-
1
-
-
0034210773
-
The ins and outs of a polyglutamine neurodegenerative disease: Spinocerebellar ataxia type 1 (SCA1)
-
Orr, H.T. (2000) The ins and outs of a polyglutamine neurodegenerative disease: spinocerebellar ataxia type 1 (SCA1). Neurobiol. Dis., 7, 129-134.
-
(2000)
Neurobiol. Dis.
, vol.7
, pp. 129-134
-
-
Orr, H.T.1
-
2
-
-
0035475788
-
SCA1 molecular genetics: A history of a 13 year collaboration against glutamines
-
Orr, H.T. and Zoghbi, H.Y. (2001) SCA1 molecular genetics: a history of a 13 year collaboration against glutamines. Hum. Mol. Genet., 10, 2307-2311.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2307-2311
-
-
Orr, H.T.1
Zoghbi, H.Y.2
-
3
-
-
0035393427
-
SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein
-
Nakamura, K., Jeong, S.Y., Uchihara, T., Anno, M., Nagashima, K., Nagashima, T., Ikeda, S., Tsuji, S. and Kanazawa, I. (2001) SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein. Hum. Mol. Genet., 10, 1441-1448.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1441-1448
-
-
Nakamura, K.1
Jeong, S.Y.2
Uchihara, T.3
Anno, M.4
Nagashima, K.5
Nagashima, T.6
Ikeda, S.7
Tsuji, S.8
Kanazawa, I.9
-
4
-
-
0033791230
-
Protein aggregation and pathogenesis of Huntington's disease: Mechanisms and correlations
-
Wanker, E.E. (2000) Protein aggregation and pathogenesis of Huntington's disease: mechanisms and correlations. Biol. Chem., 381, 937-942.
-
(2000)
Biol. Chem.
, vol.381
, pp. 937-942
-
-
Wanker, E.E.1
-
5
-
-
0030292488
-
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
-
Pulst, S.M., Nechiporuk, A., Nechiporuk, T., Gispert, S., Chen, X.N., Lopes-Cendes, I., Pearlman, S., Starkman, S., Orozco-Diaz, G., Lunkes, A. et al. (1996) Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nat. Genet., 14, 269-276.
-
(1996)
Nat. Genet.
, vol.14
, pp. 269-276
-
-
Pulst, S.M.1
Nechiporuk, A.2
Nechiporuk, T.3
Gispert, S.4
Chen, X.N.5
Lopes-Cendes, I.6
Pearlman, S.7
Starkman, S.8
Orozco-Diaz, G.9
Lunkes, A.10
-
6
-
-
0031128793
-
SCA2 trinucleotide expansion in German SCA patients
-
Riess, O., Laccone, F.A., Gispert, S., Schols, L., Zuhlke, C., Vieira-Saecker, A.M., Herlt, S., Wessel, K., Epplen, J.T., Weber, B.H. et al. (1997) SCA2 trinucleotide expansion in German SCA patients. Neurogenetics, 1, 59-64.
-
(1997)
Neurogenetics
, vol.1
, pp. 59-64
-
-
Riess, O.1
Laccone, F.A.2
Gispert, S.3
Schols, L.4
Zuhlke, C.5
Vieira-Saecker, A.M.6
Herlt, S.7
Wessel, K.8
Epplen, J.T.9
Weber, B.H.10
-
7
-
-
15444348424
-
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds
-
Schols, L., Gispert, S., Vorgerd, M., Menezes Vieira-Saecker, A.M., Blanke, P., Auburger, G., Amoiridis, G., Meves, S., Epplen, J.T., Przuntek, H. et al. (1997) Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds. Arch. Neurol., 54, 1073-1080.
-
(1997)
Arch. Neurol.
