-
1
-
-
45149107487
-
Mechanisms of neurodegeneration in Huntington's disease
-
DOI 10.1111/j.1460-9568.2008.06310.x
-
Gil, J. M. & Rego, A. C. Mechanisms of neurodegeneration in Huntington's disease. Eur. J. Neurosci. 27, 2803-2820 (2008) (Pubitemid 351832229)
-
(2008)
European Journal of Neuroscience
, vol.27
, Issue.11
, pp. 2803-2820
-
-
Gil, J.M.1
Rego, A.C.2
-
2
-
-
0030752709
-
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
-
DiFiglia, M. et al. Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain. Science 277, 1990-1993 (1997)
-
(1997)
Science
, vol.277
, pp. 1990-1993
-
-
Difiglia, M.1
-
3
-
-
18544400323
-
Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo
-
DOI 10.1016/S0092-8674(00)80514-0
-
Scherzinger, E. et al. Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo. Cell 90, 549-558 (1997) (Pubitemid 27347244)
-
(1997)
Cell
, vol.90
, Issue.3
, pp. 549-558
-
-
Scherzinger, E.1
Lurz, R.2
Turmaine, M.3
Mangiarini, L.4
Hollenbach, B.5
Hasenbank, R.6
Bates, G.P.7
Davies, S.W.8
Lehrach, H.9
Wanker, E.E.10
-
4
-
-
8144228406
-
Trinucleotide repeats and neurodegenerative disease
-
DOI 10.1093/brain/awh278
-
Everett, C. M. & Wood, N. W. Trinucleotide repeats and neurodegenerative disease. Brain 127, 2385-2405 (2004) (Pubitemid 39472967)
-
(2004)
Brain
, vol.127
, Issue.11
, pp. 2385-2405
-
-
Everett, C.M.1
Wood, N.W.2
-
5
-
-
0142181243
-
How does the Huntington's disease mutation damage cells?
-
Rubinsztein, D. C. How does the Huntington's disease mutation damage cells? Sci. Aging Knowledge Environ. PE26 (2003)
-
(2003)
Sci Aging Knowledge Environ. PE
, vol.26
-
-
Rubinsztein, D.C.1
-
6
-
-
0030850412
-
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3
-
DOI 10.1016/S0896-6273(00)80943-5
-
Paulson, H. L. et al. Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3. Neuron 19, 333-344 (1997) (Pubitemid 27374232)
-
(1997)
Neuron
, vol.19
, Issue.2
, pp. 333-344
-
-
Paulson, H.L.1
Perez, M.K.2
Trottier, Y.3
Trojanowski, J.Q.4
Subramony, S.H.5
Das, S.S.6
Vig, P.7
Mandel, J.-L.8
Fischbeck, K.H.9
Pittman, R.N.10
-
7
-
-
0037077040
-
Toxic proteins in neurodegenerative disease
-
DOI 10.1126/science.1067122
-
Taylor, J. P., Hardy, J. & Fischbeck, K. H. Toxic proteins in neurodegenerative disease. Science 296, 1991-1995 (2002) (Pubitemid 34627514)
-
(2002)
Science
, vol.296
, Issue.5575
, pp. 1991-1995
-
-
Taylor, J.P.1
Hardy, J.2
Fischbeck, K.H.3
-
8
-
-
45749147456
-
RNA toxicity is a component of ataxin-3 degeneration in Drosophila
-
DOI 10.1038/nature06909, PII NATURE06909
-
Li, L. B., Yu, Z., Teng, X. & Bonini, N. M. RNA toxicity is a component of ataxin-3 degeneration in Drosophila. Nature 453, 1107-1111 (2008) (Pubitemid 351871727)
-
(2008)
Nature
, vol.453
, Issue.7198
, pp. 1107-1111
-
-
Li, L.-B.1
Yu, Z.2
Teng, X.3
Bonini, N.M.4
-
9
-
-
13544270270
-
CAG repeats containing CAA interruptions form branched hairpin structures in spinocerebellar ataxia type 2 transcripts
-
DOI 10.1074/jbc.M409984200
-
Sobczak, K. & Krzyzosiak, W. J. CAG repeats containing CAA interruptions form branched hairpin structures in spinocerebellar ataxia type 2 transcripts. J. Biol. Chem. 280, 3898-3910 (2005) (Pubitemid 40223859)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.5
, pp. 3898-3910
-
-
Sobczak, K.1
Krzyzosiak, W.J.2
