-
1
-
-
0037385006
-
Missense mutations in the regulatory domain of PKC gamma: A new mechanism for dominant nonepisodic cerebellar ataxia
-
Chen DH, Brkanac Z, Verlinde CL, Tan XJ, Bylenok L, Nochlin D, et al. Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia. Am J Hum Genet. 2003;72:839-849.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 839-849
-
-
Chen, D.H.1
Brkanac, Z.2
Verlinde, C.L.3
Tan, X.J.4
Bylenok, L.5
Nochlin, D.6
-
2
-
-
0346734156
-
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family
-
Van De Warrenburg BP, Verbeek DS, Piersma SJ, Hennekam FA, Pearson PL, Knoers NV, et al. Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family. Neurology. 2003;61:1760-1765.
-
(2003)
Neurology
, vol.61
, pp. 1760-1765
-
-
van de Warrenburg, B.P.1
Verbeek, D.S.2
Piersma, S.J.3
Hennekam, F.A.4
Pearson, P.L.5
Knoers, N.V.6
-
3
-
-
0346754906
-
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma
-
Yabe I, Sasaki H, Chen DH, Raskind WH, Bird TD, Yamashita I, et al. Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma. Arch Neurol. 2003;60:1749-1751.
-
(2003)
Arch Neurol
, vol.60
, pp. 1749-1751
-
-
Yabe, I.1
Sasaki, H.2
Chen, D.H.3
Raskind, W.H.4
Bird, T.D.5
Yamashita, I.6
-
4
-
-
4043178555
-
Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14
-
Stevanin G, Hahn V, Lohmann E, Bouslam N, Gouttard M, Soumphonphakdy C, et al. Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14. Arch Neurol. 2004;61: 1242-1248.
-
(2004)
Arch Neurol
, vol.61
, pp. 1242-1248
-
-
Stevanin, G.1
Hahn, V.2
Lohmann, E.3
Bouslam, N.4
Gouttard, M.5
Soumphonphakdy, C.6
-
5
-
-
13544251405
-
Protein kinase C gamma mutations in spinocerebellar ataxia 14 increase kinase activity and alter membrane targeting
-
Verbeek DS, Knight MA, Harmison GG, Fischbeck KH, Howell BW. Protein kinase C gamma mutations in spinocerebellar ataxia 14 increase kinase activity and alter membrane targeting. Brain. 2005;128:436-442.
-
(2005)
Brain
, vol.128
, pp. 436-442
-
-
Verbeek, D.S.1
Knight, M.A.2
Harmison, G.G.3
Fischbeck, K.H.4
Howell, B.W.5
-
6
-
-
20344370767
-
Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population
-
Verbeek DS, Warrenburg BP, Hennekam FA, Dooijes D, Ippel PF, Verschuuren-Bemelmans CC, et al. Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population. Hum Genet. 2005;117:88-91.
-
(2005)
Hum Genet
, vol.117
, pp. 88-91
-
-
Verbeek, D.S.1
Warrenburg, B.P.2
Hennekam, F.A.3
Dooijes, D.4
Ippel, P.F.5
Verschuuren-Bemelmans, C.C.6
-
7
-
-
20144388593
-
The clinical and genetic spectrum of spinocerebellar ataxia 14
-
Chen DH, Cimino PJ, Ranum LP, Zoghbi HV, Yabe I, Schut L, et al. The clinical and genetic spectrum of spinocerebellar ataxia 14. Neurology. 2005;64:1258-1260.
-
(2005)
Neurology
, vol.64
, pp. 1258-1260
-
-
Chen, D.H.1
Cimino, P.J.2
Ranum, L.P.3
Zoghbi, H.V.4
Yabe, I.5
Schut, L.6
-
8
-
-
27644586218
-
New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14
-
Klebe S, Durr A, Rentschler A, Hahn-Barma V, Abele M, Bouslam N, et al. New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14. Ann Neurol. 2005;58:720-729.
-
(2005)
Ann Neurol
, vol.58
, pp. 720-729
-
-
Klebe, S.1
Durr, A.2
Rentschler, A.3
Hahn-Barma, V.4
Abele, M.5
Bouslam, N.6
-
9
-
-
27644562111
-
A novel H101Q mutation causes PKCgamma loss in spinocerebellar ataxia type 14
-
Alonso I, Costa C, Gomes A, Ferro A, Seixas Ai, Silva S, et al. A novel H101Q mutation causes PKCgamma loss in spinocerebellar ataxia type 14. J Hum Genet. 2005;50:523-529.
