-
3
-
-
70350455072
-
Axonal transport defects in neurodegenerative diseases
-
Morfini GA, Burns M, Binder LI, et al. Axonal transport defects in neurodegenerative diseases. J Neurosci 2009;29: 12776-12786.
-
(2009)
J Neurosci
, vol.29
, pp. 12776-12786
-
-
Morfini, G.A.1
Burns, M.2
Binder, L.I.3
-
4
-
-
0003880161
-
-
5th ed. New York NY: Garland Science
-
Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P. Molecular Biology of the Cell, 5th ed. New York, NY: Garland Science; 2008.
-
(2008)
Molecular Biology of the Cell
-
-
Alberts, B.1
Johnson, A.2
Lewis, J.3
Raff, M.4
Roberts, K.5
Walter, P.6
-
5
-
-
50349090965
-
Intracellular transport and kinesin superfamily proteins, KIFs: Structure, function, and dynamics
-
Hirokawa N, Noda Y. Intracellular transport and kinesin superfamily proteins, KIFs: structure, function, and dynamics. Physiol Rev 2008;88:1089-1118.
-
(2008)
Physiol Rev
, vol.88
, pp. 1089-1118
-
-
Hirokawa, N.1
Noda, Y.2
-
6
-
-
0037451130
-
Axonal transport of membranous and nonmembranous cargoes: A unified perspective
-
DOI 10.1083/jcb.200212017
-
Brown A. Axonal transport of membranous and nonmembranous cargoes: a unified perspective. J Cell Biol 2003; 160:817-821. (Pubitemid 36350837)
-
(2003)
Journal of Cell Biology
, vol.160
, Issue.6
, pp. 817-821
-
-
Brown, A.1
-
7
-
-
56249100084
-
Axonal transport and the delivery of pre-synaptic components
-
Goldstein AY, Wang X, Schwarz TL. Axonal transport and the delivery of pre-synaptic components. Curr Opin Neurobiol 2008;18:495-503.
-
(2008)
Curr Opin Neurobiol
, vol.18
, pp. 495-503
-
-
Goldstein, A.Y.1
Wang, X.2
Schwarz, T.L.3
-
8
-
-
58549119743
-
Bidirectional Ca2-dependent control of mitochondrial dynamics by the Miro GTPase
-
Saotome M, Safiulina D, Szabadkai G, et al. Bidirectional Ca2-dependent control of mitochondrial dynamics by the Miro GTPase. Proc Natl Acad Sci USA 2008;105: 20728-20733.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 20728-20733
-
-
Saotome, M.1
Safiulina, D.2
Szabadkai, G.3
-
9
-
-
33644507718
-
Cytoplasmic dynein/dynactin function and dysfunction in motor neurons
-
DOI 10.1016/j.ijdevneu.2005.11.013, PII S0736574805001449, Neural Signal Transduction in Health and Disease - Cytokinesd, Mitochondrial Dysfunction and Transport Processes
-
Levy JR, Holzbaur EL. Cytoplasmic dynein/dynactin function and dysfunction in motor neurons. Int J Dev Neurosci 2006;24:103-111. (Pubitemid 43294616)
-
(2006)
International Journal of Developmental Neuroscience
, vol.24
, Issue.2-3
, pp. 103-111
-
-
Levy, J.R.1
Holzbaur, E.L.F.2
-
10
-
-
0346750740
-
Myosin Function in Nervous and Sensory Systems
-
DOI 10.1002/neu.10285
-
Brown ME, Bridgman PC. Myosin function in nervous and sensory systems. J Neurobiol 2004;58:118-130. (Pubitemid 37543343)
-
(2004)
Journal of Neurobiology
, vol.58
, Issue.1
, pp. 118-130
-
-
Brown, M.E.1
Bridgman, P.C.2
-
11
-
-
73149108817
-
MicroTUB(B3)ules and brain development
-
Singh KK, Tsai LH. MicroTUB(B3)ules and brain development. Cell 2010;140:30-32.
