-
1
-
-
0022343684
-
Selective sparing of a class of striatal neuron in Huntington's disease
-
R.J. Ferrante et al. Selective sparing of a class of striatal neuron in Huntington's disease Science 230 1985 561 564
-
(1985)
Science
, vol.230
, pp. 561-564
-
-
Ferrante, R.J.1
-
2
-
-
23444458415
-
Transcriptional activation modulated by homopolymeric glutamine and proline stretches
-
H.P. Gerber et al. Transcriptional activation modulated by homopolymeric glutamine and proline stretches Science 263 1994 808 811
-
(1994)
Science
, vol.263
, pp. 808-811
-
-
Gerber, H.P.1
-
3
-
-
0030752709
-
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neuritis in brain
-
M. DiFiglia et al. Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neuritis in brain Science 277 1997 1990 1993
-
(1997)
Science
, vol.277
, pp. 1990-1993
-
-
Difiglia, M.1
-
4
-
-
48049092846
-
Activated caspase-6 and caspase-6-cleaved fragments of huntingtin specifically colocalize in the nucleus
-
S.C. Warby et al. Activated caspase-6 and caspase-6-cleaved fragments of huntingtin specifically colocalize in the nucleus Hum. Mol. Genet. 17 2008 2390 2404
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 2390-2404
-
-
Warby, S.C.1
-
5
-
-
79952615363
-
Preferential accumulation of N-terminal mutant huntingtin in the nuclei of striatal neurons is regulated by phosphorylation
-
L.S. Havel et al. Preferential accumulation of N-terminal mutant huntingtin in the nuclei of striatal neurons is regulated by phosphorylation Hum. Mol. Genet. 20 2011 1424 1437
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 1424-1437
-
-
Havel, L.S.1
-
6
-
-
84874787234
-
An N-terminal nuclear export signal regulates trafficking and aggregation of huntingtin (Htt) protein exon 1
-
Z. Zheng et al. An N-terminal nuclear export signal regulates trafficking and aggregation of huntingtin (Htt) protein exon 1 J. Biol. Chem. 288 2013 6063 6071
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 6063-6071
-
-
Zheng, Z.1
-
7
-
-
0032475931
-
Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions
-
F. Saudou et al. Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions Cell 95 1998 55 66
-
(1998)
Cell
, vol.95
, pp. 55-66
-
-
Saudou, F.1
-
8
-
-
4344636957
-
Nuclear-targeting of mutant huntingtin fragments produces Huntington's disease-like phenotypes in transgenic mice
-
DOI 10.1093/hmg/ddh175
-
G. Schilling et al. Nuclear-targeting of mutant huntingtin fragments produces Huntington's disease-like phenotypes in transgenic mice Hum. Mol. Genet. 13 2004 1599 1610 (Pubitemid 39136716)
-
(2004)
Human Molecular Genetics
, vol.13
, Issue.15
, pp. 1599-1610
-
-
Schilling, G.1
Savonenko, A.V.2
Klevytska, A.3
Morton, J.L.4
Tucker, S.M.5
Poirier, M.6
Gale, A.7
Chan, N.8
Gonzales, V.9
Slunt, H.H.10
Coonfield, M.L.11
Jenkins, N.A.12
Copeland, N.G.13
Ross, C.A.14
Borchelt, D.R.15
-
9
-
-
27544477225
-
Contribution of nuclear and extranuclear polyQ to neurological phenotypes in mouse models of Huntington's disease
-
DOI 10.1093/hmg/ddi340
-
C.L. Benn et al. Contribution of nuclear and extranuclear polyQ to neurological phenotypes in mouse models of Huntington's disease Hum. Mol. Genet. 14 2005 3065 3078 (Pubitemid 41535471)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.20
, pp. 3065-3078
-
-
Benn, C.L.1
Landles, C.2
Li, H.3
Strand, A.D.4
Woodman, B.5
Sathasivam, K.6
Li, S.-H.7
Ghazi-Noori, S.8
Hockly, E.9
Faruque, S.M.N.N.10
Cha, J.-H.J.11
Sharpe, P.T.12
Olson, J.M.13
Li, X.-J.14
Bates, G.P.15
-
10
-
-
0037101835
-
Dysregulation of gene expression in the R6/2 model of polyglutamine disease: Parallel changes in muscle and brain
-
R. Luthi-Carter et al. 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
-
11
-
-
78149487690
-
Cleavage at the 586 amino acid caspase-6 site in mutant huntingtin influences caspase-6 activation in vivo
-
R.K. Graham et al. Cleavage at the 586 amino acid caspase-6 site in mutant huntingtin influences caspase-6 activation in vivo J. Neurosci. 30 2010 15019 15029
-
(2010)