-
(2005)
J Hum Genet
, vol.50
, pp. 523-529
-
-
Alonso, I.1
Costa, C.2
Gomes, A.3
Ferro, A.4
Seixas, A.5
Silva, S.6
-
10
-
-
33750348973
-
Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4
-
Hiramoto K, Kawakami H, Inoue K, Seki T, Maruyama H, Morino H, et al. Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4. Mov Disord. 2006;21: 1355-1360.
-
(2006)
Mov Disord
, vol.21
, pp. 1355-1360
-
-
Hiramoto, K.1
Kawakami, H.2
Inoue, K.3
Seki, T.4
Maruyama, H.5
Morino, H.6
-
11
-
-
33746875548
-
Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: Expanding the phenotype
-
Vlak MH, Sinke RJ, Rabelink GM, Kremer BP, Van De Warrenburg BP. Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: expanding the phenotype. Mov Disord. 2006;21:1025-1028.
-
(2006)
Mov Disord
, vol.21
, pp. 1025-1028
-
-
Vlak, M.H.1
Sinke, R.J.2
Rabelink, G.M.3
Kremer, B.P.4
van de Warrenburg, B.P.5
-
12
-
-
33748977606
-
Mutation of the highly conserved cysteine residue 131 of the SCA14 associated PRKCG gene in a family with slow progressive cerebellar ataxia
-
Dalski A, Mitulla B, Burk K, Schattenfroh C, Schwinger E, Zuhlke C. Mutation of the highly conserved cysteine residue 131 of the SCA14 associated PRKCG gene in a family with slow progressive cerebellar ataxia. J Neurol. 2006;253:1111-1112.
-
(2006)
J Neurol
, vol.253
, pp. 1111-1112
-
-
Dalski, A.1
Mitulla, B.2
Burk, K.3
Schattenfroh, C.4
Schwinger, E.5
Zuhlke, C.6
-
13
-
-
33847739372
-
Spinocerebellar ataxia 14: Novel mutation in exon 2 of PRKCG in a German family
-
Nolte D, Landendinger M, Schmitt E, Muller U. Spinocerebellar ataxia 14: novel mutation in exon 2 of PRKCG in a German family. Mov Disord. 2007;22:265-267.
-
(2007)
Mov Disord
, vol.22
, pp. 265-267
-
-
Nolte, D.1
Landendinger, M.2
Schmitt, E.3
Muller, U.4
-
14
-
-
34250303891
-
Another mutation in cysteine 131 in protein kinase C gamma as a cause of spinocerebellar ataxia type 14
-
Klebe S, Faivre L, Forlani S, Dussert C, Tourbah A, Brice, A, et al. Another mutation in cysteine 131 in protein kinase C gamma as a cause of spinocerebellar ataxia type 14. Arch Neurol. 2007;64:913-914.
-
(2007)
Arch Neurol
, vol.64
, pp. 913-914
-
-
Klebe, S.1
Faivre, L.2
Forlani, S.3
Dussert, C.4
Tourbah, A.5
Brice, A.6
-
15
-
-
37549024558
-
Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene
-
Wieczorek S, Arning L, Gizewski ER, Alheite I, Timmann D. Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene. Mov Disord. 2007;22:2135-2136.
-
(2007)
Mov Disord
, vol.22
, pp. 2135-2136
-
-
Wieczorek, S.1
Arning, L.2
Gizewski, E.R.3
Alheite, I.4
Timmann, D.5
-
16
-
-
0023874148
-
Distribution of protein kinase C-like immunoreactive neurons in rat brain
-
Saito N, Kikkawa U, Nishizuka Y, Tanaka C. Distribution of protein kinase C-like immunoreactive neurons in rat brain. J Neurosci. 1988;8:369-382.
-
(1988)
J Neurosci
, vol.8
, pp. 369-382
-
-
Saito, N.1
Kikkawa, U.2
Nishizuka, Y.3
Tanaka, C.4
-
17
-
-
0029620817
-
Impaired motor coordination correlates with persistent multiple climbing fiber innervation in PKC gamma mutant mice
-
Chen C, Kano M, Abeliovich A, Chen L, Bao S, Kim JJ, et al. Impaired motor coordination correlates with persistent multiple climbing fiber innervation in PKC gamma mutant mice. Cell. 1995;83:1233-1242.
