-
1
-
-
78149266599
-
HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones
-
doi:10.1093/hmg/ddq398
-
Vos MJ, Zijlstra MP, Kanon B, van Waarde-Verhagen MA, Brunt ER, Oosterveld-Hut HM, Carra S, Sibon OC, Kampinga HH. 2010 HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones. Hum. Mol. Genet. 19, 4677-4693. (doi:10.1093/hmg/ddq398)
-
(2010)
Hum. Mol. Genet
, vol.19
, pp. 4677-4693
-
-
Vos, M.J.1
Zijlstra, M.P.2
Kanon, B.3
van Waarde-Verhagen, M.A.4
Brunt, E.R.5
Oosterveld-Hut, H.M.6
Carra, S.7
Sibon, O.C.8
Kampinga, H.H.9
-
2
-
-
78650187121
-
Differential expression and induction of small heat shock proteins in rat brain and cultured hippocampal neurons
-
doi:10. 1002/jnr.22536
-
Kirbach BB, Golenhofen N. 2011 Differential expression and induction of small heat shock proteins in rat brain and cultured hippocampal neurons. J. Neurosci. Res. 89, 162-175. (doi:10. 1002/jnr.22536)
-
(2011)
J. Neurosci. Res
, vol.89
, pp. 162-175
-
-
Kirbach, B.B.1
Golenhofen, N.2
-
3
-
-
42749092501
-
Expression of the small heat shock protein family in the mouse CNS: Differential anatomical and biochemical compartmentalization
-
doi:10.1016/j.neuro science.2008.01.058
-
Quraishe S, Asuni A, Boelens WC, O'Connor V, Wyttenbach A. 2008 Expression of the small heat shock protein family in the mouse CNS: differential anatomical and biochemical compartmentalization. Neuroscience 153, 483-491. (doi:10.1016/j.neuro science.2008.01.058)
-
(2008)
Neuroscience
, vol.153
, pp. 483-491
-
-
Quraishe, S.1
Asuni, A.2
Boelens, W.C.3
O'Connor, V.4
Wyttenbach, A.5
-
4
-
-
84864486839
-
The family of mammalian small heat shock proteins (HSPBs): Implications in protein deposit diseases and motor neuropathies
-
doi:10.1016/j.biocel.2012.03.011
-
Boncoraglio A, Minoia M, Carra S. 2012 The family of mammalian small heat shock proteins (HSPBs): implications in protein deposit diseases and motor neuropathies. Int. J. Biochem. Cell Biol. 14, 1657-1669. (doi:10.1016/j.biocel.2012.03.011)
-
(2012)
Int. J. Biochem. Cell Biol
, vol.14
, pp. 1657-1669
-
-
Boncoraglio, A.1
Minoia, M.2
Carra, S.3
-
5
-
-
23344452096
-
The role of heat shock proteins Hsp70 and Hsp27 in cellular protection of the central nervous system
-
doi:10.1080/02656730500069955
-
Franklin TB, Krueger-Naug AM, Clarke DB, Arrigo AP, Currie RW. 2005 The role of heat shock proteins Hsp70 and Hsp27 in cellular protection of the central nervous system. Int. J. Hyperthermia 21, 379-392. (doi:10.1080/02656730500069955)
-
(2005)
Int. J. Hyperthermia
, vol.21
, pp. 379-392
-
-
Franklin, T.B.1
Krueger-Naug, A.M.2
Clarke, D.B.3
Arrigo, A.P.4
Currie, R.W.5
-
6
-
-
0035968885
-
Differentially expressed genes in rat dorsal root ganglia following peripheral nerve injury
-
doi:10.1097/ 00001756-200110290-00050
-
Kim DS, Lee SJ, Park SY, Yoo HJ, Kim SH, Kim KJ, Cho HJ. 2001 Differentially expressed genes in rat dorsal root ganglia following peripheral nerve injury. Neuroreport 12, 3401-3405. (doi:10.1097/ 00001756-200110290-00050)
-
(2001)
Neuroreport
, vol.12
, pp. 3401-3405
-
-
Kim, D.S.1
Lee, S.J.2
Park, S.Y.3
Yoo, H.J.4
Kim, S.H.5
Kim, K.J.6
Cho, H.J.7
-
7
-
-
80455162610
-
Mechanisms of compartmental Purkinje cell death and survival in the Lurcher mutant mouse
-
doi:10.1007/s12311-010-0231-4
-
Armstrong CL, Duffin CA, McFarland R, Vogel MW. 2011 Mechanisms of compartmental Purkinje cell death and survival in the Lurcher mutant mouse. Cerebellum 10, 504-514. (doi:10.1007/s12311-010-0231-4)
-
(2011)
Cerebellum
, vol.10
, pp. 504-514
-
-
Armstrong, C.L.1
Duffin, C.A.2
McFarland, R.3
Vogel, M.W.4
-
8
-
-
0037428937
-
Patterned Purkinje cell degeneration in mouse models of Niemann-Pick type C disease
-
doi:10.1002/cne.10522
-
Sarna JR, Larouche M, Marzban H, Sillitoe RV, Rancourt DE, Hawkes R. 2003 Patterned Purkinje cell degeneration in mouse models of Niemann-Pick type C disease. J. Comp. Neurol. 456, 279-291. (doi:10.1002/cne.10522)
-
(2003)
J. Comp. Neurol
, vol.456
, pp. 279-291
-
-
Sarna, J.R.1
Larouche, M.2
Marzban, H.3
Sillitoe, R.V.4
Rancourt, D.E.5
Hawkes, R.6
-
9
-
-
0032507639
-
Heat shock, but not the reactive state per se, induces increased expression of the small stress proteins HSP25 and a B-crystallin in glial cells in vitro
-
doi:10.1097/ 00001756-199805110-00056
-
Brzyska M, Stege GJ, Renkawek K, Bosman GJ. 1998 Heat shock, but not the reactive state per se, induces increased expression of the small stress proteins HSP25 and a B-crystallin in glial cells in vitro. Neuroreport 9, 1549-1552. (doi:10.1097/ 00001756-199805110-00056)
-
(1998)
Neuroreport
, vol.9
, pp. 1549-1552
-
-
Brzyska, M.1
Stege, G.J.2
Renkawek, K.3
Bosman, G.J.4
-
10
-
-
77951975098
-
Vesicle associated membrane protein B (VAPB) is decreased in ALS spinal cord
-
doi:10. 1016/j.neurobiolaging.2008.07.005
-
Anagnostou G, Akbar MT, Paul P, Angelinetta C, Steiner TJ, de Belleroche J. 2010 Vesicle associated membrane protein B (VAPB) is decreased in ALS spinal cord. Neurobiol. Aging 31, 969-985. (doi:10. 1016/j.neurobiolaging.2008.07.005)
-
(2010)
Neurobiol. Aging
, vol.31
, pp. 969-985
-
-
Anagnostou, G.1
Akbar, M.T.2
Paul, P.3
Angelinetta, C.4
Steiner, T.J.5
de Belleroche, J.6
-
11
-
-
34447294839
-
Gene expression analysis of the Murine model of amyotrophic lateral sclerosis: Studies of the Leu126delTT mutation in SOD1
-
doi:10.1016/j. brainres.2007.05.044
-
Fukada Y, Yasui K, Kitayama M, Doi K, Nakano T, Watanabe Y, Nakashima K. 2007 Gene expression analysis of the Murine model of amyotrophic lateral sclerosis: studies of the Leu126delTT mutation in SOD1. Brain Res. 1160, 1-10. (doi:10.1016/j. brainres.2007.05.044)
-
(2007)
Brain Res
, vol.1160
, pp. 1-10
-
-
Fukada, Y.1
Yasui, K.2
Kitayama, M.3
Doi, K.4
Nakano, T.5
Watanabe, Y.6
Nakashima, K.7
-
12
-
-
3142692478
-
Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 mice
-
doi:10.1111/j.1460-9568.2004.03430
-
Maatkamp A, Vlug A, Haasdijk E, Troost D, French PJ, Jaarsma D. 2004 Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 mice. Eur. J. Neurosci. 20, 14-28. (doi:10.1111/j.1460-9568.2004.03430)
-
(2004)
Eur. J. Neurosci
, vol.20
, pp. 14-28
-
-
Maatkamp, A.1
Vlug, A.2
Haasdijk, E.3
Troost, D.4
French, P.J.5
Jaarsma, D.6
-
13
-
-
33846945050
-
The small heat shock proteins and their clients
-
doi:10.1007/s00018-006-6321-2
-
Nakamoto H, Vigh L. 2007 The small heat shock proteins and their clients. Cell Mol. Life Sci. 64, 294-306. (doi:10.1007/s00018-006-6321-2)
-
(2007)
Cell Mol. Life Sci
, vol.64
, pp. 294-306
-
-
Nakamoto, H.1
Vigh, L.2
-
14
-
-
65449181204
-
γ-Synucleinopathy: Neurodegeneration associated with overexpression of the mouse protein
-
doi:10.1093/hmg/ddp090
-
Ninkina N, Peters O, Millership S, Salem H, van der Putten H, Buchman VL. 2009 g-Synucleinopathy: neurodegeneration associated with overexpression of the mouse protein. Hum. Mol. Genet. 18, 1779-1794. (doi:10.1093/hmg/ddp090)
-
(2009)
Hum. Mol. Genet
, vol.18
, pp. 1779-1794
-
-
Ninkina, N.1
Peters, O.2
Millership, S.3
Salem, H.4
van der Putten, H.5
Buchman, V.L.6
-
15
-
-
0035424105
-
Modulation of HSP25 expression during anterior horn motor neuron degeneration in the paralyse mouse mutant
-
doi:10.1002/jnr.1148
-
Pieri I, Cifuentes-Diaz C, Oudinet JP, Blondet B, Rieger F, Gonin S, Arrigo AP, Thomas Y. 2001 Modulation of HSP25 expression during anterior horn motor neuron degeneration in the paralyse mouse mutant. J. Neurosci. Res. 65, 247-253. (doi:10.1002/jnr.1148)
-
(2001)
J. Neurosci. Res
, vol.65
, pp. 247-253
-
-
Pieri, I.1
Cifuentes-Diaz, C.2
Oudinet, J.P.3
Blondet, B.4
Rieger, F.5