J. Neurosci.
, vol.30
, pp. 15019-15029
-
-
Graham, R.K.1
-
12
-
-
0034702030
-
Decreased expression of striatal signaling genes in a mouse model of Huntington's disease
-
R. Luthi-Carter et al. Decreased expression of striatal signaling genes in a mouse model of Huntington's disease Hum. Mol. Genet. 9 2000 1259 1271 (Pubitemid 30312475)
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.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.J.15
Olson, J.M.16
-
13
-
-
33644783812
-
Regional and cellular gene expression changes in human Huntington's disease brain
-
DOI 10.1093/hmg/ddl013
-
A. Hodges et al. Regional and cellular gene expression changes in human Huntington's disease brain Hum. Mol. Genet. 15 2006 965 977 (Pubitemid 43338237)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.6
, pp. 965-977
-
-
Hodges, A.1
Strand, A.D.2
Aragaki, A.K.3
Kuhn, A.4
Sengstag, T.5
Hughes, G.6
Elliston, L.A.7
Hartog, C.8
Goldstein, D.R.9
Thu, D.10
Hollingsworth, Z.R.11
Collin, F.12
Synek, B.13
Holmans, P.A.14
Young, A.B.15
Wexler, N.S.16
Delorenzi, M.17
Kooperberg, C.18
Augood, S.J.19
Faull, R.L.M.20
Olson, J.M.21
Jones, L.22
Luthi-Carter, R.23
more..
-
14
-
-
0141828353
-
Mechanisms of transcriptional dysregulation in Huntington's disease
-
DOI 10.1016/S1566-2772(03)00059-8, PII S1566277203000598
-
R. Luthi-Carter, and J.-H.J. Cha Mechanisms of transcriptional dysregulation in Huntington's disease Clin. Neurosci. Res. 3 2003 165 177 (Pubitemid 37168738)
-
(2003)
Clinical Neuroscience Research
, vol.3
, Issue.3
, pp. 165-177
-
-
Luthi-Carter, R.1
Cha, J.-H.J.2
-
16
-
-
0035937523
-
Interference by huntingtin and atrophin-1 with CBP mediated transcription leading to cellular toxicity
-
F.C. Nucifora Jr. et al. Interference by huntingtin and atrophin-1 with CBP mediated transcription leading to cellular toxicity Science 291 2001 2423 2428
-
(2001)
Science
, vol.291
, pp. 2423-2428
-
-
Nucifora Jr., F.C.1
-
17
-
-
33745190716
-
Huntingtin inclusions do not downregulate specific genes in the R6/2 Huntington's disease mouse
-
G. Sadri-Vakili et al. Huntingtin inclusions do not downregulate specific genes in the R6/2 Huntington's disease mouse Eur. J. Neurosci. 23 2006 3171 3175
-
(2006)
Eur. J. Neurosci.
, vol.23
, pp. 3171-3175
-
-
Sadri-Vakili, G.1
-
18
-
-
0037090927
-
Huntingtin inclusions do not deplete polyglutamine-containing transcription factors in HD mice
-
Z.X. Yu et al. Huntingtin inclusions do not deplete polyglutamine- containing transcription factors in HD mice Hum. Mol. Genet. 11 2002 905 914
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 905-914
-
-
Yu, Z.X.1
-
19
-
-
0037150687
-
Sp1 and TAFII130 transcriptional activity disrupted in early Huntington's disease
-
DOI 10.1126/science.1072613
-
II130 transcriptional activity disrupted in early Huntington's disease Science 296 2002 2238 2243 (Pubitemid 34680312)
-
(2002)
Science
, vol.296
, Issue.5576
, pp. 2238-2243
-
-
Dunah, A.W.1
Jeong, H.2
Griffin, A.3
Kim, Y.-M.4
Standaert, D.G.5
Hersch, S.M.6
Mouradian, M.M.7
Young, A.B.8
Tanese, N.9
Krainc, D.10
-
20
-
-
33646137562
-
Decreased association of the transcription factor Sp1 with genes downregulated in Huntington's disease
-
A.S. Chen-Plotkin et al. Decreased association of the transcription factor Sp1 with genes downregulated in Huntington's disease Neurobiol. Dis. 22 2006 233 241
-
(2006)
Neurobiol. Dis.