-
(2010)
Cell
, vol.140
, pp. 30-32
-
-
Singh, K.K.1
Tsai, L.H.2
-
12
-
-
84882925239
-
Axonal transport: Properties mechanisms and role in nerve disease
-
Dyck PJ, Thomas PK, eds 4th ed. Philadelphia, PA: Elsevier Saunders
-
Brimijoin S. Axonal transport: properties, mechanisms, and role in nerve disease. In: Dyck PJ, Thomas PK, eds. Peripheral Neuropathy, 4th ed. Philadelphia, PA: Elsevier Saunders; 2005:2553-2583.
-
(2005)
Peripheral Neuropathy
, pp. 2553-2583
-
-
Brimijoin, S.1
-
13
-
-
34250747736
-
Neuropathy caused by drugs
-
Dyck PJ, Thomas PK, eds 4th ed. Philadelphia, PA: Elsevier Saunders
-
Herskovitz S, Schaumburg HH. Neuropathy caused by drugs. In: Dyck PJ, Thomas PK, eds. Peripheral Neuropathy, 4th ed. Philadelphia, PA: Elsevier Saunders; 2005: 2553-2583.
-
(2005)
Peripheral Neuropathy
, pp. 2553-2583
-
-
Herskovitz, S.1
Schaumburg, H.H.2
-
14
-
-
18644365196
-
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)
-
DOI 10.1086/344210
-
Reid E, Kloos M, Ashley-Koch A, et al. A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10). Am J Hum Genet 2002;71:1189-1194. (Pubitemid 35305237)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.5
, pp. 1189-1194
-
-
Reid, E.1
Kloos, M.2
Ashley-Koch, A.3
Hughes, L.4
Bevan, S.5
Svenson, I.K.6
Graham, F.L.7
Gaskell, P.C.8
Dearlove, A.9
Pericak-Vance, M.A.10
Rubinsztein, D.C.11
Marchuk, D.A.12
-
15
-
-
64049111042
-
Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10
-
Goizet C, Boukhris A, Mundwiller E, et al. Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10. Hum Mutat 2009;30:E376-385.
-
(2009)
Hum Mutat
, vol.30
-
-
Goizet, C.1
Boukhris, A.2
Mundwiller, E.3
-
16
-
-
42449095555
-
Effect of spastic paraplegia mutations in KIF5A kinesin on transport activity
-
DOI 10.1093/hmg/ddn014
-
Ebbing B, Mann K, Starosta A, et al. Effect of spastic paraplegia mutations in KIF5A kinesin on transport activity. Hum Mol Genet 2008;17:1245-1252. (Pubitemid 351566961)
-
(2008)
Human Molecular Genetics
, vol.17
, Issue.9
, pp. 1245-1252
-
-
Ebbing, B.1
Mann, K.2
Starosta, A.3
Jaud, J.4
Schols, L.5
Schule, R.6
Woehlke, G.7
-
17
-
-
0035369084
-
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bβ
-
DOI 10.1016/S0092-8674(01)00363-4
-
Zhao C, Takita J, Tanaka Y, et al. Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta. Cell 2001;105:587-597. (Pubitemid 32524112)
-
(2001)
Cell
, vol.105
, Issue.5
, pp. 587-597
-
-
Zhao, C.1
Takita, J.2
Tanaka, Y.3
Setou, M.4
Nakagawa, T.5
Takeda, S.6
Yang, H.W.7
Terada, S.8
Nakata, T.9
Takei, Y.10
Saito, M.11
Tsuji, S.12
Hayashi, Y.13
Hirokawa, N.14
-
18
-
-
0037382240
-
Mutant dynactin in motor neuron disease
-
DOI 10.1038/ng1123
-
Puls I, Jonnakuty C, LaMonte BH, et al. Mutant dynactin in motor neuron disease. Nat Genet 2003;33:455-456. (Pubitemid 36390002)
-
(2003)
Nature Genetics
, vol.33
, Issue.4
, pp. 455-456
-
-
Puls, I.1
Jonnakuty, C.2
LaMonte, B.H.3
Holzbaur, E.L.F.4
Tokito, M.5
Mann, E.6
Floeter, M.K.7
Bidus, K.8
Drayna, D.9
Oh, S.J.10
Brown Jr., R.H.11
Ludlow, C.L.12
Fischbeck, K.H.13
-
20
-
-
73349096922
-
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance
-
Tischfield MA, Baris HN, Wu C, et al. Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. Cell 2010;140:74-87.
