-
1
-
-
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 (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72, 971-983
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
2
-
-
78650031174
-
Huntington's disease: From molecular pathogenesis to clinical treatment
-
Ross, C. A., and Tabrizi, S. J. (2011) Huntington's disease: from molecular pathogenesis to clinical treatment. Lancet Neurol. 10, 83-98
-
(2011)
Lancet Neurol.
, vol.10
, pp. 83-98
-
-
Ross, C.A.1
Tabrizi, S.J.2
-
3
-
-
67349122746
-
Small molecule drug discovery for Huntington's Disease
-
Fecke, W., Gianfriddo, M., Gaviraghi, G., Terstappen, G. C., and Heitz, F. (2009) Small molecule drug discovery for Huntington's Disease. Drug Discov. Today 14, 453-464
-
(2009)
Drug Discov. Today
, vol.14
, pp. 453-464
-
-
Fecke, W.1
Gianfriddo, M.2
Gaviraghi, G.3
Terstappen, G.C.4
Heitz, F.5
-
4
-
-
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
-
5
-
-
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. (2007) Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits. Proc. Natl. Acad. Sci. U.S.A. 104, 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
-
6
-
-
44449121785
-
Artificial miRNAs mitigate shRNA-mediated toxicity in the brain: Implications for the therapeutic development of RNAi
-
McBride, J. L., Boudreau, R. L., Harper, S. Q., Staber, P. D., Monteys, A. M., Martins, I., Gilmore, B. L., Burstein, H., Peluso, R. W., Polisky, B., Carter, B. J., and Davidson, B. L. (2008) Artificial miRNAs mitigate shRNA-mediated toxicity in the brain: implications for the therapeutic development of RNAi. Proc. Natl. Acad. Sci. U.S.A. 105, 5868-5873
-
(2008)
Proc. Natl. Acad. Sci. U.S.A.
, vol.105
, pp. 5868-5873
-
-
McBride, J.L.1
Boudreau, R.L.2
Harper, S.Q.3
Staber, P.D.4
Monteys, A.M.5
Martins, I.6
Gilmore, B.L.7
Burstein, H.8
Peluso, R.W.9
Polisky, B.10
Carter, B.J.11
Davidson, B.L.12
-
7
-
-
79551530731
-
Oligonucleotide therapeutic approaches for Huntington disease
-
Sah, D. W., and Aronin, N. (2011) Oligonucleotide therapeutic approaches for Huntington disease. J. Clin. Investig. 121, 500-507
-
(2011)
J. Clin. Investig.
, vol.121
, pp. 500-507
-
-
Sah, D.W.1
Aronin, N.2
-
8
-
-
0034737299
-
Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease
-
Yamamoto, A., Lucas, J. J., and Hen, R. (2000) Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease. Cell 101, 57-66
-
(2000)
Cell
, vol.101
, pp. 57-66
-
-
Yamamoto, A.1
Lucas, J.J.2
Hen, R.3
-
9
-
-
79954992107
-
Hsp70 and its molecular role in nervous system diseases
-
Turturici, G., Sconzo, G., and Geraci, F. (2011) Hsp70 and its molecular role in nervous system diseases. Biochem. Res. Int. 2011, 618127
-
(2011)
Biochem. Res. Int.
, vol.2011
, pp. 618127
-
-
Turturici, G.1
Sconzo, G.2
Geraci, F.3
-
10
-
-
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
-
11
-
-
78649685457
-
Hsp70 and Hsp40 functionally interact with soluble mutant huntingtin oligomers in a classic ATP-dependent reaction cycle
-
Lotz, G. P., Legleiter, J., Aron, R., Mitchell, E. J., Huang, S. Y., Ng, C., Glabe, C., Thompson, L. M., and Muchowski, P. J. (2010) Hsp70 and Hsp40 functionally interact with soluble mutant huntingtin oligomers in a classic ATP-dependent reaction cycle. J. Biol. Chem. 285, 38183-38193
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 38183-38193
-
-
Lotz, G.P.1
Legleiter, J.2
Aron, R.3
Mitchell, E.J.4
Huang, S.Y.5
Ng, C.6
Glabe, C.7
Thompson, L.M.8
Muchowski, P.J.9
-
12
-
-
0034608868
-
Hsp70 and hsp40 chaperones can inhibit self-assembly of polyglutamine proteins into amyloid-like fibrils
-
Muchowski, P. J., Schaffar, G., Sittler, A., Wanker, E. E., Hayer-Hartl, M. K., and Hartl, F. U. (2000) Hsp70 and hsp40 chaperones can inhibit self-assembly of polyglutamine proteins into amyloid-like fibrils. Proc. Natl. Acad. Sci. U.S.A. 97, 7841-7846
-
(2000)
Proc. Natl. Acad. Sci. U.S.A.
