
Isaacs, J.4
Norlén, P.5
Gil, J.6
Popovic, N.7
Sundler, F.8
Bates, G.P.9
Tabrizi, S.J.10
Brundin, P.11
Mulder, H.12
-
13
-
-
0347626155
-
Exploratory activity and fear conditioning abnormalities develop early in R6/2 Huntington's disease transgenic mice
-
Bolivar V.J., Manley K., and Messer A. Exploratory activity and fear conditioning abnormalities develop early in R6/2 Huntington's disease transgenic mice. Behav. Neurosci. 117 (2003) 1233-1242
-
(2003)
Behav. Neurosci.
, vol.117
, pp. 1233-1242
-
-
Bolivar, V.J.1
Manley, K.2
Messer, A.3
-
14
-
-
1642418261
-
Early exploratory behavior abnormalities in R6/1 Huntington's disease transgenic mice
-
Bolivar V.J., Manley K., and Messer A. Early exploratory behavior abnormalities in R6/1 Huntington's disease transgenic mice. Brain Res. 1005 (2004) 29-35
-
(2004)
Brain Res.
, vol.1005
, pp. 29-35
-
-
Bolivar, V.J.1
Manley, K.2
Messer, A.3
-
16
-
-
33646421164
-
Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase
-
Borrell-Pagès M., Canals J.M., Cordelières F.P., Parker J.A., Pineda J.R., Grange G., Bryson E.A., Guillermier M., Hirsch E., Hantraye P., Cheetham M.E., Néri C., Alberch J., Brouillet E., Saudou F., and Humbert S. Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase. J. Clin. Invest. 116 (2006) 1410-1424
-
(2006)
J. Clin. Invest.
, vol.116
, pp. 1410-1424
-
-
Borrell-Pagès, M.1
Canals, J.M.2
Cordelières, F.P.3
Parker, J.A.4
Pineda, J.R.5
Grange, G.6
Bryson, E.A.7
Guillermier, M.8
Hirsch, E.9
Hantraye, P.10
Cheetham, M.E.11
Néri, C.12
Alberch, J.13
Brouillet, E.14
Saudou, F.15
Humbert, S.16
-
17
-
-
4444350918
-
Brain-derived neurotrophic factor regulates the onset and severity of motor dysfunction associated with enkephalinergic neuronal degeneration in Huntington's disease
-
Canals J.M., Pineda J.R., Torres-Peraza J.F., Bosch M., Martín-Ibañez R., Muñoz M.T., Mengod G., Ernfors P., and Alberch J. Brain-derived neurotrophic factor regulates the onset and severity of motor dysfunction associated with enkephalinergic neuronal degeneration in Huntington's disease. J. Neurosci. 24 (2004) 7727-7739
-
(2004)
J. Neurosci.
, vol.24
, pp. 7727-7739
-
-
Canals, J.M.1
Pineda, J.R.2
Torres-Peraza, J.F.3
Bosch, M.4
Martín-Ibañez, R.5
Muñoz, M.T.6
Mengod, G.7
Ernfors, P.8
Alberch, J.9
-
18
-
-
0033560924
-
Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation
-
Carter R.J., Lione L.A., Humby T., Mangiarini L., Mahal A., Bates G.P., Dunnett S.B., and Morton A.J. Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation. Neuroscience 19 (1999) 3248-3257
-
(1999)
Neuroscience
, vol.19
, pp. 3248-3257
-
-
Carter, R.J.1
Lione, L.A.2
Humby, T.3
Mangiarini, L.4
Mahal, A.5
Bates, G.P.6
Dunnett, S.B.7
Morton, A.J.8
-
19
-
-
0033819849
-
Environmental stimulation increases survival in mice transgenic for exon 1 of the Huntington's disease gene
-
Carter R.J., Hunt M.J., and Morton A.J. Environmental stimulation increases survival in mice transgenic for exon 1 of the Huntington's disease gene. Mov. Disord. 15 (2000) 925-937
-
(2000)
Mov. Disord.
, vol.15
, pp. 925-937
-
-
Carter, R.J.1
Hunt, M.J.2
Morton, A.J.3
-
20
-
-
0034283877
-
Transcriptional dysregulation in Huntington's disease
-
Cha J.H. Transcriptional dysregulation in Huntington's disease. Trends Neurosci. 23 (2000) 387-392
-
(2000)
Trends Neurosci.
, vol.23
, pp. 387-392
-
-
Cha, J.H.1
-
21
-
-
0032568517
-
Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human huntington disease gene
-
Cha J.H., Kosinski C.M., Kerner J.A., Alsdorf S.A., Mangiarini L., Davies S.W., Penney J.B., Bates G.P., and Young A.B. Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human huntington disease gene. Proc. Natl. Acad. Sci. U. S. A. 95 (1998) 6480-6485
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, pp. 6480-6485
-
-
Cha, J.H.1
Kosinski, C.M.2
Kerner, J.A.3
Alsdorf, S.A.4
Mangiarini, L.5
Davies, S.W.6
Penney, J.B.7
Bates, G.P.8
Young, A.B.9
-
22
-
-
0033912716
-
Minocycline inhibits caspase-1 and caspase-3 expression and delaus mortality in a transgenic mouse model of Huntington disease
-
Chen M., Ona V.O., Li M., Ferrante R.J., Fink K.B., Zhu S., Bian J., Guo L., Farrel L.A., Hersch S.M., Hobbs W., Vonsattel J.P., Cha J.H., and Friedlander R.M. Minocycline inhibits caspase-1 and caspase-3 expression and delaus mortality in a transgenic mouse model of Huntington disease. Nat. Med. 6 (2000) 797-801
-
(2000)
Nat. Med.
, vol.6
, pp. 797-801
-
-
Chen, M.1
Ona, V.O.2
Li, M.3
Ferrante, R.J.4
Fink, K.B.5
Zhu, S.6
Bian, J.7
Guo, L.8
Farrel, L.A.9
Hersch, S.M.10
Hobbs, W.11
Vonsattel, J.P.12
Cha, J.H.13
Friedlander, R.M.14
-
23
-
-
34948855498
-
Induction of neostriatal neurogenesis slows disease progression in a transgenic murine model of Huntington disease
-
Cho S.R., Benraiss A., Chmielnicki E., Samdani A., Economides A., and Goldman S.A. Induction of neostriatal neurogenesis slows disease progression in a transgenic murine model of Huntington disease. J. Clin. Invest. 117 (2007) 2889-2902
-
(2007)
J. Clin. Invest.
, vol.117
, pp. 2889-2902
-
-
Cho, S.R.1
Benraiss, A.2
Chmielnicki, E.3
Samdani, A.4
Economides, A.5
Goldman, S.A.6
-
24
-
-
36749022180
-
A small-molecule therapeutic lead for Huntington's disease: preclinical pharmacology and efficacy of C2-8 in the R6/2 transgenic mouse
-
Chopra V., Fox J.H., Lieberman G., Dorsey K., Matson W., Waldmeier P., Housman D.E., Kazantsev A., Young A.B., and Hersch S. A small-molecule therapeutic lead for Huntington's disease: preclinical pharmacology and efficacy of C2-8 in the R6/2 transgenic mouse. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 16685-16689
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 16685-16689
-
-
Chopra, V.1
Fox, J.H.2
Lieberman, G.3
Dorsey, K.4
Matson, W.5
Waldmeier, P.6
Housman, D.E.7
Kazantsev, A.8
Young, A.B.9
Hersch, S.10
-
25
-
-
20244362093
-
CGS21680 attenuates symptoms of Huntington's disease in a transgenic mouse model
-
Chou S.Y., Lee Y.C., Chen H.M., Chiang M.C., Lai H.L., Chang H.H., Wu Y.C., Sun C.N., Chien C.L., Lin Y.S., Wang S.C., Tung Y.Y., Chang C., and Chern Y. CGS21680 attenuates symptoms of Huntington's disease in a transgenic mouse model. J. Neurochem. 93 (2005) 310-320
-
(2005)
J. Neurochem.
, vol.93
, pp. 310-320
-
-
Chou, S.Y.1
Lee, Y.C.2
Chen, H.M.3
Chiang, M.C.4
Lai, H.L.5
Chang, H.H.6
Wu, Y.C.7
Sun, C.N.8
Chien, C.L.9
Lin, Y.S.10
Wang, S.C.11
Tung, Y.Y.12
Chang, C.13
Chern, Y.14
-
26
-
-
0037126988
-
Essential fatty acids given from conception prevent topographies of motor deficit in a transgenic model of Huntington's disease
-
Clifford J.J., Drago J., Natoli A.L., Wong J.Y.F., Kinsella A., Waddington J.L., and Vaddadi K.S. Essential fatty acids given from conception prevent topographies of motor deficit in a transgenic model of Huntington's disease. Neuroscience 109 (2002) 81-88
-
(2002)
Neuroscience
, vol.109
, pp. 81-88
-
-
Clifford, J.J.1
Drago, J.2
Natoli, A.L.3
Wong, J.Y.F.4
Kinsella, A.5
Waddington, J.L.6
Vaddadi, K.S.7
-
27
-
-
49549109150
-
Blood level of brain-derived neurotrophic factor mRNA is progressively reduced in rodent models of Huntington's disease: restoration by the neuroprotective compound CEP-1347
-
Conforti P., Ramos C., Apostol B.L., Simmons D.A., Nguyen H.P., Riess O., Thompson L.M., Zuccato C., and Cattaneo E. Blood level of brain-derived neurotrophic factor mRNA is progressively reduced in rodent models of Huntington's disease: restoration by the neuroprotective compound CEP-1347. Mol. Cell. Neurosci. 39 (2008) 1-7
-
(2008)
Mol. Cell. Neurosci.
, vol.39
, pp. 1-7
-
-
Conforti, P.1
Ramos, C.2
Apostol, B.L.3
Simmons, D.A.4
Nguyen, H.P.5
Riess, O.6
Thompson, L.M.7
Zuccato, C.8
Cattaneo, E.9
-
28
-
-
18544410106
-
Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
-
Davies S.W., Turmaine M., Cozens B.A., DiFiglia M., Sharp A.H., Ross C.A., Scherzinger E., Wanker E.E., Mangiarini L., and Bates G.P. Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation. Cell 90 (1997) 537-548
-
(1997)
Cell
, vol.90
, pp. 537-548
-
-
Davies, S.W.1
Turmaine, M.2
Cozens, B.A.3
DiFiglia, M.4
Sharp, A.H.5
Ross, C.A.6
Scherzinger, E.7
Wanker, E.E.8
Mangiarini, L.9
Bates, G.P.10
-
29
-
-
0037109665
-
Therapeutic effects of cystamine in a murine model of Huntington's disease
-
Dedeoglu A., Kubilus J.K., Jeitner T.M., Matson S.A., Bogdanov M., Kowall N.W., Matson W.R., Cooper A.J.L., Ratan R.R., Beal M.F., Hersch S.M., and Ferrante R.J. Therapeutic effects of cystamine in a murine model of Huntington's disease. J. Neurosci. 22 (2002) 8942-8950
-
(2002)
J. Neurosci.
, vol.22
, pp. 8942-8950
-
-
Dedeoglu, A.1
Kubilus, J.K.2
Jeitner, T.M.3
Matson, S.A.4
Bogdanov, M.5
Kowall, N.W.6
Matson, W.R.7
Cooper, A.J.L.8
Ratan, R.R.9
Beal, M.F.10
Hersch, S.M.11
Ferrante, R.J.12
-
30
-
-
0038115294
-
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice
-
Dedeoglu A., Kubilus J.K., Yang L., Ferrante K.L., Hersch S.M., Beal M.F., and Ferrante R.J. Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice. J. Neurochem. 85 (2003) 1359-1367
-
(2003)
J. Neurochem.
, vol.85
, pp. 1359-1367
-
-
Dedeoglu, A.1
Kubilus, J.K.2
Yang, L.3
Ferrante, K.L.4
Hersch, S.M.5
Beal, M.F.6
Ferrante, R.J.7
-
31
-
-
0025821265
-
Alterations in the levels of iron, ferritin and other trace metals in Parkinson's disease and other neurodegenerative diseases affecting the basal ganglia
-
Dexter D.T., Carayon A., Javoy-Agid F., Agid Y., Wells F.R., Daniel S.E., Lees A.J., Jenner P., and Marsden C.D. Alterations in the levels of iron, ferritin and other trace metals in Parkinson's disease and other neurodegenerative diseases affecting the basal ganglia. Brain 114 (1991) 1953-1975
-
(1991)
Brain
, vol.114
, pp. 1953-1975
-
-
Dexter, D.T.1
Carayon, A.2
Javoy-Agid, F.3
Agid, Y.4
Wells, F.R.5
Daniel, S.E.6
Lees, A.J.7
Jenner, P.8
Marsden, C.D.9
-
32
-
-
42149128233
-
The novel substituted pyrimidine, KP544, reduces motor deficits in the R6/2 transgenic mouse model of Huntington's disease
-
Dey N.D., Boersen A.J., Myers R.A., York L.R., Bombard M.C., Lu M., Sandstrom M.I., Hulce V.D., Lescaudron L., and Dunbar G.L. The novel substituted pyrimidine, KP544, reduces motor deficits in the R6/2 transgenic mouse model of Huntington's disease. Restor. Neurol. Neurosci. 25 (2007) 485-492
-
(2007)
Restor. Neurol. Neurosci.