Gonin, S.6
Arrigo, A.P.7
Thomas, Y.8
-
16
-
-
0036841876
-
Upregulation of HSP27 in a transgenic model of ALS
-
doi:10.1046/j.0179-1613.2003.00938.x
-
Vleminckx V, Van Damme P, Goffin K, Delye H, Van Den Bosch L, Robberecht W. 2002 Upregulation of HSP27 in a transgenic model of ALS. J. Neuropathol. Exp. Neurol. 61, 968-974. (doi:10.1046/j.0179-1613.2003.00938.x)
-
(2002)
J. Neuropathol. Exp. Neurol
, vol.61
, pp. 968-974
-
-
Vleminckx, V.1
van Damme, P.2
Goffin, K.3
Delye, H.4
Van Den Bosch, L.5
Robberecht, W.6
-
17
-
-
33644960735
-
Specific association of small heat shock proteins with the pathological hallmarks of Alzheimer's disease brains
-
doi:10.1111/j.1365-2990.2006.00689.x
-
Wilhelmus MM, Otte-Holler I, Wesseling P, de Waal RM, Boelens WC, Verbeek MM. 2006 Specific association of small heat shock proteins with the pathological hallmarks of Alzheimer's disease brains. Neuropathol. Appl. Neurobiol. 32, 119-130. (doi:10.1111/j.1365-2990.2006.00689.x)
-
(2006)
Neuropathol. Appl. Neurobiol
, vol.32
, pp. 119-130
-
-
Wilhelmus, M.M.1
Otte-Holler, I.2
Wesseling, P.3
de Waal, R.M.4
Boelens, W.C.5
Verbeek, M.M.6
-
18
-
-
35748947791
-
Regulation of stress-induced intracellular sorting and chaperone function of Hsp27 (HspB1) in mammalian cells
-
doi:10.1042/ BJ20070195
-
Bryantsev AL, Kurchashova SY, Golyshev SA, Polyakov VY, Wunderink HF, Kanon B, Budagova KR, Kabakov AE, Kampinga HH. 2007 Regulation of stress-induced intracellular sorting and chaperone function of Hsp27 (HspB1) in mammalian cells. Biochem. J. 407, 407-417. (doi:10.1042/ BJ20070195)
-
(2007)
Biochem. J
, vol.407
, pp. 407-417
-
-
Bryantsev, A.L.1
Kurchashova, S.Y.2
Golyshev, S.A.3
Polyakov, V.Y.4
Wunderink, H.F.5
Kanon, B.6
Budagova, K.R.7
Kabakov, A.E.8
Kampinga, H.H.9
-
19
-
-
0036566675
-
Heat shock protein 27 prevents cellular polyglutamine toxicity and suppresses the increase of reactive oxygen species caused by huntingtin
-
doi:10.1093/hmg/11.9.1137
-
Wyttenbach A, Sauvageot O, Carmichael J, Diaz-Latoud C, Arrigo AP, Rubinsztein DC. 2002 Heat shock protein 27 prevents cellular polyglutamine toxicity and suppresses the increase of reactive oxygen species caused by huntingtin. Hum. Mol. Genet. 11, 1137-1151. (doi:10.1093/hmg/11.9.1137)
-
(2002)
Hum. Mol. Genet
, vol.11
, pp. 1137-1151
-
-
Wyttenbach, A.1
Sauvageot, O.2
Carmichael, J.3
Diaz-Latoud, C.4
Arrigo, A.P.5
Rubinsztein, D.C.6
-
20
-
-
67449099354
-
Transduced HSP27 protein protects neuronal cell death by enhancing FALS-associated SOD1 mutant activity
-
doi:10.5483/BMBRep.2009.42.3.136
-
An JJ et al. 2009 Transduced HSP27 protein protects neuronal cell death by enhancing FALS-associated SOD1 mutant activity. BMB Rep. 42, 136-141. (doi:10.5483/BMBRep.2009.42.3.136)
-
(2009)
BMB Rep
, vol.42
, pp. 136-141
-
-
An, J.J.1
-
21
-
-
84883852928
-
Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders
-
doi:10.1098/ rstb.2011.0409
-
Carra S et al. 2013 Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders. Phil. Trans. R. Soc. B 368, 20110409. (doi:10.1098/ rstb.2011.0409)
-
(2013)
Phil. Trans. R. Soc. B
, vol.368
, pp. 20110409
-
-
Carra, S.1
-
22
-
-
0027482463
-
Modulation of actin microfilament dynamics and fluid phase pinocytosis by phosphorylation of heat shock protein 27
-
doi:10.1890/08-1540.1
-
Lavoie JN, Hickey E, Weber LA, Landry J. 1993 Modulation of actin microfilament dynamics and fluid phase pinocytosis by phosphorylation of heat shock protein 27. J. Biol. Chem. 268, 24210-24214. (doi:10.1890/08-1540.1)
-
(1993)
J. Biol. Chem
, vol.268
, pp. 24210-24214
-
-
Lavoie, J.N.1
Hickey, E.2
Weber, L.A.3
Landry, J.4
-
23
-
-
14044250859
-
Hsp27 consolidates intracellular redox homeostasis by upholding glutathione in its reduced form and by decreasing iron intracellular levels. Antioxid
-
doi:10.1089/ars.2005.7.414
-
Arrigo AP, Virot S, Chaufour S, Firdaus W, Kretz-Remy C, Diaz-Latoud C. 2005 Hsp27 consolidates intracellular redox homeostasis by upholding glutathione in its reduced form and by decreasing iron intracellular levels. Antioxid. Redox Signal. 7, 414-422. (doi:10.1089/ars.2005.7.414)
-
(2005)
Redox Signal
, vol.7
, pp. 414-422
-
-
Arrigo, A.P.1
Virot, S.2
Chaufour, S.3
Firdaus, W.4
Kretz-Remy, C.5
Diaz-Latoud, C.6
-
24
-
-
0032498791
-
MKBP, a novel member of the small heat shock protein family, binds and activates the myotonic dystrophy protein kinase
-
doi:10.1083/jcb.140.5.1113
-
Suzuki A, Sugiyama Y, Hayashi Y, Nyu-i N, Yoshida M, Nonaka I, Ishiura S, Arahata K, Ohno S. 1998 MKBP, a novel member of the small heat shock protein family, binds and activates the myotonic dystrophy protein kinase. J. Cell Biol. 140, 1113-1124. (doi:10.1083/jcb.140.5.1113)
-
(1998)
J. Cell Biol
, vol.140
, pp. 1113-1124
-
-
Suzuki, A.1
Sugiyama, Y.2
Hayashi, Y.3
Nyu-I, N.4
Yoshida, M.5
Nonaka, I.6
Ishiura, S.7
Arahata, K.8
Ohno, S.9
-
25
-
-
0033984092
-
Muscle develops a specific form of small heat shock protein complex composed of MKBP/HSPB2 and HSPB3 during myogenic differentiation
-
doi:10.1074/jbc.275.2.1095)
-
Sugiyama Y, Suzuki A, Kishikawa M, Akutsu R, Hirose T, Waye MM, Tsui SK, Yoshida S, Ohno S. 2000 Muscle develops a specific form of small heat shock protein complex composed of MKBP/HSPB2 and HSPB3 during myogenic differentiation. J. Biol. Chem. 275, 1095-1104. (doi:10.1074/jbc.275.2.1095)
-
(2000)
J. Biol. Chem
, vol.275
, pp. 1095-1104
-
-
Sugiyama, Y.1
Suzuki, A.2
Kishikawa, M.3
Akutsu, R.4
Hirose, T.5
Waye, M.M.6
Tsui, S.K.7
Yoshida, S.8
Ohno, S.9
-
26
-
-
70349384227
-
A novel mutation (F71L) in aA-crystallin with defective chaperone-like function associated with age-related cataract
-
doi:10.1016/j. bbadis.2009.06.011
-
Bhagyalaxmi SG, Srinivas P, Barton KA, Kumar KR, Vidyavathi M, Petrash JM, Bhanuprakash Reddy G, Padma T. 2009 A novel mutation (F71L) in aA-crystallin with defective chaperone-like function associated with age-related cataract. Biochim. Biophys. Acta 1792, 974-981. (doi:10.1016/j. bbadis.2009.06.011)
-
(2009)
Biochim. Biophys. Acta
, vol.1792
, pp. 974-981
-
-
Bhagyalaxmi, S.G.1
Srinivas, P.2
Barton, K.A.3
Kumar, K.R.4
Vidyavathi, M.5
Petrash, J.M.6
Bhanuprakash Reddy, G.7
Padma, T.8
-
27
-
-
0026567454
-
Ultrastructural identification of neurofibrillary tangles in the spinal cords in Guamanian amyotrophic lateral sclerosis and Parkinsonism-dementia complex on Guam
-
doi:10.1007/BF00296790
-
Kato S, Hirano A, Llena JF, Ito H, Yen SH. 1992 Ultrastructural identification of neurofibrillary tangles in the spinal cords in Guamanian amyotrophic lateral sclerosis and Parkinsonism-dementia complex on Guam. Acta Neuropathol. 83, 277-282. (doi:10.1007/BF00296790)
-
(1992)
Acta Neuropathol
, vol.83
, pp. 277-282
-
-
Kato, S.1
Hirano, A.2
Llena, J.F.3
Ito, H.4
Yen, S.H.5
-
28
-
-
0026782217
-
Ballooned neurons in several neurodegenerative diseases and stroke contain αB crystallin
-
doi:10.1111/j.1365-2990.1992. tb00796.x
-
Lowe J, Errington DR, Lennox G, Pike I, Spendlove I, Landon M, Mayer RJ. 1992 Ballooned neurons in several neurodegenerative diseases and stroke contain αB crystallin. Neuropathol. Appl. Neurobiol. 18, 341-350. (doi:10.1111/j.1365-2990.1992. tb00796.x)
-
(1992)
Neuropathol. Appl. Neurobiol
, vol.18
, pp. 341-350
-
-
Lowe, J.1
Errington, D.R.2
Lennox, G.3
Pike, I.4
Spendlove, I.5
Landon, M.6
Mayer, R.J.7
-
29
-
-
0034774011
-
Nerve cells expressing heat-shock proteins in Parkinson's disease
-
Braak H, Del Tredici K, Sandmann-Kiel D, Rub U, Schultz C. 2001 Nerve cells expressing heat-shock proteins in Parkinson's disease. Acta Neuropathol. 102, 449-454.