, vol.22
, pp. 233-241
-
-
Chen-Plotkin, A.S.1
-
21
-
-
33745200299
-
Sp1 is up-regulated in cellular and transgenic models of Huntington disease, and its reduction is neuroprotective
-
Z. Qiu et al. Sp1 is up-regulated in cellular and transgenic models of Huntington disease, and its reduction is neuroprotective J. Biol. Chem. 281 2006 16672 16680
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 16672-16680
-
-
Qiu, Z.1
-
22
-
-
20844455450
-
Chemotherapy for the brain: The antitumor antibiotic mithramycin prolongs survival in a mouse model of Huntington's disease
-
DOI 10.1523/JNEUROSCI.2599-04.2004
-
R.J. Ferrante et al. Chemotherapy for the brain: the antitumor antibiotic mithramycin prolongs survival in a mouse model of Huntington's disease J. Neurosci. 24 2004 10335 10342 (Pubitemid 39552617)
-
(2004)
Journal of Neuroscience
, vol.24
, Issue.46
, 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
-
23
-
-
79955755623
-
Mithramycin is a gene-selective Sp1 inhibitor that identifies a biological intersection between cancer and neurodegeneration
-
S.F. Sleiman et al. Mithramycin is a gene-selective Sp1 inhibitor that identifies a biological intersection between cancer and neurodegeneration J. Neurosci. 31 2011 6858 6870
-
(2011)
J. Neurosci.
, vol.31
, pp. 6858-6870
-
-
Sleiman, S.F.1
-
24
-
-
1042289730
-
Decreased cAMP response element-mediated transcription. An early event in exon 1 and full-length cell models of Huntington's disease that contributes to polyglutamine pathogenesis
-
DOI 10.1074/jbc.M310226200
-
K.L. Sugars et al. Decreased cAMP response element mediated transcription: an early event in exon 1 and full-length cell models of Huntington's disease that contributes to polyglutamine pathogenesis J. Biol. Chem. 279 2004 4988 4999 (Pubitemid 38199095)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.6
, pp. 4988-4999
-
-
Sugars, K.L.1
Brown, R.2
Cook, L.J.3
Swartz, J.4
Rubinsztein, D.C.5
-
25
-
-
33749042331
-
Transcriptional Repression of PGC-1α by Mutant Huntingtin Leads to Mitochondrial Dysfunction and Neurodegeneration
-
DOI 10.1016/j.cell.2006.09.015, PII S0092867406012050
-
L. Cui et al. Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration Cell 127 2006 59 69 (Pubitemid 44466642)
-
(2006)
Cell
, vol.127
, Issue.1
, pp. 59-69
-
-
Cui, L.1
Jeong, H.2
Borovecki, F.3
Parkhurst, C.N.4
Tanese, N.5
Krainc, D.6
-
26
-
-
77956949459
-
Inhibition of transglutaminase 2 mitigates transcriptional dysregulation in models of Huntington disease
-
S.J. McConoughey et al. Inhibition of transglutaminase 2 mitigates transcriptional dysregulation in models of Huntington disease EMBO Mol. Med. 2 2010 349 370
-
(2010)
EMBO Mol. Med.
