-
1
-
-
0037131567
-
The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility
-
DOI 10.1016/S0092-8674(02)01012-7
-
Liu Y, Fallon L, Lashuel HA, Liu Z, Lansbury PT, Jr. (2002) The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility. Cell 111:209-218. (Pubitemid 35292441)
-
(2002)
Cell
, vol.111
, Issue.2
, pp. 209-218
-
-
Liu, Y.1
Fallon, L.2
Lashuel, H.A.3
Liu, Z.4
Lansbury Jr., P.T.5
-
2
-
-
59649115080
-
Amyloid beta-protein assembly as a therapeutic target of Alzheimer's disease
-
Yamin G, Ono K, Inayathullah M, Teplow DB (2008) Amyloid beta-protein assembly as a therapeutic target of Alzheimer's disease. Curr Pharm Des 14:3231-3246.
-
(2008)
Curr Pharm des
, vol.14
, pp. 3231-3246
-
-
Yamin, G.1
Ono, K.2
Inayathullah, M.3
Teplow, D.B.4
-
3
-
-
16844370705
-
Connecting the dots in Huntington's disease with protein interaction networks
-
10.1186/gb-2005-6-3-210
-
Giorgini F, Muchowski PJ (2005) Connecting the dots in Huntington's disease with protein interaction networks. Genome Biol, 10.1186/gb-2005-6-3-210.
-
(2005)
Genome Biol
-
-
Giorgini, F.1
Muchowski, P.J.2
-
4
-
-
25844487226
-
Diseases of unstable repeat expansion: Mechanisms and common principles
-
DOI 10.1038/nrg1691
-
Gatchel JR, Zoghbi HY (2005) Diseases of unstable repeat expansion: Mechanisms and common principles. Nat Rev Genet 6:743-755. (Pubitemid 41400832)
-
(2005)
Nature Reviews Genetics
, vol.6
, Issue.10
, pp. 743-755
-
-
Gatchel, J.R.1
Zoghbi, H.Y.2
-
5
-
-
0033389165
-
Polyglutamine domain proteins with expanded repeats bind neurofilament, altering the neurofilament network
-
Nagai Y, Onodera O, Strittmatter WJ, Burke JR (1999) Polyglutamine domain proteins with expanded repeats bind neurofilament, altering the neurofilament network. Ann NY Acad Sci 893:192-202. (Pubitemid 30038076)
-
(1999)
Annals of the New York Academy of Sciences
, vol.893
, pp. 192-202
-
-
Nagai, Y.1
Onodera, O.2
Strittmatter, W.J.3
Burke, J.R.4
-
6
-
-
72149107077
-
Serines 13 and 16 are critical determinants of full-length human mutant huntingtin induced disease pathogenesis in HD mice
-
Gu X, et al. (2009) Serines 13 and 16 are critical determinants of full-length human mutant huntingtin induced disease pathogenesis in HD mice. Neuron 64:828-840.