-
(2001)
Acta Neuropathol
, vol.102
, pp. 449-454
-
-
Braak, H.1
Del Tredici, K.2
Sandmann-Kiel, D.3
Rub, U.4
Schultz, C.5
-
30
-
-
0025073458
-
Dementia with beta-amyloid deposition: Involvement of αB-crystallin supports two main diseases
-
doi:10. 1016/0140-6736(90)92075-S
-
Lowe J, Landon M, Pike I, Spendlove I, McDermott H, Mayer RJ. 1990 Dementia with beta-amyloid deposition: involvement of αB-crystallin supports two main diseases. Lancet 336, 515-516. (doi:10. 1016/0140-6736(90)92075-S)
-
(1990)
Lancet
, vol.336
, pp. 515-516
-
-
Lowe, J.1
Landon, M.2
Pike, I.3
Spendlove, I.4
McDermott, H.5
Mayer, R.J.6
-
31
-
-
0026541969
-
αB crystallin expression in non-lenticular tissues and selective presence in ubiquitinated inclusion bodies in human disease. J
-
doi:10.1002/path.1711660110
-
Lowe J, McDermott H, Pike I, Spendlove I, Landon M, Mayer RJ. 1992 αB crystallin expression in non-lenticular tissues and selective presence in ubiquitinated inclusion bodies in human disease. J. Pathol. 166, 61-68. (doi:10.1002/path.1711660110)
-
(1992)
Pathol
, vol.166
, pp. 61-68
-
-
Lowe, J.1
McDermott, H.2
Pike, I.3
Spendlove, I.4
Landon, M.5
Mayer, R.J.6
-
32
-
-
39049119728
-
Conformational stability of PrP amyloid fibrils controls their smallest possible fragment size
-
doi:10.1016/j.jmb.2007.12.053
-
Sun Y, Makarava N, Lee CI, Laksanalamai P, Robb FT, Baskakov IV. 2008 Conformational stability of PrP amyloid fibrils controls their smallest possible fragment size. J. Mol. Biol. 376, 1155-1167. (doi:10.1016/j.jmb.2007.12.053)
-
(2008)
J. Mol. Biol
, vol.376
, pp. 1155-1167
-
-
Sun, Y.1
Makarava, N.2
Lee, C.I.3
Laksanalamai, P.4
Robb, F.T.5
Baskakov, I.V.6
-
33
-
-
0028173755
-
Expression of a B-crystallin in Alzheimer's disease
-
doi:10.1007/BF00296185
-
Renkawek K, Voorter CE, Bosman GJ, van Workum FP, de Jong WW. 1994 Expression of a B-crystallin in Alzheimer's disease. Acta Neuropathol. 87, 155-160. (doi:10.1007/BF00296185)
-
(1994)
Acta Neuropathol
, vol.87
, pp. 155-160
-
-
Renkawek, K.1
Voorter, C.E.2
Bosman, G.J.3
van Workum, F.P.4
de Jong, W.W.5
-
34
-
-
0027330972
-
αB crystallin and HSP28 are enhanced in the cerebral cortex of patients with Alzheimer's disease
-
doi:10.1016/0022-510X(93)90135-L
-
Shinohara H, Inaguma Y, Goto S, Inagaki T, Kato K. 1993 αB crystallin and HSP28 are enhanced in the cerebral cortex of patients with Alzheimer's disease. J. Neurol. Sci. 119, 203-208. (doi:10.1016/0022-510X(93)90135-L)
-
(1993)
J. Neurol. Sci
, vol.119
, pp. 203-208
-
-
Shinohara, H.1
Inaguma, Y.2
Goto, S.3
Inagaki, T.4
Kato, K.5
-
35
-
-
3242770627
-
Interaction of the molecular chaperone αB-crystallin with alpha-synuclein: Effects on amyloid fibril formation and chaperone activity
-
doi:10. 1016/j.jmb.2004.05.054
-
Rekas A et al. 2004 Interaction of the molecular chaperone αB-crystallin with alpha-synuclein: effects on amyloid fibril formation and chaperone activity. J. Mol. Biol. 340, 1167-1183. (doi:10. 1016/j.jmb.2004.05.054)
-
(2004)
J. Mol. Biol
, vol.340
, pp. 1167-1183
-
-
Rekas, A.1
-
36
-
-
34249662262
-
GFAP and its role in Alexander disease
-
doi:10.1016/j.yexcr. 2007.04.004
-
Quinlan RA, Brenner M, Goldman JE, Messing A. 2007 GFAP and its role in Alexander disease. Exp. Cell Res. 313, 2077-2087. (doi:10.1016/j.yexcr. 2007.04.004)
-
(2007)
Exp. Cell Res
, vol.313
, pp. 2077-2087
-
-
Quinlan, R.A.1
Brenner, M.2
Goldman, J.E.3
Messing, A.4
-
37
-
-
0028365799
-
Sense and antisense modification of glial a B-crystallin production results in alterations of stress fiber formation and thermoresistance
-
doi:10.1083/jcb.125.6.1385
-
Iwaki T, Iwaki A, Tateishi J, Goldman JE. 1994 Sense and antisense modification of glial a B-crystallin production results in alterations of stress fiber formation and thermoresistance. J. Cell Biol. 125, 1385-1393. (doi:10.1083/jcb.125.6.1385)
-
(1994)
J. Cell Biol
, vol.125
, pp. 1385-1393
-
-
Iwaki, T.1
Iwaki, A.2
Tateishi, J.3
Goldman, J.E.4
-
38
-
-
0028176579
-
Chaperone activity of alpha-crystallins modulates intermediate filament assembly
-
Nicholl ID, Quinlan RA. 1994 Chaperone activity of alpha-crystallins modulates intermediate filament assembly. EMBO J. 13, 945-953.
-
(1994)
EMBO J
, vol.13
, pp. 945-953
-
-
Nicholl, I.D.1
Quinlan, R.A.2
-
39
-
-
33749184049
-
Up-regulation of heat shock protein HSP 20 in the hippocampus as an early response to hypoxia of the newborn
-
doi:10. 1111/j.1471-4159.2006.04071.x
-
David JC, Boelens WC, Grongnet JF. 2006 Up-regulation of heat shock protein HSP 20 in the hippocampus as an early response to hypoxia of the newborn. J. Neurochem. 99, 570-581. (doi:10. 1111/j.1471-4159.2006.04071.x)
-
(2006)
J. Neurochem
, vol.99
, pp. 570-581
-
-
David, J.C.1
Boelens, W.C.2
Grongnet, J.F.3
-
40
-
-
79958765896
-
The emerging role of HSP20 as a multifunctional protective agent
-
doi:10.1016/j.cellsig.2011.05.009
-
Edwards HV, Cameron RT, Baillie GS. 2011 The emerging role of HSP20 as a multifunctional protective agent. Cell Signal. 23, 1447-1454. (doi:10.1016/j.cellsig.2011.05.009)
-
(2011)
Cell Signal
, vol.23
, pp. 1447-1454
-
-
Edwards, H.V.1
Cameron, R.T.2
Baillie, G.S.3
-
41
-
-
19944432868
-
Transducible heat shock protein 20 (HSP20) phosphopeptide alters cytoskeletal dynamics
-
doi:10.1096/fj.04-2911fje
-
Dreiza CM et al. 2005 Transducible heat shock protein 20 (HSP20) phosphopeptide alters cytoskeletal dynamics. FASEB J. 19, 261-263. (doi:10.1096/fj.04-2911fje)
-
(2005)
FASEB J
, vol.19
, pp. 261-263
-
-
Dreiza, C.M.1
-
42
-
-
12944328888
-
Comparison of the small heat shock proteins alphaB-crystallin, MKBP, HSP25, HSP20, and cvHSP in heart and skeletal muscle
-
doi:10.1007/s00418-004-0711-z
-
Golenhofen N, Perng MD, Quinlan RA, Drenckhahn D. 2004 Comparison of the small heat shock proteins alphaB-crystallin, MKBP, HSP25, HSP20, and cvHSP in heart and skeletal muscle. Histochem. Cell Biol. 122, 415-425. (doi:10.1007/s00418-004-0711-z)
-
(2004)
Histochem. Cell Biol
, vol.122
, pp. 415-425
-
-
Golenhofen, N.1
Perng, M.D.2
Quinlan, R.A.3
Drenckhahn, D.4
-
43
-
-
77955365630
-
The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS)
-
doi:10.1093/hmg/ddq257
-
Crippa V et al. 2010 The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS). Hum. Mol. Genet. 19, 3440-3456. (doi:10.1093/hmg/ddq257)
-
(2010)
Hum. Mol. Genet
, vol.19
, pp. 3440-3456
-
-
Crippa, V.1
-
44
-
-
84855516743
-
The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases
-
doi:10. 1111/j.1365-2990.2011.01198.x
-
Seidel K et al. 2011 The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases. Neuropathol. Appl. Neurobiol. 38, 39-53. (doi:10. 1111/j.1365-2990.2011.01198.x)
-
(2011)
Neuropathol. Appl. Neurobiol
, vol.38
, pp. 39-53
-
-
Seidel, K.1
-
45
-
-
77949876309
-
Small heat shock proteins and protein-misfolding diseases
-
doi:10.2174/138920110790909669
-
Laskowska E, Matuszewska E, Kuczynska-Wisnik D. 2010 Small heat shock proteins and protein-misfolding diseases. Curr. Pharm. Biotechnol. 11, 146-157. (doi:10.2174/138920110790909669)
-
(2010)
Curr. Pharm. Biotechnol
, vol.11
, pp. 146-157
-
-
Laskowska, E.1
Matuszewska, E.2
Kuczynska-Wisnik, D.3
-
46
-
-
38349105324
-
HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy
-
doi:10.1074/jbc.M706304200
-
Carra S, Seguin SJ, Lambert H, Landry J. 2008 HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy. J. Biol. Chem. 283, 1437-1444. (doi:10.1074/jbc.M706304200)
-
(2008)