, vol.54
, pp. 1073-1080
-
-
Schols, L.1
Gispert, S.2
Vorgerd, M.3
Menezes Vieira-Saecker, A.M.4
Blanke, P.5
Auburger, G.6
Amoiridis, G.7
Meves, S.8
Epplen, J.T.9
Przuntek, H.10
-
8
-
-
0033046989
-
Spinocerebellar ataxia 2 (SCA2): Morphometric analyses in 11 autopsies
-
Estrada, R., Galarraga, J., Orozco, G., Nodarse, A. and Auburger, G. (1999) Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies. Acta Neuropathol. (Berl.), 97, 306-310.
-
(1999)
Acta Neuropathol. (Berl.)
, vol.97
, pp. 306-310
-
-
Estrada, R.1
Galarraga, J.2
Orozco, G.3
Nodarse, A.4
Auburger, G.5
-
9
-
-
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. (1997) Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation. Cell, 90, 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
-
10
-
-
0030752709
-
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
-
DiFiglia, M., Sapp, E., Chase, K.O., Davies, S.W., Bates, G.P., Vonsattel, J.P. and Aronin, N. (1997) Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain. Science, 277, 1990-1993.
-
(1997)
Science
, vol.277
, pp. 1990-1993
-
-
DiFiglia, M.1
Sapp, E.2
Chase, K.O.3
Davies, S.W.4
Bates, G.P.5
Vonsattel, J.P.6
Aronin, N.7
-
11
-
-
0030669689
-
Polyglutamines, nuclear inclusions and neurodegeneration
-
Lunkes, A. and Mandel, J.L. (1997) Polyglutamines, nuclear inclusions and neurodegeneration. Nat. Med., 3, 1201-1202.
-
(1997)
Nat. Med.
, vol.3
, pp. 1201-1202
-
-
Lunkes, A.1
Mandel, J.L.2
-
12
-
-
0030850412
-
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3
-
Paulson, H.L., Perez, M.K., Trottier, Y., Trojanowski, J.Q., Subramony, S.H., Das, S.S., Vig, P., Mandel, J.L., Fischbeck, K.H. and Pittman, R.N. (1997b) Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3. Neuron, 19, 333-344.
-
(1997)
Neuron
, vol.19
, 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
-
13
-
-
0033044001
-
Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia type 2
-
Huynh, D.P., DelBigio, M.R., Ho, D.H. and Pulst, S.M. (1999) Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia type 2. Ann. Neurol., 45, 232-241.
-
(1999)
Ann. Neurol.
, vol.45
, pp. 232-241
-
-
Huynh, D.P.1
DelBigio, M.R.2
Ho, D.H.3
Pulst, S.M.4
-
14
-
-
0037096365
-
Polyglutamine-expanded ataxin-7 promotes non-cell-autonomous purkinje cell degeneration and displays proteolytic cleavage in ataxic transgenic mice
-
Garden, G.A., Libby, R.T., Fu, Y.H., Kinoshita, Y., Huang, J., Possin, D.E., Smith, A.C., Martinez, R.A., Fine, G.C., Grote, S.K. et al. (2002) Polyglutamine-expanded ataxin-7 promotes non-cell-autonomous purkinje cell degeneration and displays proteolytic cleavage in ataxic transgenic mice. J. Neurosci., 22, 4897-4905.
-
(2002)
J. Neurosci.
, vol.22
, pp. 4897-4905
-
-
Garden, G.A.1
Libby, R.T.2
Fu, Y.H.3
Kinoshita, Y.4
Huang, J.5
Possin, D.E.6
Smith, A.C.7
Martinez, R.A.8
Fine, G.C.9
Grote, S.K.10
-
15
-
-
0037047123
-
Live-cell imaging reveals divergent intracellular dynamics of polyglutamine disease proteins and supports a sequestration model of pathogenesis
-
Chai, Y., Shao, J., Miller, V.M., Williams, A. and Paulson, H.L. (2002) Live-cell imaging reveals divergent intracellular dynamics of polyglutamine disease proteins and supports a sequestration model of pathogenesis. Proc. Natl Acad. Sci. USA, 99, 9310-9315.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 9310-9315
-
-
Chai, Y.1
Shao, J.2
Miller, V.M.3
Williams, A.4
Paulson, H.L.5
-
16
-
-
0032475931
-
Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions
-
Saudou, F., Finkbeiner, S., Devys, D. and Greenberg, M.E. (1998) Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions. Cell, 95, 55-66.