-
(2009)
Neuron
, vol.64
, pp. 828-840
-
-
Gu, X.1
-
7
-
-
33745003424
-
Cleavage at the Caspase-6 Site Is Required for Neuronal Dysfunction and Degeneration Due to Mutant Huntingtin
-
DOI 10.1016/j.cell.2006.04.026, PII S0092867406005587
-
Graham RK, et al. (2006) Cleavage at the caspase-6 site is required for neuronal dysfunction and degeneration due to mutant huntingtin. Cell 125:1179-1191. (Pubitemid 43866195)
-
(2006)
Cell
, vol.125
, Issue.6
, pp. 1179-1191
-
-
Graham, R.K.1
Deng, Y.2
Slow, E.J.3
Haigh, B.4
Bissada, N.5
Lu, G.6
Pearson, J.7
Shehadeh, J.8
Bertram, L.9
Murphy, Z.10
Warby, S.C.11
Doty, C.N.12
Roy, S.13
Wellington, C.L.14
Leavitt, B.R.15
Raymond, L.A.16
Nicholson, D.W.17
Hayden, M.R.18
-
8
-
-
0032898311
-
Kennedy's disease: Caspase cleavage of the androgen receptor is a crucial event in cytotoxicity
-
DOI 10.1046/j.1471-4159.1999.0720185.x
-
Ellerby LM, et al. (1999) Kennedy's disease: Caspase cleavage of the androgen receptor is a crucial event in cytotoxicity. J Neurochem 72:185-195. (Pubitemid 29013892)
-
(1999)
Journal of Neurochemistry
, vol.72
, Issue.1
, pp. 185-195
-
-
Ellerby, L.M.1
Hackam, A.S.2
Propp, S.S.3
Ellerby, H.M.4
Rabizadeh, S.5
Cashman, N.R.6
Trifiro, M.A.7
Pinsky, L.8
Wellington, C.L.9
Salvesen, G.S.10
Hayden, M.R.11
Bredesen, D.E.12
-
9
-
-
0032475941
-
Ataxin-1 nuclear localization and aggregation: Role in polyglutarnine- Induced disease in SCA1 transgenic mice
-
DOI 10.1016/S0092-8674(00)81781-X
-
Klement IA, et al. (1998) Ataxin-1 nuclear localization and aggregation: Role in polyglutamine-induced disease in SCA1 transgenic mice. Cell 95:41-53. (Pubitemid 28458023)
-
(1998)
Cell
, vol.95
, Issue.1
, 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
-
10
-
-
23944438950
-
The AXH domain of ataxin-1 mediates neurodegeneration through its interaction with Gfi-1/senseless proteins
-
DOI 10.1016/j.cell.2005.06.012, PII S0092867405005957
-
Tsuda H, et al. (2005) The AXH domain of Ataxin-1 mediates neurodegeneration through its interaction with Gfi-1/Senseless proteins. Cell 122:633-644. (Pubitemid 41191160)
-
(2005)
Cell
, vol.122
, Issue.4
, pp. 633-644
-
-
Tsuda, H.1
Jafar-Nejad, H.2
Patel, A.J.3
Sun, Y.4
Chen, H.-K.5
Rose, M.F.6
Venken, K.J.T.7
Botas, J.8
Orr, H.T.9
Bellen, H.J.10
Zoghbi, H.Y.11
-
11
-
-
28444444502
-
Polyglutamine is not all: The functional role of the AXH domain in the ataxin-1 protein
-
DOI 10.1016/j.jmb.2005.09.083, PII S0022283605011629
-
de Chiara C, Menon RP, Dal Piaz F, Calder L, Pastore A (2005) Polyglutamine is not all: The functional role of the AXH domain in the ataxin-1 protein. J Mol Biol 354:883-893. (Pubitemid 41735509)
-
(2005)
Journal of Molecular Biology
, vol.354
, Issue.4
, pp. 883-893
-
-
De, C.C.1
Menon, R.P.2
Dal, P.F.3
Calder, L.4
Pastore, A.5
-
12
-
-
0037846441
-
Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice
-
DOI 10.1016/S0896-6273(03)00258-7
-
Emamian ES, et al. (2003) Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice. Neuron 38:375-387. (Pubitemid 36579141)
-
(2003)
Neuron
, vol.38
, Issue.3
, pp. 375-387
-
-
Emamian, E.S.1
Kaytor, M.D.2
Duvick, L.A.3
Zu, T.4
Tousey, S.K.5
Zoghbi, H.Y.6
Clark, H.B.7
Orr, H.T.8
-
14
-
-
78649371716
-
Subclinical pulmonary dysfunction in spinocerebellar ataxias 1, 2 and 3
-
Sriranjini SJ, Pal PK, Krishna N, Sathyaprabha TN (2010) Subclinical pulmonary dysfunction in spinocerebellar ataxias 1, 2 and 3. Acta Neurol Scand 122:323-328.