J. Biol. Chem
, vol.283
, pp. 1437-1444
-
-
Carra, S.1
Seguin, S.J.2
Lambert, H.3
Landry, J.4
-
47
-
-
21244489544
-
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells
-
doi:10.1093/hmg/ddi174
-
Carra S, Sivilotti M, Chavez Zobel AT, Lambert H, Landry J. 2005 HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells. Hum. Mol. Genet. 14, 1659-1669. (doi:10.1093/hmg/ddi174)
-
(2005)
Hum. Mol. Genet
, vol.14
, pp. 1659-1669
-
-
Carra, S.1
Sivilotti, M.2
Chavez Zobel, A.T.3
Lambert, H.4
Landry, J.5
-
48
-
-
65549101724
-
HspB8 participates in protein quality control by a non-chaperone-like mechanism that requires eIF2a phosphorylation
-
doi:10.1074/jbc.M807440200
-
Carra S, Brunsting JF, Lambert H, Landry J, Kampinga HH. 2009 HspB8 participates in protein quality control by a non-chaperone-like mechanism that requires eIF2a phosphorylation. J. Biol. Chem. 284, 5523-5532. (doi:10.1074/jbc.M807440200)
-
(2009)
J. Biol. Chem
, vol.284
, pp. 5523-5532
-
-
Carra, S.1
Brunsting, J.F.2
Lambert, H.3
Landry, J.4
Kampinga, H.H.5
-
49
-
-
0033515597
-
HSP27 multimerization mediated by phosphorylation-sensitive intermolecular interactions at the amino terminus
-
doi:10.1074/jbc.274.14.9378
-
Lambert H, Charette SJ, Bernier AF, Guimond A, Landry J. 1999 HSP27 multimerization mediated by phosphorylation-sensitive intermolecular interactions at the amino terminus. J. Biol. Chem. 274, 9378-9385. (doi:10.1074/jbc.274.14.9378)
-
(1999)
J. Biol. Chem
, vol.274
, pp. 9378-9385
-
-
Lambert, H.1
Charette, S.J.2
Bernier, A.F.3
Guimond, A.4
Landry, J.5
-
50
-
-
4744353967
-
Testis-specific human small heat shock protein HSPB9 is a cancer/testis antigen, and potentially interacts with the dynein subunit TCTEL1
-
doi:10.1078/0171-9335-00396
-
de Wit NJ, Verschuure P, Kappe G, King SM, de Jong WW, van Muijen GN, Boelens WC. 2004 Testis-specific human small heat shock protein HSPB9 is a cancer/testis antigen, and potentially interacts with the dynein subunit TCTEL1. Eur. J. Cell Biol. 83, 337-345. (doi:10.1078/0171-9335-00396)
-
(2004)
Eur. J. Cell Biol
, vol.83
, pp. 337-345
-
-
de Wit, N.J.1
Verschuure, P.2
Kappe, G.3
King, S.M.4
de Jong, W.W.5
van Muijen, G.N.6
Boelens, W.C.7
-
51
-
-
0037359564
-
The sperm outer dense fiber protein is the 10th member of the superfamily of mammalian small stress proteins
-
doi:10.1379/1466-1268
-
Fontaine JM, Rest JS, Welsh MJ, Benndorf R. 2003 The sperm outer dense fiber protein is the 10th member of the superfamily of mammalian small stress proteins. Cell Stress Chaperones 8, 62-69. (doi:10.1379/1466-1268)
-
(2003)
Cell Stress Chaperones
, vol.8
, pp. 62-69
-
-
Fontaine, J.M.1
Rest, J.S.2
Welsh, M.J.3
Benndorf, R.4
-
52
-
-
0037358061
-
The human genome encodes 10 a-crystallin-related small heat shock proteins: HspB1-10
-
doi:10.1379/1466-1268
-
Kappe G, Franck E, Verschuure P, Boelens WC, Leunissen JA, de Jong WW. 2003 The human genome encodes 10 a-crystallin-related small heat shock proteins: HspB1-10. Cell Stress Chaperones 8, 53-61. (doi:10.1379/1466-1268)
-
(2003)
Cell Stress Chaperones
, vol.8
, pp. 53-61
-
-
Kappe, G.1
Franck, E.2
Verschuure, P.3
Boelens, W.C.4
Leunissen, J.A.5
de Jong, W.W.6
-
53
-
-
0034009392
-
Characterization of alpha-crystallin-plasma membrane binding
-
doi:10.1074/jbc. 275.9.6664
-
Cobb BA, Petrash JM. 2000 Characterization of alpha-crystallin-plasma membrane binding. J. Biol. Chem. 275, 6664-6672. (doi:10.1074/jbc. 275.9.6664)
-
(2000)
J. Biol. Chem
, vol.275
, pp. 6664-6672
-
-
Cobb, B.A.1
Petrash, J.M.2
-
54
-
-
0035191639
-
Crystal structure and assembly of a eukaryotic small heat shock protein
-
doi:10.1038/nsb722
-
van Montfort RL, Basha E, Friedrich KL, Slingsby C, Vierling E. 2001 Crystal structure and assembly of a eukaryotic small heat shock protein. Nat. Struct. Biol. 8, 1025-1030. (doi:10.1038/nsb722)
-
(2001)
Nat. Struct. Biol
, vol.8
, pp. 1025-1030
-
-
van Montfort, R.L.1
Basha, E.2
Friedrich, K.L.3
Slingsby, C.4
Vierling, E.5
-
55
-
-
0035718677
-
Structure and function of the small heat shock protein/alpha-crystallin family of molecular chaperones
-
oi:10.1016/S0065-3233(01)59004.X
-
Van Montfort R, Slingsby C, Vierling E. 2001 Structure and function of the small heat shock protein/alpha-crystallin family of molecular chaperones. Adv. Protein Chem. 59, 105-156. (doi:10.1016/S0065-3233(01)59004.X)
-
(2001)
Adv. Protein Chem
, vol.59
, pp. 105-156
-
-
van Montfort, R.1
Slingsby, C.2
Vierling, E.3
-
56
-
-
0035895908
-
Phosphorylation-induced change of the oligomerization state of a B-crystallin
-
doi:10.1074/jbc. M009004200
-
Ito H, Kamei K, Iwamoto I, Inaguma Y, Nohara D, Kato K. 2001 Phosphorylation-induced change of the oligomerization state of a B-crystallin. J. Biol. Chem. 276, 5346-5352. (doi:10.1074/jbc. M009004200)
-
(2001)
J. Biol. Chem
, vol.276
, pp. 5346-5352
-
-
Ito, H.1
Kamei, K.2
Iwamoto, I.3
Inaguma, Y.4
Nohara, D.5
Kato, K.6
-
57
-
-
78650843219
-
Small heat shock proteins, protein degradation and protein aggregation diseases
-
doi:10.4161/auto. 7.1.13935
-
Vos MJ, Zijlstra MP, Carra S, Sibon OC, Kampinga HH. 2011 Small heat shock proteins, protein degradation and protein aggregation diseases. Autophagy 7, 101-103. (doi:10.4161/auto. 7.1.13935)
-
(2011)
Autophagy
, vol.7
, pp. 101-103
-
-
Vos, M.J.1
Zijlstra, M.P.2
Carra, S.3
Sibon, O.C.4
Kampinga, H.H.5
-
58
-
-
0026483279
-
α-Crystallin can function as a molecular chaperone
-
doi:10.1073/pnas. 89.21.10449
-
Horwitz J. 1992 α-Crystallin can function as a molecular chaperone. Proc. Natl Acad. Sci. USA 89, 10449-10453. (doi:10.1073/pnas. 89.21.10449)
-
(1992)
Proc. Natl Acad. Sci. USA
, vol.89
, pp. 10449-10453
-
-
Horwitz, J.1
-
59
-
-
0030826325
-
Structure-function studies on small heat shock protein oligomeric assembly and interaction with unfolded polypeptides
-
doi:10.1074/jbc.272.39.24646
-
Leroux MR, Melki R, Gordon B, Batelier G, Candido EP. 1997 Structure-function studies on small heat shock protein oligomeric assembly and interaction with unfolded polypeptides. J. Biol. Chem. 272, 24646-24656. (doi:10.1074/jbc.272.39.24646)
-
(1997)
J. Biol. Chem
, vol.272
, pp. 24646-24656
-
-
Leroux, M.R.1
Melki, R.2
Gordon, B.3
Batelier, G.4
Candido, E.P.5
-
60
-
-
33644842178
-
Differences in the chaperone-like activities of the four main small heat shock proteins of Drosophila melanogaster
-
doi:10.1379/CSC-166.1
-
Morrow G, Heikkila JJ, Tanguay RM. 2006 Differences in the chaperone-like activities of the four main small heat shock proteins of Drosophila melanogaster. Cell Stress Chaperones. 11, 51-60. (doi:10.1379/CSC-166.1)
-
(2006)
Cell Stress Chaperones
, vol.11
, pp. 51-60
-
-
Morrow, G.1
Heikkila, J.J.2
Tanguay, R.M.3
-
61
-
-
2642563501
-
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy
-
doi:10.1038/ng1354
-
Evgrafov OV et al. 2004 Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. Nat. Genet. 36, 602-606. (doi:10.1038/ng1354)
-
(2004)
Nat. Genet
, vol.36
, pp. 602-606
-
-
Evgrafov, O.V.1
-
62
-
-
0028924759
-
Modulation of cellular thermoresistance and actin filament stability accompanies phosphorylation-induced changes in the oligomeric structure of heat shock protein 27
-
Lavoie JN, Lambert H, Hickey E, Weber LA, Landry J. 1995 Modulation of cellular thermoresistance and actin filament stability accompanies phosphorylation-induced changes in the oligomeric structure of heat shock protein 27. Mol. Cell. Biol. 15, 505-516.