, vol.25
, pp. 485-492
-
-
Dey, N.D.1
Boersen, A.J.2
Myers, R.A.3
York, L.R.4
Bombard, M.C.5
Lu, M.6
Sandstrom, M.I.7
Hulce, V.D.8
Lescaudron, L.9
Dunbar, G.L.10
-
33
-
-
36749033738
-
Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits
-
DiFiglia M., Sena-Esteves M., Chase K., Sapp E., Pfister E., Sass M., Yoder J., Reeves P., Pandey R.K., Rajeev K.G., Manoharan M., Sah D.W., Zamore P.D., and Aronin N. Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 17204-17209
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 17204-17209
-
-
DiFiglia, M.1
Sena-Esteves, M.2
Chase, K.3
Sapp, E.4
Pfister, E.5
Sass, M.6
Yoder, J.7
Reeves, P.8
Pandey, R.K.9
Rajeev, K.G.10
Manoharan, M.11
Sah, D.W.12
Zamore, P.D.13
Aronin, N.14
-
34
-
-
0029753270
-
The pharmacology and mechanism of action of riluzole
-
Doble A. The pharmacology and mechanism of action of riluzole. Neurology 47 (1996) S233-S241
-
(1996)
Neurology
, vol.47
-
-
Doble, A.1
-
35
-
-
35348983910
-
Behavioral and electrophysiological effects of the adenosine A2A receptor antagonist SCH 58261 in R6/2 Huntington's disease mice
-
Domenici M.R., Scattoni M.L., Martire A., Lastoria G., Potenza R.L., Borioni A., Venerosi A., Calamandrei G., and Popoli P. Behavioral and electrophysiological effects of the adenosine A2A receptor antagonist SCH 58261 in R6/2 Huntington's disease mice. Neurobiol. Dis. 28 (2007) 197-205
-
(2007)
Neurobiol. Dis.
, vol.28
, pp. 197-205
-
-
Domenici, M.R.1
Scattoni, M.L.2
Martire, A.3
Lastoria, G.4
Potenza, R.L.5
Borioni, A.6
Venerosi, A.7
Calamandrei, G.8
Popoli, P.9
-
36
-
-
43649106471
-
Sertraline slows disease progression and increases neurogenesis in N171-82Q mouse model of Huntington's disease
-
Duan W., Peng Q., Masuda N., Ford E., Tryggestad E., Ladenheim B., Zhao M., Cadet J.L., Wong J., and Ross C.A. Sertraline slows disease progression and increases neurogenesis in N171-82Q mouse model of Huntington's disease. Neurobiol. Dis. 30 (2008) 312-322
-
(2008)
Neurobiol. Dis.
, vol.30
, pp. 312-322
-
-
Duan, W.1
Peng, Q.2
Masuda, N.3
Ford, E.4
Tryggestad, E.5
Ladenheim, B.6
Zhao, M.7
Cadet, J.L.8
Wong, J.9
Ross, C.A.10
-
37
-
-
0032211289
-
Striatal transplantation in a transgenic mouse model of Huntington's disease
-
Dunnett S.B., Carter R.J., Watts C., Torres E.M., Mahal A., Mangiarini L., Bates G., and Morton A.J. Striatal transplantation in a transgenic mouse model of Huntington's disease. Exp. Neurol. 154 (1998) 31-40
-
(1998)
Exp. Neurol.
, vol.154
, pp. 31-40
-
-
Dunnett, S.B.1
Carter, R.J.2
Watts, C.3
Torres, E.M.4
Mahal, A.5
Mangiarini, L.6
Bates, G.7
Morton, A.J.8
-
38
-
-
0037974734
-
Asialoerythropoietin is a nonerythropoietic cytokine with broad neuroprotective activity in vivo
-
Erbayraktar S., Grasso G., Sfacteria A., Xie Q.W., Coleman T., Kreilgaard M., Torup L., Sager T., Erbayraktar Z., Gokmen N., Yilmaz O., Ghezzi P., Villa P., Fratelli M., Casagrande S., Leist M., Helboe L., Gerwein J., Christensen S., Geist M.A., Pedersen L.Ø., Cerami-Hand C., Wuerth J.P., Cerami A., and Brines M. Asialoerythropoietin is a nonerythropoietic cytokine with broad neuroprotective activity in vivo. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 6741-6746
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 6741-6746
-
-
Erbayraktar, S.1
Grasso, G.2
Sfacteria, A.3
Xie, Q.W.4
Coleman, T.5
Kreilgaard, M.6
Torup, L.7
Sager, T.8
Erbayraktar, Z.9
Gokmen, N.10
Yilmaz, O.11
Ghezzi, P.12
Villa, P.13
Fratelli, M.14
Casagrande, S.15
Leist, M.16
Helboe, L.17
Gerwein, J.18
Christensen, S.19
Geist, M.A.20
Pedersen, L.Ø.21
Cerami-Hand, C.22
Wuerth, J.P.23
Cerami, A.24
Brines, M.25
more..
-
39
-
-
0021927818
-
Diabetes mellitus in Huntington disease
-
Farrer L.A. Diabetes mellitus in Huntington disease. Clin. Genet. 27 (1985) l62-167
-
(1985)
Clin. Genet.
, vol.27
-
-
Farrer, L.A.1
-
40
-
-
0029988363
-
Assessment of coenzyme Q10 tolerability in Huntington's disease
-
Feigin A., Kieburtz K., Como P., Hickey C., Claude K., Abwender D., Zimmerman C., Steinberg K., and Shoulson I. Assessment of coenzyme Q10 tolerability in Huntington's disease. Mov. Disord. 11 (1996) 321-323
-
(1996)
Mov. Disord.
, vol.11
, pp. 321-323
-
-
Feigin, A.1
Kieburtz, K.2
Como, P.3
Hickey, C.4
Claude, K.5
Abwender, D.6
Zimmerman, C.7
Steinberg, K.8
Shoulson, I.9
-
41
-
-
0034660457
-
Neuroprotective effects of creatine in a transgenic mouse model of Huntington's disease
-
Ferrante R.J., Andreassen O.A., Jenkins B.G., Dedeoglu A., Kuemmerle S., Kubilus J.K., Kaddurah-Daouk R., Hersch S.M., and Beal M.F. Neuroprotective effects of creatine in a transgenic mouse model of Huntington's disease. J. Neurosci. 20 (2000) 4389-4397
-
(2000)
J. Neurosci.
, vol.20
, pp. 4389-4397
-
-
Ferrante, R.J.1
Andreassen, O.A.2
Jenkins, B.G.3
Dedeoglu, A.4
Kuemmerle, S.5
Kubilus, J.K.6
Kaddurah-Daouk, R.7
Hersch, S.M.8
Beal, M.F.9
-
43
-
-
0142157600
-
Histone deacetylase inhibition by sodium butyrate chemotherapy ameliorates the neurodegenerative phenotype in Huntington's disease mice
-
Ferrante R.J., Kubilus J.K., Lee J., Ryu H., Beesen A., Zucker B., Smith K., Kowall N.W., Ratan R.R., Luthi-Carter R., and Hersch S.M. Histone deacetylase inhibition by sodium butyrate chemotherapy ameliorates the neurodegenerative phenotype in Huntington's disease mice. J. Neurosci. 23 (2003) 9418-9427
-
(2003)
J. Neurosci.
, vol.23
, pp. 9418-9427
-
-
Ferrante, R.J.1
Kubilus, J.K.2
Lee, J.3
Ryu, H.4
Beesen, A.5
Zucker, B.6
Smith, K.7
Kowall, N.W.8
Ratan, R.R.9
Luthi-Carter, R.10
Hersch, S.M.11
-
44
-
-
20844455450
-
Chemotherapy for the brain: the antitumor antibiotic mithramycin prolongs survival in a mouse model of Huntington's disease
-
Ferrante R.J., Ryu H., Kubilus J.K., D, Mello S., Sugars K.L., Lee J., Lu P., Smith K., Browne S., Beal M.F., Kristal B.S., Stavrovskaya I.G., Hewett S., Rubinsztein D.C., Langley B., and Ratan R.R. Chemotherapy for the brain: the antitumor antibiotic mithramycin prolongs survival in a mouse model of Huntington's disease. J Neurosci. 24 (2004) 10335-10342
-
(2004)
J Neurosci.
, vol.24
, pp. 10335-10342
-
-
Ferrante, R.J.1
Ryu, H.2
Kubilus, J.K.3
D'Mello, S.4
Sugars, K.L.5
Lee, J.6
Lu, P.7
Smith, K.8
Browne, S.9
Beal, M.F.10
Kristal, B.S.11
Stavrovskaya, I.G.12
Hewett, S.13
Rubinsztein, D.C.14
Langley, B.15
Ratan, R.R.16
-
45
-
-
0035808264
-
Anti-amyloidogenic activity of tetracyclines: studies in vitro
-
Forloni G., Colombo L., Girola L., Tagliavini F., and Salmona M. Anti-amyloidogenic activity of tetracyclines: studies in vitro. FEBS Lett. 487 (2001) 404-487
-
(2001)
FEBS Lett.
, vol.487
, pp. 404-487
-
-
Forloni, G.1
Colombo, L.2
Girola, L.3
Tagliavini, F.4
Salmona, M.5
-
46
-
-
45149107487
-
Mechanisms of neurodegeneration in Huntington's disease
-
Gil J.M., and Rego A.C. Mechanisms of neurodegeneration in Huntington's disease. Eur. J. Neurosci. 27 (2008) 2803-2820
-
(2008)
Eur. J. Neurosci.
, vol.27
, pp. 2803-2820
-
-
Gil, J.M.1
Rego, A.C.2
-
47
-
-
2642545019
-
Asialoerythropoietin is not effective in the R6/2 line of Huntington's disease mice
-
Gil J.M., Leist M., Popovic N., Brundin P., and Petersén Å. Asialoerythropoietin is not effective in the R6/2 line of Huntington's disease mice. BMC Neurosci. 5 (2004) 17-27
-
(2004)
BMC Neurosci.
, vol.5
, pp. 17-27
-
-
Gil, J.M.1
Leist, M.2
Popovic, N.3
Brundin, P.4
Petersén, Å.5
-
48
-
-
27644485740
-
Reduced hippocampal neurogenesis in R6/2 transgenic Huntington's disease mice
-
Gil J.M., Mohapel P., Araújo I.M., Popovic N., Li J.Y., Brundin P., and Petersén Å. Reduced hippocampal neurogenesis in R6/2 transgenic Huntington's disease mice. Neurobiol. Dis. 20 (2005) 744-751
-
(2005)
Neurobiol. Dis.