, vol.97
, pp. 7841-7846
-
-
Muchowski, P.J.1
Schaffar, G.2
Sittler, A.3
Wanker, E.E.4
Hayer-Hartl, M.K.5
Hartl, F.U.6
-
13
-
-
77953916528
-
HSP90 at the hub of protein homeostasis: Emerging mechanistic insights
-
Taipale, M., Jarosz, D. F., and Lindquist, S. (2010) HSP90 at the hub of protein homeostasis: emerging mechanistic insights. Nat. Rev. Mol. Cell Biol. 11, 515-528
-
(2010)
Nat. Rev. Mol. Cell Biol.
, vol.11
, pp. 515-528
-
-
Taipale, M.1
Jarosz, D.F.2
Lindquist, S.3
-
14
-
-
0037315208
-
Regulation of signaling protein function and trafficking by the hsp90/hsp70-based chaperone machinery
-
Pratt, W. B., and Toft, D. O. (2003) Regulation of signaling protein function and trafficking by the hsp90/hsp70-based chaperone machinery. Exp. Biol. Med. 228, 111-133
-
(2003)
Exp. Biol. Med.
, vol.228
, pp. 111-133
-
-
Pratt, W.B.1
Toft, D.O.2
-
15
-
-
0032569851
-
Hsp90 as a capacitor for morphological evolution
-
Rutherford, S. L., and Lindquist, S. (1998) Hsp90 as a capacitor for morphological evolution. Nature 396, 336-342
-
(1998)
Nature
, vol.396
, pp. 336-342
-
-
Rutherford, S.L.1
Lindquist, S.2
-
16
-
-
77953012604
-
Heat shock protein 90 in neurodegenerative diseases
-
Luo, W., Sun, W., Taldone, T., Rodina, A., and Chiosis, G. (2010) Heat shock protein 90 in neurodegenerative diseases. Mol. Neurodegener. 5, 24
-
(2010)
Mol. Neurodegener.
, vol.5
, pp. 24
-
-
Luo, W.1
Sun, W.2
Taldone, T.3
Rodina, A.4
Chiosis, G.5
-
17
-
-
79959985492
-
Hsp90 inhibitors as selective anticancer drugs
-
Kamal, A., and Burrows, F. J. (2004) Hsp90 inhibitors as selective anticancer drugs. Discov. Med. 4, 277-280
-
(2004)
Discov. Med.