, vol.2
, pp. 349-370
-
-
McConoughey, S.J.1
-
27
-
-
28844499005
-
Mitochondrial cyclic AMP response element-binding protein (CREB) mediates mitochondrial gene expression and neuronal survival
-
DOI 10.1074/jbc.C500140200
-
J. Lee et al. Mitochondrial cyclic AMP response element-binding protein (CREB) mediates mitochondrial gene expression and neuronal survival J. Biol. Chem. 280 2005 40398 40401 (Pubitemid 41780525)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.49
, pp. 40398-40401
-
-
Lee, J.1
Kim, C.-H.2
Simon, D.K.3
Aminova, L.R.4
Andreyev, A.Y.5
Kushnareva, Y.E.6
Murphy, A.N.7
Lonze, B.E.8
Kim, K.-S.9
Ginty, D.D.10
Ferrante, R.J.11
Ryu, H.12
Ratan, R.R.13
-
28
-
-
0035909330
-
Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila
-
DOI 10.1038/35099568
-
J.S. Steffan et al. Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila Nature 413 2001 739 743 (Pubitemid 33009952)
-
(2001)
Nature
, vol.413
, Issue.6857
, 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
Housman, D.E.12
Jackson, G.R.13
Marsh, J.L.14
Thompson, L.M.15
-
29
-
-
84857674697
-
Long-term memory deficits in Huntington's disease are associated with reduced CBP histone acetylase activity
-
A. Giralt et al. Long-term memory deficits in Huntington's disease are associated with reduced CBP histone acetylase activity Hum. Mol. Genet. 21 2012 1203 1216
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 1203-1216
-
-
Giralt, A.1
-
30
-
-
33744504676
-
Mechanisms of disease: Histone modifications in Huntington's disease
-
DOI 10.1038/ncpneuro0199, PII N0199
-
G. Sadri-Vakili, and J.H. Cha Mechanisms of disease: histone modifications in Huntington's disease Nat. Clin. Pract. Neurol. 2 2006 330 338 (Pubitemid 43811543)
-
(2006)
Nature Clinical Practice Neurology
, vol.2
, Issue.6
, pp. 330-338
-
-
Sadri-Vakili, G.1
Cha, J.-H.J.2
-
31
-
-
70450192073
-
Transcriptional dysregulation of coding and non-coding genes in cellular models of Huntington's disease
-
A. Bithell et al. Transcriptional dysregulation of coding and non-coding genes in cellular models of Huntington's disease Biochem. Soc. Trans. 37 2009 1270 1275
-
(2009)
Biochem. Soc. Trans.
, vol.37
, pp. 1270-1275
-
-
Bithell, A.1
-
32
-
-
0035919701
-
Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease
-
DOI 10.1126/science.1059581
-
C. Zuccato et al. Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease Science 293 2001 493 498 (Pubitemid 32679077)
-
(2001)
Science
, vol.293
, Issue.5529
, pp. 493-498
-
-
Zuccato, C.1
Ciammola, A.2
Rigamonti, D.3
Leavitt, B.R.4
Goffredo, D.5
Conti, L.6
MacDonald, M.E.7
Friedlander, R.M.8
Silani, V.9
Hayden, M.R.10
Timmusk, T.11
Sipione, S.12
Cattaneo, E.13
-
33
-
-
0041353535
-
Huntingtin interacts with REST/NRSF to modulate the transcription of NRSE-controlled neuronal genes
-
DOI 10.1038/ng1219
-
C. Zuccato et al. Huntingtin interacts with REST/NRSF to modulate the transcription of NRSE-controlled neuronal genes Nat. Genet. 35 2003 76 83 (Pubitemid 37048599)
-
(2003)
Nature Genetics
, vol.35
, Issue.1
, pp. 76-83
-
-
Zuccato, C.1
Tartari, M.2
Crotti, A.3
Goffredo, D.4
Valenza, M.5
Conti, L.6
Cataudella, T.7
Leavitt, B.R.8
Hayden, M.R.9
Timmusk, T.10
Rigamonti, D.11
Cattaneo, E.12
-
34
-
-
39649092720
-
A microRNA-based gene dysregulation pathway in Huntington's disease
-
R. Johnson et al. A microRNA-based gene dysregulation pathway in Huntington's disease Neurobiol. Dis. 29 2008 438 445
-
(2008)
Neurobiol. Dis.