-
(1995)
Cell
, vol.83
, pp. 1233-1242
-
-
Chen, C.1
Kano, M.2
Abeliovich, A.3
Chen, L.4
Bao, S.5
Kim, J.J.6
-
18
-
-
0029591742
-
Impaired synapse elimination during cerebellar development in PKC gamma mutant mice
-
Kano M, Hashimoto K, Chen C, Abeliovich A, Aiba A, Kurihara H, et al. Impaired synapse elimination during cerebellar development in PKC gamma mutant mice. Cell. 1995;83:1223-1231.
-
(1995)
Cell
, vol.83
, pp. 1223-1231
-
-
Kano, M.1
Hashimoto, K.2
Chen, C.3
Abeliovich, A.4
Aiba, A.5
Kurihara, H.6
-
19
-
-
15844395343
-
Phosphorylation of PKC activation loop plays an important role in receptor-mediated translocation of PKC
-
Seki T, Matsubayashi H, Amano T, Shirai Y, Saito N, Sakai N. Phosphorylation of PKC activation loop plays an important role in receptor-mediated translocation of PKC. Genes Cells. 2005; 10:225-239.
-
(2005)
Genes Cells
, vol.10
, pp. 225-239
-
-
Seki, T.1
Matsubayashi, H.2
Amano, T.3
Shirai, Y.4
Saito, N.5
Sakai, N.6
-
20
-
-
58149490769
-
Mutant γPKC found in spinocerebellar ataxia type 14 induces aggregate-independent maldevelopment of dendrites in primary cultured Purkinje cells
-
Seki T, Shimahara T, Yamamoto K, Abe N, Amano T, Adachi N, et al. Mutant γPKC found in spinocerebellar ataxia type 14 induces aggregate-independent maldevelopment of dendrites in primary cultured Purkinje cells. Neurobiol Dis. 2009;33:260-273.
-
(2009)
Neurobiol Dis
, vol.33
, pp. 260-273
-
-
Seki, T.1
Shimahara, T.2
Yamamoto, K.3
Abe, N.4
Amano, T.5
Adachi, N.6
-
21
-
-
36248998804
-
Aggregate formation of mutant protein kinase C gamma found in spinocerebellar ataxia type 14 impairs ubiquitin-proteasome system and induces endoplasmic reticulum stress
-
Seki T, Takahashi H, Adachi N, Abe N, Shimahara T, Saito N, et al. Aggregate formation of mutant protein kinase C gamma found in spinocerebellar ataxia type 14 impairs ubiquitin-proteasome system and induces endoplasmic reticulum stress. Eur J Neurosci. 2007;26:3126-3140.
-
(2007)
Eur J Neurosci
, vol.26
, pp. 3126-3140
-
-
Seki, T.1
Takahashi, H.2
Adachi, N.3
Abe, N.4
Shimahara, T.5
Saito, N.6
-
22
-
-
0037077040
-
Toxic proteins in neurodegenerative disease
-
Taylor JP, Hardy J, Fischbeck KH. Toxic proteins in neurodegenerative disease. Science. 2002;296:1991-1995.
-
(2002)
Science
, vol.296
, pp. 1991-1995
-
-
Taylor, J.P.1
Hardy, J.2
Fischbeck, K.H.3
-
23
-
-
3142514201
-
Protein aggregation and neurodegenerative disease
-
Ross CA, Poirier MA. Protein aggregation and neurodegenerative disease. Nat Med. 2004;10 Suppl:S10-S17.
-
(2004)
Nat Med
, vol.10
, Issue.SUPPL.
-
-
Ross, C.A.1
Poirier, M.A.2
-
24
-
-
33845192482
-
Congo red and protein aggregation in neurodegenerative diseases
-
Frid P, Anisimov SV, Popovic N. Congo red and protein aggregation in neurodegenerative diseases. Brain Res Rev. 2007;53: 135-160.
-
(2007)
Brain Res Rev
, vol.53
, pp. 135-160
-
-
Frid, P.1
Anisimov, S.V.2
Popovic, N.3
-
25
-
-
77950486751
-
Amyloidosis-where are we now and where are we heading?
-
Picken MM. Amyloidosis-where are we now and where are we heading? Arch Pathol Lab Med. 2010;134:545-551.