, vol.4
, pp. 277-280
-
-
Kamal, A.1
Burrows, F.J.2
-
18
-
-
0141484615
-
A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors
-
Kamal, A., Thao, L., Sensintaffar, J., Zhang, L., Boehm, M. F., Fritz, L. C., and Burrows, F. J. (2003) A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors. Nature 425, 407-410
-
(2003)
Nature
, vol.425
, pp. 407-410
-
-
Kamal, A.1
Thao, L.2
Sensintaffar, J.3
Zhang, L.4
Boehm, M.F.5
Fritz, L.C.6
Burrows, F.J.7
-
19
-
-
0035363805
-
Geldanamycin activates a heat shock response and inhibits huntingtin aggregation in a cell culture model of Huntington's disease
-
Sittler, A., Lurz, R., Lueder, G., Priller, J., Lehrach, H., Hayer-Hartl, M. K., Hartl, F. U., and Wanker, E. E. (2001) Geldanamycin activates a heat shock response and inhibits huntingtin aggregation in a cell culture model of Huntington's disease. Hum. Mol. Genet. 10, 1307-1315
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1307-1315
-
-
Sittler, A.1
Lurz, R.2
Lueder, G.3
Priller, J.4
Lehrach, H.5
Hayer-Hartl, M.K.6
Hartl, F.U.7
Wanker, E.E.8
-
20
-
-
67650745109
-
Loss of Hsp70 exacerbates pathogenesis but not levels of fibrillar aggregates in a mouse model of Huntington's disease
-
Wacker, J. L., Huang, S. Y., Steele, A. D., Aron, R., Lotz, G. P., Nguyen, Q., Giorgini, F., Roberson, E. D., Lindquist, S., Masliah, E., and Muchowski, P. J. (2009) Loss of Hsp70 exacerbates pathogenesis but not levels of fibrillar aggregates in a mouse model of Huntington's disease. J. Neurosci. 29, 9104-9114
-
(2009)
J. Neurosci.
, vol.29
, pp. 9104-9114
-
-
Wacker, J.L.1
Huang, S.Y.2
Steele, A.D.3
Aron, R.4
Lotz, G.P.5
Nguyen, Q.6
Giorgini, F.7
Roberson, E.D.8
Lindquist, S.9
Masliah, E.10
Muchowski, P.J.11
-
21
-
-
70349087428
-
Development of a method for the high-throughput quantification of cellular proteins
-
Paganetti, P., Weiss, A., Trapp, M., Hammerl, I., Bleckmann, D., Bodner, R. A., Coven-Easter, S., Housman, D. E., and Parker, C. N. (2009) Development of a method for the high-throughput quantification of cellular proteins. Chembiochem 10, 1678-1688
-
(2009)
Chembiochem
, vol.10
, pp. 1678-1688
-
-
Paganetti, P.1
Weiss, A.2
Trapp, M.3
Hammerl, I.4
Bleckmann, D.5
Bodner, R.A.6
Coven-Easter, S.7
Housman, D.E.8
Parker, C.N.9
-
22
-
-
60849106643
-
Inducible mutant huntingtin expression in HN10 cells reproduces Huntington's disease-like neuronal dysfunction
-
Weiss, A., Roscic, A., and Paganetti, P. (2009) Inducible mutant huntingtin expression in HN10 cells reproduces Huntington's disease-like neuronal dysfunction. Mol. Neurodegener. 4, 11
-
(2009)
Mol. Neurodegener.
, vol.4
, pp. 11
-
-
Weiss, A.1
Roscic, A.2
Paganetti, P.3
-
23
-
-
0035862896
-
Neurological abnormalities in a knock-in mouse model of Huntington's disease
-
Lin, C. H., Tallaksen-Greene, S., Chien, W. M., Cearley, J. A., Jackson, W. S., Crouse, A. B., Ren, S., Li, X. J., Albin, R. L., and Detloff, P. J. (2001) Neurological abnormalities in a knock-in mouse model of Huntington's disease. Hum. Mol. Genet. 10, 137-144
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 137-144
-
-
Lin, C.H.1
Tallaksen-Greene, S.2
Chien, W.M.3
Cearley, J.A.4
Jackson, W.S.5
Crouse, A.B.6
Ren, S.7
Li, X.J.8
Albin, R.L.9
Detloff, P.J.10
-
24
-
-
44349170450
-
The ground state of embryonic stem cell self-renewal
-
Ying, Q. L., Wray, J., Nichols, J., Batlle-Morera, L., Doble, B., Woodgett, J., Cohen, P., and Smith, A. (2008) The ground state of embryonic stem cell self-renewal. Nature 453, 519-523
-
(2008)
Nature
, vol.453
, pp. 519-523
-
-
Ying, Q.L.1
Wray, J.2
Nichols, J.3
Batlle-Morera, L.4
Doble, B.5
Woodgett, J.6
Cohen, P.7
Smith, A.8
-
25
-
-
34250192881
-
Generation of a defined and uniform population of CNS progenitors and neurons from mouse embryonic stem cells
-
Bibel, M., Richter, J., Lacroix, E., and Barde, Y. A. (2007) Generation of a defined and uniform population of CNS progenitors and neurons from mouse embryonic stem cells. Nat. Protoc. 2, 1034-1043
-
(2007)
Nat. Protoc.