-
(2010)
Cell
, vol.140
, pp. 74-87
-
-
Tischfield, M.A.1
Baris, H.N.2
Wu, C.3
-
21
-
-
62849088641
-
The amino terminus of tau inhibits kinesin-dependent axonal transport: Implications for filament toxicity
-
LaPointe NE, Morfini G, Pigino G, et al. The amino terminus of tau inhibits kinesin-dependent axonal transport: implications for filament toxicity. J Neurosci Res 2009;87: 440-451.
-
(2009)
J Neurosci Res
, vol.87
, pp. 440-451
-
-
Lapointe, N.E.1
Morfini, G.2
Pigino, G.3
-
22
-
-
65249161745
-
Disruption of fast axonal transport is a pathogenic mechanism for intraneuronal amyloid beta
-
Pigino G, Morfini G, Atagi Y, et al. Disruption of fast axonal transport is a pathogenic mechanism for intraneuronal amyloid beta. Proc Natl Acad Sci USA 2009;106: 5907-5912.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 5907-5912
-
-
Pigino, G.1
Morfini, G.2
Atagi, Y.3
-
23
-
-
67649826155
-
Pathogenic huntingtin inhibits fast axonal transport by activating JNK3 and phosphorylating kinesin
-
Morfini GA, You YM, Pollema SL, et al. Pathogenic huntingtin inhibits fast axonal transport by activating JNK3 and phosphorylating kinesin. Nat Neurosci 2009;12:864-871.
-
(2009)
Nat Neurosci
, vol.12
, pp. 864-871
-
-
Morfini, G.A.1
You, Y.M.2
Pollema, S.L.3
-
24
-
-
3142636768
-
Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules
-
DOI 10.1016/j.cell.2004.06.018, PII S0092867404006191
-
Gauthier LR, Charrin BC, Borrell-Pages M, et al. Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules. Cell 2004;118:127-138. (Pubitemid 38902819)
-
(2004)
Cell
, vol.118
, Issue.1
, pp. 127-138
-
-
Gauthier, L.R.1
Charrin, B.C.2
Borrell-Pages, M.3
Dompierre, J.P.4
Rangone, H.5
Cordelieres, F.P.6
De Mey, J.7
MacDonald, M.E.8
Lessmann, V.9
Humbert, S.10
Saudou, F.11
-
25
-
-
34047175919
-
Histone deacetylase 6 inhibition compensates for the transport deficit in Huntington's disease by increasing tubulin acetylation
-
DOI 10.1523/JNEUROSCI.0037-07.2007
-
Dompierre JP, Godin JD, Charrin BC, et al. Histone deacetylase 6 inhibition compensates for the transport deficit in Huntington's disease by increasing tubulin acetylation. J Neurosci 2007;27:3571-3583. (Pubitemid 46515140)
-
(2007)
Journal of Neuroscience
, vol.27
, Issue.13
, pp. 3571-3583
-
-
Dompierre, J.P.1
Godin, J.D.2
Charrin, B.C.3
Cordelieres, F.P.4
King, S.J.5
Humbert, S.6
Saudou, F.7
-
26
-
-
11144353869
-
Parkinson's disease α-synuclein mutations exhibit defective axonal transport in cultured neurons
-
DOI 10.1242/jcs.00967
-
Saha AR, Hill J, Utton MA, et al. Parkinson's disease alpha-synuclein mutations exhibit defective axonal transport in cultured neurons. J Cell Sci 2004;117:1017-1024. (Pubitemid 38456084)
-
(2004)
Journal of Cell Science
, vol.117
, Issue.7
, pp. 1017-1024
-
-
Saha, A.R.1
Hill, J.2
Utton, M.A.3
Asuni, A.A.4
Ackerley, S.5
Grierson, A.J.6
Miller, C.C.7
Davies, A.M.8
Buchman, V.L.9
Anderton, B.H.10
Hanger, D.P.11
-
27
-
-
33847770318
-
1-Methyl-4-phenylpyridinium affects fast axonal transport by activation of caspase and protein kinase C
-
DOI 10.1073/pnas.0611231104
-