-
(2010)
Arch Pathol Lab Med
, vol.134
, pp. 545-551
-
-
Picken, M.M.1
-
26
-
-
0034612220
-
Inhibition of huntingtin fibrillogenesis by specific antibodies and small molecules: Implications for Huntington's disease therapy
-
Heiser V, Scherzinger E, Boeddrich A, Nordhoff E, Lurz R, Schugardt N, et al. Inhibition of huntingtin fibrillogenesis by specific antibodies and small molecules: implications for Huntington's disease therapy. Proc Natl Acad Sci U S A. 2000;97: 6739-6744.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 6739-6744
-
-
Heiser, V.1
Scherzinger, E.2
Boeddrich, A.3
Nordhoff, E.4
Lurz, R.5
Schugardt, N.6
-
27
-
-
0035668573
-
Inhibition of polyglutamine aggregation in R6/2 HD brain slices-complex dose-response profiles
-
Smith DL, Portier R, Woodman B, Hockly E, Mahal A, Klunk WE, et al. Inhibition of polyglutamine aggregation in R6/2 HD brain slices-complex dose-response profiles. Neurobiol Dis. 2001;8:1017-1026.
-
(2001)
Neurobiol Dis
, vol.8
, pp. 1017-1026
-
-
Smith, D.L.1
Portier, R.2
Woodman, B.3
Hockly, E.4
Mahal, A.5
Klunk, W.E.6
-
28
-
-
0037461730
-
Pivotal role of oligomerization in expanded polyglutamine neurodegenerative disorders
-
Sanchez I, Mahlke C, Yuan J. Pivotal role of oligomerization in expanded polyglutamine neurodegenerative disorders. Nature. 2003;421:373-379.
-
(2003)
Nature
, vol.421
, pp. 373-379
-
-
Sanchez, I.1
Mahlke, C.2
Yuan, J.3
-
29
-
-
69749090512
-
On the mechanism of nonspecific inhibitors of protein aggregation: Dissecting the interactions of alpha-synuclein with Congo red and Lacmoid
-
Lendel C, Bertoncini CW, Cremades N, Waudby CA, Vendruscolo M, Dobson CM, et al. On the mechanism of nonspecific inhibitors of protein aggregation: dissecting the interactions of alpha-synuclein with Congo red and Lacmoid. Biochemistry. 2009;48:8322-8334.
-
(2009)
Biochemistry
, vol.48
, pp. 8322-8334
-
-
Lendel, C.1
Bertoncini, C.W.2
Cremades, N.3
Waudby, C.A.4
Vendruscolo, M.5
Dobson, C.M.6
-
30
-
-
0036262777
-
Inducible and brain region-specific CREB transgenic mice
-
Sakai N, Thome J, Newton SS, Chen J, Kelz MB, Steffen C, et al. Inducible and brain region-specific CREB transgenic mice. Mol Pharmacol. 2002;61:1453-1464.
-
(2002)
Mol Pharmacol
, vol.61
, pp. 1453-1464
-
-
Sakai, N.1
Thome, J.2
Newton, S.S.3
Chen, J.4
Kelz, M.B.5
Steffen, C.6
-
31
-
-
23844524453
-
Mutant protein kinase Cγ found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death
-
Seki T, Adachi N, Ono Y, Mochizuki H, Hiramoto K, Amano T, et al. Mutant protein kinase Cγ found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death. J Biol Chem. 2005;280:29096-29106.
-
(2005)
J Biol Chem
, vol.280
, pp. 29096-29106
-
-
Seki, T.1
Adachi, N.2
Ono, Y.3
Mochizuki, H.4
Hiramoto, K.5
Amano, T.6
-
32
-
-
33747478593
-
Fused protein of dPKC activation loop and PDK1-interacting fragment (dAL-PIF) functions as a pseudosubstrate and an inhibitory molecule for PDK1 when expressed in cells
-
Seki T, Irie N, Nakamura K, Sakaue H, Ogawa W, Kasuga M, et al. Fused protein of dPKC activation loop and PDK1-interacting fragment (dAL-PIF) functions as a pseudosubstrate and an inhibitory molecule for PDK1 when expressed in cells. Genes Cells. 2006;11:1051-1070.