, vol.2
, pp. 1034-1043
-
-
Bibel, M.1
Richter, J.2
Lacroix, E.3
Barde, Y.A.4
-
26
-
-
78651318329
-
Co-chaperones are limiting in a depleted chaperone network
-
Heldens, L., Dirks, R. P., Hensen, S. M., Onnekink, C., van Genesen, S. T., Rustenburg, F., and Lubsen, N. H. (2010) Co-chaperones are limiting in a depleted chaperone network. Cell. Mol. Life Sci. 67, 4035-4048
-
(2010)
Cell. Mol. Life Sci.
, vol.67
, pp. 4035-4048
-
-
Heldens, L.1
Dirks, R.P.2
Hensen, S.M.3
Onnekink, C.4
Van Genesen, S.T.5
Rustenburg, F.6
Lubsen, N.H.7
-
27
-
-
0035502934
-
New anti-huntingtin monoclonal antibodies: Implications for huntingtin conformation and its binding proteins
-
Ko, J., Ou, S., and Patterson, P. H. (2001) New anti-huntingtin monoclonal antibodies: implications for huntingtin conformation and its binding proteins. Brain Res. Bull. 56, 319-329
-
(2001)
Brain Res. Bull.
, vol.56
, pp. 319-329
-
-
Ko, J.1
Ou, S.2
Patterson, P.H.3
-
28
-
-
70349103737
-
Single-step detection of mutant huntingtin in animal and human tissues: A bioassay for Huntington's disease
-
Weiss, A., Abramowski, D., Bibel, M., Bodner, R., Chopra, V., DiFiglia, M., Fox, J., Kegel, K., Klein, C., Grueninger, S., Hersch, S., Housman, D., Régulier, E., Rosas, H. D., Stefani, M., Zeitlin, S., Bilbe, G., and Paganetti, P. (2009) Single-step detection of mutant huntingtin in animal and human tissues: a bioassay for Huntington's disease. Anal. Biochem. 395, 8-15
-
(2009)
Anal. Biochem.
, vol.395
, pp. 8-15
-
-
Weiss, A.1
Abramowski, D.2
Bibel, M.3
Bodner, R.4
Chopra, V.5
DiFiglia, M.6
Fox, J.7
Kegel, K.8
Klein, C.9
Grueninger, S.10
Hersch, S.11
Housman, D.12
Régulier, E.13
Rosas, H.D.14
Stefani, M.15
Zeitlin, S.16
Bilbe, G.17
Paganetti, P.18
-
29
-
-
79551567075
-
Microtiter plate quantification of mutant and wild-type huntingtin normalized to cell count
-
Weiss, A., Grueninger, S., Abramowski, D., Giorgio, F. P., Lopatin, M. M., Rosas, H. D., Hersch, S., and Paganetti, P. (2011) Microtiter plate quantification of mutant and wild-type huntingtin normalized to cell count. Anal. Biochem. 410, 304-306
-
(2011)
Anal. Biochem.
, vol.410
, pp. 304-306
-
-
Weiss, A.1
Grueninger, S.2
Abramowski, D.3
Giorgio, F.P.4
Lopatin, M.M.5
Rosas, H.D.6
Hersch, S.7
Paganetti, P.8
-
30
-
-
17044392973
-
Development and implementation of a highly miniaturized confocal 2D-FIDA-based high-throughput screening assay to search for active site modulators of the human heat shock protein 90beta
-
Schilb, A., Riou, V., Schoepfer, J., Ottl, J., Müller, K., Chene, P., Mayr, L. M., and Filipuzzi, I. (2004) Development and implementation of a highly miniaturized confocal 2D-FIDA-based high-throughput screening assay to search for active site modulators of the human heat shock protein 90beta. J. Biomol. Screen. 9, 569-577
-
(2004)