-
10
-
-
0142009656
-
RNA structure of trinucleotide repeats associated with human neurological diseases
-
DOI 10.1093/nar/gkg766
-
Sobczak, K., de Mezer, M., Michlewski, G., Krol, J. & Krzyzosiak, W. J. RNA structure of trinucleotide repeats associated with human neurological diseases. Nucleic Acids Res. 31, 5469-5482 (2003) (Pubitemid 37441917)
-
(2003)
Nucleic Acids Research
, vol.31
, Issue.19
, pp. 5469-5482
-
-
Sobczak, K.1
De Mezer, M.2
Michlewski, G.3
Krol, J.4
Krzyzosiak, W.J.5
-
11
-
-
78650483521
-
Atomic resolution structure of CAG RNA repeats: Structural insights and implications for the trinucleotide repeat expansion diseases
-
Kiliszek, A., Kierzek, R., Krzyzosiak, W. J. & Rypniewski, W. Atomic resolution structure of CAG RNA repeats: structural insights and implications for the trinucleotide repeat expansion diseases. Nucleic Acids Res. 38, 8370-8376 (2010)
-
(2010)
Nucleic Acids Res.
, vol.38
, pp. 8370-8376
-
-
Kiliszek, A.1
Kierzek, R.2
Krzyzosiak, W.J.3
Rypniewski, W.4
-
12
-
-
79956023002
-
Mutant CAG repeats of Huntingtin transcript fold into hairpins, form nuclear foci and are targets for RNA interference
-
de Mezer, M., Wojciechowska, M., Napierala, M., Sobczak, K. & Krzyzosiak, W. J. Mutant CAG repeats of Huntingtin transcript fold into hairpins, form nuclear foci and are targets for RNA interference. Nucleic Acids Res. 39, 3852-3863 (2011)
-
(2011)
Nucleic Acids Res.
, vol.39
, pp. 3852-3863
-
-
De Mezer, M.1
Wojciechowska, M.2
Napierala, M.3
Sobczak, K.4
Krzyzosiak, W.J.5
-
13
-
-
0029762012
-
CAG trinucleotide RNA repeats interact with RNA-binding proteins
-
McLaughlin, B. A., Spencer, C. & Eberwine, J. CAG trinucleotide RNA repeats interact with RNA-binding proteins. Am. J. Hum. Genet. 59, 561-569 (1996) (Pubitemid 26269034)
-
(1996)
American Journal of Human Genetics
, vol.59
, Issue.3
, pp. 561-569
-
-
McLaughlin, B.A.1
Spencer, C.2
Eberwine, J.3
-
14
-
-
33748373580
-
RNA-mediated neuromuscular disorders
-
DOI 10.1146/annurev.neuro.29.051605.113014
-
Ranum, L. P. & Cooper, T. A. RNA-mediated neuromuscular disorders. Annu. Rev. Neurosci. 29, 259-277 (2006) (Pubitemid 44476846)
-
(2006)
Annual Review of Neuroscience
, vol.29
, pp. 259-277
-
-
Ranum, L.P.W.1
Cooper, T.A.2
-
15
-
-
10044282898
-
A systems view of mRNP biology
-
DOI 10.1101/gad.1256904
-
Hieronymus, H. & Silver, P. A. A systems view of mRNP biology. Genes Dev. 18, 2845-2860 (2004) (Pubitemid 39602303)
-
(2004)
Genes and Development
, vol.18
, Issue.23
, pp. 2845-2860
-
-
Hieronymus, H.1
Silver, P.A.2
-
16
-
-
81155154296
-
The PP2a-specific ubiquitin ligase Mid1 is a sequence-dependent regulator of translation efficiency controlling 3-phosphoinositide dependent protein kinase-1 (PDPK-1)
-
Aranda-Orgilles, B. et al. The PP2a-specific ubiquitin ligase Mid1 is a sequence-dependent regulator of translation efficiency controlling 3-phosphoinositide dependent protein kinase-1 (PDPK-1). J. Biol. Chem. 286, 39945-39957 (2011)
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 39945-39957
-
-
Aranda-Orgilles, B.1
-
17
-
-
39549091711
-
The opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complex
-
Aranda-Orgilles, B. et al. The opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complex. Hum. Genet. 123, 163-176 (2008)
-
(2008)
Hum. Genet.