Morfini G, Pigino G, Opalach K, et al. 1-Methyl-4-phenylpyridinium affects fast axonal transport by activation of caspase and protein kinase C. Proc Natl Acad Sci USA 2007;104:2442-2447. (Pubitemid 46391416)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.7
, pp. 2442-2447
-
-
Morfini, G.1
Pigino, G.2
Opalach, K.3
Serulle, Y.4
Moreira, J.E.5
Sugimori, M.6
Llinas, R.R.7
Brady, S.T.8
-
28
-
-
0033585832
-
Selective impairment of fast anterograde axonal transport in the peripheral nerves of asymptomatic transgenic mice with a G93A mutant SOD1 gene
-
DOI 10.1016/S0006-8993(98)01351-1, PII S0006899398013511
-
Warita H, Itoyama Y, Abe K. Selective impairment of fast anterograde axonal transport in the peripheral nerves of asymptomatic transgenic mice with a G93A mutant SOD1 gene. Brain Res 1999;819:120-131. (Pubitemid 29225463)
-
(1999)
Brain Research
, vol.819
, Issue.1-2
, pp. 120-131
-
-
Warita, H.1
Itoyama, Y.2
Abe, K.3
-
29
-
-
0033366384
-
Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons
-
DOI 10.1038/4553
-
Williamson TL, Cleveland DW. Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons. Nat Neurosci 1999;2: 50-56. (Pubitemid 30488940)
-
(1999)
Nature Neuroscience
, vol.2
, Issue.1
, pp. 50-56
-
-
Williamson, T.L.1
Cleveland, D.W.2
-
30
-
-
4644362726
-
P38α stress-activated protein kinase phosphorylates neurofilaments and is associated with neurofilament pathology in amyotrophic lateral sclerosis
-
DOI 10.1016/j.mcn.2004.02.009, PII S104474310400051X
-
Ackerley S, Grierson AJ, Banner S, et al. p38alpha stressactivated protein kinase phosphorylates neurofilaments and is associated with neurofilament pathology in amyotrophic lateral sclerosis. Mol Cell Neurosci 2004;26:354-364. (Pubitemid 38781091)
-
(2004)
Molecular and Cellular Neuroscience
, vol.26
, Issue.2
, pp. 354-364
-
-
Ackerley, S.1
Grierson, A.J.2
Banner, S.3
Perkinton, M.S.4
Brownlees, J.5
Byers, H.L.6
Ward, M.7
Thornhill, P.8
Hussain, K.9
Waby, J.S.10
Anderton, B.H.11
Cooper, J.D.12
Dingwall, C.13
Leigh, P.N.14
Shaw, C.E.15
Miller, C.C.J.16
-
31
-
-
35548991459
-
Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content
-
DOI 10.1093/hmg/ddm226
-
De Vos KJ, Chapman AL, Tennant ME, et al. Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content. Hum Mol Genet 2007;16:2720-2728. (Pubitemid 350018514)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.22
, pp. 2720-2728
-
-
De Vos, K.J.1
Chapman, A.L.2
Tennant, M.E.3
Manser, C.4
Tudor, E.L.5
Lau, K.-F.6
Brownlees, J.7
Ackerley, S.8
Shaw, P.J.9
Mcloughlin, D.M.10
Shaw, C.E.11
Leigh, P.N.12
Miller, C.C.J.13
Grierson, A.J.14
-
32
-
-
0034631964
-
Glutamate slows axonal transport of neurofilaments in transfected neurons
-
Ackerley S, Grierson AJ, Brownlees J, et al. Glutamate slows axonal transport of neurofilaments in transfected neurons. J Cell Biol 2000;150:165-176.
-
(2000)
J Cell Biol
, vol.150
, pp. 165-176
-
-
Ackerley, S.1
Grierson, A.J.2
Brownlees, J.3
-
33
-
-
62949103631
-
Riluzole protects against glutamate-induced slowing of neurofilament axonal transport
-
Stevenson A, Yates DM, Manser C, et al. Riluzole protects against glutamate-induced slowing of neurofilament axonal transport. Neurosci Lett 2009;454:161-164.