-
(2006)
Genes Cells
, vol.11
, pp. 1051-1070
-
-
Seki, T.1
Irie, N.2
Nakamura, K.3
Sakaue, H.4
Ogawa, W.5
Kasuga, M.6
-
33
-
-
34347358526
-
Protein kinase C gamma mutations in the C1B domain cause caspase-3-linked apoptosis in lens epithelial cells through gap junctions
-
Lin D, Shanks D, Prakash O, Takemoto DJ. Protein kinase C gamma mutations in the C1B domain cause caspase-3-linked apoptosis in lens epithelial cells through gap junctions. Exp Eye Res. 2007;85:113-122.
-
(2007)
Exp Eye Res
, vol.85
, pp. 113-122
-
-
Lin, D.1
Shanks, D.2
Prakash, O.3
Takemoto, D.J.4
-
34
-
-
49649093191
-
PKCgamma; mutations in spinocerebellar ataxia type 14 affect C1 domain accessibility and kinase activity leading to aberrant MAPK signaling
-
Verbeek DS, Goedhart J, Bruinsma L, Sinke RJ, Reits EA. PKCγ mutations in spinocerebellar ataxia type 14 affect C1 domain accessibility and kinase activity leading to aberrant MAPK signaling. J Cell Sci. 2008;121:2339-2349.
-
(2008)
J Cell Sci
, vol.121
, pp. 2339-2349
-
-
Verbeek, D.S.1
Goedhart, J.2
Bruinsma, L.3
Sinke, R.J.4
Reits, E.A.5
-
35
-
-
70350754464
-
Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxiarelated aprataxin
-
Asai H, Hirano M, Shimada K, Kiriyama T, Furiya Y, Ikeda M, et al. Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxiarelated aprataxin. Hum Mol Genet. 2009;18:3533-3543.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3533-3543
-
-
Asai, H.1
Hirano, M.2
Shimada, K.3
Kiriyama, T.4
Furiya, Y.5
Ikeda, M.6
-
36
-
-
50349095449
-
Enzymological analysis of mutant protein kinase Cgamma; causing spinocerebellar ataxia Type 14 and dysfunction in Ca2+ homeostasis
-
Adachi N, Kobayashi T, Takahashi H, Kawasaki T, Shirai Y, Ueyama T, et al. Enzymological analysis of mutant protein kinase Cgamma; causing spinocerebellar ataxia Type 14 and dysfunction in Ca2+ homeostasis. J Biol Chem. 2008;283:19854-19863.
-
(2008)
J Biol Chem
, vol.283
, pp. 19854-19863
-
-
Adachi, N.1
Kobayashi, T.2
Takahashi, H.3
Kawasaki, T.4
Shirai, Y.5
Ueyama, T.6
-
37
-
-
33745088678
-
Molecular pathogenesis of spinocerebellar ataxias
-
Duenas AM, Goold R, Giunti P. Molecular pathogenesis of spinocerebellar ataxias. Brain. 2006;129:1357-1370.
-
(2006)
Brain
, vol.129
, pp. 1357-1370
-
-
Duenas, A.M.1
Goold, R.2
Giunti, P.3
-
38
-
-
0030996676
-
A beta deposition inhibitor screen using synthetic amyloid
-
Esler WP, Stimson ER, Ghilardi JR, Felix AM, Lu YA, Vinters HV, et al. A beta deposition inhibitor screen using synthetic amyloid. Nat Biotechnol. 1997;15:258-263.
-
(1997)
Nat Biotechnol
, vol.15
, pp. 258-263
-
-
Esler, W.P.1
Stimson, E.R.2
Ghilardi, J.R.3
Felix, A.M.4
Lu, Y.A.5
Vinters, H.V.6
-
39
-
-
34548227453
-
Detection of polyglutamine protein oligomers in cells by fluorescence correlation spectroscopy
-
Takahashi Y, Okamoto Y, Popiel HA, Fujikake N, Toda T, Kinjo M, et al. Detection of polyglutamine protein oligomers in cells by fluorescence correlation spectroscopy. J Biol Chem. 2007; 282:24039-24048.
-
(2007)
J Biol Chem
, vol.282
, pp. 24039-24048
-
-
Takahashi, Y.1
Okamoto, Y.2
Popiel, H.A.3
Fujikake, N.4
Toda, T.5
Kinjo, M.6
-
40
-
-
0031466995
-
Direct visualization of the translocation of the gamma-subspecies of protein kinase C in living cells using fusion proteins with green fluorescent protein
-
Sakai N, Sasaki K, Ikegaki N, Shirai Y, Ono Y, Saito N. Direct visualization of the translocation of the gamma-subspecies of protein kinase C in living cells using fusion proteins with green fluorescent protein. J Cell Biol. 1997;139:1465-1476.