-
(1998)
Cell
, vol.95
, pp. 55-66
-
-
Saudou, F.1
Finkbeiner, S.2
Devys, D.3
Greenberg, M.E.4
-
17
-
-
0033391428
-
Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice
-
Cummings, C.J., Reinstein, E., Sun, Y., Antalffy, B., Jiang, Y., Ciechanover, A., Orr, H.T., Beaudet, A.L. and Zoghbi, H.Y. (1999) Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice. Neuron, 24, 879-892.
-
(1999)
Neuron
, vol.24
, pp. 879-892
-
-
Cummings, C.J.1
Reinstein, E.2
Sun, Y.3
Antalffy, B.4
Jiang, Y.5
Ciechanover, A.6
Orr, H.T.7
Beaudet, A.L.8
Zoghbi, H.Y.9
-
18
-
-
0032475941
-
Ataxin-1 nuclear localization and aggregation: Role in polyglutamine-induced disease in SCA1 transgenic mice
-
Klement, I.A., Skinner, P.J., Kaytor, M.D., Yi, H., Hersch, S.M., Clark, H.B., Zoghbi, H.Y. and Orr, H.T. (1998) Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice. Cell, 95, 41-53.
-
(1998)
Cell
, vol.95
, pp. 41-53
-
-
Klement, I.A.1
Skinner, P.J.2
Kaytor, M.D.3
Yi, H.4
Hersch, S.M.5
Clark, H.B.6
Zoghbi, H.Y.7
Orr, H.T.8
-
19
-
-
0031838352
-
Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1
-
Cummings, C.J., Mancini, M.A., Antalffy, B., DeFranco, D.B., Orr, H.T. and Zoghbi, H.Y. (1998) Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1. Nat. Genet., 19, 148-154.
-
(1998)
Nat. Genet.
, vol.19
, pp. 148-154
-
-
Cummings, C.J.1
Mancini, M.A.2
Antalffy, B.3
DeFranco, D.B.4
Orr, H.T.5
Zoghbi, H.Y.6
-
20
-
-
0035394668
-
Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice
-
Cummings, C.J., Sun, Y., Opal, P., Antalffy, B., Mestril, R., Orr, H.T., Dillmann, W.H. and Zoghbi, H.Y. (2001) Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice. Hum. Mol. Genet., 10, 1511-1518.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1511-1518
-
-
Cummings, C.J.1
Sun, Y.2
Opal, P.3
Antalffy, B.4
Mestril, R.5
Orr, H.T.6
Dillmann, W.H.7
Zoghbi, H.Y.8
-
21
-
-
0032945938
-
Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone
-
Stenoien, D.L., Cummings, C.J., Adams, H.P., Mancini, M.G., Patel, K., DeMartino, G.N., Marcelli, M., Weigel, N.L. and Mancini, M.A. (1999) Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone. Hum. Mol. Genet., 8, 731-741.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 731-741
-
-
Stenoien, D.L.1
Cummings, C.J.2
Adams, H.P.3
Mancini, M.G.4
Patel, K.5
DeMartino, G.N.6
Marcelli, M.7
Weigel, N.L.8
Mancini, M.A.9
-
22
-
-
0033499931
-
Analysis of the role of heatshock protein (Hsp) molecular chaperones in polyglutamine disease
-
Chai, Y., Koppenhafer, S.L., Bonini, N.M. and Paulson, H.L. (1999) Analysis of the role of heatshock protein (Hsp) molecular chaperones in polyglutamine disease. J. Neurosci., 19, 10338-10347.