-
(2009)
Neurosci Lett
, vol.454
, pp. 161-164
-
-
Stevenson, A.1
Yates, D.M.2
Manser, C.3
-
34
-
-
67649400910
-
Ultramicroscopy reveals axonal transport impairments in cortical motor neurons at prion disease
-
Ermolayev V, Friedrich M, Nozadze R, et al. Ultramicroscopy reveals axonal transport impairments in cortical motor neurons at prion disease. Biophys J 2009;96:3390-3398.
-
(2009)
Biophys J
, vol.96
, pp. 3390-3398
-
-
Ermolayev, V.1
Friedrich, M.2
Nozadze, R.3
-
35
-
-
55549094109
-
Hereditary spastic paraplegia: Clinical features and pathogenetic mechanisms
-
Salinas S, Proukakis C, Crosby A, Warner TT. Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms. Lancet Neurol 2008;7:1127-1138.
-
(2008)
Lancet Neurol
, vol.7
, pp. 1127-1138
-
-
Salinas, S.1
Proukakis, C.2
Crosby, A.3
Warner, T.T.4
-
36
-
-
39849101639
-
Quantitative and functional analyses of spastin in the nervous system: Implications for hereditary spastic paraplegia
-
DOI 10.1523/JNEUROSCI.3159-07.2008
-
Solowska JM, Morfini G, Falnikar A, et al. Quantitative and functional analyses of spastin in the nervous system: implications for hereditary spastic paraplegia. J Neurosci 2008;28:2147-2157. (Pubitemid 351317638)
-
(2008)
Journal of Neuroscience
, vol.28
, Issue.9
, pp. 2147-2157
-
-
Solowska, J.M.1
Morfini, G.2
Falnikar, A.3
Himes, B.T.4
Brady, S.T.5
Huang, D.6
Baas, P.W.7
-
37
-
-
2642563501
-
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy
-
DOI 10.1038/ng1354
-
Evgrafov OV, Mersiyanova I, Irobi J, et al. Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. Nat Genet 2004;36:602-606. (Pubitemid 38715987)
-
(2004)
Nature Genetics
, vol.36
, Issue.6
, pp. 602-606
-
-
Evgrafov, O.V.1
Mersiyanova, I.2
Irobi, J.3
Van Den Bosch, L.V.4
Dierick, I.5
Leung, C.L.6
Schagina, O.7
Verpoorten, N.8
Van Impe, K.9
Fedotov, V.10
Dadali, E.11
Auer-Grumbach, M.12
Windpassinger, C.13
Wagner, K.14
Mitrovic, Z.15
Hilton-Jones, D.16
Talbot, K.17
Martin, J.-J.18
Vasserman, N.19
Tverskaya, S.20
Polyakov, A.21
Liem, R.K.H.22
Gettemans, J.23
Robberecht, W.24
De Jonghe, P.25
Timmerman, V.26
more..
-
38
-
-
2642539919
-
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy
-
DOI 10.1038/ng1328
-
Irobi J, Van Impe K, Seeman P, et al. Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy. Nat Genet 2004;36:597-601. (Pubitemid 38715986)
-
(2004)
Nature Genetics
, vol.36
, Issue.6
, pp. 597-601
-
-
Irobi, J.1
Van Impe, K.2
Seeman, P.3
Jordanova, A.4
Dierick, I.5
Verpoorten, N.6
Michalik, A.7
De Vriendt, E.8
Jacobs, A.9
Van Gerwen, V.10
Vennekens, K.11
Mazanec, R.12
Tournev, I.13
Hilton-Jones, D.14
Talbot, K.15
Kremensky, I.16
Van Den Bosch, L.17
Robberecht, W.18
Vandekerckhove, J.19
Van Broeckhoven, C.20
Gettemans, J.21
De Jonghe, P.22
Timmerman, V.23
more..
-
39
-
-
76649105116
-
Mutant small heat shock protein B3 causes motor neuropathy: Utility of a candidate gene approach
-
Kolb SJ, Snyder PJ, Poi EJ, et al. Mutant small heat shock protein B3 causes motor neuropathy: utility of a candidate gene approach. Neurology 2010;74:502-506.