, vol.123
, pp. 163-176
-
-
Aranda-Orgilles, B.1
-
18
-
-
0035184651
-
MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation
-
DOI 10.1038/ng762
-
Trockenbacher, A. et al. MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation. Nat. Genet. 29, 287-294 (2001) (Pubitemid 33096453)
-
(2001)
Nature Genetics
, vol.29
, Issue.3
, pp. 287-294
-
-
Trockenbacher, A.1
Suckow, V.2
Foerster, J.3
Winter, J.4
Krauss, S.5
Ropers, H.-H.6
Schneider, R.7
Schweiger, S.8
-
19
-
-
79957722643
-
Control of mTORC1 signaling by the Opitz syndrome protein MID1
-
Liu, E., Knutzen, C. A., Krauss, S., Schweiger, S. & Chiang, G. G. Control of mTORC1 signaling by the Opitz syndrome protein MID1. Proc. Natl Acad. Sci. USA 108, 8680-8685 (2011)
-
(2011)
Proc. Natl Acad. Sci. USA
, vol.108
, pp. 8680-8685
-
-
Liu, E.1
Knutzen, C.A.2
Krauss, S.3
Schweiger, S.4
Chiang, G.G.5
-
20
-
-
0037178786
-
MTOR interacts with raptor to form a nutrient-sensitive complex that signals to the cell growth machinery
-
Kim, D. H. et al. mTOR interacts with raptor to form a nutrient-sensitive complex that signals to the cell growth machinery. Cell 110, 163-175 (2002)
-
(2002)
Cell
, vol.110
, pp. 163-175
-
-
Kim, D.H.1
-
21
-
-
27744569843
-
MTOR and S6K1 mediate assembly of the translation preinitiation complex through dynamic protein interchange and ordered phosphorylation events
-
DOI 10.1016/j.cell.2005.10.024, PII S0092867405011578
-
Holz, M. K., Ballif, B. A., Gygi, S. P. & Blenis, J. mTOR and S6K1 mediate assembly of the translation preinitiation complex through dynamic protein interchange and ordered phosphorylation events. Cell 123, 569-580 (2005) (Pubitemid 41608461)
-
(2005)
Cell
, vol.123
, Issue.4
, pp. 569-580
-
-
Holz, M.K.1
Ballif, B.A.2
Gygi, S.P.3
Blenis, J.4
-
22
-
-
0030949304
-
Translational controls impinging on the 5'-untranslated region and initiation factor proteins
-
DOI 10.1016/S0959-437X(97)80133-5
-
Jackson, R. J. & Wickens, M. Translational controls impinging on the 5'-untranslated region and initiation factor proteins. Curr. Opin. Genet. Dev. 7, 233-241 (1997) (Pubitemid 27206762)
-
(1997)
Current Opinion in Genetics and Development
, vol.7
, Issue.2
, pp. 233-241
-
-
Jackson, R.J.1
Wickens, M.2
-
23
-
-
0028982138
-
Growth-dependent translation of IGF-II mRNA by a rapamycin-sensitive pathway
-
Nielsen, F. C., Ostergaard, L., Nielsen, J. & Christiansen, J. Growth-dependent translation of IGF-II mRNA by a rapamycin-sensitive pathway. Nature 377, 358-362 (1995)
-
(1995)
Nature
, vol.377
, pp. 358-362
-
-
Nielsen, F.C.1
Ostergaard, L.2
Nielsen, J.3
Christiansen, J.4
-
24
-
-
5044229348
-
Molecular mechanisms of translational control
-
DOI 10.1038/nrm1488
-
Gebauer, F. & Hentze, M. W. Molecular mechanisms of translational control. Nat. Rev. Mol. Cell. Biol. 5, 827-835 (2004) (Pubitemid 39336276)
-
(2004)
Nature Reviews Molecular Cell Biology
, vol.5
, Issue.10
, pp. 827-835
-
-
Gebauer, F.1
Hentze, M.W.2
-
25
-
-
67349217986
-
Molecular mechanisms of mTOR-mediated translational control
-
Ma, X. M. & Blenis, J. Molecular mechanisms of mTOR-mediated translational control. Nat. Rev. Mol. Cell. Biol. 10, 307-318 (2009)
-
(2009)
Nat. Rev. Mol. Cell. Biol.