-
(1999)
J. Neurosci.
, vol.19
, pp. 10338-10347
-
-
Chai, Y.1
Koppenhafer, S.L.2
Bonini, N.M.3
Paulson, H.L.4
-
23
-
-
0033030565
-
Evidence for proteasome involvement in polyglutamine disease: Localization to nuclear inclusions in SCA3/MJD and suppression of polygutamine aggregation in vitro
-
Chai, Y., Koppenhafer, S.L., Shoesmitth, S.J., Perez, M.K. and Paulson, H.L. (1999) Evidence for proteasome involvement in polyglutamine disease: localization to nuclear inclusions in SCA3/MJD and suppression of polygutamine aggregation in vitro. Hum. Mol. Genet., 8, 673-682.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 673-682
-
-
Chai, Y.1
Koppenhafer, S.L.2
Shoesmitth, S.J.3
Perez, M.K.4
Paulson, H.L.5
-
24
-
-
14344276400
-
Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions
-
Lebre, A.S., Jamot, L., Takahashi, J., Spassky, N., Leprince, C., Ravise, N., Zander, C., Fujigasaki, H., Kussel-Andermann, P., Duyckaerts, C. et al. (2001) Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions. Hum. Mol. Genet., 10, 1201-1213.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1201-1213
-
-
Lebre, A.S.1
Jamot, L.2
Takahashi, J.3
Spassky, N.4
Leprince, C.5
Ravise, N.6
Zander, C.7
Fujigasaki, H.8
Kussel-Andermann, P.9
Duyckaerts, C.10
-
25
-
-
0035937523
-
Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity
-
Nucifora, F.C. Jr, Sasaki, M., Peters, M.F., Huang, H., Cooper, J.K., Yamada, M., Takahashi, H., Tsuji, S., Troncoso, J., Dawson, V.L. et al. (2001) Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity. Science, 291, 2423-2428.
-
(2001)
Science
, vol.291
, pp. 2423-2428
-
-
Nucifora F.C., Jr.1
Sasaki, M.2
Peters, M.F.3
Huang, H.4
Cooper, J.K.5
Yamada, M.6
Takahashi, H.7
Tsuji, S.8
Troncoso, J.9
Dawson, V.L.10
-
26
-
-
0033587128
-
Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease
-
Ona, V.O., Li, M., Vonsattel, J.P., Andrews, L.J., Khan, S.Q., Chung, W.M., Frey, A.S., Menon, A.S., Li, X.J., Stieg, P.E. et al. (1999) Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease. Nature, 399, 263-267.
-
(1999)
Nature
, vol.399
, pp. 263-267
-
-
Ona, V.O.1
Li, M.2
Vonsattel, J.P.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
-
27
-
-
0033103523
-
Caspase-8 is required for cell death induced by expanded polyglutamine repeats
-
Sanchez, I., Xu, C.J., Juo, P., Kakizaka, A., Blenis, J. and Yuan, J. (1999) Caspase-8 is required for cell death induced by expanded polyglutamine repeats. Neuron, 22, 623-633.
-
(1999)
Neuron
, vol.22
, pp. 623-633
-
-
Sanchez, I.1
Xu, C.J.2
Juo, P.3
Kakizaka, A.4
Blenis, J.5
Yuan, J.6
-
28
-
-
0032851595
-
Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization
-
Sawa, A., Wiegand, G.W., Cooper, J., Margolis, R.L., Sharp, A.H., Lawler, J.F. Jr, Greenamyre, J.T., Snyder, S.H. and Ross, C.A. (1999) Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization. Nat. Med., 5, 1194-1198.
-
(1999)
Nat. Med.