, vol.29
, pp. 438-445
-
-
Johnson, R.1
-
35
-
-
58149375393
-
The bifunctional microRNA miR-9/miR-9* regulates REST and CoREST and is downregulated in Huntington's disease
-
A. Packer et al. The bifunctional microRNA miR-9/miR-9* regulates REST and CoREST and is downregulated in Huntington's disease J. Neurosci. 28 2008 14341 14346
-
(2008)
J. Neurosci.
, vol.28
, pp. 14341-14346
-
-
Packer, A.1
-
36
-
-
84863877748
-
Sp1 regulates human huntingtin gene expression
-
R. Wang et al. Sp1 regulates human huntingtin gene expression J. Mol. Neurosci. 47 2012 311 321
-
(2012)
J. Mol. Neurosci.
, vol.47
, pp. 311-321
-
-
Wang, R.1
-
37
-
-
0037101837
-
Polyglutamine and transcription: Gene expression changes shared by DRPLA and Huntington's disease mouse models reveals context-independent effects
-
R. Luthi-Carter et al. Polyglutamine and transcription: gene expression changes shared by DRPLA and Huntington's disease mouse models reveal context independent effects Hum. Mol. Genet. 11 2002 1927 1937 (Pubitemid 34919269)
-
(2002)
Human Molecular Genetics
, vol.11
, Issue.17
, pp. 1927-1937
-
-
Luthi-Carter, R.1
Strand, A.D.2
Hanson, S.A.3
Kooperberg, C.4
Schilling, G.5
La Spada, A.R.6
Merry, D.E.7
Young, A.B.8
Ross, C.A.9
Borchelt, D.R.10
Olson, J.M.11
-
39
-
-
29244462838
-
In vitro analysis of huntingtin-mediated transcriptional repression reveals multiple transcription factor targets
-
DOI 10.1016/j.cell.2005.10.030, PII S0092867405012286
-
W. Zhai et al. In vitro analysis of huntingtin-mediated transcriptional repression reveals multiple transcription factor targets Cell 123 2005 1241 1253 (Pubitemid 41821782)
-
(2005)
Cell
, vol.123
, Issue.7
, pp. 1241-1253
-
-
Zhai, W.1
Jeong, H.2
Cui, L.3
Krainc, D.4
Tjian, R.5
-
40
-
-
19944431703
-
Neuroprotective effects of phenylbutyrate in the N171-82Q transgenic mouse model of Huntington's disease
-
DOI 10.1074/jbc.M410210200
-
G. Gardian et al. Neuroprotective effects of phenylbutyrate in the N171-82Q transgenic mouse model of Huntington's disease J. Biol. Chem. 280 2005 556 563 (Pubitemid 40165021)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.1
, pp. 556-563
-
-
Gardian, G.1
Browne, S.E.2
Choi, D.-K.3
Klivenyi, P.4
Gregorio, J.5
Kubilus, J.K.6
Ryu, H.7
Langley, B.8
Ratan, R.R.9
Ferrante, R.J.10
Beal, M.F.11
-
41
-
-
84864409298
-
Genome-wide histone acetylation is altered in a transgenic mouse model of Huntington's disease
-
K.N. McFarland et al. Genome-wide histone acetylation is altered in a transgenic mouse model of Huntington's disease PLoS ONE 7 2012 e41423
-
(2012)
PLoS ONE
, vol.7
, pp. 41423
-
-
McFarland, K.N.1
-
42
-
-
12944263711
-
The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription
-
DOI 10.1073/pnas.100110097
-
J.S. Steffan et al. The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription Proc. Natl. Acad. Sci. U. S. A. 97 2000 6763 6768 (Pubitemid 30412788)
-
(2000)
Proceedings of the National Academy of Sciences of the United States of America
, vol.97
, Issue.12
, pp. 6763-6768
-
-
Steffan, J.S.1
Kazantsev, A.2
Spasic-Boskovic, O.3
Greenwald, M.4
Zhu, Y.-Z.5
Gohler, H.6
Wanker, E.E.7
Bates, G.P.8
Housman, D.E.9
Thompson, L.M.10
-
43
-
-
34447312020
-
ESET/SETDB1 gene expression and histone H3 (K9) trimethylation in Huntington's disease
-
DOI 10.1073/pnas.0606373103
-
H. Ryu et al. ESET/SETDB1 gene expression and histone H3 (K9) trimethylation in Huntington's disease Proc. Natl. Acad. Sci. U. S. A. 103 2006 19176 19181 (Pubitemid 350002846)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.50
, pp. 19176-19181
-
-
Ryu, H.1
Lee, J.2
Hagerty, S.W.3
Byoung, Y.S.4
McAlpin, S.E.5
Cormier, K.A.6
Smith, K.M.7
Ferrante, R.J.8
-
44
-
-
43049168861
-
Altered histone monoubiquitylation mediated by mutant huntingtin induces transcriptional dysregulation
-
M.O. Kim et al. Altered histone monoubiquitylation mediated by mutant huntingtin induces transcriptional dysregulation J. Neurosci. 28 2008 3947 3957
-
(2008)