, vol.20
, pp. 744-751
-
-
Gil, J.M.1
Mohapel, P.2
Araújo, I.M.3
Popovic, N.4
Li, J.Y.5
Brundin, P.6
Petersén, Å.7
-
49
-
-
0034081681
-
The pattern of neurodegeneration in Huntington's disease: a comparative study of cannabinoid, dopamine, adenosine and GABA(A) receptor alterations in the human basal ganglia in Huntington's disease
-
Glass M., Dragunow M., and Faull R.L. The pattern of neurodegeneration in Huntington's disease: a comparative study of cannabinoid, dopamine, adenosine and GABA(A) receptor alterations in the human basal ganglia in Huntington's disease. Neuroscience 97 (2000) 505-519
-
(2000)
Neuroscience
, vol.97
, pp. 505-519
-
-
Glass, M.1
Dragunow, M.2
Faull, R.L.3
-
50
-
-
0345118102
-
Delayed onset of Huntington's disease in mice in an enriched environment correlates with delayed loss of cannabinoid CB1 receptors
-
Glass M., van Dellen A., Blakemore C., Hannan A.J., and Faull R.L. Delayed onset of Huntington's disease in mice in an enriched environment correlates with delayed loss of cannabinoid CB1 receptors. Neuroscience 123 (2004) 207-212
-
(2004)
Neuroscience
, vol.123
, pp. 207-212
-
-
Glass, M.1
van Dellen, A.2
Blakemore, C.3
Hannan, A.J.4
Faull, R.L.5
-
51
-
-
0033363319
-
Learning enhances adult neurogenesis in the hippocampal formation
-
Gould E., Beylin A., Tanapat P., Reeves A., and Shors T.J. Learning enhances adult neurogenesis in the hippocampal formation. Nat. Neurosci. 2 (1999) 260-265
-
(1999)
Nat. Neurosci.
, vol.2
, pp. 260-265
-
-
Gould, E.1
Beylin, A.2
Tanapat, P.3
Reeves, A.4
Shors, T.J.5
-
52
-
-
27644524469
-
Cognitive disorders and neurogenesis deficits in Huntington's disease mice are rescued by fluoxetine
-
Grote H.E., Bull N.D., Howard M.L., van Dellen A., Blakemore C., Bartlett P.F., and Hannan A.J. Cognitive disorders and neurogenesis deficits in Huntington's disease mice are rescued by fluoxetine. Eur. J. Neurosci. 22 (2005) 2081-2088
-
(2005)
Eur. J. Neurosci.
, vol.22
, pp. 2081-2088
-
-
Grote, H.E.1
Bull, N.D.2
Howard, M.L.3
van Dellen, A.4
Blakemore, C.5
Bartlett, P.F.6
Hannan, A.J.7
-
53
-
-
0033042929
-
(R)-alpha-lipoic acid-supplemented old rats have improved mitochondrial function, decreased oxidative damage, and increased metabolic rate
-
Hagen T.M., Ingersoll R.T., Lykkesfeldt J., Liu J., Wehr C.M., Vinarsky V., Bartholomew J.C., and Ames A.B. (R)-alpha-lipoic acid-supplemented old rats have improved mitochondrial function, decreased oxidative damage, and increased metabolic rate. FASEB J. 13 (1999) 411-418
-
(1999)
FASEB J.
, vol.13
, pp. 411-418
-
-
Hagen, T.M.1
Ingersoll, R.T.2
Lykkesfeldt, J.3
Liu, J.4
Wehr, C.M.5
Vinarsky, V.6
Bartholomew, J.C.7
Ames, A.B.8
-
54
-
-
3242748968
-
Molecular mediators, environmental modulators and experience-dependent synaptic dysfunction in Huntington's disease
-
Hannan A.J. Molecular mediators, environmental modulators and experience-dependent synaptic dysfunction in Huntington's disease. Acta Biochim. Pol. 51 (2004) 415-430
-
(2004)
Acta Biochim. Pol.
, vol.51
, pp. 415-430
-
-
Hannan, A.J.1
-
55
-
-
0347928859
-
Overexpression of heat shock protein 70 in R6/2 Huntington's disease mice has only modest effects on disease progression
-
Hansson O., Nylandsted J., Castilho R.F., Leist M., Jäättelä M., and Brundin P. Overexpression of heat shock protein 70 in R6/2 Huntington's disease mice has only modest effects on disease progression. Brain Res. 970 (2003) 47-57
-
(2003)
Brain Res.
, vol.970
, pp. 47-57
-
-
Hansson, O.1
Nylandsted, J.2
Castilho, R.F.3
Leist, M.4
Jäättelä, M.5
Brundin, P.6
-
56
-
-
0034612220
-
Inhibition of huntingtin fibrillogenesis by specific antibodies and small molecules: implications for Huntington's disease therapy
-
Heiser V., Scherzinger E., Boeddrich A., Nordhoff E., Lurz R., Schugardt N., Lehrach H., and Wanker E.E. Inhibition of huntingtin fibrillogenesis by specific antibodies and small molecules: implications for Huntington's disease therapy. Proc. Natl. Acad. Sci. U. S. A. 97 (2000) 6739-6744
-
(2000)
Proc. Natl. Acad. Sci. U. S. A.
, vol.97
, pp. 6739-6744
-
-
Heiser, V.1
Scherzinger, E.2
Boeddrich, A.3
Nordhoff, E.4
Lurz, R.5
Schugardt, N.6
Lehrach, H.7
Wanker, E.E.8
-
57
-
-
0037115495
-
Progressive retinal degeneration and dysfunction in R6 Huntington's disease mice
-
Helmlinger D., Yvert G., Picaud S., Merienne K., Sahel J., Mandel J.L., and Devys D. Progressive retinal degeneration and dysfunction in R6 Huntington's disease mice. Hum. Mol. Genet. 11 (2002) 3351-3359
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 3351-3359
-
-
Helmlinger, D.1
Yvert, G.2
Picaud, S.3
Merienne, K.4
Sahel, J.5
Mandel, J.L.6
Devys, D.7
-
58
-
-
0027724925
-
Functional aspects of creatine kinase in brain
-
Hemmer W., and Wallimann T. Functional aspects of creatine kinase in brain. Dev. Neurosci. 15 (1993) 249-260
-
(1993)
Dev. Neurosci.
, vol.15
, pp. 249-260
-
-
Hemmer, W.1
Wallimann, T.2
-
59
-
-
24044442568
-
Early behavioral deficits in R6/2 mice suitable for use in preclinical drug testing
-
Hickey M.A., Gallant K., Gross G.G., Levine M.S., and Chesselet M.F. Early behavioral deficits in R6/2 mice suitable for use in preclinical drug testing. Neurobiol. Dis. 20 (2005) 1-11
-
(2005)
Neurobiol. Dis.
, vol.20
, pp. 1-11
-
-
Hickey, M.A.1
Gallant, K.2
Gross, G.G.3
Levine, M.S.4
Chesselet, M.F.5
-
60
-
-
0036152343
-
Environmental enrichment slows disease progression in R6/2 Huntington's disease mice
-
Hockly E., Cordery P.M., Woodman B., Mahal A., van Dellen A., Blakemore C., Lewis C.M., Hannan A.J., and Bates G.P. Environmental enrichment slows disease progression in R6/2 Huntington's disease mice. Ann. Neurol. 51 (2002) 235-242
-
(2002)
Ann. Neurol.
, vol.51
, pp. 235-242
-
-
Hockly, E.1
Cordery, P.M.2
Woodman, B.3
Mahal, A.4
van Dellen, A.5
Blakemore, C.6
Lewis, C.M.7
Hannan, A.J.8
Bates, G.P.9
-
61
-
-
0037452775
-
Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease
-
Hockly E., Richon V.M., Woodman B., Smith D.L., Zhou X., Rosa E., Sathasivam K., Ghazi-Noori S., Mahal A., Lowden P.A., Steffan J.S., Marsh J.L., Thompson L.M., Lewis C.M., Marks P.A., and Bates G.P. Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 2041-2046
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 2041-2046
-
-
Hockly, E.1
Richon, V.M.2
Woodman, B.3
Smith, D.L.4
Zhou, X.5
Rosa, E.6
Sathasivam, K.7
Ghazi-Noori, S.8
Mahal, A.9
Lowden, P.A.10
Steffan, J.S.11
Marsh, J.L.12
Thompson, L.M.13
Lewis, C.M.14
Marks, P.A.15
Bates, G.P.16
-
62
-
-
0141678246
-
Standardization and statistical approaches to therapeutic trials in the R6/2 mouse
-
Hockly E., Woodman B., Mahal A., Lewis C.M., and Bates G. Standardization and statistical approaches to therapeutic trials in the R6/2 mouse. Brain Res. Bull. 61 (2003) 469-479
-
(2003)
Brain Res. Bull.
, vol.61
, pp. 469-479
-
-
Hockly, E.1
Woodman, B.2
Mahal, A.3
Lewis, C.M.4
Bates, G.5
-
63
-
-
29144498271
-
Evaluation of the benzothiazole aggregation inhibitors riluzole and PGL-135 as therapeutics for Huntington's disease
-
Hockly E., Tse J., Barker A.L., Moolman D.L., Beunard J.L., Revington A.P., Holt K., Sunshine S., Moffitt H., Sathasivam K., Woodman B., Wanker E.E., Lowden P.A., and Bates G.P. Evaluation of the benzothiazole aggregation inhibitors riluzole and PGL-135 as therapeutics for Huntington's disease. Neurobiol. Dis. 21 (2006) 228-236
-
(2006)
Neurobiol. Dis.
, vol.21
, pp. 228-236
-
-
Hockly, E.1
Tse, J.2
Barker, A.L.3
Moolman, D.L.4
Beunard, J.L.5
Revington, A.P.6
Holt, K.7
Sunshine, S.8
Moffitt, H.9
Sathasivam, K.10
Woodman, B.11
Wanker, E.E.12
Lowden, P.A.13
Bates, G.P.14
-
64
-
-
34248146697
-
High-capacity adenoviral vector-mediated reduction of huntingtin aggregate load in vitro and in vivo
-
Huang B., Schiefer J., Sass C., Landwehrmeyer G.B., Kosinski C.M., and Kochanek S. High-capacity adenoviral vector-mediated reduction of huntingtin aggregate load in vitro and in vivo. Hum. Gene Ther. 18 (2007) 303-311
-
(2007)
Hum. Gene Ther.
, vol.18
, pp. 303-311
-
-
Huang, B.1
Schiefer, J.2
Sass, C.3
Landwehrmeyer, G.B.4
Kosinski, C.M.5
Kochanek, S.6
-
65
-
-
26044473385
-
Atypical diabetes associated with inclusion formation in the R6/2 mouse model of Huntington's disease is not improved by treatment with hypoglycaemic agents
-
Hunt M.J., and Morton A.J. Atypical diabetes associated with inclusion formation in the R6/2 mouse model of Huntington's disease is not improved by treatment with hypoglycaemic agents. Exp. Brain Res. 166 (2005) 220-229
-
(2005)
Exp. Brain Res.