J. Biomol. Screen.
, vol.9
, pp. 569-577
-
-
Schilb, A.1
Riou, V.2
Schoepfer, J.3
Ottl, J.4
Müller, K.5
Chene, P.6
Mayr, L.M.7
Filipuzzi, I.8
-
31
-
-
38349157746
-
4,5-Diarylisoxazole Hsp90 chaperone inhibitors: Potential therapeutic agents for the treatment of cancer
-
Brough, P. A., Aherne, W., Barril, X., Borgognoni, J., Boxall, K., Cansfield, J. E., Cheung, K. M., Collins, I., Davies, N. G., Drysdale, M. J., Dymock, B., Eccles, S. A., Finch, H., Fink, A., Hayes, A., Howes, R., Hubbard, R. E., James, K., Jordan, A. M., Lockie, A., Martins, V., Massey, A., Matthews, T. P., McDonald, E., Northfield, C. J., Pearl, L. H., Prodromou, C., Ray, S., Raynaud, F. I., Roughley, S. D., Sharp, S. Y., Surgenor, A., Walmsley, D. L., Webb, P., Wood, M., Workman, P., and Wright, L. (2008) 4,5-Diarylisoxazole Hsp90 chaperone inhibitors: potential therapeutic agents for the treatment of cancer. J. Med. Chem. 51, 196-218
-
(2008)
J. Med. Chem.
, vol.51
, pp. 196-218
-
-
Brough, P.A.1
Aherne, W.2
Barril, X.3
Borgognoni, J.4
Boxall, K.5
Cansfield, J.E.6
Cheung, K.M.7
Collins, I.8
Davies, N.G.9
Drysdale, M.J.10
Dymock, B.11
Eccles, S.A.12
Finch, H.13
Fink, A.14
Hayes, A.15
Howes, R.16
Hubbard, R.E.17
James, K.18
Jordan, A.M.19
Lockie, A.20
Martins, V.21
Massey, A.22
Matthews, T.P.23
McDonald, E.24
Northfield, C.J.25
Pearl, L.H.26
Prodromou, C.27
Ray, S.28
Raynaud, F.I.29
Roughley, S.D.30
Sharp, S.Y.31
Surgenor, A.32
Walmsley, D.L.33
Webb, P.34
Wood, M.35
Workman, P.36
Wright, L.37
more..
-
32
-
-
42349084306
-
NVP-AUY922: A novel heat shock protein 90 inhibitor active against xenograft tumor growth, angiogenesis, and metastasis
-
Eccles, S. A., Massey, A., Raynaud, F. I., Sharp, S. Y., Box, G., Valenti, M., Patterson, L., de Haven, B. A., Gowan, S., Boxall, F., Aherne, W., Rowlands, M., Hayes, A., Martins, V., Urban, F., Boxall, K., Prodromou, C., Pearl, L., James, K., Matthews, T. P., Cheung, K. M., Kalusa, A., Jones, K., McDonald, E., Barril, X., Brough, P. A., Cansfield, J. E., Dymock, B., Drysdale, M. J., Finch, H., Howes, R., Hubbard, R. E., Surgenor, A., Webb, P., Wood, M., Wright, L., and Workman, P. (2008) NVP-AUY922: a novel heat shock protein 90 inhibitor active against xenograft tumor growth, angiogenesis, and metastasis. Cancer Res. 68, 2850-2860
-
(2008)
Cancer Res.
, vol.68
, pp. 2850-2860
-
-
Eccles, S.A.1
Massey, A.2
Raynaud, F.I.3
Sharp, S.Y.4
Box, G.5
Valenti, M.6
Patterson, L.7
De Haven, B.A.8
Gowan, S.9
Boxall, F.10
Aherne, W.11
Rowlands, M.12
Hayes, A.13
Martins, V.14
Urban, F.15
Boxall, K.16
Prodromou, C.17
Pearl, L.18
James, K.19
Matthews, T.P.20
Cheung, K.M.21
Kalusa, A.22
Jones, K.23
McDonald, E.24
Barril, X.25
Brough, P.A.26
Cansfield, J.E.27
Dymock, B.28
Drysdale, M.J.29
Finch, H.30
Howes, R.31
Hubbard, R.E.32
Surgenor, A.33
Webb, P.34
Wood, M.35
Wright, L.36
Workman, P.37
more..