-
(2010)
Acta Neurol Scand
, vol.122
, pp. 323-328
-
-
Sriranjini, S.J.1
Pal, P.K.2
Krishna, N.3
Sathyaprabha, T.N.4
-
15
-
-
18444386197
-
A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration
-
DOI 10.1016/S0896-6273(02)00733-X
-
Watase K, et al. (2002) A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration. Neuron 34:905-919. (Pubitemid 34722281)
-
(2002)
Neuron
, vol.34
, Issue.6
, pp. 905-919
-
-
Watase, K.1
Weeber, E.J.2
Xu, B.3
Antalffy, B.4
Yuva-Paylor, L.5
Hashimoto, K.6
Kano, M.7
Atkinson, R.8
Sun, Y.9
Armstrong, D.L.10
Sweatt, J.D.11
Orr, H.T.12
Paylor, R.13
Zoghbi, H.Y.14
-
16
-
-
42049086100
-
Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1
-
DOI 10.1038/nature06731, PII NATURE06731
-
Lim J, et al. (2008) Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1. Nature 452:713-718. (Pubitemid 351521076)
-
(2008)
Nature
, vol.452
, Issue.7188
, pp. 713-718
-
-
Lim, J.1
Crespo-Barreto, J.2
Jafar-Nejad, P.3
Bowman, A.B.4
Richman, R.5
Hill, D.E.6
Orr, H.T.7
Zoghbi, H.Y.8
-
17
-
-
33847290297
-
Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes
-
DOI 10.1038/ng1977, PII NG1977
-
Bowman AB, et al. (2007) Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes. Nat Genet 39:373-379. (Pubitemid 46328494)
-
(2007)
Nature Genetics
, vol.39
, Issue.3
, pp. 373-379
-
-
Bowman, A.B.1
Lam, Y.C.2
Jafar-Nejad, P.3
Chen, H.-K.4
Richman, R.5
Samaco, R.C.6
Fryer, J.D.7
Kahle, J.J.8
Orr, H.T.9
Zoghbi, H.Y.10
-
18
-
-
0037726598
-
Interaction of Akt-phosphorylated ataxin-1 with 14-3-3 mediates neurodegeneration in spinocerebellar ataxia type 1
-
Chen HK, et al. (2003) Interaction of Akt-phosphorylated ataxin-1 with 14-3-3 mediates neurodegeneration in spinocerebellar ataxia type 1. Cell 113:457-468.
-
(2003)
Cell
, vol.113
, pp. 457-468
-
-
Chen, H.K.1
-
19
-
-
33845657872
-
ATAXIN-1 Interacts with the Repressor Capicua in Its Native Complex to Cause SCA1 Neuropathology
-
DOI 10.1016/j.cell.2006.11.038, PII S0092867406015431
-
Lam YC, et al. (2006) ATAXIN-1 interacts with the repressor Capicua in its native complex to cause SCA1 neuropathology. Cell 127:1335-1347. (Pubitemid 44960413)
-
(2006)
Cell
, vol.127
, Issue.7
, pp. 1335-1347
-
-
Lam, Y.C.1
Bowman, A.B.2
Jafar-Nejad, P.3
Lim, J.4
Richman, R.5
Fryer, J.D.6
Hyun, E.D.7
Duvick, L.A.8
Orr, H.T.9
Botas, J.10
Zoghbi, H.Y.11
-
20
-
-
0038724088
-
The 14-3-3 proteins: Gene, gene expression, and function
-
Takahashi Y (2003) The 14-3-3 proteins: Gene, gene expression, and function. Neurochem Res 28:1265-1273.
-
(2003)
Neurochem Res
, vol.28
, pp. 1265-1273
-
-
Takahashi, Y.1
-
21
-
-
0026494876
-
14-3-3 proteins: A highly conserved, widespread family of eukaryotic proteins
-
Aitken A, et al. (1992) 14-3-3 proteins: A highly conserved, widespread family of eukaryotic proteins. Trends Biochem Sci 17:498-501.