, vol.5
, pp. 1194-1198
-
-
Sawa, A.1
Wiegand, G.W.2
Cooper, J.3
Margolis, R.L.4
Sharp, A.H.5
Lawler J.F., Jr.6
Greenamyre, J.T.7
Snyder, S.H.8
Ross, C.A.9
-
29
-
-
0032840052
-
Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: Triple-labeling immunofluorescent study
-
Koyano, S., Uchihara, T., Fujigasaki, H., Nakamura, A., Yagishita, S. and Iwabuchi, K. (1999) Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study. Neurosci. Lett., 273, 117-120.
-
(1999)
Neurosci. Lett.
, vol.273
, pp. 117-120
-
-
Koyano, S.1
Uchihara, T.2
Fujigasaki, H.3
Nakamura, A.4
Yagishita, S.5
Iwabuchi, K.6
-
30
-
-
0036185711
-
Neuronal intranuclear inclusions in SCA2: A genetic, morphological and immunohistochemical study of two cases
-
Pang, J.T., Giunti, P., Chamberlain, S., An, S.F., Vitaliani, R., Scaravilli, T., Martinian, L., Wood, N.W., Scaravilli, F. and Ansorge, O. (2002) Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases. Brain, 125, 656-663.
-
(2002)
Brain
, vol.125
, pp. 656-663
-
-
Pang, J.T.1
Giunti, P.2
Chamberlain, S.3
An, S.F.4
Vitaliani, R.5
Scaravilli, T.6
Martinian, L.7
Wood, N.W.8
Scaravilli, F.9
Ansorge, O.10
-
31
-
-
0033811788
-
Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human
-
Huynh, D.P, Figueroa, K., Hoang, N. and Pulst, S.M. (2000) Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human. Nat. Genet., 26, 44-50.
-
(2000)
Nat. Genet.
, vol.26
, pp. 44-50
-
-
Huynh, D.P.1
Figueroa, K.2
Hoang, N.3
Pulst, S.M.4
-
32
-
-
0034701797
-
A novel protein with RNA-binding motifs interacts with ataxin-2
-
Shibata, H., Huynh, D.P. and Pulst, S.M. (2000) A novel protein with RNA-binding motifs interacts with ataxin-2. Hum. Mol. Genet., 9, 1303-1313.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1303-1313
-
-
Shibata, H.1
Huynh, D.P.2
Pulst, S.M.3
-
34
-
-
9344227302
-
Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract
-
Goldberg, Y.P., Nicholson, D.W., Rasper, D.M., Kalchman, M.A., Koide, H.B., Graham, R.K., Bromm, M., Kazemi-Esfarjani, P., Thornberry, N.A., Vaillancourt, J.P. et al. (1996) Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract. Nat. Genet., 13, 442-449.
-
(1996)
Nat. Genet.
, vol.13
, pp. 442-449
-
-
Goldberg, Y.P.1
Nicholson, D.W.2
Rasper, D.M.3
Kalchman, M.A.4
Koide, H.B.5
Graham, R.K.6
Bromm, M.7
Kazemi-Esfarjani, P.8
Thornberry, N.A.9
Vaillancourt, J.P.10
-
35
-
-
0031446233
-
Intranuclear neuronal inclusions: A common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?
-
Ross, C.A. (1997) Intranuclear neuronal inclusions: a common pathogenic mechanism for glutamine-repeat neurodegenerative diseases? Neuron, 19, 1147-1150.