-
(1995)
Mol. Cell. Biol
, vol.15
, pp. 505-516
-
-
Lavoie, J.N.1
Lambert, H.2
Hickey, E.3
Weber, L.A.4
Landry, J.5
-
63
-
-
0030802287
-
Molecular chaperones and the cytoskeleton
-
Liang P, MacRae TH. 1997 Molecular chaperones and the cytoskeleton. J. Cell Sci. 110, 1431-1440.
-
(1997)
J. Cell Sci
, vol.110
, pp. 1431-1440
-
-
Liang, P.1
Macrae, T.H.2
-
64
-
-
0032818827
-
Intermediate filament interactions can be altered by HSP27 and alphaB-crystallin
-
Perng MD, Cairns L, van den IJssel P, Prescott A, Hutcheson AM, Quinlan RA. 1999 Intermediate filament interactions can be altered by HSP27 and alphaB-crystallin. J. Cell Sci. 112, 2099-2112.
-
(1999)
J. Cell Sci
, vol.112
, pp. 2099-2112
-
-
Perng, M.D.1
Cairns, L.2
van den Ijssel, P.3
Prescott, A.4
Hutcheson, A.M.5
Quinlan, R.A.6
-
65
-
-
0036186869
-
Hsp27: Novel regulator of intracellular redox state
-
doi:10.1080/152165401317291165
-
Arrigo AP. 2001 Hsp27: novel regulator of intracellular redox state. IUBMB Life. 52, 303-307. (doi:10.1080/152165401317291165)
-
(2001)
IUBMB Life
, vol.52
, pp. 303-307
-
-
Arrigo, A.P.1
-
66
-
-
0036143720
-
Hsp27 as a negative regulator of cytochrome C release
-
doi:10.1128/MCB.22.3.816-834.2002
-
Paul C, Manero F, Gonin S, Kretz-Remy C, Virot S, Arrigo AP. 2002 Hsp27 as a negative regulator of cytochrome C release. Mol. Cell. Biol. 22, 816-834. (doi:10.1128/MCB.22.3.816-834.2002)
-
(2002)
Mol. Cell. Biol
, vol.22
, pp. 816-834
-
-
Paul, C.1
Manero, F.2
Gonin, S.3
Kretz-Remy, C.4
Virot, S.5
Arrigo, A.P.6
-
67
-
-
77952890212
-
Dynamic processes that reflect anti-apoptotic strategies set up by HspB1 (Hsp27)
-
doi:10.1016/j.yexcr. 2010.03.006
-
Paul C, Simon S, Gibert B, Virot S, Manero F, Arrigo AP. 2010 Dynamic processes that reflect anti-apoptotic strategies set up by HspB1 (Hsp27). Exp. Cell. Res. 316, 1535-1552. (doi:10.1016/j.yexcr. 2010.03.006)
-
(2010)
Exp. Cell. Res
, vol.316
, pp. 1535-1552
-
-
Paul, C.1
Simon, S.2
Gibert, B.3
Virot, S.4
Manero, F.5
Arrigo, A.P.6
-
68
-
-
11144243412
-
Modulation of neurodegeneration by molecular chaperones
-
doi:10.1038/nrn1587)
-
Muchowski PJ, Wacker JL. 2005 Modulation of neurodegeneration by molecular chaperones. Nat. Rev. Neurosci. 6, 11-22. (doi:10.1038/nrn1587)
-
(2005)
Nat. Rev. Neurosci
, vol.6
, pp. 11-22
-
-
Muchowski, P.J.1
Wacker, J.L.2
-
69
-
-
78651499280
-
Dysregulation of axonal transport and motorneuron diseases
-
doi:10.1042/BC20100093
-
Sau D, Rusmini P, Crippa V, Onesto E, Bolzoni E, Ratti A, Poletti A. 2011 Dysregulation of axonal transport and motorneuron diseases. Biol. Cell 103, 87-107. (doi:10.1042/BC20100093)
-
(2011)
Biol. Cell
, vol.103
, pp. 87-107
-
-
Sau, D.1
Rusmini, P.2
Crippa, V.3
Onesto, E.4
Bolzoni, E.5
Ratti, A.6
Poletti, A.7
-
70
-
-
7244236320
-
Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
-
doi:10.1038/ nature02998
-
Arrasate M, Mitra S, Schweitzer ES, Segal MR, Finkbeiner S. 2004 Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death. Nature 431, 805-810. (doi:10.1038/ nature02998)
-
(2004)
Nature
, vol.431
, pp. 805-810
-
-
Arrasate, M.1
Mitra, S.2
Schweitzer, E.S.3
Segal, M.R.4
Finkbeiner, S.5
-
71
-
-
0032475941
-
Ataxin-1 nuclear localization and aggregation: Role in polyglutamine-induced disease in SCA1 transgenic mice
-
doi:10.1016/S0092-8674(00)81781-X
-
Klement IA, Skinner PJ, Kaytor MD, Yi H, Hersch SM, Clark HB, Zoghbi HY, Orr HT. 1998 Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice. Cell 95, 41-53. (doi:10.1016/S0092-8674(00)81781-X)
-
(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
-
72
-
-
0034098057
-
Motoneuronal cell death is not correlated with aggregate formation of androgen receptors containing an elongated polyglutamine tract
-
doi:10.1093/ hmg/9.1.133
-
Simeoni S, Mancini MA, Stenoien DL, Marcelli M, Weigel NL, Zanisi M, Martini L, Poletti A. 2000 Motoneuronal cell death is not correlated with aggregate formation of androgen receptors containing an elongated polyglutamine tract. Hum. Mol. Genet. 9, 133-144. (doi:10.1093/ hmg/9.1.133)
-
(2000)
Hum. Mol. Genet
, vol.9
, pp. 133-144
-
-
Simeoni, S.1
Mancini, M.A.2
Stenoien, D.L.3
Marcelli, M.4
Weigel, N.L.5
Zanisi, M.6
Martini, L.7
Poletti, A.8
-
73
-
-
34247365603
-
Aggregation and proteasome: The case of elongated polyglutamine aggregation in spinal and bulbar muscular atrophy
-
doi:10.1016/j.neurobiolaging.2006.05.015
-
Rusmini P, Sau D, Crippa V, Palazzolo I, Simonini F, Onesto E, Martini L, Poletti A. 2007 Aggregation and proteasome: the case of elongated polyglutamine aggregation in spinal and bulbar muscular atrophy. Neurobiol. Aging 28, 1099-1111. (doi:10.1016/j.neurobiolaging.2006.05.015)
-
(2007)
Neurobiol. Aging
, vol.28
, pp. 1099-1111
-
-
Rusmini, P.1
Sau, D.2
Crippa, V.3
Palazzolo, I.4
Simonini, F.5
Onesto, E.6
Martini, L.7
Poletti, A.8
-
74
-
-
0032475931
-
Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions
-
doi:10.1016/S0092-8674(00)81782-1
-
Saudou F, Finkbeiner S, Devys D, Greenberg ME. 1998 Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions. Cell 95, 55-66. (doi:10.1016/S0092-8674(00)81782-1)
-
(1998)
Cell
, vol.95
, pp. 55-66
-
-
Saudou, F.1
Finkbeiner, S.2
Devys, D.3
Greenberg, M.E.4
-
75
-
-
19244384530
-
Distinct aggregation and cell death patterns among different types of primary neurons induced by mutant huntingtin protein
-
doi:10.1111/j.1471-4159.2004.02372.x
-
Tagawa K et al. 2004 Distinct aggregation and cell death patterns among different types of primary neurons induced by mutant huntingtin protein. J. Neurochem. 89, 974-987. (doi:10.1111/j.1471-4159.2004.02372.x)
-
(2004)
J. Neurochem
, vol.89
, pp. 974-987
-
-
Tagawa, K.1
-
76
-
-
7944233158
-
Cell biology of protein misfolding: The examples of Alzheimer's and Parkinson's diseases
-
doi:10. 1038/ncb1104-1054
-
Selkoe DJ. 2004 Cell biology of protein misfolding: the examples of Alzheimer's and Parkinson's diseases. Nat. Cell Biol. 6, 1054-1061. (doi:10. 1038/ncb1104-1054)
-
(2004)
Nat. Cell Biol
, vol.6
, pp. 1054-1061
-
-
Selkoe, D.J.1
-
77
-
-
0037388418
-
Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing protein
-
doi:10. 1093/hmg/ddg074
-
Taylor JP, Tanaka F, Robitschek J, Sandoval CM, Taye A, Markovic-Plese S, Fischbeck KH. 2003 Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing protein. Hum. Mol. Genet. 12, 749-757. (doi:10. 1093/hmg/ddg074)
-
(2003)
Hum. Mol. Genet
, vol.12
, pp. 749-757
-
-
Taylor, J.P.1
Tanaka, F.2
Robitschek, J.3
Sandoval, C.M.4
Taye, A.5
Markovic-Plese, S.6
Fischbeck, K.H.7
-
78
-
-
0037444446
-
Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor protein
-
Adachi H et al. 2003 Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor protein. J. Neurosci. 23, 2203-2211.
