-
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. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72, 971-983 (1993).
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
2
-
-
28644433087
-
Normal huntingtin function: An alternative approach to Huntington's disease
-
DOI 10.1038/nrn1806
-
Cattaneo, E., Zuccato, C. & Tartari, M. Normal huntingtin function: an alternative approach to Huntington's disease. Nat. Rev. Neurosci. 6, 919-930 (2005). (Pubitemid 41753086)
-
(2005)
Nature Reviews Neuroscience
, vol.6
, Issue.12
, pp. 919-930
-
-
Cattaneo, E.1
Zuccato, C.2
Tartari, M.3
-
3
-
-
84855499458
-
Huntington's disease: Molecular basis of neurodegeneration
-
Rubinsztein, D.C. & Carmichael, J. Huntington's disease: molecular basis of neurodegeneration. Expert Rev. Mol. Med. 5, 1-21 (2003).
-
(2003)
Expert Rev. Mol. Med
, vol.5
, pp. 1-21
-
-
Rubinsztein, D.C.1
Carmichael, J.2
-
4
-
-
33846225133
-
Huntington's disease
-
DOI 10.1016/S0140-6736(07)60111-1, PII S0140673607601111
-
Walker, F.O. Huntington's disease. Lancet 369, 218-228 (2007). (Pubitemid 46107685)
-
(2007)
Lancet
, vol.369
, Issue.9557
, pp. 218-228
-
-
Walker, F.O.1
-
5
-
-
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
-
6
-
-
80051951102
-
FAT10 protein binds to polyglutamine proteins and modulates their solubility
-
Nagashima, Y., Kowa, H., Tsuji, S. & Iwata, A. FAT10 protein binds to polyglutamine proteins and modulates their solubility. J. Biol. Chem. 286, 29594-29600 (2011).
-
(2011)
J. Biol. Chem
, vol.286
, pp. 29594-29600
-
-
Nagashima, Y.1
Kowa, H.2
Tsuji, S.3
Iwata, A.4
-
7
-
-
66749167799
-
Rhes a striatal specific protein, mediates mutant-huntingtin cytotoxicity
-
Subramaniam, S., Sixt, K.M., Barrow, R. & Snyder, S.H. Rhes, a striatal specific protein, mediates mutant-huntingtin cytotoxicity. Science 324, 1327-1330 (2009).
-
(2009)
Science
, vol.324
, pp. 1327-1330
-
-
Subramaniam, S.1
Sixt, K.M.2
Barrow, R.3
Snyder, S.H.4
-
8
-
-
72149124383
-
IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosome
-
Thompson, L.M. et al. IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosome. J. Cell Biol. 187, 1083-1099 (2009).
-
(2009)
J. Cell Biol
, vol.187
, pp. 1083-1099
-
-
Thompson, L.M.1
-
9
-
-
0034737299
-
Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease
-
Yamamoto, A., Lucas, J.J. & Hen, R. Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease. Cell 101, 57-66 (2000).
-
(2000)
Cell
, vol.101
, pp. 57-66
-
-
Yamamoto, A.1
Lucas, J.J.2
Hen, R.3
-
10
-
-
36749033738
-
Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits
-
DiFiglia, M. et al. Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits. Proc. Natl. Acad. Sci. USA 104, 17204-17209 (2007).