-
33
-
-
0029075280
-
Binding of p23 and hsp90 during assembly with the progesterone receptor
-
Johnson, J. L., and Toft, D. O. (1995) Binding of p23 and hsp90 during assembly with the progesterone receptor. Mol. Endocrinol. 9, 670-678
-
(1995)
Mol. Endocrinol.
, vol.9
, pp. 670-678
-
-
Johnson, J.L.1
Toft, D.O.2
-
34
-
-
0029082383
-
Inactivation of the mouse Huntington's disease gene homolog Hdh
-
Duyao, M. P., Auerbach, A. B., Ryan, A., Persichetti, F., Barnes, G. T., McNeil, S. M., Ge, P., Vonsattel, J. P., Gusella, J. F., and Joyner, A. L. (1995) Inactivation of the mouse Huntington's disease gene homolog Hdh. Science 269, 407-410
-
(1995)
Science
, vol.269
, pp. 407-410
-
-
Duyao, M.P.1
Auerbach, A.B.2
Ryan, A.3
Persichetti, F.4
Barnes, G.T.5
McNeil, S.M.6
Ge, P.7
Vonsattel, J.P.8
Gusella, J.F.9
Joyner, A.L.10
-
35
-
-
0037198547
-
Neuronal cells show regulatory differences in the hsp70 gene response
-
Kaarniranta, K., Oksala, N., Karjalainen, H. M., Suuronen, T., Sistonen, L., Helminen, H. J., Salminen, A., and Lammi, M. J. (2002) Neuronal cells show regulatory differences in the hsp70 gene response. Brain Res. Mol. Brain Res. 101, 136-140
-
(2002)
Brain Res. Mol. Brain Res.
, vol.101
, pp. 136-140
-
-
Kaarniranta, K.1
Oksala, N.2
Karjalainen, H.M.3
Suuronen, T.4
Sistonen, L.5
Helminen, H.J.6
Salminen, A.7
Lammi, M.J.8
-
36
-
-
27144503120
-
17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration
-
Waza, M., Adachi, H., Katsuno, M., Minamiyama, M., Sang, C., Tanaka, F., Inukai, A., Doyu, M., and Sobue, G. (2005) 17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration. Nat. Med. 11, 1088-1095
-
(2005)
Nat. Med.
, vol.11
, pp. 1088-1095
-
-
Waza, M.1
Adachi, H.2
Katsuno, M.3
Minamiyama, M.4
Sang, C.5
Tanaka, F.6
Inukai, A.7
Doyu, M.8
Sobue, G.9
-
37
-
-
60549084901
-
17-DMAG ameliorates polyglutamine-mediated motor neuron degeneration through well-preserved proteasome function in an SBMA model mouse
-
Tokui, K., Adachi, H., Waza, M., Katsuno, M., Minamiyama, M., Doi, H., Tanaka, K., Hamazaki, J., Murata, S., Tanaka, F., and Sobue, G. (2009) 17-DMAG ameliorates polyglutamine-mediated motor neuron degeneration through well-preserved proteasome function in an SBMA model mouse. Hum. Mol. Genet. 18, 898-910
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 898-910
-
-
Tokui, K.1
Adachi, H.2
Waza, M.3
Katsuno, M.4
Minamiyama, M.5
Doi, H.6
Tanaka, K.7
Hamazaki, J.8
Murata, S.9
Tanaka, F.10
Sobue, G.11
-
38
-
-
33744770333
-
Pharmacologic and genetic inhibition of hsp90- dependent trafficking reduces aggregation and promotes degradation of the expanded glutamine androgen receptor without stress protein induction
-
Thomas, M., Harrell, J. M., Morishima, Y., Peng, H. M., Pratt, W. B., and Lieberman, A. P. (2006) Pharmacologic and genetic inhibition of hsp90- dependent trafficking reduces aggregation and promotes degradation of the expanded glutamine androgen receptor without stress protein induction. Hum. Mol. Genet. 15, 1876-1883
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 1876-1883
-
-
Thomas, M.1
Harrell, J.M.2
Morishima, Y.3
Peng, H.M.4
Pratt, W.B.5
Lieberman, A.P.6
-
39
-
-
79961013560
-
Altered chromatin architecture underlies progressive impairment of the heat shock response in mouse models of Huntington disease
-
Labbadia, J., Cunliffe, H., Weiss, A., Katsyuba, E., Sathasivam, K., Seredenina, T., Woodman, B., Moussaoui, S., Frentzel, S., Luthi-Carter, R., Paganetti, P., and Bates, G. P. (2011) Altered chromatin architecture underlies progressive impairment of the heat shock response in mouse models of Huntington disease. J. Clin. Investig. 121, 3306-3319
-
(2011)