-
(2003)
J. Neurosci
, vol.23
, pp. 2203-2211
-
-
Adachi, H.1
-
79
-
-
0036501074
-
Molecular chaperones enhance the degradation of expanded polyglutamine repeat androgen receptor in a cellular model of spinal and bulbar muscular atrophy
-
doi:10.1093/hmg/11.5.515
-
Bailey CK, Andriola IF, Kampinga HH, Merry DE. 2002 Molecular chaperones enhance the degradation of expanded polyglutamine repeat androgen receptor in a cellular model of spinal and bulbar muscular atrophy. Hum. Mol. Genet. 11, 515-523. (doi:10.1093/hmg/11.5.515)
-
(2002)
Hum. Mol. Genet
, vol.11
, pp. 515-523
-
-
Bailey, C.K.1
Andriola, I.F.2
Kampinga, H.H.3
Merry, D.E.4
-
80
-
-
0033499931
-
Analysis of the role of heat shock protein (HSP) molecular chaperones in polyglutamine disease
-
Chai Y, Koppenhafer SL, Bonini NM, Paulson HL. 1999 Analysis of the role of heat shock 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
-
81
-
-
0035394668
-
Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice
-
doi:10.1093/hmg/10.14.1511
-
Cummings CJ, Sun Y, Opal P, Antalffy B, Mestril R, Orr HT, Dillmann WH, Zoghbi HY. 2001 Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice. Hum. Mol. Genet. 10, 1511-1518. (doi:10.1093/hmg/10.14.1511)
-
(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
-
82
-
-
28044469532
-
Pharmacological induction of heat-shock proteins alleviates polyglutamine-mediated motor neuron disease
-
doi:10.1073/pnas.0506249102
-
Katsuno M, Sang C, Adachi H, Minamiyama M, Waza M, Tanaka F, Doyu M, Sobue G. 2005 Pharmacological induction of heat-shock proteins alleviates polyglutamine-mediated motor neuron disease. Proc. Natl Acad. Sci. USA 102, 16801-16806. (doi:10.1073/pnas.0506249102)
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 16801-16806
-
-
Katsuno, M.1
Sang, C.2
Adachi, H.3
Minamiyama, M.4
Waza, M.5
Tanaka, F.6
Doyu, M.7
Sobue, G.8
-
83
-
-
0035504859
-
Protective effect of chaperones on polyglutamine diseases
-
doi:10.1016/S0361-9230(01) 00593-7
-
Kobayashi Y, Sobue G. 2001 Protective effect of chaperones on polyglutamine diseases. Brain Res. Bull. 56, 165-168. (doi:10.1016/S0361-9230(01) 00593-7)
-
(2001)
Brain Res. Bull
, vol.56
, pp. 165-168
-
-
Kobayashi, Y.1
Sobue, G.2
-
84
-
-
33645897980
-
Alteration of familial ALS-linked mutant SOD1 solubility with disease progression: Its modulation by the proteasome and Hsp70
-
doi:10.1016/j.bbrc.2006.02.170
-
Koyama S et al. 2006 Alteration of familial ALS-linked mutant SOD1 solubility with disease progression: its modulation by the proteasome and Hsp70. Biochem. Biophys. Res. Commun. 343, 719-730. (doi:10.1016/j.bbrc.2006.02.170)
-
(2006)
Biochem. Biophys. Res. Commun
, vol.343
, pp. 719-730
-
-
Koyama, S.1
-
85
-
-
17044403380
-
Hsp27 and Hsp70 administered in combination have a potent protective effect against FALS-associated SOD1-mutant-induced cell death in mammalian neuronal cells
-
doi:10.1016/j. molbrainres.2004.10.028
-
Patel YJ, Payne Smith MD, de Belleroche J, Latchman DS. 2005 Hsp27 and Hsp70 administered in combination have a potent protective effect against FALS-associated SOD1-mutant-induced cell death in mammalian neuronal cells. Brain Res. Mol. Brain Res. 134, 256-274. (doi:10.1016/j. molbrainres.2004.10.028)
-
(2005)
Brain Res. Mol. Brain Res
, vol.134
, pp. 256-274
-
-
Patel, Y.J.1
Payne Smith, M.D.2
de Belleroche, J.3
Latchman, D.S.4
-
86
-
-
78349309239
-
Poletti A. 2011 17-AAG increases autophagic removal of mutant androgen receptor in spinal and bulbar muscular atrophy
-
doi:10.1016/j.nbd. 2010.08.023
-
Rusmini P, Simonini F, Crippa V, Bolzoni E, Onesto E, Cagnin M, Sau D, Ferri N, Poletti A. 2011 17-AAG increases autophagic removal of mutant androgen receptor in spinal and bulbar muscular atrophy. Neurobiol. Dis. 41, 83-95. (doi:10.1016/j.nbd. 2010.08.023)
-
Neurobiol. Dis
, vol.41
, pp. 83-95
-
-
Rusmini, P.1
Simonini, F.2
Crippa, V.3
Bolzoni, E.4
Onesto, E.5
Cagnin, M.6
Sau, D.7
Ferri, N.8
-
87
-
-
0032727617
-
Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70
-
doi:10.1038/70532
-
Warrick JM, Chan HY, Gray-Board GL, Chai Y, Paulson HL, Bonini NM. 1999 Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70. Nat. Genet. 23, 425-428. (doi:10.1038/70532)
-
(1999)
Nat. Genet
, vol.23
, pp. 425-428
-
-
Warrick, J.M.1
Chan, H.Y.2
Gray-Board, G.L.3
Chai, Y.4
Paulson, H.L.5
Bonini, N.M.6
-
88
-
-
27144503120
-
17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration
-
doi:10.1038/nm1298
-
Waza M, Adachi H, Katsuno M, Minamiyama M, Sang C, Tanaka F, Inukai A, Doyu M, Sobue G. 2005 17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration. Nat. Med. 11, 1088-1095. (doi:10.1038/nm1298)
-
(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
-
89
-
-
33746724745
-
Modulation of Hsp90 function in neurodegenerative disorders: A molecular-targeted therapy against disease-causing protein
-
doi:10.1007/ s00109-006-0066-0
-
Waza M, Adachi H, Katsuno M, Minamiyama M, Tanaka F, Doyu M, Sobue G. 2006 Modulation of Hsp90 function in neurodegenerative disorders: a molecular-targeted therapy against disease-causing protein. J. Mol. Med. 84, 635-646. (doi:10.1007/ s00109-006-0066-0)
-
(2006)
J. Mol. Med
, vol.84
, pp. 635-646
-
-
Waza, M.1
Adachi, H.2
Katsuno, M.3
Minamiyama, M.4
Tanaka, F.5
Doyu, M.6
Sobue, G.7
-
90
-
-
34547893834
-
Heat-shock protein 105 interacts with and suppresses aggregation of mutant Cu/Zn superoxide dismutase: Clues to a possible strategy for treating ALS
-
doi:10.1111/j.1471-4159. 2007.04534.x
-
Yamashita H, Kawamata J, Okawa K, Kanki R, Nakamizo T, Hatayama T, Yamanaka K, Takahashi R, Shimohama S. 2007 Heat-shock protein 105 interacts with and suppresses aggregation of mutant Cu/Zn superoxide dismutase: clues to a possible strategy for treating ALS. J. Neurochem. 102, 1497-1505. (doi:10.1111/j.1471-4159. 2007.04534.x)
-
(2007)
J. Neurochem
, vol.102
, pp. 1497-1505
-
-
Yamashita, H.1
Kawamata, J.2
Okawa, K.3
Kanki, R.4
Nakamizo, T.5
Hatayama, T.6
Yamanaka, K.7
Takahashi, R.8
Shimohama, S.9
-
91
-
-
75949094261
-
A DNAJB chaperone subfamily with HDAC-dependent activities suppresses toxic protein aggregation
-
doi:10.1016/j.molcel. 2010.01.001
-
Hageman J, Rujano MA, van Waarde MA, Kakkar V, Dirks RP, Govorukhina N, Oosterveld-Hut HM, Lubsen NH, Kampinga HH. 2010 A DNAJB chaperone subfamily with HDAC-dependent activities suppresses toxic protein aggregation. Mol. Cell 37, 355-369. (doi:10.1016/j.molcel. 2010.01.001)
-
(2010)
Mol. Cell
, vol.37
, pp. 355-369
-
-
Hageman, J.1
Rujano, M.A.2
van Waarde, M.A.3
Kakkar, V.4
Dirks, R.P.5
Govorukhina, N.6
Oosterveld-Hut, H.M.7
Lubsen, N.H.8
Kampinga, H.H.9
-
92
-
-
46849116411
-
Structural and functional diversities between members of the human HSPB, HSPH, HSPA, and DNAJ chaperone families
-
doi:10.1021/bi800639z
-
Vos MJ, Hageman J, Carra S, Kampinga HH. 2008 Structural and functional diversities between members of the human HSPB, HSPH, HSPA, and DNAJ chaperone families. Biochemistry 47, 7001-7011. (doi:10.1021/bi800639z)
-
(2008)
Biochemistry
, vol.47
, pp. 7001-7011
-
-
Vos, M.J.1
Hageman, J.2
Carra, S.3
Kampinga, H.H.4
-
93
-
-
77449132101
-
The small heat shock protein, HSPB6, in muscle function and disease
-
doi:10.1007/s12192-009-0127-8
-
Dreiza CM, Komalavilas P, Furnish EJ, Flynn CR, Sheller MR, Smoke CC, Lopes LB, Brophy CM. 2010 The small heat shock protein, HSPB6, in muscle function and disease. Cell Stress Chaperones 15, 1-11. (doi:10.1007/s12192-009-0127-8)
-
(2010)
Cell Stress Chaperones
, vol.15
, pp. 1-11
-
-
Dreiza, C.M.1
Komalavilas, P.2
Furnish, E.J.3
Flynn, C.R.4
Sheller, M.R.5
Smoke, C.C.6
Lopes, L.B.7
Brophy, C.M.8
-
94
-
-
0037179756
-
Hsp27 upregulation and phosphorylation is required for injured sensory and motor neuron survival
-
doi:10.1016/S0896-6273(02)00941-8
-
Benn SC, Perrelet D, Kato AC, Scholz J, Decosterd I, Mannion RJ, Bakowska JC, Woolf CJ. 2002 Hsp27 upregulation and phosphorylation is required for injured sensory and motor neuron survival. Neuron 36, 45-56. (doi:10.1016/S0896-6273(02)00941-8)
-
(2002)
Neuron
, vol.36
, pp. 45-56
-
-
Benn, S.C.1
Perrelet, D.2
Kato, A.C.3
Scholz, J.4
Decosterd, I.5
Mannion, R.J.6
Bakowska, J.C.7
Woolf, C.J.8
-
95
-
-
77957665681
-
A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases
-
doi:10.4161/auto. 6.7.13042
-
Crippa V, Carra S, Rusmini P, Sau D, Bolzoni E, Bendotti C, De Biasi S, Poletti A. 2010 A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases. Autophagy 6, 958-960. (doi:10.4161/auto. 6.7.13042)
-
(2010)
Autophagy
, vol.6
, pp. 958-960
-
-
Crippa, V.1
Carra, S.2
Rusmini, P.3
Sau, D.4
Bolzoni, E.5
Bendotti, C.6
de Biasi, S.7
Poletti, A.8
-
96
-
-
33744798774
-
Onset and progression in inherited ALS determined by motor neurons and microglia
-
doi:10.1126/science. 1123511
-
Boillee S, Yamanaka K, Lobsiger CS, Copeland NG, Jenkins NA, Kassiotis G, Kollias G, Cleveland DW. 2006 Onset and progression in inherited ALS determined by motor neurons and microglia. Science 312, 1389-1392. (doi:10.1126/science. 1123511)
-
(2006)
Science
, vol.312
, pp. 1389-1392
-
-
Boillee, S.1
Yamanaka, K.2
Lobsiger, C.S.3
Copeland, N.G.4
Jenkins, N.A.5
Kassiotis, G.6
Kollias, G.7
Cleveland, D.W.8
-
97
-
-
0033366461
-
SOD1 mutants linked to amyotrophic lateral sclerosis selectively inactivate a glial glutamate transporter
-
doi:10.1038/8091