, vol.166
, pp. 220-229
-
-
Hunt, M.J.1
Morton, A.J.2
-
66
-
-
85009226418
-
10 and remacemide in Huntington's disease
-
Huntington Study Group
-
10 and remacemide in Huntington's disease. Neurology 57 (2001) 397-404
-
(2001)
Neurology
, vol.57
, pp. 397-404
-
-
-
67
-
-
0345600893
-
Dosage effects of riluzole in Huntington's disease: a multicenter placebo-controlled study
-
Huntington Study Group
-
Huntington Study Group. Dosage effects of riluzole in Huntington's disease: a multicenter placebo-controlled study. Neurology 61 (2003) 1551-1556
-
(2003)
Neurology
, vol.61
, pp. 1551-1556
-
-
-
68
-
-
3543092682
-
Minocycline safety and tolerability in Huntington disease
-
Huntington Study Group
-
Huntington Study Group. Minocycline safety and tolerability in Huntington disease. Neurology 63 (2004) 547-549
-
(2004)
Neurology
, vol.63
, pp. 547-549
-
-
-
69
-
-
0033009587
-
Mice transgenic for an expanded CAG repeat in the Huntington's disease gene develop diabetes
-
Hurlbert M.S., Zhou W., Wasmeier C., Kaddis F.G., Hutton J.C., and Freed C.R. Mice transgenic for an expanded CAG repeat in the Huntington's disease gene develop diabetes. Diabetes 48 (1999) 649-651
-
(1999)
Diabetes
, vol.48
, pp. 649-651
-
-
Hurlbert, M.S.1
Zhou, W.2
Wasmeier, C.3
Kaddis, F.G.4
Hutton, J.C.5
Freed, C.R.6
-
70
-
-
0033914470
-
Early alterations in gene expression and cell morphology in a mouse model of Huntington's disease
-
Iannicola C., Moreno S., Oliverio S., Nardacci R., Ciofi-Luzzatto A., and Piacentini M. Early alterations in gene expression and cell morphology in a mouse model of Huntington's disease. J. Neurochem. 75 (2000) 830-839
-
(2000)
J. Neurochem.
, vol.75
, pp. 830-839
-
-
Iannicola, C.1
Moreno, S.2
Oliverio, S.3
Nardacci, R.4
Ciofi-Luzzatto, A.5
Piacentini, M.6
-
71
-
-
29144517660
-
FGF-2 promotes neurogenesis and neuroprotection and prolongs survival in a transgenic mouse model of Huntington's disease
-
Jin K., LaFevre-Bernt M., Sun Y., Chen S., Gafni J., Crippen D., Logvinova A., Ross C.A., Greenberg D.A., and Ellerby L.M. FGF-2 promotes neurogenesis and neuroprotection and prolongs survival in a transgenic mouse model of Huntington's disease. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 18189-18194
-
(2005)
Proc. Natl. Acad. Sci. U. S. A.
, vol.102
, pp. 18189-18194
-
-
Jin, K.1
LaFevre-Bernt, M.2
Sun, Y.3
Chen, S.4
Gafni, J.5
Crippen, D.6
Logvinova, A.7
Ross, C.A.8
Greenberg, D.A.9
Ellerby, L.M.10
-
72
-
-
0030024623
-
Functional outcome in rats transferred to an enriched environment 15 days after focal brain ischemia
-
Johansson B.B. Functional outcome in rats transferred to an enriched environment 15 days after focal brain ischemia. Stroke 27 (1996) 324-326
-
(1996)
Stroke
, vol.27
, pp. 324-326
-
-
Johansson, B.B.1
-
73
-
-
0032014092
-
Transglutaminase action imitates Huntington's disease: selective polymerization of Huntingtin containing expanded polyglutamine
-
Kahlem P., Green H., and Djian P. Transglutaminase action imitates Huntington's disease: selective polymerization of Huntingtin containing expanded polyglutamine. Mol. Cell 1 (1998) 595-601
-
(1998)
Mol. Cell
, vol.1
, pp. 595-601
-
-
Kahlem, P.1
Green, H.2
Djian, P.3
-
74
-
-
0036172346
-
Prolonged survival and decreased abnormal movements in transgenic model of Huntington disease, with administration of the transglutaminase inhibitor cystamine
-
Karpuj M.V., Becher M.W., Springer J.E., Chabas D., Youssef S., Pedotti R., Mitchell D., and Steinman L. Prolonged survival and decreased abnormal movements in transgenic model of Huntington disease, with administration of the transglutaminase inhibitor cystamine. Nat. Med. 8 (2002) 143-149
-
(2002)
Nat. Med.
, vol.8
, pp. 143-149
-
-
Karpuj, M.V.1
Becher, M.W.2
Springer, J.E.3
Chabas, D.4
Youssef, S.5
Pedotti, R.6
Mitchell, D.7
Steinman, L.8
-
75
-
-
0036677435
-
Tauroursodeoxycholic acid, a bile acid, is neuroprotective in a transgenic animal model of Huntington's disease
-
Keene C.D., Rodrigues C.M., Eich T., Chhabra M.S., Steer C.J., and Low W.C. Tauroursodeoxycholic acid, a bile acid, is neuroprotective in a transgenic animal model of Huntington's disease. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 10671-10676
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 10671-10676
-
-
Keene, C.D.1
Rodrigues, C.M.2
Eich, T.3
Chhabra, M.S.4
Steer, C.J.5
Low, W.C.6
-
76
-
-
0030937293
-
More hippocampal neurons in adult mice living in an enriched environment
-
Kempermann G., Kuhn H.G., and Gage F.H. More hippocampal neurons in adult mice living in an enriched environment. Nature 386 (1997) 493-495
-
(1997)
Nature
, vol.386
, pp. 493-495
-
-
Kempermann, G.1
Kuhn, H.G.2
Gage, F.H.3
-
77
-
-
0037971143
-
Increased survival and neuroprotective effects of BN82451 in a transgenic mouse model of Huntington's disease
-
Klivenyi P., Ferrante R.J., Gardian G., Browne S., Chabrier P.E., and Beal M.F. Increased survival and neuroprotective effects of BN82451 in a transgenic mouse model of Huntington's disease. J. Neurochem. 86 (2003) 267-272
-
(2003)
J. Neurochem.
, vol.86
, pp. 267-272
-
-
Klivenyi, P.1
Ferrante, R.J.2
Gardian, G.3
Browne, S.4
Chabrier, P.E.5
Beal, M.F.6
-
78
-
-
0024352110
-
Quantitative evaluation of Congo red binding to amyloid-like proteins with a beta-pleated sheet conformation
-
Klunk W.E., Pettegrew J.W., and Abraham D.J. Quantitative evaluation of Congo red binding to amyloid-like proteins with a beta-pleated sheet conformation. J. Histochem. Cytochem. 37 (1989) 1273-1281
-
(1989)
J. Histochem. Cytochem.
, vol.37
, pp. 1273-1281
-
-
Klunk, W.E.1
Pettegrew, J.W.2
Abraham, D.J.3
-
79
-
-
34249986143
-
Physical activity fails to rescue hippocampal neurogenesis deficits in the R6/2 mouse model of Huntington's disease
-
Kohl Z., Kandasamy M., Winner B., Aigner R., Gross C., Couillard-Despres S., Bogdahn U., Aigner L., and Winkler J. Physical activity fails to rescue hippocampal neurogenesis deficits in the R6/2 mouse model of Huntington's disease. Brain Res. 1155 (2007) 24-33
-
(2007)
Brain Res.
, vol.1155
, pp. 24-33
-
-
Kohl, Z.1
Kandasamy, M.2
Winner, B.3
Aigner, R.4
Gross, C.5
Couillard-Despres, S.6
Bogdahn, U.7
Aigner, L.8
Winkler, J.9
-
80
-
-
34948838383
-
Riluzole in Huntington's disease: a 3-year, randomized controlled study
-
European Huntington's Disease Initiative Study Group
-
Landwehrmeyer G.B., Dubois B., de Yébenes J.G., Kremer B., Gaus W., Kraus P.H., Przuntek H., Dib M., Doble A., Fischer W., Ludolph A.C., and European Huntington's Disease Initiative Study Group. Riluzole in Huntington's disease: a 3-year, randomized controlled study. Ann. Neurol. 62 (2007) 262-272
-
(2007)
Ann. Neurol.
, vol.62
, pp. 262-272
-
-
Landwehrmeyer, G.B.1
Dubois, B.2
de Yébenes, J.G.3
Kremer, B.4
Gaus, W.5
Kraus, P.H.6
Przuntek, H.7
Dib, M.8
Doble, A.9
Fischer, W.10
Ludolph, A.C.11
-
81
-
-
1842608950
-
Decreased hippocampal cell proliferation in R6/1 Huntington's mice
-
Lazic S.E., Grote H., Armstrong R.J., Blakemore C., Hannan A.J., van Dellen A., and Barker R.A. Decreased hippocampal cell proliferation in R6/1 Huntington's mice. NeuroReport 15 (2004) 811-813
-
(2004)
NeuroReport
, vol.15
, pp. 811-813
-
-
Lazic, S.E.1
Grote, H.2
Armstrong, R.J.3
Blakemore, C.4
Hannan, A.J.5
van Dellen, A.6
Barker, R.A.7
-
82
-
-
33645452859
-
Neurogenesis in the R6/1 transgenic mouse model of Huntington's disease: effects of environmental enrichment
-
Lazic S.E., Grote H.E., Blakemore C., Hannan A.J., van Dellen A., Phillips W., and Barker R.A. Neurogenesis in the R6/1 transgenic mouse model of Huntington's disease: effects of environmental enrichment. Eur. J. Neurosci. 23 (2006) 1829-1838
-
(2006)
Eur. J. Neurosci.
, vol.23
, pp. 1829-1838
-
-
Lazic, S.E.1
Grote, H.E.2
Blakemore, C.3
Hannan, A.J.4
van Dellen, A.5
Phillips, W.6
Barker, R.A.7
-
83
-
-
0032811511
-
Ultrastructural localization and progressive formation of neuropil aggregates in Huntington's disease transgenic mice
-
Li H., Li S.H., Cheng A.L., Mangiarini L., Bates G.P., and Li X.J. Ultrastructural localization and progressive formation of neuropil aggregates in Huntington's disease transgenic mice. Hum. Mol. Genet. 8 (1999) 1227-1236
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1227-1236
-
-
Li, H.1
Li, S.H.2
Cheng, A.L.3
Mangiarini, L.4
Bates, G.P.5
Li, X.J.6
-
84
-
-
3142521479
-
Stem cell therapy for human neurodegenerative disorders-how to make it work
-
Lindvall O., Kokaia Z., and Martinez-Serrano A. Stem cell therapy for human neurodegenerative disorders-how to make it work. Nat. Med. 10 (2004) S42-S50
-
(2004)
Nat. Med.
, vol.10
-
-
Lindvall, O.1
Kokaia, Z.2
Martinez-Serrano, A.3
-
85
-
-
0033500593
-
Selective discrimination learning impairments in mice expressing the human Huntington's disease mutation
-
Lione L.A., Carter R.J., Hunt M.J., Bates G.P., Morton A.J., and Dunnett S.B. Selective discrimination learning impairments in mice expressing the human Huntington's disease mutation. J. Neurosci. 19 (1999) 10428-10437
-
(1999)
J. Neurosci.
, vol.19
, pp. 10428-10437
-
-
Lione, L.A.1
Carter, R.J.2
Hunt, M.J.3
Bates, G.P.4
Morton, A.J.5
Dunnett, S.B.6
-
86
-
-
0035969336
-
Evaluation of R6/2 HD transgenic mice for therapeutic studies in Huntington's disease: behavioral testing and impact of diabetes mellitus
-
Luesse H.G., Schiefer J., Spruenken A., Puls C., Block F., and Kosinski C.M. Evaluation of R6/2 HD transgenic mice for therapeutic studies in Huntington's disease: behavioral testing and impact of diabetes mellitus. Behav. Brain Res. 126 (2001) 185-195
-
(2001)
Behav. Brain Res.