J. Neurosci.
, vol.28
, pp. 3947-3957
-
-
Kim, M.O.1
-
45
-
-
84881472626
-
Targeting H3K4 trimethylation in Huntington disease
-
M. Vashishtha et al. Targeting H3K4 trimethylation in Huntington disease Proc. Natl. Acad. Sci. U. S. A. 110 2013 E3027 E3036
-
(2013)
Proc. Natl. Acad. Sci. U. S. A.
, vol.110
-
-
Vashishtha, M.1
-
47
-
-
54849422301
-
Huntingtin modulates transcription, occupies gene promoters in vivo, and binds directly to DNA in a polyglutamine-dependent manner
-
C.L. Benn et al. Huntingtin modulates transcription, occupies gene promoters in vivo, and binds directly to DNA in a polyglutamine-dependent manner J. Neurosci. 28 2008 10720 10733
-
(2008)
J. Neurosci.
, vol.28
, pp. 10720-10733
-
-
Benn, C.L.1
-
48
-
-
84864008352
-
Promoters are differentially sensitive to N-terminal mutant huntingtin-mediated transcriptional repression
-
M. Hogel et al. Promoters are differentially sensitive to N-terminal mutant huntingtin-mediated transcriptional repression PLoS ONE 7 2012 e41152
-
(2012)
PLoS ONE
, vol.7
, pp. 41152
-
-
Hogel, M.1
-
49
-
-
24744444740
-
Mitochondrial respiration and ATP production are significantly impaired in striatal cells expressing mutant huntingtin
-
DOI 10.1074/jbc.M504749200
-
T. Milakovic, and G.V. Johnson Mitochondrial respiration and ATP production are significantly impaired in striatal cells expressing mutant huntingtin J. Biol. Chem. 280 2005 30773 30782 (Pubitemid 41291807)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.35
, pp. 30773-30782
-
-
Milakovic, T.1
Johnson, G.V.W.2
-
50
-
-
33845933438
-
Mutant Huntingtin expression induces mitochondrial calcium handling defects in clonal striatal cells: Functional consequences
-
DOI 10.1074/jbc.M603845200
-
T. Milakovic et al. Mutant huntingtin expression induces mitochondrial calcium handling defects in clonal striatal cells: functional consequences J. Biol. Chem. 281 2006 34785 34795 (Pubitemid 46036517)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.46
, pp. 34785-34795
-
-
Milakovic, T.1
Quintanilla, R.A.2
Johnson, G.V.W.3
-
51
-
-
71849091297
-
Impaired mitochondrial trafficking in Huntington's disease
-
X.J. Li et al. Impaired mitochondrial trafficking in Huntington's disease Biochim. Biophys. Acta 1802 2010 62 65
-
(2010)
Biochim. Biophys. Acta
, vol.1802
, pp. 62-65
-
-
Li, X.J.1
-
52
-
-
31544446034
-
Severe ultrastructural mitochondrial changes in lymphoblasts homozygous for Huntington disease mutation
-
DOI 10.1016/j.mad.2005.09.010, PII S0047637405002289, Dementias and Cognitive Sidorders: New Insights and Approaches
-
F. Squitieri et al. Severe ultrastructural mitochondrial changes in lymphoblasts homozygous for huntington disease mutation Mech. Ageing Dev. 127 2006 217 220 (Pubitemid 43165622)
-
(2006)
Mechanisms of Ageing and Development
, vol.127
, Issue.2
, pp. 217-220
-
-
Squitieri, F.1
Cannella, M.2
Sgarbi, G.3
Maglione, V.4
Falleni, A.5
Lenzi, P.6
Baracca, A.7
Cislaghi, G.8
Saft, C.9
Ragona, G.10
Russo, M.A.11
Thompson, L.M.12
Solaini, G.13
Fornai, F.14