J. Clin. Investig.
, vol.121
, pp. 3306-3319
-
-
Labbadia, J.1
Cunliffe, H.2
Weiss, A.3
Katsyuba, E.4
Sathasivam, K.5
Seredenina, T.6
Woodman, B.7
Moussaoui, S.8
Frentzel, S.9
Luthi-Carter, R.10
Paganetti, P.11
Bates, G.P.12
-
40
-
-
34547807613
-
Global changes to the ubiquitin system in Huntington's disease
-
Bennett, E. J., Shaler, T. A., Woodman, B., Ryu, K. Y., Zaitseva, T. S., Becker, C. H., Bates, G. P., Schulman, H., and Kopito, R. R. (2007) Global changes to the ubiquitin system in Huntington's disease. Nature 448, 704-708
-
(2007)
Nature
, vol.448
, 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
-
41
-
-
14644419638
-
Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation
-
Bowman, A. B., Yoo, S. Y., Dantuma, N. P., and Zoghbi, H. Y. (2005) Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation. Hum. Mol. Genet. 14, 679-691
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 679-691
-
-
Bowman, A.B.1
Yoo, S.Y.2
Dantuma, N.P.3
Zoghbi, H.Y.4
-
42
-
-
34249802905
-
Ubiquitin-proteasome system alterations in a striatal cell model of Huntington's disease
-
Hunter, J. M., Lesort, M., and Johnson, G. V. (2007) Ubiquitin-proteasome system alterations in a striatal cell model of Huntington's disease. J. Neurosci. Res. 85, 1774-1788
-
(2007)
J. Neurosci. Res.
, vol.85
, pp. 1774-1788
-
-
Hunter, J.M.1
Lesort, M.2
Johnson, G.V.3
-
43
-
-
77949352928
-
Acute polyglutamine expression in inducible mouse model unravels ubiquitin/proteasome system impairment and permanent recovery attributable to aggregate formation
-
Ortega, Z., Díaz-Hernández, M., Maynard, C. J., Hernández, F., Dantuma, N. P., and Lucas, J. J. (2010) Acute polyglutamine expression in inducible mouse model unravels ubiquitin/proteasome system impairment and permanent recovery attributable to aggregate formation. J. Neurosci. 30, 3675-3688
-
(2010)
J. Neurosci.
, vol.30
, pp. 3675-3688
-
-
Ortega, Z.1
Díaz-Hernández, M.2
Maynard, C.J.3
Hernández, F.4
Dantuma, N.P.5
Lucas, J.J.6
-
44
-
-
29644433718
-
Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington's disease mice: Exclusion of proteasome activator REGgamma as a therapeutic target
-
Bett, J. S., Goellner, G. M., Woodman, B., Pratt, G., Rechsteiner, M., and Bates, G. P. (2006) Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington's disease mice: exclusion of proteasome activator REGgamma as a therapeutic target. Hum. Mol. Genet. 15, 33-44
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 33-44
-
-
Bett, J.S.1
Goellner, G.M.2
Woodman, B.3
Pratt, G.4
Rechsteiner, M.5
Bates, G.P.6
|