-
(2007)
Proc. Natl. Acad. Sci. USA
, vol.104
, pp. 17204-17209
-
-
Difiglia, M.1
-
11
-
-
20244378556
-
RNA interference improves motor and neuropathological abnormalities in a Huntington's disease mouse model
-
DOI 10.1073/pnas.0501507102
-
Harper, S.Q. et al. RNA interference improves motor and neuropathological abnormalities in a Huntington's disease mouse model. Proc. Natl. Acad. Sci. USA 102, 5820-5825 (2005). (Pubitemid 40559643)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.16
, pp. 5820-5825
-
-
Harper, S.Q.1
Staber, P.D.2
He, X.3
Eliason, S.L.4
Martins, I.H.5
Mao, Q.6
Yang, L.7
Kotin, R.M.8
Paulson, H.L.9
Davidson, B.L.10
-
12
-
-
25144464388
-
Intrastriatal rAAV-mediated delivery of anti-huntingtin shRNAs induces partial reversal of disease progression in R6/1 Huntington's disease transgenic mice
-
DOI 10.1016/j.ymthe.2005.05.006, PII S1525001605002005
-
Rodriguez-Lebron, E., Denovan-Wright, E.M., Nash, K., Lewin, A.S. & Mandel, R.J. Intrastriatal rAAV-mediated delivery of anti-huntingtin shRNAs induces partial reversal of disease progression in R6/1 Huntington's disease transgenic mice. Mol. Ther. 12, 618-633 (2005). (Pubitemid 41350143)
-
(2005)
Molecular Therapy
, vol.12
, Issue.4
, pp. 618-633
-
-
Rodriguez-Lebron, E.1
Denovan-Wright, E.M.2
Nash, K.3
Lewin, A.S.4
Mandel, R.J.5
-
13
-
-
67349100160
-
Nonallele-specific silencing of mutant and wild-type huntingtin demonstrates therapeutic efficacy in Huntington's disease mice
-
Boudreau, R.L. et al. Nonallele-specific silencing of mutant and wild-type huntingtin demonstrates therapeutic efficacy in Huntington's disease mice. Mol. Ther. 17, 1053-1063 (2009).
-
(2009)
Mol. Ther
, vol.17
, pp. 1053-1063
-
-
Boudreau, R.L.1
-
14
-
-
65249131740
-
Sustained effects of nonallele-specific Huntingtin silencing
-
Drouet, V. et al. Sustained effects of nonallele-specific Huntingtin silencing. Ann. Neurol. 65, 276-285 (2009).
-
(2009)
Ann. Neurol
, vol.65
, pp. 276-285
-
-
Drouet, V.1
-
15
-
-
77749319356
-
Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein
-
Bauer, P.O. et al. Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein. Nat. Biotechnol. 28, 256-263 (2010).
-
(2010)
Nat. Biotechnol
, vol.28
, pp. 256-263
-
-
Bauer, P.O.1
-
16
-
-
57649227693
-
Rapamycin and mTOR-independent autophagy inducers ameliorate toxicity of polyglutamine-expanded huntingtin and related proteinopathies
-
Sarkar, S., Ravikumar, B., Floto, R.A. & Rubinsztein, D.C. Rapamycin and mTOR-independent autophagy inducers ameliorate toxicity of polyglutamine-expanded huntingtin and related proteinopathies. Cell Death Differ. 16, 46-56 (2009).
-
(2009)
Cell Death Differ
, vol.16
, pp. 46-56
-
-
Sarkar, S.1
Ravikumar, B.2
Floto, R.A.3
Rubinsztein, D.C.4
-
17
-
-
77950903972
-
The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy
-
Filimonenko, M. et al. The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy. Mol. Cell 38, 265-279 (2010).
-
(2010)
Mol. Cell
, vol.38
, pp. 265-279
-
-
Filimonenko, M.1
-
18
-
-
15744387323
-
Co-chaperone CHIP associates with expanded polyglutamine protein and promotes their degradation by proteasomes
-
DOI 10.1074/jbc.M412042200
-
Jana, N.R. et al. Co-chaperone CHIP associates with expanded polyglutamine protein and promotes their degradation by proteasomes. J. Biol. Chem. 280, 11635-11640 (2005). (Pubitemid 40418477)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.12
, pp. 11635-11640
-
-
Jana, N.R.1
Dikshit, P.2
Goswami, A.3
Kotliarova, S.4
Murata, S.5
Tanaka, K.6
Nukina, N.7
-
19
-
-
34249715853
-
Huntingtin interacting proteins are genetic modifiers of neurodegeneration
-
Kaltenbach, L.S. et al. Huntingtin interacting proteins are genetic modifiers of neurodegeneration. PLoS Genet. 3, e82 (2007).