-
(1997)
Neuron
, vol.19
, pp. 1147-1150
-
-
Ross, C.A.1
-
36
-
-
0035976953
-
The role of protein composition in specifying nuclear inclusion formation in polyglutamine disease
-
Chai, Y., Wu, L., Griffin, J.D. and Paulson, H.L. (2001) The role of protein composition in specifying nuclear inclusion formation in polyglutamine disease. J. Biol. Chem., 276, 4489-4497.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 4489-4497
-
-
Chai, Y.1
Wu, L.2
Griffin, J.D.3
Paulson, H.L.4
-
37
-
-
0030936575
-
Machado-Joseph disease gene product is a cytoplasmic protein widely expressed in brain
-
Paulson, H.L., Das, S.S., Crino, P.B., Perez, M.K., Patel, S.C., Gotsdiner, D., Fischbeck, K.H. and Pittman, R.N. (1997) Machado-Joseph disease gene product is a cytoplasmic protein widely expressed in brain. Ann. Neurol., 41, 453-462.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 453-462
-
-
Paulson, H.L.1
Das, S.S.2
Crino, P.B.3
Perez, M.K.4
Patel, S.C.5
Gotsdiner, D.6
Fischbeck, K.H.7
Pittman, R.N.8
-
38
-
-
0032517816
-
Recruitment and the role of nuclear localization in polyglutamine-mediated aggregation
-
Perez, M.K., Paulson, H.L., Pendse, S.J, Saionz, S.J. Bonini, N.M, Pittman, R.N. (1998) Recruitment and the role of nuclear localization in polyglutamine-mediated aggregation. J. Cell Biol., 143, 1457-1470.
-
(1998)
J. Cell Biol.
, vol.143
, pp. 1457-1470
-
-
Perez, M.K.1
Paulson, H.L.2
Pendse, S.J.3
Saionz, S.J.4
Bonini, N.M.5
Pittman, R.N.6
-
39
-
-
0034646426
-
Effects of heat shock, heat shock protein 40 (HDJ-2), and proteasome inhibition on protein aggregation in cellular models of Huntington's disease
-
Wyttenbach, A., Carmichael, J., Swartz, J., Furlong, R.A., Narain, Y., Rankin, J. and Rubinsztein, D.C. (2000) 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)
Proc. Natl. Acad. Sci. USA
, vol.97
, 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
-
40
-
-
0032837943
-
Ataxin-1 and ataxin-3 in neuronal intranuclear inclusion disease
-
Lieberman, A.P., Trojanowski, J.Q., Leonard, D.G., Chen, K.L., Barnett, J.L., Leverenz, J.B., Bird, T.D., Robitaille, Y., Malandrini, A. and Fishbeck, K.H. (1999) Ataxin-1 and ataxin-3 in neuronal intranuclear inclusion disease. Ann. Neurol., 46, 271-273.
-
(1999)
Ann. Neurol.
, vol.46
, pp. 271-273
-
-
Lieberman, A.P.1
Trojanowski, J.Q.2
Leonard, D.G.3
Chen, K.L.4
Barnett, J.L.5
Leverenz, J.B.6
Bird, T.D.7
Robitaille, Y.8
Malandrini, A.9
Fishbeck, K.H.10
-
41
-
-
0037017405
-
Caspase-mediated cleavage of the stacking protein GRASP65 is required for Golgi fragmentation during apoptosis
-
Lane, J.D., Lucocq, J., Pryde, J., Barr, F.A., Woodman, P.G., Allan, V.J. and Lowe, M. (2002) Caspase-mediated cleavage of the stacking protein GRASP65 is required for Golgi fragmentation during apoptosis. J. Cell Biol., 156, 495-509.
-
(2002)
J. Cell Biol.
, vol.156
, pp. 495-509
-
-
Lane, J.D.1
Lucocq, J.2
Pryde, J.3
Barr, F.A.4
Woodman, P.G.5
Allan, V.J.6
Lowe, M.7
-
42
-
-
0034307476
-
Huntingtin experession stimulates endosomal-lysosomal activity, endosome tubulation, and autophagy
-
Kegel, K.B., Kim, M., Sapp, E., McIntyre-Castano, J.G., Aronin, N. and DiFiglia, M. (2000) Huntingtin experession stimulates endosomal-lysosomal activity, endosome tubulation, and autophagy. J. Neurosci., 20, 7268-7278.
-
(2000)
J. Neurosci.
, vol.20
, pp. 7268-7278
-
-
Kegel, K.B.1
Kim, M.2
Sapp, E.3
McIntyre-Castano, J.G.4
Aronin, N.5
DiFiglia, M.6
|