-
53
-
-
36849087900
-
Harnessing hypoxic adaptation to prevent, treat, and repair stroke
-
DOI 10.1007/s00109-007-0283-1, Special Issue (Ed. G. Semenza): Hypoxia and Human Disease
-
R.R. Ratan et al. Harnessing hypoxic adaptation to prevent, treat, and repair stroke J. Mol. Med. 85 2007 1331 1338 (Pubitemid 50005503)
-
(2007)
Journal of Molecular Medicine
, vol.85
, Issue.12
, pp. 1331-1338
-
-
Ratan, R.R.1
Siddiq, A.2
Smirnova, N.3
Karpisheva, K.4
Haskew-Layton, R.5
McConoughey, S.6
Langley, B.7
Estevez, A.8
Huerta, P.T.9
Volpe, B.10
Roy, S.11
Sen, C.K.12
Gazaryan, I.13
Cho, S.14
Fink, M.15
LaManna, J.16
-
54
-
-
84863923855
-
PGC-1α rescues Huntington's disease proteotoxicity by preventing oxidative stress and promoting TFEB function
-
T. Tsunemi et al. PGC-1α rescues Huntington's disease proteotoxicity by preventing oxidative stress and promoting TFEB function Sci. Transl. Med. 4 2012 142ra97
-
(2012)
Sci. Transl. Med.
, vol.4
-
-
Tsunemi, T.1
-
55
-
-
33846386124
-
Beneficial effects of rolipram in a quinolinic acid model of striatal excitotoxicity
-
Z. DeMarch et al. Beneficial effects of rolipram in a quinolinic acid model of striatal excitotoxicity Neurobiol. Dis. 25 2007 266 273
-
(2007)
Neurobiol. Dis.
, vol.25
, pp. 266-273
-
-
Demarch, Z.1
-
56
-
-
67349165136
-
Phosphodiesterase 10 inhibition reduces striatal excitotoxicity in the quinolinic acid model of Huntington's disease
-
C. Giampa et al. Phosphodiesterase 10 inhibition reduces striatal excitotoxicity in the quinolinic acid model of Huntington's disease Neurobiol. Dis. 34 2009 450 456
-
(2009)
Neurobiol. Dis.
, vol.34
, pp. 450-456
-
-
Giampa, C.1
-
57
-
-
84884906692
-
Binding of the repressor complex REST-mSIN3b by small molecules restores neuronal gene transcription in Huntington's disease models
-
10.1111/jnc.12348
-
P. Conforti et al. Binding of the repressor complex REST-mSIN3b by small molecules restores neuronal gene transcription in Huntington's disease models J. Neurochem 2013 10.1111/jnc.12348
-
(2013)
J. Neurochem
-
-
Conforti, P.1
-
58
-
-
84882239332
-
In vivo delivery of DN:REST improves transcriptional changes of REST-regulated genes in HD mice
-
P. Conforti et al. In vivo delivery of DN:REST improves transcriptional changes of REST-regulated genes in HD mice Gene Ther. 20 2013 678 685
-
(2013)
Gene Ther.
, vol.20
, pp. 678-685
-
-
Conforti, P.1
-
59
-
-
78651318398
-
Rescue of gene expression by modified REST decoy oligonucleotides in a cellular model of Huntington's disease
-
C. Soldati et al. Rescue of gene expression by modified REST decoy oligonucleotides in a cellular model of Huntington's disease J. Neurochem. 116 2011 415 425
-
(2011)
J. Neurochem.
, vol.116
, pp. 415-425
-
-
Soldati, C.1
-
60
-
-
84876665921
-
Neuroprotective effects of PPAR-γ agonist rosiglitazone in N171-82Q mouse model of Huntington's disease
-
J. Jin et al. Neuroprotective effects of PPAR-γ agonist rosiglitazone in N171-82Q mouse model of Huntington's disease J. Neurochem. 125 2013 410 419
-
(2013)