-
(2007)
PLoS Genet
, vol.3
-
-
Kaltenbach, L.S.1
-
20
-
-
84863833900
-
Network organization of the huntingtin proteomic interactome in mammalian brain
-
Shirasaki, D.I. et al. Network organization of the huntingtin proteomic interactome in mammalian brain. Neuron 75, 41-57 (2012).
-
(2012)
Neuron
, vol.75
, pp. 41-57
-
-
Shirasaki, D.I.1
-
21
-
-
70349675573
-
RNAi screening in Drosophila cells identifies new modifiers of mutant huntingtin aggregation
-
Doumanis, J., Wada, K., Kino, Y., Moore, A.W. & Nukina, N. RNAi screening in Drosophila cells identifies new modifiers of mutant huntingtin aggregation. PLoS ONE 4, e7275 (2009).
-
(2009)
PLoS ONE
, vol.4
-
-
Doumanis, J.1
Wada, K.2
Kino, Y.3
Moore, A.W.4
Nukina, N.5
-
22
-
-
77955870526
-
A genomewide RNA interference screen for modifiers of aggregates formation by mutant Huntingtin in Drosophila
-
Zhang, S., Binari, R., Zhou, R. & Perrimon, N. A genomewide RNA interference screen for modifiers of aggregates formation by mutant Huntingtin in Drosophila. Genetics 184, 1165-1179 (2010).
-
(2010)
Genetics
, vol.184
, pp. 1165-1179
-
-
Zhang, S.1
Binari, R.2
Zhou, R.3
Perrimon, N.4
-
23
-
-
77955500335
-
Matrix metalloproteinases are modifiers of huntingtin proteolysis and toxicity in Huntington's disease
-
Miller, J.P. et al. Matrix metalloproteinases are modifiers of huntingtin proteolysis and toxicity in Huntington's disease. Neuron 67, 199-212 (2010).
-
(2010)
Neuron
, vol.67
, pp. 199-212
-
-
Miller, J.P.1
-
24
-
-
67650258745
-
Enhanced degradation of mutant huntingtin by rho kinase inhibition is mediated through activation of proteasome and macroautophagy
-
Bauer, P.O. & Nukina, N. Enhanced degradation of mutant huntingtin by rho kinase inhibition is mediated through activation of proteasome and macroautophagy. Autophagy 5, 747-748 (2009).
-
(2009)
Autophagy
, vol.5
, pp. 747-748
-
-
Bauer, P.O.1
Nukina, N.2
-
25
-
-
0027160708
-
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
-
Brand, A.H. & Perrimon, N. Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 118, 401-415 (1993). (Pubitemid 23214028)
-
(1993)
Development
, vol.118
, Issue.2
, pp. 401-415
-
-
Brand, A.H.1
Perrimon, N.2
-
26
-
-
33746644725
-
NUB1 suppresses the formation of Lewy body-like inclusions by proteasomal degradation of synphilin-1
-
DOI 10.2353/ajpath.2006.051067
-
Tanji, K. et al. NUB1 suppresses the formation of Lewy body-like inclusions by proteasomal degradation of synphilin-1. Am. J. Pathol. 169, 553-565 (2006). (Pubitemid 44156314)
-
(2006)
American Journal of Pathology
, vol.169
, Issue.2
, pp. 553-565
-
-
Tanji, K.1
Tanaka, T.2
Mori, F.3
Kito, K.4
Takahashi, H.5
Wakabayashi, K.6
Kamitani, T.7
-
27
-
-
0035827621
-
NUB1 a NEDD8-interacting protein, is induced by interferon and down-regulates the NEDD8 expression
-
Kito, K., Yeh, E.T. & Kamitani, T. NUB1, a NEDD8-interacting protein, is induced by interferon and down-regulates the NEDD8 expression. J. Biol. Chem. 276, 20603-20609 (2001).