, vol.126
, pp. 185-195
-
-
Luesse, H.G.1
Schiefer, J.2
Spruenken, A.3
Puls, C.4
Block, F.5
Kosinski, C.M.6
-
87
-
-
0034702030
-
Decreased expression of striatal signaling genes in a mouse model of Huntington's disease
-
Luthi-Carter R., Strand A., Peters N.L., Solano S.M., Hollingsworth Z.R., Menon A.S., Frey A.S., Spektor B.S., Penney E.B., Schilling G., Ross C.A., Borchelt D.R., Tapscott S.J., Young A.B., Cha J.H., and Olson J.M. Decreased expression of striatal signaling genes in a mouse model of Huntington's disease. Hum. Mol. Genet. 9 (2000) 1259-1271
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1259-1271
-
-
Luthi-Carter, R.1
Strand, A.2
Peters, N.L.3
Solano, S.M.4
Hollingsworth, Z.R.5
Menon, A.S.6
Frey, A.S.7
Spektor, B.S.8
Penney, E.B.9
Schilling, G.10
Ross, C.A.11
Borchelt, D.R.12
Tapscott, S.J.13
Young, A.B.14
Cha, J.H.15
Olson, J.M.16
-
88
-
-
0037101835
-
Dysregulation of gene expression in the R6/2 model of polyglutamine disease: parallel changes in muscle and brain
-
Luthi-Carter R., Hanson S.A., Strand A.D., Bergstrom D.A., Chun W., Peters N.L., Woods A.M., Chan E.Y., Kooperberg C., Krainc D., Young A.B., Tapscott S.J., and Olson J.M. Dysregulation of gene expression in the R6/2 model of polyglutamine disease: parallel changes in muscle and brain. Hum. Mol. Genet. 11 (2002) 1911-1926
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 1911-1926
-
-
Luthi-Carter, R.1
Hanson, S.A.2
Strand, A.D.3
Bergstrom, D.A.4
Chun, W.5
Peters, N.L.6
Woods, A.M.7
Chan, E.Y.8
Kooperberg, C.9
Krainc, D.10
Young, A.B.11
Tapscott, S.J.12
Olson, J.M.13
-
89
-
-
10744223572
-
Complex alteration of NMDA receptors in transgenic Huntington's disease mouse brain: analysis of mRNA and protein expression, plasma membrane association, interacting proteins, and phosphorylation
-
Luthi-Carter R., Apostol B.L., Dunah A.W., DeJohn M.M., Farrell L.A., Bates G.P., Young A.B., Standaert D.G., Thompson L.M., and Cha J.H. Complex alteration of NMDA receptors in transgenic Huntington's disease mouse brain: analysis of mRNA and protein expression, plasma membrane association, interacting proteins, and phosphorylation. Neurobiol. Dis. 14 (2003) 624-636
-
(2003)
Neurobiol. Dis.
, vol.14
, pp. 624-636
-
-
Luthi-Carter, R.1
Apostol, B.L.2
Dunah, A.W.3
DeJohn, M.M.4
Farrell, L.A.5
Bates, G.P.6
Young, A.B.7
Standaert, D.G.8
Thompson, L.M.9
Cha, J.H.10
-
90
-
-
34548095002
-
Metformin therapy in a transgenic mouse model of Huntington's disease
-
Ma T.C., Buescher J.L., Oatis B., Funk J.A., Nash A.J., Carrier R.L., and Hoyt K.R. Metformin therapy in a transgenic mouse model of Huntington's disease. Neurosci. Lett. 411 (2007) 98-103
-
(2007)
Neurosci. Lett.
, vol.411
, pp. 98-103
-
-
Ma, T.C.1
Buescher, J.L.2
Oatis, B.3
Funk, J.A.4
Nash, A.J.5
Carrier, R.L.6
Hoyt, K.R.7
-
91
-
-
16044373842
-
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
-
Mangiarini L., Sathasivam K., Seller M., Cozens B., Harper A., Hetherington C., Lawton M., Trottier Y., Lehrach H., Davies S.W., and Bates G.P. Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell 87 (1996) 493-506
-
(1996)
Cell
, vol.87
, pp. 493-506
-
-
Mangiarini, L.1
Sathasivam, K.2
Seller, M.3
Cozens, B.4
Harper, A.5
Hetherington, C.6
Lawton, M.7
Trottier, Y.8
Lehrach, H.9
Davies, S.W.10
Bates, G.P.11
-
92
-
-
0036715380
-
Tissue' transglutaminase ablation reduces neuronal death and prolongs survival in a mouse model of Huntington's disease
-
Mastroberardino P.G., Iannicola C., Nardacci R., Bernassola F., De Laurenzi V., Melino G., Moreno S., Pavone F., Oliverio S., Fesus L., and Piacentini M. Tissue' transglutaminase ablation reduces neuronal death and prolongs survival in a mouse model of Huntington's disease. Cell Death Differ. 9 (2002) 873-880
-
(2002)
Cell Death Differ.
, vol.9
, pp. 873-880
-
-
Mastroberardino, P.G.1
Iannicola, C.2
Nardacci, R.3
Bernassola, F.4
De Laurenzi, V.5
Melino, G.6
Moreno, S.7
Pavone, F.8
Oliverio, S.9
Fesus, L.10
Piacentini, M.11
-
93
-
-
43649101278
-
Tiagabine is neuroprotective in the N171-82Q and R6/2 mouse models of Huntington's disease
-
Masuda N., Peng Q., Li Q., Jiang M., Liang Y., Wang X., Zhao M., Wang W., Ross C.A., and Duan W. Tiagabine is neuroprotective in the N171-82Q and R6/2 mouse models of Huntington's disease. Neurobiol. Dis. 30 (2008) 293-302
-
(2008)
Neurobiol. Dis.
, vol.30
, pp. 293-302
-
-
Masuda, N.1
Peng, Q.2
Li, Q.3
Jiang, M.4
Liang, Y.5
Wang, X.6
Zhao, M.7
Wang, W.8
Ross, C.A.9
Duan, W.10
-
94
-
-
0037194221
-
Cellular localization and development of neuronal intranuclear inclusions in striatal and cortical neurons in R6/2 transgenic mice
-
Meade C.A., Deng Y.P., Fusco F.R., Del Mar N., Hersch S., Goldowitz D., and Reiner A. Cellular localization and development of neuronal intranuclear inclusions in striatal and cortical neurons in R6/2 transgenic mice. J. Comp. Neurol. 449 (2002) 241-269
-
(2002)
J. Comp. Neurol.
, vol.449
, pp. 241-269
-
-
Meade, C.A.1
Deng, Y.P.2
Fusco, F.R.3
Del Mar, N.4
Hersch, S.5
Goldowitz, D.6
Reiner, A.7
-
95
-
-
0037562002
-
DNA vaccination against mutant huntingtin ameliorates the HDR6/2 diabetic phenotype
-
Miller T.W., Shirley T.L., Wolfgang W.J., Kang X., and Messer A. DNA vaccination against mutant huntingtin ameliorates the HDR6/2 diabetic phenotype. Mol. Ther. 7 (2003) 572-579
-
(2003)
Mol. Ther.
, vol.7
, pp. 572-579
-
-
Miller, T.W.1
Shirley, T.L.2
Wolfgang, W.J.3
Kang, X.4
Messer, A.5
-
96
-
-
41949104569
-
Up-regulation of GLT1 expression increases glutamate uptake and attenuates the Huntington's disease phenotype in the R6/2 mouse
-
Miller B.R., Dorner J.L., Shou M., Sari Y., Barton S.J., Sengelaub D.R., Kennedy R.T., and Rebec G.V. Up-regulation of GLT1 expression increases glutamate uptake and attenuates the Huntington's disease phenotype in the R6/2 mouse. Neuroscience 153 (2008) 329-337
-
(2008)
Neuroscience
, vol.153
, pp. 329-337
-
-
Miller, B.R.1
Dorner, J.L.2
Shou, M.3
Sari, Y.4
Barton, S.J.5
Sengelaub, D.R.6
Kennedy, R.T.7
Rebec, G.V.8
-
97
-
-
16244384501
-
A combination drug therapy improves cognition and reverses gene expression changes in a mouse model of Huntington's disease
-
Morton A.J., Hunt M.J., Hodges A.K., Lewis P.D., Redfern A.J., Dunnett S.B., and Jones L. A combination drug therapy improves cognition and reverses gene expression changes in a mouse model of Huntington's disease. Eur. J. Neurosci. 21 (2005) 855-870
-
(2005)
Eur. J. Neurosci.
, vol.21
, pp. 855-870
-
-
Morton, A.J.1
Hunt, M.J.2
Hodges, A.K.3
Lewis, P.D.4
Redfern, A.J.5
Dunnett, S.B.6
Jones, L.7
-
98
-
-
12144273983
-
Disintegration of the sleep-wake cycle and circadian timing in Huntington's disease
-
Morton A.J., Wood N.I., Hastings M.H., Hurelbrink C., Barker R.A., and Maywood E.S. Disintegration of the sleep-wake cycle and circadian timing in Huntington's disease. J. Neurosci. 25 (2005) 157-163
-
(2005)
J. Neurosci.
, vol.25
, pp. 157-163
-
-
Morton, A.J.1
Wood, N.I.2
Hastings, M.H.3
Hurelbrink, C.4
Barker, R.A.5
Maywood, E.S.6
-
99
-
-
0034234519
-
Abnormal synaptic plasticity and impaired spatial cognition in mice transgenic for exon 1 of the human Huntington's disease gene
-
Murphy K.P., Carter R.J., Lione L.A., Mangiarini L., Mahal A., Bates G.P., Dunnett S.B., and Morton A.J. Abnormal synaptic plasticity and impaired spatial cognition in mice transgenic for exon 1 of the human Huntington's disease gene. J. Neurosci. 20 (2000) 5115-5123
-
(2000)
J. Neurosci.
, vol.20
, pp. 5115-5123
-
-
Murphy, K.P.1
Carter, R.J.2
Lione, L.A.3
Mangiarini, L.4
Mahal, A.5
Bates, G.P.6
Dunnett, S.B.7
Morton, A.J.8
-
100
-
-
23844482456
-
Clioquinol down-regulates mutant huntingtin expression in vitro and mitigates pathology in a Huntington's disease mouse model
-
Nguyen T., Hamby A., and Massa S.M. Clioquinol down-regulates mutant huntingtin expression in vitro and mitigates pathology in a Huntington's disease mouse model. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 1840-11845
-
(2005)
Proc. Natl. Acad. Sci. U. S. A.
, vol.102
, pp. 1840-11845
-
-
Nguyen, T.1
Hamby, A.2
Massa, S.M.3
-
101
-
-
5144223534
-
Anti-inflammatory treatment with acetylsalicylate or rofecoxib is not neuroprotective in Huntington's disease transgenic mice
-
Norflus F., Nanje A., Gutekunst C.A., Shi G., Cohen J., Bejarano M., Fox J., Ferrante R.J., and Hersch S.M. Anti-inflammatory treatment with acetylsalicylate or rofecoxib is not neuroprotective in Huntington's disease transgenic mice. Neurobiol. Dis. 17 (2004) 319-325
-
(2004)
Neurobiol. Dis.