-
(1997)
J Cell Biol
, vol.139
, pp. 1465-1476
-
-
Sakai, N.1
Sasaki, K.2
Ikegaki, N.3
Shirai, Y.4
Ono, Y.5
Saito, N.6
-
41
-
-
5644277698
-
Propagation of γPKC translocation along the dendrites of Purkinje cell in γPKC-GFP transgenic mice
-
Sakai N, Tsubokawa H, Matsuzaki M, Kajimoto T, Takahashi E, Ren Y, et al. Propagation of γPKC PKCPKC translocation along the dendrites of Purkinje cell in γPKC-GFP transgenic mice. Genes Cells. 2004;9:945-957.
-
(2004)
Genes Cells
, vol.9
, pp. 945-957
-
-
Sakai, N.1
Tsubokawa, H.2
Matsuzaki, M.3
Kajimoto, T.4
Takahashi, E.5
Ren, Y.6
-
42
-
-
0028172886
-
Beta-amyloid neurotoxicity requires fibril formation and is inhibited by congo red
-
Lorenzo A, Yankner BA. Beta-amyloid neurotoxicity requires fibril formation and is inhibited by congo red. Proc Natl Acad Sci U S A. 1994;91:12243-12247.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 12243-12247
-
-
Lorenzo, A.1
Yankner, B.A.2
-
43
-
-
0030569357
-
Betaamyloid induces apoptosis in human-derived neurotypic SHSY5Y cells
-
Li YP, Bushnell AF, Lee CM, Perlmutter LS, Wong SK. Betaamyloid induces apoptosis in human-derived neurotypic SHSY5Y cells. Brain Res. 1996;738:196-204.
-
(1996)
Brain Res
, vol.738
, pp. 196-204
-
-
Li, Y.P.1
Bushnell, A.F.2
Lee, C.M.3
Perlmutter, L.S.4
Wong, S.K.5
-
44
-
-
0036340697
-
A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter
-
Brkanac Z, Bylenok L, Fernandez M, Matsushita M, Lipe H, Wolff J, et al. A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter. Arch Neurol. 2002;59:1291-1295.
-
(2002)
Arch Neurol
, vol.59
, pp. 1291-1295
-
-
Brkanac, Z.1
Bylenok, L.2
Fernandez, M.3
Matsushita, M.4
Lipe, H.5
Wolff, J.6
-
45
-
-
77953254167
-
Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagy
-
Yamamoto K, Seki T, Adachi N, Takahashi T, Tanaka S, Hide I, et al. Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagy. Genes Cells. 2010;15:425-437.
-
(2010)
Genes Cells
, vol.15
, pp. 425-437
-
-
Yamamoto, K.1
Seki, T.2
Adachi, N.3
Takahashi, T.4
Tanaka, S.5
Hide, I.6
-
47
-
-
0001944263
-
How do intracellular proteolytic systems change with age?
-
Cuervo AM, Dice JF. How do intracellular proteolytic systems change with age? Front Biosci. 1998;3:d25-d43.
-
(1998)
Front Biosci
, vol.3
-
-
Cuervo, A.M.1
Dice, J.F.2
-
48
-
-
33846295583
-
Systemic administration of Congo red does not improve motor or cognitive function in R6/2 mice
-
Wood NI, Pallier PN, Wanderer J, Morton AJ. Systemic administration of Congo red does not improve motor or cognitive function in R6/2 mice. Neurobiol Dis. 2007;25:342-353.
-
(2007)
Neurobiol Dis
, vol.25
, pp. 342-353
-
-
Wood, N.I.1
Pallier, P.N.2
Wanderer, J.3
Morton, A.J.4
-
49
-
-
20044370990
-
Curcumin inhibits formation of amyloid beta oligomers and fibrils, binds plaques, and reduces amyloid in vivo
-
Yang F, Lim GP, Begum AN, Ubeda OJ, Simmons MR, Ambegaokar SS, et al. Curcumin inhibits formation of amyloid beta oligomers and fibrils, binds plaques, and reduces amyloid in vivo. J Biol Chem. 2005;280:5892-5901.
-
(2005)
J Biol Chem
, vol.280
, pp. 5892-5901
-
-
Yang, F.1
Lim, G.P.2
Begum, A.N.3
Ubeda, O.J.4
Simmons, M.R.5
Ambegaokar, S.S.6
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