-
(2001)
J. Biol. Chem
, vol.276
, pp. 20603-20609
-
-
Kito, K.1
Yeh, E.T.2
Kamitani, T.3
-
28
-
-
84863178573
-
TR-FRET-based duplex immunoassay reveals an inverse correlation of soluble and aggregated mutant huntingtin in Huntington's disease
-
Baldo, B. et al. TR-FRET-based duplex immunoassay reveals an inverse correlation of soluble and aggregated mutant huntingtin in Huntington's disease. Chem. Biol. 19, 264-275 (2012).
-
(2012)
Chem. Biol
, vol.19
, pp. 264-275
-
-
Baldo, B.1
-
29
-
-
0033119123
-
Nuclear and neuropil aggregates in Huntington's disease: Relationship to neuropathology
-
Gutekunst, C.A. et al. Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology. J. Neurosci. 19, 2522-2534 (1999).
-
(1999)
J. Neurosci
, vol.19
, pp. 2522-2534
-
-
Gutekunst, C.A.1
-
30
-
-
84877139837
-
A novel human embryonic stem cell-derived Huntington's disease neuronal model exhibits mutant huntingtin (mHTT) aggregates and soluble mHTT-dependent neurodegeneration
-
doi:10.1096/fj.12-219220 16 January 2013
-
Lu, B. & Palacino, J. A novel human embryonic stem cell-derived Huntington's disease neuronal model exhibits mutant huntingtin (mHTT) aggregates and soluble mHTT-dependent neurodegeneration. FASEB J . doi:10.1096/fj.12- 219220 (16 January 2013).
-
FASEB J
-
-
Lu, B.1
Palacino, J.2
-
31
-
-
84864628471
-
Induced pluripotent stem cells from patients with Huntington's disease show CAG-repeat-expansion-associated phenotypes
-
The HD iPSC Consortium
-
The HD iPSC Consortium. Induced pluripotent stem cells from patients with Huntington's disease show CAG-repeat-expansion-associated phenotypes. Cell Stem Cell 11, 264-278 (2012).
-
(2012)
Cell Stem Cell
, vol.11
, pp. 264-278
-
-
-
32
-
-
0035824559
-
Targeting of NEDD8 and its conjugates for proteasomal degradation by NUB1
-
Kamitani, T., Kito, K., Fukuda-Kamitani, T. & Yeh, E.T. Targeting of NEDD8 and its conjugates for proteasomal degradation by NUB1. J. Biol. Chem. 276, 46655-46660 (2001).
-
(2001)
J. Biol. Chem
, vol.276
, pp. 46655-46660
-
-
Kamitani, T.1
Kito, K.2
Fukuda-Kamitani, T.3
Yeh, E.T.4
-
33
-
-
0041856380
-
Regulation of the NEDD8 conjugation system by a splicing variant, NUB1L
-
DOI 10.1074/jbc.M212057200
-
Tanaka, T., Kawashima, H., Yeh, E.T. & Kamitani, T. Regulation of the NEDD8 conjugation system by a splicing variant, NUB1L. J. Biol. Chem. 278, 32905-32913 (2003). (Pubitemid 37055733)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.35
, pp. 32905-32913
-
-
Tanaka, T.1
Kawashima, H.2
Yeh, E.T.H.3
Kamitani, T.4
-
34
-
-
1942533448
-
NEDD8 ultimate buster-1l interacts with the ubiquitin-like protein fat10 and accelerates its degradation
-
DOI 10.1074/jbc.M310114200
-
Hipp, M.S., Raasi, S., Groettrup, M. & Schmidtke, G. NEDD8 ultimate buster-1L interacts with the ubiquitin-like protein FAT10 and accelerates its degradation. J. Biol. Chem. 279, 16503-16510 (2004). (Pubitemid 38509349)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.16
, pp. 16503-16510
-
-
Hipp, M.S.1
Raasi, S.2
Groettrup, M.3
Schmidtke, G.4
-
35
-
-
64749098830
-
An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer
-
Soucy, T.A. et al. An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer. Nature 458, 732-736 (2009).