-
(1992)
Trends Biochem Sci
, vol.17
, pp. 498-501
-
-
Aitken, A.1
-
22
-
-
0029871708
-
Interaction of 14-3-3 with signaling proteins is mediated by the recognition of phosphoserine
-
DOI 10.1016/S0092-8674(00)81067-3
-
Muslin AJ, Tanner JW, Allen PM, Shaw AS (1996) Interaction of 14-3-3 with signaling proteins is mediated by the recognition of phosphoserine. Cell 84:889-897. (Pubitemid 26106858)
-
(1996)
Cell
, vol.84
, Issue.6
, pp. 889-897
-
-
Muslin, A.J.1
Tanner, J.W.2
Allen, P.M.3
Shaw, A.S.4
-
23
-
-
0036479325
-
14-3-3 Proteins: Active cofactors in cellular regulation by serine/threonine phosphorylation
-
DOI 10.1074/jbc.R100059200
-
Tzivion G, Avruch J (2002) 14-3-3 proteins: Active cofactors in cellular regulation by serine/threonine phosphorylation. J Biol Chem 277:3061-3064. (Pubitemid 34953163)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.5
, pp. 3061-3064
-
-
Tzivion, G.1
Avruch, J.2
-
24
-
-
0038757833
-
14-3-3epsilon is important for neuronal migration by binding to NUDEL: Amolecular explanation for Miller-Dieker syndrome
-
Toyo-oka K, et al. (2003) 14-3-3epsilon is important for neuronal migration by binding to NUDEL: Amolecular explanation for Miller-Dieker syndrome. Nat Genet 34:274-285.
-
(2003)
Nat Genet
, vol.34
, pp. 274-285
-
-
Toyo-oka, K.1
-
25
-
-
0036914288
-
Functional specificity in 14-3-3 isoform interactions through dimer formation and phosphorylation. Chromosome location of mammalian isoforms and variants
-
Aitken A (2002) Functional specificity in 14-3-3 isoform interactions through dimer formation and phosphorylation. Chromosome location of mammalian isoforms and variants. Plant Mol Biol 50:993-1010.
-
(2002)
Plant Mol Biol
, vol.50
, pp. 993-1010
-
-
Aitken, A.1
-
26
-
-
0029067231
-
Isoforms of 14-3-3 protein can form homo- and heterodimers in vivo and in vitro: Implications for function as adapter proteins
-
Jones DH, Ley S, Aitken A (1995) Isoforms of 14-3-3 protein can form homo- and heterodimers in vivo and in vitro: Implications for function as adapter proteins. FEBS Lett 368:55-58.
-
(1995)
FEBS Lett
, vol.368
, pp. 55-58
-
-
Jones, D.H.1
Ley, S.2
Aitken, A.3
-
28
-
-
33644877400
-
14-3-3 proteins: A number of functions for a numbered protein
-
10.1126/stke.2962005re10
-
Bridges D, Moorhead GB (2005) 14-3-3 proteins: A number of functions for a numbered protein. Sci STKE, 10.1126/stke.2962005re10.
-
(2005)
Sci STKE
-
-
Bridges, D.1
Moorhead, G.B.2
-
29
-
-
0029163222
-
SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat
-
Burright EN, et al. (1995) SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat. Cell 82:937-948.