, vol.10
, pp. 307-318
-
-
Ma, X.M.1
Blenis, J.2
-
27
-
-
77955107974
-
RNase-assisted RNA chromatography
-
Michlewski, G. & Caceres, J. F. RNase-assisted RNA chromatography. RNA 16, 1673-1678 (2010)
-
(2010)
RNA
, vol.16
, pp. 1673-1678
-
-
Michlewski, G.1
Caceres, J.F.2
-
28
-
-
57649227693
-
Rapamycin and mTOR-independent autophagy inducers ameliorate toxicity of polyglutamineexpanded huntingtin and related proteinopathies
-
Sarkar, S., Ravikumar, B., Floto, R. A. & Rubinsztein, D. C. Rapamycin and mTOR-independent autophagy inducers ameliorate toxicity of polyglutamineexpanded huntingtin and related proteinopathies. Cell Death Differ. 16, 46-56 (2008)
-
(2008)
Cell Death Differ.
, vol.16
, pp. 46-56
-
-
Sarkar, S.1
Ravikumar, B.2
Floto, R.A.3
Rubinsztein, D.C.4
-
29
-
-
11144245626
-
The role of autophagy during the early neonatal starvation period
-
DOI 10.1038/nature03029
-
Kuma, A. et al. The role of autophagy during the early neonatal starvation period. Nature 432, 1032-1036 (2004) (Pubitemid 40052234)
-
(2004)
Nature
, vol.432
, Issue.7020
, pp. 1032-1036
-
-
Kuma, A.1
Hatano, M.2
Matsui, M.3
Yamamoto, A.4
Nakaya, H.5
Yoshimori, T.6
Ohsumi, Y.7
Tokuhisa, T.8
Mizushima, N.9
-
30
-
-
4744366210
-
Imperfect CAG repeats form diverse structures in SCA1 transcripts
-
DOI 10.1074/jbc.M405130200
-
Sobczak, K. & Krzyzosiak, W. J. Imperfect CAG repeats form diverse structures in SCA1 transcripts. J. Biol. Chem. 279, 41563-41572 (2004) (Pubitemid 39313598)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.40
, pp. 41563-41572
-
-
Sobczak, K.1
Krzyzosiak, W.J.2
-
31
-
-
2942587013
-
Mouse Huntington's disease homolog mRNA levels: Variation and allele effects
-
Dixon, K. T., Cearley, J. A., Hunter, J. M. & Detloff, P. J. Mouse Huntington's disease homolog mRNA levels: variation and allele effects. Gene Expr. 11, 221-231 (2004) (Pubitemid 38735922)
-
(2003)
Gene Expression
, vol.11
, Issue.5-6
, pp. 221-231
-
-
Dixon, K.T.1
Cearley, J.A.2
Hunter, J.M.3
Detloff, P.J.4
-
32
-
-
60849109193
-
CAG repeat lengths4or 335 attenuate the phenotype in the R6/2 Huntington's disease transgenic mouse
-
Dragatsis, I. et al. CAG repeat lengths4or 335 attenuate the phenotype in the R6/2 Huntington's disease transgenic mouse. Neurobiol. Dis. 33, 315-330 (2009)
-
(2009)
Neurobiol. Dis.