-
(2009)
Nature
, vol.458
, pp. 732-736
-
-
Soucy, T.A.1
-
36
-
-
34447135496
-
Substrate-mediated regulation of cullin neddylation
-
DOI 10.1074/jbc.M701153200
-
Chew, E.H. & Hagen, T. Substrate-mediated regulation of cullin neddylation. J. Biol. Chem. 282, 17032-17040 (2007). (Pubitemid 47093199)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.23
, pp. 17032-17040
-
-
Chew, E.-H.1
Hagen, T.2
-
37
-
-
0027521002
-
Interferon beta-1b is effective in relapsing-remitting multiple sclerosis. II. MRI analysis results of a multicenter, randomized, double-blind, placebo- controlled trial
-
Paty, D.W., Li, D.K. & the UBC MS/MRI Study Group & the IFNB Multiple Sclerosis Study Group. Interferon beta-1b is effective in relapsing-remitting multiple sclerosis. II. MRI analysis results of a multicenter, randomized, double-blind, placebo-controlled trial. Neurology 43, 662-667 (1993). (Pubitemid 23121952)
-
(1993)
Neurology
, vol.43
, Issue.4
, pp. 662-667
-
-
Paty, D.W.1
Li, D.K.B.2
-
38
-
-
12644263394
-
Targeted inactivation of the mouse Huntington's disease gene homolog Hdh
-
MacDonald, M.E. et al. Targeted inactivation of the mouse Huntington's disease gene homolog Hdh. Cold Spring Harb. Symp. Quant. Biol. 61, 627-638 (1996).
-
(1996)
Cold Spring Harb. Symp. Quant. Biol
, vol.61
, pp. 627-638
-
-
MacDonald, M.E.1
-
39
-
-
0029082383
-
Inactivation of the mouse Huntington's disease gene homolog Hdh
-
Duyao, M.P. et al. Inactivation of the mouse Huntington's disease gene homolog Hdh. Science 269, 407-410 (1995).
-
(1995)
Science
, vol.269
, pp. 407-410
-
-
Duyao, M.P.1
-
40
-
-
84860192454
-
Six-month partial suppression of Huntingtin is well tolerated in the adult rhesus striatum
-
Grondin, R. et al. Six-month partial suppression of Huntingtin is well tolerated in the adult rhesus striatum. Brain 135, 1197-1209 (2012).
-
(2012)
Brain
, vol.135
, pp. 1197-1209
-
-
Grondin, R.1
-
41
-
-
34848892367
-
Immunohistochemical localization of NUB1, a synphilin-1-binding protein, in neurodegenerative disorders
-
DOI 10.1007/s00401-007-0238-1
-
Tanji, K. et al. Immunohistochemical localization of NUB1, a synphilin-1-binding protein, in neurodegenerative disorders. Acta Neuropathol. 114, 365-371 (2007). (Pubitemid 47500348)
-
(2007)
Acta Neuropathologica
, vol.114
, Issue.4
, pp. 365-371
-
-
Tanji, K.1
Mori, F.2
Kakita, A.3
Zhang, H.4
Kito, K.5
Kamitani, T.6
Takahashi, H.7
Wakabayashi, K.8
-
42
-
-
60849106643
-
Inducible mutant huntingtin expression in HN10 cells reproduces Huntington's disease-like neuronal dysfunction
-
Weiss, A., Roscic, A. & Paganetti, P. Inducible mutant huntingtin expression in HN10 cells reproduces Huntington's disease-like neuronal dysfunction. Mol. Neurodegener. 4, 11 (2009).
-
(2009)
Mol. Neurodegener
, vol.4
, pp. 11
-
-
Weiss, A.1
Roscic, A.2
Paganetti, P.3
-
43
-
-
69249232195
-
An efficient and reversible transposable system for gene delivery and lineage-specific differentiation in human embryonic stem cells
-
Lacoste, A., Berenshteyn, F. & Brivanlou, A.H. An efficient and reversible transposable system for gene delivery and lineage-specific differentiation in human embryonic stem cells. Cell Stem Cell 5, 332-342 (2009).
-
(2009)
Cell Stem Cell
, vol.5
, pp. 332-342
-
-
Lacoste, A.1
Berenshteyn, F.2
Brivanlou, A.H.3
-
44
-
-
62149125434
-
Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling
-
Chambers, S.M. et al. Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling. Nat. Biotechnol. 27, 275-280 (2009).