J. Neurochem.
, vol.125
, pp. 410-419
-
-
Jin, J.1
-
61
-
-
0037386621
-
Histone deacetylase inhibitors prevent oxidative neuronal death independent of expanded polyglutamine repeats via an Sp1-dependent pathway
-
DOI 10.1073/pnas.0737363100
-
H. Ryu et al. Histone deacetylase inhibitors prevent oxidative neuronal death independent of expanded polyglutamine repeats via an Sp1-dependent pathway Proc. Natl. Acad. Sci. U. S. A. 100 2003 4281 4286 (Pubitemid 36418194)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.7
, pp. 4281-4286
-
-
Ryu, H.1
Lee, J.2
Olofsson, B.A.3
Mwidau, A.4
Deodoglu, A.5
Escudero, M.6
Flemington, E.7
Azizkhan-Clifford, J.8
Ferrante, R.J.9
Ratan, R.R.10
-
62
-
-
0142157600
-
Histone Deacetylase Inhibition by Sodium Butyrate Chemotherapy Ameliorates the Neurodegenerative Phenotype in Huntington's Disease Mice
-
R.J. Ferrante et al. Histone deacetylase inhibition by sodium butyrate chemotherapy ameliorates the neurodegenerative phenotype in Huntington's disease mice J. Neurosci. 23 2003 9418 9427 (Pubitemid 37323042)
-
(2003)
Journal of Neuroscience
, vol.23
, Issue.28
, 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
-
63
-
-
33644830913
-
Differential contributions of Caenorhabditis elegans histone deacetylases to Huntingtin polyglutamine toxicity
-
DOI 10.1523/JNEUROSCI.3344-05.2006
-
E.A. Bates et al. Differential contributions of Caenorhabditis elegans histone deacetylases to huntingtin polyglutamine toxicity J. Neurosci. 26 2006 2830 2838 (Pubitemid 43357867)
-
(2006)
Journal of Neuroscience
, vol.26
, Issue.10
, pp. 2830-2838
-
-
Bates, E.A.1
Victor, M.2
Jones, A.K.3
Shi, Y.4
Hart, A.C.5
-
64
-
-
53249114029
-
Inhibition of specific HDACs and sirtuins suppresses pathogenesis in a Drosophila model of Huntington's disease
-
J. Pallos et al. Inhibition of specific HDACs and sirtuins suppresses pathogenesis in a Drosophila model of Huntington's disease Hum. Mol. Genet. 17 2008 3767 3775
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 3767-3775
-
-
Pallos, J.1
-
65
-
-
55749103407
-
The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic mice
-
E.A. Thomas et al. The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic mice Proc. Natl. Acad. Sci. U. S. A. 105 2008 15564 15569
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 15564-15569
-
-
Thomas, E.A.1
-
66
-
-
84871706585
-
The Sirtuin 2 inhibitor AK-7 is neuroprotective in huntington disease mouse models
-
V. Chopra et al. The Sirtuin 2 inhibitor AK-7 is neuroprotective in huntington disease mouse models Cell Rep. 2 2013 1492 1497
-
(2013)
Cell Rep.
, vol.2
, pp. 1492-1497
-
-
Chopra, V.1
-
67
-
-
78349291479
-
Nicotinamide improves motor deficits and upregulates PGC-1alpha and BDNF gene expression in a mouse model of Huntington's disease
-
T. Hathorn et al. Nicotinamide improves motor deficits and upregulates PGC-1alpha and BDNF gene expression in a mouse model of Huntington's disease Neurobiol. Dis. 41 2011 43 50
-
(2011)
Neurobiol. Dis.
, vol.41
, pp. 43-50
-
-
Hathorn, T.1
-
68
-
-
79955654901
-
The influence of synaptic activity on neuronal health
-
K.F.S. Bell, and G.E. Hardingham The influence of synaptic activity on neuronal health Curr. Opin. Neurobiol. 21 2011 299 305
-
(2011)
Curr. Opin. Neurobiol.
, vol.21
, pp. 299-305
-
-
Bell, K.F.S.1
Hardingham, G.E.2
|