-
Trotti D, Rolfs A, Danbolt NC, Brown Jr RH, Hediger MA. 1999 SOD1 mutants linked to amyotrophic lateral sclerosis selectively inactivate a glial glutamate transporter. Nat. Neurosci. 2, 427-433. (doi:10.1038/8091)
-
(1999)
Nat. Neurosci
, vol.2
, pp. 427-433
-
-
Trotti, D.1
Rolfs, A.2
Danbolt, N.C.3
Brown, R.H.4
Hediger, M.A.5
-
98
-
-
79959982281
-
Muscle cells and motoneurons differentially remove mutant SOD1 causing familial amyotrophic lateral sclerosis
-
doi:10.1111/j.1471-4159.2011.07298.x
-
Onesto E, Rusmini P, Crippa V, Ferri N, Zito A, Galbiati M, Poletti A. 2011 Muscle cells and motoneurons differentially remove mutant SOD1 causing familial amyotrophic lateral sclerosis. J. Neurochem. 118, 266-280. (doi:10.1111/j.1471-4159.2011.07298.x)
-
(2011)
J. Neurochem
, vol.118
, pp. 266-280
-
-
Onesto, E.1
Rusmini, P.2
Crippa, V.3
Ferri, N.4
Zito, A.5
Galbiati, M.6
Poletti, A.7
-
99
-
-
54849404282
-
Skeletal muscle is a primary target of SOD1G93A-mediated toxicity
-
doi:10.1016/j.cmet. 2008.09.002
-
Dobrowolny G et al. 2008 Skeletal muscle is a primary target of SOD1G93A-mediated toxicity. Cell Metab. 8, 425-436. (doi:10.1016/j.cmet. 2008.09.002)
-
(2008)
Cell Metab
, vol.8
, pp. 425-436
-
-
Dobrowolny, G.1
-
100
-
-
77953530958
-
Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice
-
doi:10.1093/hmg/ddq106
-
Wong M, Martin LJ. 2010 Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice. Hum. Mol. Genet. 19, 2284-2302. (doi:10.1093/hmg/ddq106)
-
(2010)
Hum. Mol. Genet
, vol.19
, pp. 2284-2302
-
-
Wong, M.1
Martin, L.J.2
-
101
-
-
78549246252
-
Identification of the Drosophila ortholog of HSPB8: Implication of HSPB8 loss of function in protein folding diseases
-
doi:10.1074/jbc. M110.127498
-
Carra S et al. 2010 Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. J. Biol. Chem. 285, 37811-37822. (doi:10.1074/jbc. M110.127498)
-
(2010)
J. Biol. Chem
, vol.285
, pp. 37811-37822
-
-
Carra, S.1
-
102
-
-
65249153614
-
The stress-inducible HspB8-Bag3 complex induces the eIF2a kinase pathway: Implications for protein quality control and viral factory degradation?
-
Carra S. 2009 The stress-inducible HspB8-Bag3 complex induces the eIF2a kinase pathway: implications for protein quality control and viral factory degradation? Autophagy 5, 428-429. (doi:10.4161/auto.5.3.7894)
-
(2009)
Autophagy
, vol.5
, pp. 428-429
-
-
Carra, S.1
-
103
-
-
38949108670
-
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes
-
Klionsky DJ et al. 2008 Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes. Autophagy 4, 151-175.
-
(2008)
Autophagy
, vol.4
, pp. 151-175
-
-
Klionsky, D.J.1
-
104
-
-
74549133523
-
Chaperone-assisted selective autophagy is essential for muscle maintenance
-
doi:10.1016/j.cub. 2009.11.022
-
Arndt V et al. 2010 Chaperone-assisted selective autophagy is essential for muscle maintenance. Curr. Biol. 20, 143-148. (doi:10.1016/j.cub. 2009.11.022)
-
(2010)
Curr. Biol
, vol.20
, pp. 143-148
-
-
Arndt, V.1
-
105
-
-
50649116818
-
Misfolded proteins partition between two distinct quality control compartments
-
doi:10.1038/nature07195
-
Kaganovich D, Kopito R, Frydman J. 2008 Misfolded proteins partition between two distinct quality control compartments. Nature 454, 1088-1095. (doi:10.1038/nature07195)
-
(2008)
Nature
, vol.454
, pp. 1088-1095
-
-
Kaganovich, D.1
Kopito, R.2
Frydman, J.3
-
106
-
-
84860668972
-
Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins
-
doi:10.1016/j.pneurobio. 2011.09.009
-
Carra S, Crippa V, Rusmini P, Boncoraglio A, Minoia M, Giorgetti E, Kampinga HH, Poletti A. 2012 Alteration of protein folding and degradation in motor neuron diseases: implications and protective functions of small heat shock proteins. Prog. Neurobiol. 97, 83-100. (doi:10.1016/j.pneurobio. 2011.09.009)
-
(2012)
Prog. Neurobiol
, vol.97
, pp. 83-100
-
-
Carra, S.1
Crippa, V.2
Rusmini, P.3
Boncoraglio, A.4
Minoia, M.5
Giorgetti, E.6
Kampinga, H.H.7
Poletti, A.8
-
107
-
-
72449141635
-
Identification of the key structural motifs involved in
-
doi:10. 1042/BJ20090907
-
Fuchs M, Poirier DJ, Seguin SJ, Lambert H, Carra S, Charette SJ, Landry J. 2010 Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction. Biochem. J. 425, 245-255. (doi:10. 1042/BJ20090907)
-
(2010)
HspB8/HspB6-Bag3 Interaction. Biochem. J
, vol.425
, pp. 245-255
-
-
Fuchs, M.1
Poirier, D.J.2
Seguin, S.J.3
Lambert, H.4
Carra, S.5
Charette, S.J.6
Landry, J.7
-
108
-
-
73349134699
-
Blockade of Hsp20 phosphorylation exacerbates cardiac ischemia/reperfusion injury by suppressed autophagy and increased cell death
-
doi:10.1161/CIRCRESAHA.109.200378
-
Qian J, Ren X, Wang X, Zhang P, Jones WK, Molkentin JD, Fan GC, Kranias EG. 2009 Blockade of Hsp20 phosphorylation exacerbates cardiac ischemia/reperfusion injury by suppressed autophagy and increased cell death. Circ. Res. 105, 1223-1231. (doi:10.1161/CIRCRESAHA.109.200378)
-
(2009)
Circ. Res
, vol.105
, pp. 1223-1231
-
-
Qian, J.1
Ren, X.2
Wang, X.3
Zhang, P.4
Jones, W.K.5
Molkentin, J.D.6
Fan, G.C.7
Kranias, E.G.8
-
109
-
-
77950903972
-
The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy
-
doi:10.1016/j.molcel. 2010.04.007
-
Filimonenko M et al. 2010 The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy. Mol. Cell 38, 265-279. (doi:10.1016/j.molcel. 2010.04.007)
-
(2010)
Mol. Cell
, vol.38
, pp. 265-279
-
-
Filimonenko, M.1
-
110
-
-
33645214602
-
Huntingtin and mutant SOD1 form aggregate structures with distinct molecular properties in human cells
-
doi:10.1074/jbc. M509201200
-
Matsumoto G, Kim S, Morimoto RI. 2006 Huntingtin and mutant SOD1 form aggregate structures with distinct molecular properties in human cells. J. Biol. Chem. 281, 4477-4485. (doi:10.1074/jbc. M509201200)
-
(2006)
J. Biol. Chem
, vol.281
, pp. 4477-4485
-
-
Matsumoto, G.1
Kim, S.2
Morimoto, R.I.3
-
111
-
-
0037015081
-
Huntington's disease age-of-onset linked to polyglutamine aggregation nucleation
-
doi:10.1073/pnas.182276099
-
Chen S, Ferrone FA, Wetzel R. 2002 Huntington's disease age-of-onset linked to polyglutamine aggregation nucleation. Proc. Natl Acad. Sci. USA 99, 11884-11889. (doi:10.1073/pnas.182276099)
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 11884-11889
-
-
Chen, S.1
Ferrone, F.A.2
Wetzel, R.3
-
112
-
-
33947586837
-
Mechanisms of ataxin-3 misfolding and fibril formation: Kinetic analysis of a disease-associated polyglutamine protein
-
doi:10.1016/j.jmb.2007.02.058
-
Ellisdon AM, Pearce MC, Bottomley SP. 2007 Mechanisms of ataxin-3 misfolding and fibril formation: kinetic analysis of a disease-associated polyglutamine protein. J. Mol. Biol. 368, 595-605. (doi:10.1016/j.jmb.2007.02.058)
-
(2007)
J. Mol. Biol
, vol.368
, pp. 595-605
-
-
Ellisdon, A.M.1
Pearce, M.C.2
Bottomley, S.P.3
-
113
-
-
0037135111
-
The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeutics
-
doi:10.1126/science.1072994
-
Hardy J, Selkoe DJ. 2002 The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics. Science 297, 353-356. (doi:10.1126/science.1072994)
-
(2002)
Science
, vol.297
, pp. 353-356
-
-
Hardy, J.1
Selkoe, D.J.2
-
114
-
-
33744952750
-
Extended polyglutamine tracts cause aggregation and structural perturbation of an adjacent beta barrel protein
-
doi:10.1074/jbc.M511523200
-
Ignatova Z, Gierasch LM. 2006 Extended polyglutamine tracts cause aggregation and structural perturbation of an adjacent beta barrel protein. J. Biol. Chem. 281, 12959-12967. (doi:10.1074/jbc.M511523200)
-
(2006)
J. Biol. Chem. 281
, pp. 12959-12967
-
-
Ignatova, Z.1
Gierasch, L.M.2
-
115
-
-
0028985267
-
The precursor protein of non-A b component of Alzheimer's disease amyloid is a presynaptic protein of the central nervous system
-
doi:10.1016/0896-6273(95)90302-X
-
Iwai A, Masliah E, Yoshimoto M, Ge N, Flanagan L, de Silva HA, Kittel A, Saitoh T. 1995 The precursor protein of non-A b component of Alzheimer's disease amyloid is a presynaptic protein of the central nervous system. Neuron 14, 467-475. (doi:10.1016/0896-6273(95)90302-X)
-
(1995)
Neuron
, vol.14
, pp. 467-475
-
-
Iwai, A.1
Masliah, E.2
Yoshimoto, M.3
Ge, N.4
Flanagan, L.5
de Silva, H.A.6
Kittel, A.7
Saitoh, T.8
-
116
-
-
0034681471
-
Dopaminergic loss and inclusion body formation in a-synuclein mice: Implications for neurodegenerative disorders
-
doi:10.1126/science.287.5456.1265
-
Masliah E, Rockenstein E, Veinbergs I, Mallory M, Hashimoto M, Takeda A, Sagara Y, Sisk A, Mucke L. 2000 Dopaminergic loss and inclusion body formation in a-synuclein mice: implications for neurodegenerative disorders. Science 287, 1265-1269. (doi:10.1126/science.287.5456.1265)
-
(2000)
Science
, vol.287
, pp. 1265-1269
-
-
Masliah, E.1
Rockenstein, E.2
Veinbergs, I.3
Mallory, M.4
Hashimoto, M.5
Takeda, A.6
Sagara, Y.7
Sisk, A.8
Mucke, L.9
-
117
-
-
18544400323
-
Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo
-
doi:10.1016/S0092-8674(00)80514-0
-
Scherzinger E et al. 1997 Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo. Cell 90, 549-558. (doi:10.1016/S0092-8674(00)80514-0)
-
(1997)
Cell
, vol.90
, pp. 549-558
-
-
Scherzinger, E.1
-
118
-
-
3142514201
-
Protein aggregation and neurodegenerative disease
-
(doi:10.1038/nm1066)
-
Ross CA, Poirier MA. 2004 Protein aggregation and neurodegenerative disease. Nat. Med. 10(Suppl.), S10-S17. (doi:10.1038/nm1066)
-
(2004)
Nat. Med
, vol.10
, Issue.SUPPL.