, vol.17
, pp. 319-325
-
-
Norflus, F.1
Nanje, A.2
Gutekunst, C.A.3
Shi, G.4
Cohen, J.5
Bejarano, M.6
Fox, J.7
Ferrante, R.J.8
Hersch, S.M.9
-
102
-
-
0033587128
-
Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease
-
Ona V.O., Li M., Vonsattel J.P.G., Andrews L.J., Khan S.Q., Chung W.M., Frey A.S., Menon A.S., Li X.J., Stieg P.E., Yuan J., Penney J.B., Young A.B., Cha J.H., and Friedlander R.M. Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease. Nature 399 (1999) 263-267
-
(1999)
Nature
, vol.399
, pp. 263-267
-
-
Ona, V.O.1
Li, M.2
Vonsattel, J.P.G.3
Andrews, L.J.4
Khan, S.Q.5
Chung, W.M.6
Frey, A.S.7
Menon, A.S.8
Li, X.J.9
Stieg, P.E.10
Yuan, J.11
Penney, J.B.12
Young, A.B.13
Cha, J.H.14
Friedlander, R.M.15
-
103
-
-
34447637430
-
Pharmacological imposition of sleep slows cognitive decline and reverses dysregulation of circadian gene expression in a transgenic mouse model of Huntington's disease
-
Pallier P.N., Maywood E.S., Zheng Z., Chesham J.E., Inyushkin A.N., Dyball R., Hastings M.H., and Morton A.J. Pharmacological imposition of sleep slows cognitive decline and reverses dysregulation of circadian gene expression in a transgenic mouse model of Huntington's disease. J. Neurosci. 27 (2007) 7869-7878
-
(2007)
J. Neurosci.
, vol.27
, pp. 7869-7878
-
-
Pallier, P.N.1
Maywood, E.S.2
Zheng, Z.3
Chesham, J.E.4
Inyushkin, A.N.5
Dyball, R.6
Hastings, M.H.7
Morton, A.J.8
-
104
-
-
0035449745
-
Infusion of brain-derived neurotrophic factor into the lateral ventricle of the adult rat leads to new neurons in the parenchyma of the striatum, septum, thalamus, and hypothalamus
-
Pencea V., Bingaman K.D., Wiegand S.J., and Luskin M.B. Infusion of brain-derived neurotrophic factor into the lateral ventricle of the adult rat leads to new neurons in the parenchyma of the striatum, septum, thalamus, and hypothalamus. J. Neurosci. 21 (2001) 6706-6717
-
(2001)
J. Neurosci.
, vol.21
, pp. 6706-6717
-
-
Pencea, V.1
Bingaman, K.D.2
Wiegand, S.J.3
Luskin, M.B.4
-
105
-
-
39249084415
-
The antidepressant sertraline improves the phenotype, promotes neurogenesis and increases BDNF levels in the R6/2 Huntington's disease mouse model
-
Peng Q., Masuda N., Jiang M., Li Q., Zhao M., Ross C.A., and Duan W. The antidepressant sertraline improves the phenotype, promotes neurogenesis and increases BDNF levels in the R6/2 Huntington's disease mouse model. Exp. Neurol. 210 (2008) 154-163
-
(2008)
Exp. Neurol.
, vol.210
, pp. 154-163
-
-
Peng, Q.1
Masuda, N.2
Jiang, M.3
Li, Q.4
Zhao, M.5
Ross, C.A.6
Duan, W.7
-
106
-
-
33747602312
-
Hypothalamic-endocrine aspects in Huntington's disease
-
Petersén Å., and Björkqvist M. Hypothalamic-endocrine aspects in Huntington's disease. Eur. J. Neurosci. 24 (2006) 961-967
-
(2006)
Eur. J. Neurosci.
, vol.24
, pp. 961-967
-
-
Petersén, Å.1
Björkqvist, M.2
-
107
-
-
19944427749
-
Orexin loss in Huntington's disease
-
Petersén Å., Gil J., Maat-Schieman M.L.C., Björkqvist M., Tanila H., Araújo I.M., Smith R., Popovic N., Wierup N., Norlén P., Li J.Y., Roos R.A.C., Sundler F., Mulder H., and Brundin P. Orexin loss in Huntington's disease. Hum. Mol. Genet. 14 (2005) 39-47
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 39-47
-
-
Petersén, Å.1
Gil, J.2
Maat-Schieman, M.L.C.3
Björkqvist, M.4
Tanila, H.5
Araújo, I.M.6
Smith, R.7
Popovic, N.8
Wierup, N.9
Norlén, P.10
Li, J.Y.11
Roos, R.A.C.12
Sundler, F.13
Mulder, H.14
Brundin, P.15
-
108
-
-
33845976361
-
Neuroprotection by GDNF-secreting stem cells in a Huntington's disease model: optical neuroimage tracking of brain-grafted cells
-
Pineda J.R., Rubio N., Akerud P., Urbán N., Badimon L., Arenas E., Alberch J., Blanco J., and Canals J.M. Neuroprotection by GDNF-secreting stem cells in a Huntington's disease model: optical neuroimage tracking of brain-grafted cells. Gene Ther. 14 (2007) 118-128
-
(2007)
Gene Ther.
, vol.14
, pp. 118-128
-
-
Pineda, J.R.1
Rubio, N.2
Akerud, P.3
Urbán, N.4
Badimon, L.5
Arenas, E.6
Alberch, J.7
Blanco, J.8
Canals, J.M.9
-
109
-
-
0015521813
-
Increased frequency of diabetes mellitus in patients with Huntington's chorea
-
Podolsky S., Leopold N.A., and Sax D.S. Increased frequency of diabetes mellitus in patients with Huntington's chorea. Lancet 1 (1972) 1356-1358
-
(1972)
Lancet
, vol.1
, pp. 1356-1358
-
-
Podolsky, S.1
Leopold, N.A.2
Sax, D.S.3
-
110
-
-
16244373680
-
Lentiviral gene delivery of GDNF into the striatum of R6/2 Huntington mice fails to attenuate behavioral and neuropathological changes
-
Popovic N., Maingay M., Kirik D., and Brundin P. Lentiviral gene delivery of GDNF into the striatum of R6/2 Huntington mice fails to attenuate behavioral and neuropathological changes. Exp.Neurol. 193 (2005) 65-74
-
(2005)
Exp.Neurol.
, vol.193
, pp. 65-74
-
-
Popovic, N.1
Maingay, M.2
Kirik, D.3
Brundin, P.4
-
111
-
-
0037082198
-
Dysregulation of ascorbate release in the striatum of behaving mice expressing the Huntington's disease gene
-
Rebec G.V., Barton S.J., and Ennis M.D. Dysregulation of ascorbate release in the striatum of behaving mice expressing the Huntington's disease gene. J. Neurosci. 22 (2002) RC202
-
(2002)
J. Neurosci.
, vol.22
-
-
Rebec, G.V.1
Barton, S.J.2
Ennis, M.D.3
-
112
-
-
0042243499
-
Ascorbate treatment attenuates the Huntington behavioral phenotype in mice
-
Rebec G.V., Barton S.J., Marseilles A.M., and Collins K. Ascorbate treatment attenuates the Huntington behavioral phenotype in mice. Neuroreport 14 (2003) 1263-1265
-
(2003)
Neuroreport
, vol.14
, pp. 1263-1265
-
-
Rebec, G.V.1
Barton, S.J.2
Marseilles, A.M.3
Collins, K.4
-
113
-
-
29744431726
-
Hyperactive striatal neurons in symptomatic Huntington R6/2 mice: variations with behavioral state and repeated ascorbate treatment
-
Rebec G.V., Conroy S.K., and Barton S.J. Hyperactive striatal neurons in symptomatic Huntington R6/2 mice: variations with behavioral state and repeated ascorbate treatment. Neuroscience 137 (2006) 327-336
-
(2006)
Neuroscience
, vol.137
, pp. 327-336
-
-
Rebec, G.V.1
Conroy, S.K.2
Barton, S.J.3
-
114
-
-
0033437155
-
Riluzole therapy in Huntington's disease (HD)
-
Rosas H.D., Koroshetz W.J., Jenkins B.G., Chen Y.I., Hayden D.L., Beal M.F., and Cudkowicz M.E. Riluzole therapy in Huntington's disease (HD). Mov. Disord. 14 (1999) 326-330
-
(1999)
Mov. Disord.
, vol.14
, pp. 326-330
-
-
Rosas, H.D.1
Koroshetz, W.J.2
Jenkins, B.G.3
Chen, Y.I.4
Hayden, D.L.5
Beal, M.F.6
Cudkowicz, M.E.7
-
115
-
-
3142514201
-
Protein aggregation and neurodegenerative disease
-
Ross C.A., and Poirier M.A. Protein aggregation and neurodegenerative disease. Nat. Med. 10 (2004) S10-S17
-
(2004)
Nat. Med.
, vol.10
-
-
Ross, C.A.1
Poirier, M.A.2
-
116
-
-
34447312020
-
ESET/SETDB1 gene expression and histone H3 (K9) trimethylation in Huntington's disease
-
Ryu H., Lee J., Hagerty S.W., Soh B.Y., McAlpin S.E., Cormier K.A., Smith K.M., and Ferrante R.J. ESET/SETDB1 gene expression and histone H3 (K9) trimethylation in Huntington's disease. Proc. Natl. Acad. Sci. USA 103 (2006) 19176-19181
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 19176-19181
-
-
Ryu, H.1
Lee, J.2
Hagerty, S.W.3
Soh, B.Y.4
McAlpin, S.E.5
Cormier, K.A.6
Smith, K.M.7
Ferrante, R.J.8
-
117
-
-
0037461730
-
Pivotal role of oligomerization in expanded polyglutamine neurodegenerative disorders
-
Sánchez I., Mahlke C., and Yuan J. Pivotal role of oligomerization in expanded polyglutamine neurodegenerative disorders. Nature 421 (2003) 373-379
-
(2003)
Nature
, vol.421
, pp. 373-379
-
-
Sánchez, I.1
Mahlke, C.2
Yuan, J.3
-
118
-
-
0344875113
-
Oral uridine pro-drug PN401 decreases neurodegeneration, behavioral impairment, weight loss and mortality in the 3-nitropropionic acid mitochondrial toxin model of Huntington's disease
-
Saydoff J.A., Liu L.S., Garcia R.A., Hu Z., Li D., and von Borstel R.W. Oral uridine pro-drug PN401 decreases neurodegeneration, behavioral impairment, weight loss and mortality in the 3-nitropropionic acid mitochondrial toxin model of Huntington's disease. Brain Res. 994 (2003) 44-54
-
(2003)
Brain Res.
, vol.994
, pp. 44-54
-
-
Saydoff, J.A.1
Liu, L.S.2
Garcia, R.A.3
Hu, Z.4
Li, D.5
von Borstel, R.W.6
-
119
-
-
33750831549
-
Oral uridine pro-drug PN401 is neuroprotective in the R6/2 and N171-82Q mouse models of Huntington's disease
-
Saydoff J.A., Garcia R.A., Browne S.E., Liu L., Sheng J., Brenneman D., Hu Z., Cardin S., Gonzalez A., von Borstel R.W., Gregorio J., Burr H., and Beal M.F. Oral uridine pro-drug PN401 is neuroprotective in the R6/2 and N171-82Q mouse models of Huntington's disease. Neurobiol. Dis. 24 (2006) 455-465
-
(2006)
Neurobiol. Dis.
, vol.24
, pp. 455-465
-
-
Saydoff, J.A.1
Garcia, R.A.2
Browne, S.E.3
Liu, L.4
Sheng, J.5
Brenneman, D.6
Hu, Z.7
Cardin, S.8
Gonzalez, A.9
von Borstel, R.W.10
Gregorio, J.11
Burr, H.12
Beal, M.F.13
-
120
-
-
10744226569
-
Minocycline inhibits caspase activation and reactivation, increases the ratio of XIAP to smac/DIABLO, and reduces the mitochondrial leakage of cytochrome C and smac/DIABLO
-
Scarabelli T.M., Stephanou A., Pasini E., Gitti G., Townsend P., Lawrence K., Chen-Scarabelli C., Saravolatz L., Latchman D., Knight R., and Gardin J. Minocycline inhibits caspase activation and reactivation, increases the ratio of XIAP to smac/DIABLO, and reduces the mitochondrial leakage of cytochrome C and smac/DIABLO. J. Am. Coll. Cardiol. 43 (2004) 865-874
-
(2004)
J. Am. Coll. Cardiol.
, vol.43
, pp. 865-874
-
-
Scarabelli, T.M.1
Stephanou, A.2
Pasini, E.3
Gitti, G.4
Townsend, P.5
Lawrence, K.6
Chen-Scarabelli, C.7
Saravolatz, L.8
Latchman, D.9
Knight, R.10
Gardin, J.11
-
121
-
-
0036652765
-
Riluzole prolongs survival time and alters nuclear inclusion formation in a transgenic mouse model of Huntington's disease
-
Schiefer J., Landwehrmeyer G.B., Lüesse H.G., Sprünken A., Puls C., Milkereit A., Milkereit E., and Kosinski C.M. Riluzole prolongs survival time and alters nuclear inclusion formation in a transgenic mouse model of Huntington's disease. Mov. Disord. 17 (2002) 748-757
-
(2002)
Mov. Disord.