, vol.33
, pp. 315-330
-
-
Dragatsis, I.1
-
33
-
-
0032879437
-
Membrane filter assay for detection of amyloid-like polyglutamine- containing protein aggregates
-
DOI 10.1016/S0076-6879(99)09026-6
-
Wanker, E. E. et al. Membrane filter assay for detection of amyloid-like polyglutamine-containing protein aggregates. Methods Enzymol. 309, 375-386 (1999) (Pubitemid 29446461)
-
(1999)
Methods in Enzymology
, vol.309
, pp. 375-386
-
-
Wanker, E.E.1
Scherzinger, E.2
Heiser, V.3
Sittler, A.4
Eickhoff, H.5
Lehrach, H.6
-
34
-
-
4143120231
-
Muscleblind proteins regulate alternative splicing
-
DOI 10.1038/sj.emboj.7600300
-
Ho, T. H. et al. Muscleblind proteins regulate alternative splicing. EMBO J. 23, 3103-3112 (2004) (Pubitemid 39093604)
-
(2004)
EMBO Journal
, vol.23
, Issue.15
, pp. 3103-3112
-
-
Ho, T.H.1
Charlet-B, N.2
Poulos, M.G.3
Singh, G.4
Swanson, M.S.5
Cooper, T.A.6
-
35
-
-
0346243804
-
A Muscleblind Knockout Model for Myotonic Dystrophy
-
DOI 10.1126/science.1088583
-
Kanadia, R. N. et al. A muscleblind knockout model for myotonic dystrophy. Science 302, 1978-1980 (2003) (Pubitemid 37523508)
-
(2003)
Science
, vol.302
, Issue.5652
, pp. 1978-1980
-
-
Kanadia, R.N.1
Johnstone, K.A.2
Mankodi, A.3
Lungu, C.4
Thornton, C.A.5
Esson, D.6
Timmers, A.M.7
Hauswirth, W.W.8
Swanson, M.S.9
-
37
-
-
34548718165
-
Muscleblind-like 1 interacts with RNA hairpins in splicing target and pathogenic RNAs
-
DOI 10.1093/nar/gkm601
-
Yuan, Y. et al. Muscleblind-like 1 interacts with RNA hairpins in splicing target and pathogenic RNAs. Nucleic Acids Res. 35, 5474-5486 (2007) (Pubitemid 47423921)
-
(2007)
Nucleic Acids Research
, vol.35
, Issue.16
, pp. 5474-5486
-
-
Yuan, Y.1
Compton, S.A.2
Sobczak, K.3
Stenberg, M.G.4
Thornton, C.A.5
Griffith, J.D.6
Swanson, M.S.7
-
38
-
-
23744450059
-
Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy
-
DOI 10.1242/jcs.02404
-
Ho, T. H. et al. Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy. J. Cell Sci. 118, 2923-2933 (2005) (Pubitemid 41136369)
-
(2005)
Journal of Cell Science
, vol.118
, Issue.13
, pp. 2923-2933
-
-
Ho, T.H.1
Savkur, R.S.2
Poulos, M.G.3
Mancini, M.A.4
Swanson, M.S.5
Cooper, T.A.6
-
39
-
-
80455168268
-
CAG repeats mimic CUG repeats in the misregulation of alternative splicing
-
Mykowska, A., Sobczak, K., Wojciechowska, M., Kozlowski, P. & Krzyzosiak, W. J. CAG repeats mimic CUG repeats in the misregulation of alternative splicing. Nucleic Acids Res. 39, 8938-8951 (2011)
-
(2011)
Nucleic Acids Res.
, vol.39
, pp. 8938-8951
-
-
Mykowska, A.1
Sobczak, K.2
Wojciechowska, M.3
Kozlowski, P.4
Krzyzosiak, W.J.5
-
40
-
-
84855259402
-
Triplet repeat RNA structure and its role as pathogenic agent and therapeutic target
-
Krzyzosiak, W. J. et al. Triplet repeat RNA structure and its role as pathogenic agent and therapeutic target. Nucleic Acids Res. 40, 11-26 (2012)
-
(2012)
Nucleic Acids Res.
, vol.40
, pp. 11-26
-
-
Krzyzosiak, W.J.1
-
41
-
-
5444231258
-
Huntingtin processing in pathogenesis of Huntington disease
-
Qin, Z. H. & Gu, Z. L. Huntingtin processing in pathogenesis of Huntington disease. Acta. Pharmacol. Sin. 25, 1243-1249 (2004)
-
(2004)
Acta. Pharmacol. Sin.