-
(2009)
Nat. Biotechnol
, vol.27
, pp. 275-280
-
-
Chambers, S.M.1
-
45
-
-
0035502934
-
New anti-huntingtin monoclonal antibodies: Implications for huntingtin conformation and its binding proteins
-
DOI 10.1016/S0361-9230(01)00599-8, PII S0361923001005998
-
Ko, J., Ou, S. & Patterson, P.H. New anti-huntingtin monoclonal antibodies: implications for huntingtin conformation and its binding proteins. Brain Res. Bull. 56, 319-329 (2001). (Pubitemid 33062356)
-
(2001)
Brain Research Bulletin
, vol.56
, Issue.3-4
, pp. 319-329
-
-
Ko, J.1
Ou, S.2
Patterson, P.H.3
-
46
-
-
70349103737
-
Single-step detection of mutant huntingtin in animal and human tissues: A bioassay for Huntington's disease
-
Weiss, A. et al. Single-step detection of mutant huntingtin in animal and human tissues: a bioassay for Huntington's disease. Anal. Biochem. 395, 8-15 (2009).
-
(2009)
Anal. Biochem
, vol.395
, pp. 8-15
-
-
Weiss, A.1
-
47
-
-
84867148826
-
Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression
-
Weiss, A. et al. Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression. J. Clin. Invest. 122, 3731-3736 (2012).
-
(2012)
J. Clin. Invest
, vol.122
, pp. 3731-3736
-
-
Weiss, A.1
-
48
-
-
33748741301
-
CHIP protects from the neurotoxicity of expanded and wild-type ataxin-1 and promotes their ubiquitination and degradation
-
DOI 10.1074/jbc.M601603200
-
Al-Ramahi, I. et al. CHIP protects from the neurotoxicity of expanded and wild-type ataxin-1 and promotes their ubiquitination and degradation. J. Biol. Chem. 281, 26714-26724 (2006). (Pubitemid 44401880)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.36
, pp. 26714-26724
-
-
Al-Ramahi, I.1
Lam, Y.C.2
Chen, H.-K.3
De Gouyon, B.4
Zhang, M.5
Perez, A.M.6
Branco, J.7
De Haro, M.8
Patterson, C.9
Zoghbi, H.Y.10
Botas, J.11
-
49
-
-
0041691176
-
Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats
-
DOI 10.1002/cne.10776
-
Menalled, L.B., Sison, J.D., Dragatsis, I., Zeitlin, S. & Chesselet, M.F. Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats. J. Comp. Neurol. 465, 11-26 (2003). (Pubitemid 37075677)
-
(2003)
Journal of Comparative Neurology
, vol.465
, Issue.1
, pp. 11-26
-
-
Menalled, L.B.1
Sison, J.D.2
Dragatsis, I.3
Zeitlin, S.4
Chesselet, M.-F.5
-
50
-
-
73949155373
-
Mutant huntingtin and glycogen synthase kinase 3-beta accumulate in neuronal lipid rafts of a presymptomatic knock-in mouse model of Huntington's disease
-
Valencia, A. et al. Mutant huntingtin and glycogen synthase kinase 3-beta accumulate in neuronal lipid rafts of a presymptomatic knock-in mouse model of Huntington's disease. J. Neurosci. Res. 88, 179-190 (2010).
-
(2010)
J. Neurosci. Res
, vol.88
, pp. 179-190
-
-
Valencia, A.1
-
51
-
-
77955284657
-
The pseudokinase tribbles homolog 3 interacts with ATF4 to negatively regulate insulin exocytosis in human and mouse beta cells
-
Liew, C.W. et al. The pseudokinase tribbles homolog 3 interacts with ATF4 to negatively regulate insulin exocytosis in human and mouse beta cells. J. Clin. Invest. 120, 2876-2888 (2010).
-
(2010)
J. Clin. Invest
, vol.120
, pp. 2876-2888
-
-
Liew, C.W.1
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