, vol.17
, pp. 748-757
-
-
Schiefer, J.1
Landwehrmeyer, G.B.2
Lüesse, H.G.3
Sprünken, A.4
Puls, C.5
Milkereit, A.6
Milkereit, E.7
Kosinski, C.M.8
-
122
-
-
4043164771
-
The metabotropic glutamate receptor 5 antagonist MPEP and the mGluR2 agonist LY379268 modify disease progression in a transgenic mouse model of Huntington's disease
-
Schiefer J., Sprünken A., Puls C., Lüesse H.G., Milkereit A., Milkereit E., Johann V., and Kosinski C.M. The metabotropic glutamate receptor 5 antagonist MPEP and the mGluR2 agonist LY379268 modify disease progression in a transgenic mouse model of Huntington's disease. Brain Res. 1019 (2004) 246-254
-
(2004)
Brain Res.
, vol.1019
, pp. 246-254
-
-
Schiefer, J.1
Sprünken, A.2
Puls, C.3
Lüesse, H.G.4
Milkereit, A.5
Milkereit, E.6
Johann, V.7
Kosinski, C.M.8
-
123
-
-
0034796483
-
Riluzole in Huntington's disease (HD): an open label study with one year follow up
-
Seppi K., Mueller J., Bodner T., Brandauer E., Benke T., Weirich-Schwaiger H., Poewe W., and Wenning G.K. Riluzole in Huntington's disease (HD): an open label study with one year follow up. J. Neurol. 248 (2001) 866-869
-
(2001)
J. Neurol.
, vol.248
, pp. 866-869
-
-
Seppi, K.1
Mueller, J.2
Bodner, T.3
Brandauer, E.4
Benke, T.5
Weirich-Schwaiger, H.6
Poewe, W.7
Wenning, G.K.8
-
124
-
-
0042845880
-
Minocycline and doxycycline are not beneficial in a model of Huntington's disease
-
Smith D.L., Woodman B., Mahal A., Sathasivam K., Ghazi-Noori S., Lowden P.A., Bates G.P., and Hockly E. Minocycline and doxycycline are not beneficial in a model of Huntington's disease. Ann. Neurol. 54 (2003) 186-196
-
(2003)
Ann. Neurol.
, vol.54
, pp. 186-196
-
-
Smith, D.L.1
Woodman, B.2
Mahal, A.3
Sathasivam, K.4
Ghazi-Noori, S.5
Lowden, P.A.6
Bates, G.P.7
Hockly, E.8
-
125
-
-
33745120560
-
10 formulations in Huntington's disease mice
-
10 formulations in Huntington's disease mice. Biochim. Biophys. Acta 1762 (2006) 616-626
-
(2006)
Biochim. Biophys. Acta
, vol.1762
, pp. 616-626
-
-
Smith, K.M.1
Matson, S.2
Matson, W.R.3
Cormier, K.4
Del Signore, S.J.5
Hagerty, S.W.6
Stack, E.C.7
Ryu, H.8
Ferrante, R.J.9
-
126
-
-
1542286877
-
Environmental enrichment rescues protein deficits in a mouse model of Huntington's disease, indicating a possible disease mechanism
-
Spires T.L., Grote H.E., Varshney N.K., Cordery P.M., van Dellen A., Blakemore C., and Hannan A.J. Environmental enrichment rescues protein deficits in a mouse model of Huntington's disease, indicating a possible disease mechanism. J. Neurosci. 24 (2004) 2270-2276
-
(2004)
J. Neurosci.
, vol.24
, pp. 2270-2276
-
-
Spires, T.L.1
Grote, H.E.2
Varshney, N.K.3
Cordery, P.M.4
van Dellen, A.5
Blakemore, C.6
Hannan, A.J.7
-
127
-
-
0036756963
-
CAG mutation effect on rate of progression in Huntington's disease
-
Squitieri F., Cannella M., and Simonelli M. CAG mutation effect on rate of progression in Huntington's disease. Neurol. Sci. 23 (2002) S107-S108
-
(2002)
Neurol. Sci.
, vol.23
-
-
Squitieri, F.1
Cannella, M.2
Simonelli, M.3
-
128
-
-
24144475005
-
Chronology of behavioral symptoms and neuropathological sequela in R6/2 Huntington's disease transgenic mice
-
Stack E.C., Kubilus J.K., Smith K., Cormier K., Del Signore S.J., Guelin E., Ryu H., Hersch S.M., and Ferrante R.J. Chronology of behavioral symptoms and neuropathological sequela in R6/2 Huntington's disease transgenic mice. J. Comp. Neurol. 490 (2005) 354-370
-
(2005)
J. Comp. Neurol.
, vol.490
, pp. 354-370
-
-
Stack, E.C.1
Kubilus, J.K.2
Smith, K.3
Cormier, K.4
Del Signore, S.J.5
Guelin, E.6
Ryu, H.7
Hersch, S.M.8
Ferrante, R.J.9
-
129
-
-
31644439986
-
10 in R6/2 transgenic Huntington's disease mice
-
10 in R6/2 transgenic Huntington's disease mice. Biochim. Biophys. Acta 1762 (2006) 373-380
-
(2006)
Biochim. Biophys. Acta
, vol.1762
, pp. 373-380
-
-
Stack, E.C.1
Smith, K.M.2
Ryu, H.3
Cormier, K.4
Chen, M.5
Hagerty, S.W.6
Del Signore, S.J.7
Cudkowicz, M.E.8
Friedlander, R.M.9
Ferrante, R.J.10
-
130
-
-
36348937388
-
Neuroprotective effects of synaptic modulation in Huntington's disease R6/2 mice
-
Stack E.C., Dedeoglu A., Smith K.M., Cormier K., Kubilus J.K., Bogdanov M., Matson W.R., Yang L., Jenkins B.G., Luthi-Carter R., Kowall N.W., Hersch S.M., Beal M.F., and Ferrante R.J. Neuroprotective effects of synaptic modulation in Huntington's disease R6/2 mice. J. Neurosci. 27 (2007) 12908-12915
-
(2007)
J. Neurosci.
, vol.27
, pp. 12908-12915
-
-
Stack, E.C.1
Dedeoglu, A.2
Smith, K.M.3
Cormier, K.4
Kubilus, J.K.5
Bogdanov, M.6
Matson, W.R.7
Yang, L.8
Jenkins, B.G.9
Luthi-Carter, R.10
Kowall, N.W.11
Hersch, S.M.12
Beal, M.F.13
Ferrante, R.J.14
-
131
-
-
34447302317
-
Modulation of nucleosome dynamics in Huntington's disease
-
Stack E.C., Del Signore S.J., Luthi-Carter R., Soh B.Y., Goldstein D.R., Matson S., Goodrich S., Markey A.L., Cormier K., Hagerty S.W., Smith K., Ryu H., and Ferrante R.J. Modulation of nucleosome dynamics in Huntington's disease. Hum. Mol. Genet. 16 (2007) 1164-1175
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 1164-1175
-
-
Stack, E.C.1
Del Signore, S.J.2
Luthi-Carter, R.3
Soh, B.Y.4
Goldstein, D.R.5
Matson, S.6
Goodrich, S.7
Markey, A.L.8
Cormier, K.9
Hagerty, S.W.10
Smith, K.11
Ryu, H.12
Ferrante, R.J.13
-
132
-
-
0035909330
-
Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila
-
Steffan J.S., Bodai L., Pallos J., Poelman M., McCampbell A., Apostol B.L., Kazantsev A., Schmidt E., Zhu Y.Z., Greenwald M., Kurokawa R., Housma D.E., Jackson G.R., Marsh J.L., and Thompson L.M. Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila. Nature 413 (2001) 739-743
-
(2001)
Nature
, vol.413
, pp. 739-743
-
-
Steffan, J.S.1
Bodai, L.2
Pallos, J.3
Poelman, M.4
McCampbell, A.5
Apostol, B.L.6
Kazantsev, A.7
Schmidt, E.8
Zhu, Y.Z.9
Greenwald, M.10
Kurokawa, R.11
Housma, D.E.12
Jackson, G.R.13
Marsh, J.L.14
Thompson, L.M.15
-
133
-
-
1642633757
-
Trehalose alleviates polyglutamine-mediated pathology in a mouse model of Huntington disease
-
Tanaka M., Machida Y., Niu S., Ikeda T., Jana N.R., Doi H., Kurosawa M., Nekooki M., and Nukina N. Trehalose alleviates polyglutamine-mediated pathology in a mouse model of Huntington disease. Nat. Med. 10 (2004) 148-154
-
(2004)
Nat. Med.
, vol.10
, pp. 148-154
-
-
Tanaka, M.1
Machida, Y.2
Niu, S.3
Ikeda, T.4
Jana, N.R.5
Doi, H.6
Kurosawa, M.7
Nekooki, M.8
Nukina, N.9
-
134
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
The Huntington's Disease Collaborative Research Group
-
The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72 (1993) 971-983
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
135
-
-
4444233214
-
Minocycline in Huntington's disease: a pilot study
-
Thomas M., Ashizawa T., and Jankovic J. Minocycline in Huntington's disease: a pilot study. Mov. Disord. 19 (2004) 692-695
-
(2004)
Mov. Disord.
, vol.19
, pp. 692-695
-
-
Thomas, M.1
Ashizawa, T.2
Jankovic, J.3
-
136
-
-
0034608857
-
Nonapoptotic neurodegeneration in a transgenic mouse model of Huntington's disease
-
Turmaine M., Raza A., Mahal A., Mangiarini L., Bates G.P., and Davies S.W. Nonapoptotic neurodegeneration in a transgenic mouse model of Huntington's disease. Proc. Natl. Acad. Sci. U. S. A. 97 (2000) 8093-8097
-
(2000)
Proc. Natl. Acad. Sci. U. S. A.
, vol.97
, pp. 8093-8097
-
-
Turmaine, M.1
Raza, A.2
Mahal, A.3
Mangiarini, L.4
Bates, G.P.5
Davies, S.W.6
-
137
-
-
0034643362
-
Delaying the onset of Huntington's in mice
-
van Dellen A., Blakemore C., Deacon R., York D., and Hannan A.J. Delaying the onset of Huntington's in mice. Nature 404 (2000) 721-722
-
(2000)
Nature
, vol.404
, pp. 721-722
-
-
van Dellen, A.1
Blakemore, C.2
Deacon, R.3
York, D.4
Hannan, A.J.5
-
138
-
-
0035503912
-
Anterior cingulate cortical transplantation in transgenic Huntington's disease mice
-
van Dellen A., Deacon R., York D., Blakemore C., and Hannan A.J. Anterior cingulate cortical transplantation in transgenic Huntington's disease mice. Brain. Res. Bull. 56 (2001) 313-318
-
(2001)
Brain. Res. Bull.
, vol.56
, pp. 313-318
-
-
van Dellen, A.1
Deacon, R.2
York, D.3
Blakemore, C.4
Hannan, A.J.5
-
139
-
-
0033539607
-
Running enhances neurogenesis, learning, and long-term potentiation in mice
-
van Praag H., Christie B.R., Sejnowski T.J., and Gage F.H. Running enhances neurogenesis, learning, and long-term potentiation in mice. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 13427-13431
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 13427-13431
-
-
van Praag, H.1
Christie, B.R.2
Sejnowski, T.J.3
Gage, F.H.4
-
140
-
-
0141959170
-
Creatine supplementation in Huntington's disease: a placebo-controlled pilot trial
-
Verbessem P., Lemiere J., Eijnde B.O., Swinnen S., Vanhees L., Van Leemputte M., Hespel P., and Dom R. Creatine supplementation in Huntington's disease: a placebo-controlled pilot trial. Neurology 61 (2003) 925-930
-
(2003)
Neurology
, vol.61
, pp. 925-930
-
-
Verbessem, P.1
Lemiere, J.2
Eijnde, B.O.3
Swinnen, S.4
Vanhees, L.5
Van Leemputte, M.6
Hespel, P.7
Dom, R.8
-
141
-
-
0041335559
-
Minocycline inhibits caspase-independent and -dependent mitochondrial cell death pathways in models of Huntington's disease
-
Wang X., Zhu S., Drozda M., Zhang W., Stavrovskaya I.G., Cattaneo E., Ferrante R.J., Kristal B.S., and Friedlander R.M. Minocycline inhibits caspase-independent and -dependent mitochondrial cell death pathways in models of Huntington's disease. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 10483-10487
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 10483-10487
-
-
Wang, X.1
Zhu, S.2
Drozda, M.3
Zhang, W.4
Stavrovskaya, I.G.5
Cattaneo, E.6
Ferrante, R.J.7
Kristal, B.S.8
Friedlander, R.M.9
-
142
-
-
26944458863
-
Compounds blocking mutant huntingtin toxicity identified using a Huntington's disease neuronal cell model
-
Wang W., Duan W., Igarashi S., Morita H., Nakamura M., and Ross C.A. Compounds blocking mutant huntingtin toxicity identified using a Huntington's disease neuronal cell model. Neurobiol. Dis. 20 (2005) 500-508
-
(2005)
Neurobiol. Dis.