, vol.25
, pp. 1243-1249
-
-
Qin, Z.H.1
Gu, Z.L.2
-
42
-
-
77950584656
-
Proteolysis of mutant huntingtin produces an exon 1 fragment that accumulates as an aggregated protein in neuronal nuclei in Huntington disease
-
Landles, C. et al. Proteolysis of mutant huntingtin produces an exon 1 fragment that accumulates as an aggregated protein in neuronal nuclei in Huntington disease. J. Biol. Chem. 285, 8808-8823 (2010)
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 8808-8823
-
-
Landles, C.1
-
43
-
-
67449094981
-
Mutant huntingtin N-terminal fragments of specific size mediate aggregation and toxicity in neuronal cells
-
Ratovitski, T. et al. Mutant huntingtin N-terminal fragments of specific size mediate aggregation and toxicity in neuronal cells. J. Biol. Chem. 284, 10855-10867 (2009)
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 10855-10867
-
-
Ratovitski, T.1
-
44
-
-
38649110478
-
Increased caspase-2, calpain activations and decreased mitochondrial complex II activity in cells expressing exogenous huntingtin exon 1 containing CAG repeat in the pathogenic range
-
DOI 10.1007/s10571-007-9220-7
-
Majumder, P., Raychaudhuri, S., Chattopadhyay, B. & Bhattacharyya, N. P. Increased caspase-2, calpain activations and decreased mitochondrial complex II activity in cells expressing exogenous huntingtin exon 1 containing CAG repeat in the pathogenic range. Cell. Mol. Neurobiol. 27, 1127-1145 (2007) (Pubitemid 351170078)
-
(2007)
Cellular and Molecular Neurobiology
, vol.27
, Issue.8
, pp. 1127-1145
-
-
Majumder, P.1
Raychaudhuri, S.2
Chattopadhyay, B.3
Bhattacharyya, N.P.4
-
45
-
-
79551645514
-
Perturbation with intrabodies reveals that calpain cleavage is required for degradation of huntingtin exon 1
-
Southwell, A. L. et al. Perturbation with intrabodies reveals that calpain cleavage is required for degradation of huntingtin exon 1. PLoS ONE 6, e16676 (2011)
-
(2011)
PLoS ONE
, vol.6
-
-
Southwell, A.L.1
-
46
-
-
0034646426
-
Effects of heat shock, heat shock protein 40 (HDJ-2), and proteasome inhibition on protein aggregation in cellular models of Huntington's disease
-
DOI 10.1073/pnas.97.6.2898
-
Wyttenbach, A. et al. Effects of heat shock, heat shock protein 40 (HDJ-2), and proteasome inhibition on protein aggregation in cellular models of Huntington's disease. Proc. Natl Acad. Sci. USA 97, 2898-2903 (2000) (Pubitemid 30159269)
-
(2000)
Proceedings of the National Academy of Sciences of the United States of America
, vol.97
, Issue.6
, pp. 2898-2903
-
-
Wyttenbach, A.1
Carmichael, J.2
Swartz, J.3
Furlong, R.A.4
Narain, Y.5
Rankin, J.6
Rubinsztein, D.C.7
-
47
-
-
0035336658
-
Altered proteasomal function due to the expression of polyglutamine-expanded truncated N-terminal huntingtin induces apoptosis by caspase activation through mitochondrial cytochrome c release
-
Jana, N. R., Zemskov, E. A., Wang, G. & Nukina, N. Altered proteasomal function due to the expression of polyglutamine-expanded truncated N-terminal huntingtin induces apoptosis by caspase activation through mitochondrial cytochrome c release. Hum. Mol. Genet. 10, 1049-1059 (2001) (Pubitemid 32447782)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.10
, pp. 1049-1059
-
-
Jana, N.R.1
Zemskov, E.A.2
Wang, G.-H.3
Nukina, N.4
-
48
-
-
0035947372
-
Impairment of the ubiquitin-proteasome system by protein aggregation
-
DOI 10.1126/science.292.5521.1552
-
Bence, N. F., Sampat, R. M. & Kopito, R. R. Impairment of the ubiquitinproteasome system by protein aggregation. Science 292, 1552-1555 (2001) (Pubitemid 32493425)
-
(2001)
Science