-
-
Ross, C.A.1
Poirier, M.A.2
-
119
-
-
77749240461
-
The interaction of alphaB-crystallin with mature alpha-synuclein amyloid fibrils inhibits their elongation
-
doi:10.1016/j.bpj.2009. 10.056
-
Waudby CA et al. 2010 The interaction of alphaB-crystallin with mature alpha-synuclein amyloid fibrils inhibits their elongation. Biophys. J. 98, 843-851. (doi:10.1016/j.bpj.2009. 10.056)
-
(2010)
Biophys. J
, vol.98
, pp. 843-851
-
-
Waudby, C.A.1
-
120
-
-
36749037242
-
Monitoring the prevention of amyloid fibril formation by alpha-crystallin. Temperature dependence and the nature of the aggregating species
-
doi:10.1111/j. 1742-4658.2007.06144.x
-
Rekas A, Jankova L, Thorn DC, Cappai R, Carver JA. 2007 Monitoring the prevention of amyloid fibril formation by alpha-crystallin. Temperature dependence and the nature of the aggregating species. FEBS J. 274, 6290-6304. (doi:10.1111/j. 1742-4658.2007.06144.x)
-
(2007)
FEBS J
, vol.274
, pp. 6290-6304
-
-
Rekas, A.1
Jankova, L.2
Thorn, D.C.3
Cappai, R.4
Carver, J.A.5
-
121
-
-
77953799932
-
Small heat-shock proteins interact with a flanking domain to suppress polyglutamine aggregation
-
doi:10.1073/ pnas.0914773107
-
Robertson AL, Headey SJ, Saunders HM, Ecroyd H, Scanlon MJ, Carver JA, Bottomley SP. 2010 Small heat-shock proteins interact with a flanking domain to suppress polyglutamine aggregation. Proc. Natl Acad. Sci. USA 107, 10424-10429. (doi:10.1073/ pnas.0914773107)
-
(2010)
Proc. Natl Acad. Sci. USA 107
, pp. 10424-10429
-
-
Robertson, A.L.1
Headey, S.J.2
Saunders, H.M.3
Ecroyd, H.4
Scanlon, M.J.5
Carver, J.A.6
Bottomley, S.P.7
-
122
-
-
8544260320
-
Characterization of the structure and the amyloidogenic properties of the Josephin domain of the polyglutamine-containing protein ataxin-3
-
doi:10. 1016/j.jmb.2004.09.065
-
Masino L, Nicastro G, Menon RP, Dal Piaz F, Calder L, Pastore A. 2004 Characterization of the structure and the amyloidogenic properties of the Josephin domain of the polyglutamine-containing protein ataxin-3. J. Mol. Biol. 344, 1021-1035. (doi:10. 1016/j.jmb.2004.09.065)
-
(2004)
J. Mol. Biol
, vol.344
, pp. 1021-1035
-
-
Masino, L.1
Nicastro, G.2
Menon, R.P.3
Dal Piaz, F.4
Calder, L.5
Pastore, A.6
-
123
-
-
0034652143
-
Subcellular localization of proteasomes and their regulatory complexes in mammalian cells
-
doi:10.1042/0264-6021:3460155
-
Brooks P et al. 2000 Subcellular localization of proteasomes and their regulatory complexes in mammalian cells. Biochem. J. 346, 155-161. (doi:10.1042/0264-6021:3460155)
-
(2000)
Biochem. J
, vol.346
, pp. 155-161
-
-
Brooks, P.1
-
124
-
-
34848886914
-
Autophagosome formation: Core machinery and adaptations
-
doi:10.1038/ncb1007-1102
-
Xie Z, Klionsky DJ. 2007. Autophagosome formation: core machinery and adaptations. Nat. Cell Biol. 9, 1102-1109. (doi:10.1038/ncb1007-1102)
-
(2007)
Nat. Cell Biol
, vol.9
, pp. 1102-1109
-
-
Xie, Z.1
Klionsky, D.J.2
-
125
-
-
65549163327
-
Cytoplasmic retention of polyglutamine-expanded androgen receptor ameliorates disease via autophagy in a mouse model of spinal and bulbar muscular atrophy
-
doi:10.1093/ hmg/ddp115
-
Montie HL, Cho MS, Holder L, Liu Y, Tsvetkov AS, Finkbeiner S, Merry DE. 2009 Cytoplasmic retention of polyglutamine-expanded androgen receptor ameliorates disease via autophagy in a mouse model of spinal and bulbar muscular atrophy. Hum. Mol. Genet. 18, 1937-1950. (doi:10.1093/ hmg/ddp115)
-
(2009)
Hum. Mol. Genet
, vol.18
, pp. 1937-1950
-
-
Montie, H.L.1
Cho, M.S.2
Holder, L.3
Liu, Y.4
Tsvetkov, A.S.5
Finkbeiner, S.6
Merry, D.E.7
-
126
-
-
23044507689
-
Decreased expression of Hsp27 and Hsp70 in transformed lymphoblastoid cells from patients with spinocerebellar ataxia type 7
-
doi:10.1016/j.bbrc.2005.06.207
-
Tsai HF, Lin SJ, Li C, Hsieh M. 2005 Decreased expression of Hsp27 and Hsp70 in transformed lymphoblastoid cells from patients with spinocerebellar ataxia type 7. Biochem. Biophys. Res. Comm. 334, 1279-1286. (doi:10.1016/j.bbrc.2005.06.207)
-
(2005)
Biochem. Biophys. Res. Comm
, vol.334
, pp. 1279-1286
-
-
Tsai, H.F.1
Lin, S.J.2
Li, C.3
Hsieh, M.4
-
127
-
-
17844361953
-
HSP27 and cell death in spinocerebellar ataxia type 3
-
doi:10.1080/14734220410026248
-
Hsieh M, Tsai HF, Chang WH. 2005 HSP27 and cell death in spinocerebellar ataxia type 3. Cerebellum 4, 31-36. (doi:10.1080/14734220410026248)
-
(2005)
Cerebellum
, vol.4
, pp. 31-36
-
-
Hsieh, M.1
Tsai, H.F.2
Chang, W.H.3
-
128
-
-
70350432944
-
Activation of gene transcription by heat shock protein 27 may contribute to its neuronal protection
-
doi:10.1074/jbc.M109.037937
-
Friedman MJ, Li S, Li XJ. 2009. Activation of gene transcription by heat shock protein 27 may contribute to its neuronal protection. J. Biol. Chem. 284, 27944-27951. (doi:10.1074/jbc.M109.037937)
-
(2009)
J. Biol. Chem
, vol.284
, pp. 27944-27951
-
-
Friedman, M.J.1
Li, S.2
Li, X.J.3
-
129
-
-
34447331291
-
Hsp27 overexpression in the R6/2 mouse model of Huntington's disease: Chronic neurodegeneration does not induce Hsp27 activation
-
doi:10.1093/hmg/ddm057
-
Zourlidou A et al. 2007. Hsp27 overexpression in the R6/2 mouse model of Huntington's disease: chronic neurodegeneration does not induce Hsp27 activation. Hum. Mol. Genet. 16, 1078-1090. (doi:10.1093/hmg/ddm057)
-
(2007)
Hum. Mol. Genet
, vol.16
, pp. 1078-1090
-
-
Zourlidou, A.1
|