-
(1995)
Cell
, vol.82
, pp. 937-948
-
-
Burright, E.N.1
-
30
-
-
0037127035
-
Immunolocalisation of 14-3-3 isoforms in normal and scrapie-infected murine brain
-
DOI 10.1016/S0306-4522(01)00492-4, PII S0306452201004924
-
Baxter HC, Liu WG, Forster JL, Aitken A, Fraser JR (2002) Immunolocalisation of 14-3-3 isoforms in normal and scrapie-infected murine brain. Neuroscience 109:5-14. (Pubitemid 34088143)
-
(2002)
Neuroscience
, vol.109
, Issue.1
, pp. 5-14
-
-
Baxter, H.C.1
Liu, W.-G.2
Forster, J.L.3
Aitken, A.4
Fraser, J.R.5
-
31
-
-
33847064609
-
Intranuclear immunolocalization of 14-3-3 protein isoforms in brains with spinocerebellar ataxia type 1
-
DOI 10.1016/j.neulet.2006.12.026, PII S030439400601322X
-
Umahara T, et al. (2007) Intranuclear immunolocalization of 14-3-3 protein isoforms in brains with spinocerebellar ataxia type 1. Neurosci Lett 414:130-135. (Pubitemid 46273989)
-
(2007)
Neuroscience Letters
, vol.414
, Issue.2
, pp. 130-135
-
-
Umahara, T.1
Uchihara, T.2
Yagishita, S.3
Nakamura, A.4
Tsuchiya, K.5
Iwamoto, T.6
-
32
-
-
0034701278
-
Repeat instability and motor incoordination in mice with a targeted expanded CAG repeat in the Sca1 locus
-
Lorenzetti D, et al. (2000) Repeat instability and motor incoordination in mice with a targeted expanded CAG repeat in the Sca1 locus. Hum Mol Genet 9:779-785. (Pubitemid 30162762)
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.5
, pp. 779-785
-
-
Lorenzetti, D.1
Watase, K.2
Xu, B.3
Matzuk, M.M.4
Orr, H.T.5
Zoghbi, H.Y.6
-
33
-
-
33746267019
-
Swallowing in degenerative ataxias
-
DOI 10.1007/s00415-006-0122-2
-
Ramio-Torrentia L, Gomez E, Genis D (2006) Swallowing in degenerative ataxias. J Neurol 253:875-881. (Pubitemid 44100440)
-
(2006)
Journal of Neurology
, vol.253
, Issue.7
, pp. 875-881
-
-
Ramio-Torrentia, L.1
Gomez, E.2
Genis, D.3
-
34
-
-
0032883528
-
Vocal cord abductor paralysis in spinocerebellar ataxia type 1 [5]
-
Shiojiri T, et al. (1999) Vocal cord abductor paralysis in spinocerebellar ataxia type 1. J Neurol Neurosurg Psychiatry 67:695. (Pubitemid 29486232)
-
(1999)
Journal of Neurology Neurosurgery and Psychiatry
, vol.67
, Issue.5
, pp. 695
-
-
Shiojiri, T.1
Tsunemi, T.2
Matsunaga, T.3
Sasaki, H.4
Yabe, I.5
Tashiro, K.6
Nishizawa, N.7
Takamoto, K.8
Yokota, T.9
Mizusawa, H.10
-
35
-
-
34547692622
-
Trinucleotide repeat disorders
-
DOI 10.1146/annurev.neuro.29.051605.113042
-
Orr HT, Zoghbi HY (2007) Trinucleotide repeat disorders. Annu Rev Neurosci 30: 575-621. (Pubitemid 47218768)
-
(2007)
Annual Review of Neuroscience
, vol.30
, pp. 575-621
-
-
Orr, H.T.1
Zoghbi, H.Y.2
-
36
-
-
33745588863
-
Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins
-
DOI 10.1093/hmg/ddl121
-
Spencer CM, et al. (2006) Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins. Hum Mol Genet 15:1984-1994. (Pubitemid 43983272)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.12
, pp. 1984-1994
-
-
Spencer, C.M.1
Serysheva, E.2
Yuva-Paylor, L.A.3
Oostra, B.A.4
Nelson, D.L.5
Paylor, R.6
-
37
-
-
77957007354
-
SCA1-like disease in mice expressing wild type ataxin-1 with a serine to aspartic acid replacement at residue 776
-
Duvick L, et al. (2010) SCA1-like disease in mice expressing wild type ataxin-1 with a serine to aspartic acid replacement at residue 776. Neuron 67:929-935.
-
(2010)
Neuron
, vol.67
, pp. 929-935
-
-
Duvick, L.1
|