, vol.292
, Issue.5521
, pp. 1552-1555
-
-
Bence, N.F.1
Sampat, R.M.2
Kopito, R.R.3
-
49
-
-
34547807613
-
Global changes to the ubiquitin system in Huntington's disease
-
DOI 10.1038/nature06022, PII NATURE06022
-
Bennett, E. J. et al. Global changes to the ubiquitin system in Huntington's disease. Nature 448, 704-708 (2007) (Pubitemid 47236860)
-
(2007)
Nature
, vol.448
, Issue.7154
, pp. 704-708
-
-
Bennett, E.J.1
Shaler, T.A.2
Woodman, B.3
Ryu, K.-Y.4
Zaitseva, T.S.5
Becker, C.H.6
Bates, G.P.7
Schulman, H.8
Kopito, R.R.9
-
50
-
-
77955291545
-
Inhibiting the ubiquitin-proteasome system leads to preferential accumulation of toxic N-terminal mutant huntingtin fragments
-
Li, X. et al. Inhibiting the ubiquitin-proteasome system leads to preferential accumulation of toxic N-terminal mutant huntingtin fragments. Hum. Mol. Genet. 19, 2445-2455 (2010)
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 2445-2455
-
-
Li, X.1
-
51
-
-
80053563760
-
Induction of autophagy with catalytic mTOR inhibitors reduces huntingtin aggregates in a neuronal cell model
-
Roscic, A., Baldo, B., Crochemore, C., Marcellin, D. O & Paganetti, P. Induction of autophagy with catalytic mTOR inhibitors reduces huntingtin aggregates in a neuronal cell model. J. Neurochem. 119, 398-407 (2011)
-
(2011)
J. Neurochem.
, vol.119
, pp. 398-407
-
-
Roscic, A.1
Baldo, B.2
Crochemore, C.3
Marcellin, D.O.4
Paganetti, P.5
-
52
-
-
2642586352
-
Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease
-
DOI 10.1038/ng1362
-
Ravikumar, B. et al. Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease. Nat. Genet. 36, 585-595 (2004) (Pubitemid 38715985)
-
(2004)
Nature Genetics
, vol.36
, Issue.6
, pp. 585-595
-
-
Ravikumar, B.1
Vacher, C.2
Berger, Z.3
Davies, J.E.4
Luo, S.5
Oroz, L.G.6
Scaravilli, F.7
Easton, D.F.8
Duden, R.9
O'Kane, C.J.10
Rubinsztein, D.C.11
-
53
-
-
78049231804
-
A small-molecule scaffold induces autophagy in primary neurons and protects against toxicity in a Huntington disease model
-
Tsvetkov, A. S. et al. A small-molecule scaffold induces autophagy in primary neurons and protects against toxicity in a Huntington disease model. Proc. Natl Acad. Sci. USA 107, 16982-16987 (2010)
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 16982-16987
-
-
Tsvetkov, A.S.1
-
54
-
-
30744459353
-
Levels of mutant huntingtin influence the phenotypic severity of Huntington disease in YAC128 mouse models
-
DOI 10.1016/j.nbd.2005.08.007, PII S0969996105002317
-
Graham, R. K. et al. Levels of mutant huntingtin influence the phenotypic severity of Huntington disease in YAC128 mouse models. Neurobiol. Dis. 21, 444-455 (2006) (Pubitemid 43099867)
-
(2006)
Neurobiology of Disease
, vol.21
, Issue.2
, pp. 444-455
-
-
Graham, R.K.1
Slow, E.J.2
Deng, Y.3
Bissada, N.4
Lu, G.5
Pearson, J.6
Shehadeh, J.7
Leavitt, B.R.8
Raymond, L.A.9
Hayden, M.R.10
-
55
-
-
0033591465
-
Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure
-
DOI 10.1006/jmbi.1999.2700
-
Mathews, D. H., Sabina, J., Zuker, M. & Turner, D. H. Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure. J. Mol. Biol. 288, 911-940 (1999) (Pubitemid 29248642)
-
(1999)
Journal of Molecular Biology
, vol.288
, Issue.5
, pp. 911-940
-
-
Mathews, D.H.1
Sabina, J.2
Zuker, M.3
Turner, D.H.4
-
56
-
-
0042121256
-
Mfold web server for nucleic acid folding and hybridization prediction
-
DOI 10.1093/nar/gkg595
-
Zuker, M. Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res. 31, 3406-3415 (2003). (Pubitemid 37442169)
-
(2003)
Nucleic Acids Research
, vol.31
, Issue.13
, pp. 3406-3415
-
-
Zuker, M.1
|