, vol.20
, pp. 500-508
-
-
Wang, W.1
Duan, W.2
Igarashi, S.3
Morita, H.4
Nakamura, M.5
Ross, C.A.6
-
143
-
-
15944409947
-
Cerebral PET imaging and histological evidence of transglutaminase inhibitor cystamine induced neuroprotection in transgenic R6/2 mouse model of Huntington's disease
-
Wang X., Sarkar A., Cicchetti F., Yu M., Zhu A., Jokivarsi K., Saint-Pierre M., and Brownell A.L. Cerebral PET imaging and histological evidence of transglutaminase inhibitor cystamine induced neuroprotection in transgenic R6/2 mouse model of Huntington's disease. J. Neurol. Sci. 231 (2005) 57-66
-
(2005)
J. Neurol. Sci.
, vol.231
, pp. 57-66
-
-
Wang, X.1
Sarkar, A.2
Cicchetti, F.3
Yu, M.4
Zhu, A.5
Jokivarsi, K.6
Saint-Pierre, M.7
Brownell, A.L.8
-
144
-
-
26844494370
-
Clinico-pathological rescue of a model mouse of Huntington's disease by siRNA
-
Wang Y.L., Liu W., Wada E., Murata M., Wada K., and Kanazawa I. Clinico-pathological rescue of a model mouse of Huntington's disease by siRNA. Neurosci. Res. 53 (2005) 241-249
-
(2005)
Neurosci. Res.
, vol.53
, pp. 241-249
-
-
Wang, Y.L.1
Liu, W.2
Wada, E.3
Murata, M.4
Wada, K.5
Kanazawa, I.6
-
145
-
-
0032727617
-
Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70
-
Warrick J.M., Chan H.Y., Gray-Board G.L., Chai Y., Paulson H.L., and Bonini N.M. Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70. Nat. Genet. 23 (1999) 425-428
-
(1999)
Nat. Genet.
, vol.23
, pp. 425-428
-
-
Warrick, J.M.1
Chan, H.Y.2
Gray-Board, G.L.3
Chai, Y.4
Paulson, H.L.5
Bonini, N.M.6
-
146
-
-
0032502715
-
Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract
-
Wellington C.L., Ellerby L.M., Hackam A.S., Margolis R.L., Trifiro M.A., Singaraja R., McCutcheon K., Salvesen S., Propp S.S., Bromm M., Rowland K.J., Zhang T., Rasper D., Roy S., Thornberry N., Pinsky L., Kakizuka A., Ross C.A., Nicholson D.W., Bredesen D.E., and Hayden M.R. Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract. J. Biol. Chem. 273 (1998) 9158-9167
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 9158-9167
-
-
Wellington, C.L.1
Ellerby, L.M.2
Hackam, A.S.3
Margolis, R.L.4
Trifiro, M.A.5
Singaraja, R.6
McCutcheon, K.7
Salvesen, S.8
Propp, S.S.9
Bromm, M.10
Rowland, K.J.11
Zhang, T.12
Rasper, D.13
Roy, S.14
Thornberry, N.15
Pinsky, L.16
Kakizuka, A.17
Ross, C.A.18
Nicholson, D.W.19
Bredesen, D.E.20
Hayden, M.R.21
more..
-
147
-
-
33747074341
-
Predict-HD and the future of therapeutic trials
-
Wild E.J., and Tabrizi S.J. Predict-HD and the future of therapeutic trials. Lancet Neurol. 5 (2006) 724-725
-
(2006)
Lancet Neurol.
, vol.5
, pp. 724-725
-
-
Wild, E.J.1
Tabrizi, S.J.2
-
148
-
-
0042666901
-
Chronic lithium chloride treatment has variable effects on motor behaviour and survival of mice transgenic for the Huntington's disease mutation
-
Wood N.I., and Morton A.J. Chronic lithium chloride treatment has variable effects on motor behaviour and survival of mice transgenic for the Huntington's disease mutation. Brain Res. Bull. 61 (2003) 375-383
-
(2003)
Brain Res. Bull.
, vol.61
, pp. 375-383
-
-
Wood, N.I.1
Morton, A.J.2
-
149
-
-
33846295583
-
Systemic administration of Congo red does not improve motor or cognitive function in R6/2 mice
-
Wood N.I., Pallier P.N., Wanderer J., and Morton A.J. Systemic administration of Congo red does not improve motor or cognitive function in R6/2 mice. Neurobiol. Dis. 25 (2007) 342-353
-
(2007)
Neurobiol. Dis.
, vol.25
, pp. 342-353
-
-
Wood, N.I.1
Pallier, P.N.2
Wanderer, J.3
Morton, A.J.4
-
150
-
-
0034737299
-
Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease
-
Yamamoto A., Lucas J.J., and Hen R. Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease. Cell 101 (2000) 57-66
-
(2000)
Cell
, vol.101
, pp. 57-66
-
-
Yamamoto, A.1
Lucas, J.J.2
Hen, R.3
-
151
-
-
60549106602
-
Intracerebral transplantation of neural stem cells combined with trehalose ingestion alleviates pathology in a mouse model of Huntington's disease
-
Yang C.R., and Yu R.K. Intracerebral transplantation of neural stem cells combined with trehalose ingestion alleviates pathology in a mouse model of Huntington's disease. J. Neurosci. Res. 87 (2009) 26-33
-
(2009)
J. Neurosci. Res.
, vol.87
, pp. 26-33
-
-
Yang, C.R.1
Yu, R.K.2
-
152
-
-
0032957382
-
Environmental enrichment inhibits spontaneous apoptosis, prevents seizures and is neuroprotective
-
Young D., Lawlor P.A., Leone P., Dragunow M., and During M.J. Environmental enrichment inhibits spontaneous apoptosis, prevents seizures and is neuroprotective. Nat. Med. 5 (1999) 448-453
-
(1999)
Nat. Med.
, vol.5
, pp. 448-453
-
-
Young, D.1
Lawlor, P.A.2
Leone, P.3
Dragunow, M.4
During, M.J.5
-
153
-
-
0037444445
-
Mutant huntingtin causes context-dependent neurodegeneration in mice with Huntington's disease
-
Yu Z.X., Li S.H., Evans J., Pillarisetti A., Li H., and Li X.J. Mutant huntingtin causes context-dependent neurodegeneration in mice with Huntington's disease. J. Neurosci. 23 (2003) 2193-2202
-
(2003)
J. Neurosci.
, vol.23
, pp. 2193-2202
-
-
Yu, Z.X.1
Li, S.H.2
Evans, J.3
Pillarisetti, A.4
Li, H.5
Li, X.J.6
-
154
-
-
0344010993
-
Sequential activation of individual caspases, and of alterations in Bcl-2 proapoptotic signals in a mouse model of Huntington's disease
-
Zhang Y., Ona V.O., Li M., Drozda M., Dubois-Dauphin M., Przedborski S., Ferrante R.J., and Friedlander R.M. Sequential activation of individual caspases, and of alterations in Bcl-2 proapoptotic signals in a mouse model of Huntington's disease. J. Neurochem. 87 (2003) 1184-1192
-
(2003)
J. Neurochem.
, vol.87
, pp. 1184-1192
-
-
Zhang, Y.1
Ona, V.O.2
Li, M.3
Drozda, M.4
Dubois-Dauphin, M.5
Przedborski, S.6
Ferrante, R.J.7
Friedlander, R.M.8
-
155
-
-
20044390015
-
A potent small molecule inhibits polyglutamine aggregation in Huntington's disease neurons and suppresses neurodegeneration in vivo
-
Zhang X., Smith D.L., Meriin A.B., Engemann S., Russel D.E., Roark M., Washington S.L., Maxwell M.M., Marsh J.L., Thompson L.M., Wanker E.E., Young A.B., Housman D.E., Bates G.P., Sherman M.Y., and Kazantsev A.G. A potent small molecule inhibits polyglutamine aggregation in Huntington's disease neurons and suppresses neurodegeneration in vivo. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 892-897
-
(2005)
Proc. Natl. Acad. Sci. U. S. A.
, vol.102
, pp. 892-897
-
-
Zhang, X.1
Smith, D.L.2
Meriin, A.B.3
Engemann, S.4
Russel, D.E.5
Roark, M.6
Washington, S.L.7
Maxwell, M.M.8
Marsh, J.L.9
Thompson, L.M.10
Wanker, E.E.11
Young, A.B.12
Housman, D.E.13
Bates, G.P.14
Sherman, M.Y.15
Kazantsev, A.G.16
-
156
-
-
34447331291
-
Hsp27 overexpression in the R6/2 mouse model of Huntington's disease: chronic neurodegeneration does not induce Hsp27 activation
-
Zourlidou A., Gidalevitz T., Kristiansen M., Landles C., Woodman B., Wells D.J., Latchman D.S., de Belleroche J., Tabrizi S.J., Morimoto R.I., and Bates G.P. Hsp27 overexpression in the R6/2 mouse model of Huntington's disease: chronic neurodegeneration does not induce Hsp27 activation. Hum. Mol. Genet. 16 (2007) 1078-1090
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 1078-1090
-
-
Zourlidou, A.1
Gidalevitz, T.2
Kristiansen, M.3
Landles, C.4
Woodman, B.5
Wells, D.J.6
Latchman, D.S.7
de Belleroche, J.8
Tabrizi, S.J.9
Morimoto, R.I.10
Bates, G.P.11
-
157
-
-
4544310434
-
Gabapentin-lactam, but not gabapentin, reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington's disease
-
Zucker B., Ludin D.E., Gerds T.A., Lücking C.H., Landwehrmeyer G.B., and Feuerstein T.J. Gabapentin-lactam, but not gabapentin, reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington's disease. Naunyn Schmiedebergs Arch. Pharmacol. 370 (2004) 131-139
-
(2004)
Naunyn Schmiedebergs Arch. Pharmacol.
, vol.370
, pp. 131-139
-
-
Zucker, B.1
Ludin, D.E.2
Gerds, T.A.3
Lücking, C.H.4
Landwehrmeyer, G.B.5
Feuerstein, T.J.6
-
158
-
-
12744279625
-
Transcriptional dysregulation in striatal projection- and interneurons in a mouse model of Huntington's disease: neuronal selectivity and potential neuroprotective role of HAP1
-
Zucker B., Luthi-Carter R., Kama J.A., Dunah A.W., Stern E.A., Fox J.H., Standaert D.G., Young A.B., and Augood S.J. Transcriptional dysregulation in striatal projection- and interneurons in a mouse model of Huntington's disease: neuronal selectivity and potential neuroprotective role of HAP1. Hum. Mol. Genet. 14 (2005) 179-189
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 179-189
-
-
Zucker, B.1
Luthi-Carter, R.2
Kama, J.A.3
Dunah, A.W.4
Stern, E.A.5
Fox, J.H.6
Standaert, D.G.7
Young, A.B.8
Augood, S.J.9
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