-
(2010)
Neurology
, vol.74
, pp. 502-506
-
-
Kolb, S.J.1
Snyder, P.J.2
Poi, E.J.3
-
40
-
-
64549164076
-
Gigaxonin controls vimentin organization through a tubulin chaperone-independent pathway
-
Cleveland DW, Yamanaka K, Bomont P. Gigaxonin controls vimentin organization through a tubulin chaperone-independent pathway. Hum Mol Genet 2009;18:1384-1394.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1384-1394
-
-
Cleveland, D.W.1
Yamanaka, K.2
Bomont, P.3
-
41
-
-
27744494043
-
Gigaxonin-controlled degradation of MAP1B light chain is critical to neuronal survival
-
DOI 10.1038/nature04256, PII N04256
-
Allen E, Ding J, Wang W, et al. Gigaxonin-controlled degradation of MAP1B light chain is critical to neuronal survival. Nature 2005;438:224-228. (Pubitemid 41599874)
-
(2005)
Nature
, vol.438
, Issue.7065
, pp. 224-228
-
-
Allen, E.1
Ding, J.2
Wang, W.3
Pramanik, S.4
Chou, J.5
Yau, V.6
Yang, Y.7
-
42
-
-
33749620373
-
Rab5 and Rab7 Control Endocytic Sorting along the Axonal Retrograde Transport Pathway
-
DOI 10.1016/j.neuron.2006.08.018, PII S0896627306006404
-
Deinhardt K, Salinas S, Verastegui C, et al. Rab5 and Rab7 control endocytic sorting along the axonal retrograde transport pathway. Neuron 2006;52:293-305. (Pubitemid 44548343)
-
(2006)
Neuron
, vol.52
, Issue.2
, pp. 293-305
-
-
Deinhardt, K.1
Salinas, S.2
Verastegui, C.3
Watson, R.4
Worth, D.5
Hanrahan, S.6
Bucci, C.7
Schiavo, G.8
-
43
-
-
18844446126
-
Mutations in the neurofilament light gene linked to Charcot-Marie-Tooth disease cause defects in transport
-
DOI 10.1111/j.1471-4159.2005.03095.x
-
Perez-Olle R, Lopez-Toledano MA, Goryunov D, et al. Mutations in the neurofilament light gene linked to Charcot-Marie-Tooth disease cause defects in transport. J Neurochem 2005;93:861-874. (Pubitemid 40695745)
-
(2005)
Journal of Neurochemistry
, vol.93
, Issue.4
, pp. 861-874
-
-
Perez-Olle, R.1
Lopez-Toledano, M.A.2
Goryunov, D.3
Cabrera-Poch, N.4
Stefanis, L.5
Brown, K.6
Liem, R.K.H.7
-
44
-
-
0026580004
-
Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells
-
De Waegh SM, Lee VM, Brady ST. Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells. Cell 1992; 68:451-463.
-
(1992)
Cell
, vol.68
, pp. 451-463
-
-
De Waegh, S.M.1
Lee, V.M.2
Brady, S.T.3
-
45
-
-
33750347347
-
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
-
DOI 10.1038/nature05292, PII NATURE05292
-
Lin MT, Beal MF. Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases. Nature 2006;443: 787-795. (Pubitemid 44622683)
-
(2006)
Nature
, vol.443
, Issue.7113
, pp. 787-795
-
-
Lin, M.T.1
Beal, M.F.2
-
46
-
-
77949801029
-
Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex
-
Misko A, Jiang S, Wegorzewska I, Milbrandt J, Baloh RH. Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex. J Neurosci 2010;30:4232-4240.
-
(2010)
J Neurosci
, vol.30
, pp. 4232-4240
-
-
Misko, A.1
Jiang, S.2
Wegorzewska, I.3
Milbrandt, J.4
Baloh, R.H.5
-
47
-
-
39349083915
-
Adapting proteostasis for disease intervention
-
DOI 10.1126/science.1141448
-
Balch WE, Morimoto RI, Dillin A, Kelly JW. Adapting proteostasis for disease intervention. Science 2008;319: 916-919. (Pubitemid 351263754)
-
(2008)
Science
, vol.319
, Issue.5865
, pp. 916-919
-
-
Balch, W.E.1
Morimoto, R.I.2
Dillin, A.3
Kelly, J.W.4
|