-
1
-
-
49249118746
-
TDP- 43 is a culprit in human neurodegeneration, and not just an innocent bystander
-
Banks, G.T., Kuta, A., Isaacs, A.M. and Fisher, E.M. (2008) TDP- 43 is a culprit in human neurodegeneration, and not just an innocent bystander. Mamm. Genome, 19, 299-305.
-
(2008)
Mamm. Genome
, vol.19
, pp. 299-305
-
-
Banks, G.T.1
Kuta, A.2
Isaacs, A.M.3
Fisher, E.M.4
-
2
-
-
84882687005
-
c9RAN translation: a potential therapeutic target for the treatment of amyotrophic lateral sclerosis and frontotemporal dementia
-
Gendron, T.F., Cosio, D.M. and Petrucelli, L. (2013) c9RAN translation: a potential therapeutic target for the treatment of amyotrophic lateral sclerosis and frontotemporal dementia. Expert Opin. Ther. Targets, 17, 991-995.
-
(2013)
Expert Opin. Ther. Targets
, vol.17
, pp. 991-995
-
-
Gendron, T.F.1
Cosio, D.M.2
Petrucelli, L.3
-
3
-
-
84875441083
-
The changing scene of amyotrophic lateral sclerosis
-
Robberecht, W. and Philips, T. (2013) The changing scene of amyotrophic lateral sclerosis. Nat. Rev. Neurosci., 14, 248-264.
-
(2013)
Nat. Rev. Neurosci.
, vol.14
, pp. 248-264
-
-
Robberecht, W.1
Philips, T.2
-
4
-
-
62149141328
-
Rethinking ALS: the FUS about TDP-43
-
Lagier-Tourenne, C. and Cleveland, D.W. (2009) Rethinking ALS: the FUS about TDP-43. Cell, 136, 1001-1004.
-
(2009)
Cell
, vol.136
, pp. 1001-1004
-
-
Lagier-Tourenne, C.1
Cleveland, D.W.2
-
5
-
-
84881490873
-
Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis
-
Ling, S.C., Polymenidou, M. and Cleveland, D.W. (2013) Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis. Neuron, 79, 416-438.
-
(2013)
Neuron
, vol.79
, pp. 416-438
-
-
Ling, S.C.1
Polymenidou, M.2
Cleveland, D.W.3
-
6
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann, M., Sampathu, D.M., Kwong, L.K., Truax, A.C., Micsenyi, M.C., Chou, T.T., Bruce, J., Schuck, T., Grossman, M., Clark, C.M. et al. (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science, 314, 130-133.
-
(2006)
Science
, vol.314
, pp. 130-133
-
-
Neumann, M.1
Sampathu, D.M.2
Kwong, L.K.3
Truax, A.C.4
Micsenyi, M.C.5
Chou, T.T.6
Bruce, J.7
Schuck, T.8
Grossman, M.9
Clark, C.M.10
-
7
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
Sreedharan, J., Blair, I.P., Tripathi, V.B., Hu, X., Vance, C., Rogelj, B., Ackerley, S., Durnall, J.C., Williams, K.L., Buratti, E. et al. (2008) TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science, 319, 1668-1672.
-
(2008)
Science
, vol.319
, pp. 1668-1672
-
-
Sreedharan, J.1
Blair, I.P.2
Tripathi, V.B.3
Hu, X.4
Vance, C.5
Rogelj, B.6
Ackerley, S.7
Durnall, J.C.8
Williams, K.L.9
Buratti, E.10
-
8
-
-
41949100148
-
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
-
Van Deerlin, V.M., Leverenz, J.B., Bekris, L.M., Bird, T.D., Yuan, W., Elman, L.B., Clay, D., Wood, E.M., Chen-Plotkin, A.S., Martinez- Lage, M. et al. (2008) TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. Lancet Neurol., 7, 409-416.
-
(2008)
Lancet Neurol.
, vol.7
, pp. 409-416
-
-
Van Deerlin, V.M.1
Leverenz, J.B.2
Bekris, L.M.3
Bird, T.D.4
Yuan, W.5
Elman, L.B.6
Clay, D.7
Wood, E.M.8
Chen-Plotkin, A.S.9
Martinez-Lage, M.10
-
9
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
Kabashi, E., Valdmanis, P.N., Dion, P., Spiegelman, D., McConkey, B.J., Vande Velde, C., Bouchard, J.P., Lacomblez, L., Pochigaeva, K., Salachas, F. et al. (2008) TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat. Genet., 40, 572-574.
-
(2008)
Nat. Genet.
, vol.40
, pp. 572-574
-
-
Kabashi, E.1
Valdmanis, P.N.2
Dion, P.3
Spiegelman, D.4
McConkey, B.J.5
Vande Velde, C.6
Bouchard, J.P.7
Lacomblez, L.8
Pochigaeva, K.9
Salachas, F.10
-
10
-
-
84884777626
-
Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders
-
Janssens, J. and Van Broeckhoven, C. (2013) Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders. Hum. Mol. Genet., 22, R77-R87.
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. R77-R87
-
-
Janssens, J.1
Van Broeckhoven, C.2
-
11
-
-
67749133873
-
TDP-43 is intrinsically aggregationprone and ALS-linked mutations accelerate aggregation and increase toxicity
-
Johnson, B.S., Snead, D., Lee, J.J., McCaffery, J.M., Shorter, J. and Gitler, A.D. (2009) TDP-43 is intrinsically aggregationprone and ALS-linked mutations accelerate aggregation and increase toxicity. J. Biol. Chem., 284, 20329-20339.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 20329-20339
-
-
Johnson, B.S.1
Snead, D.2
Lee, J.J.3
McCaffery, J.M.4
Shorter, J.5
Gitler, A.D.6
-
12
-
-
84155171976
-
Understanding the role of TDP-43 and FUS/TLS in ALS and beyond
-
Da Cruz, S. and Cleveland, D.W. (2011) Understanding the role of TDP-43 and FUS/TLS in ALS and beyond. Curr. Opin. Neurobiol., 21, 904-919.
-
(2011)
Curr. Opin. Neurobiol.
, vol.21
, pp. 904-919
-
-
Da Cruz, S.1
Cleveland, D.W.2
-
13
-
-
84862908655
-
A yeast functional screen predicts new candidate ALS disease genes
-
Couthouis, J., Hart, M.P., Shorter, J., DeJesus-Hernandez, M., Erion, R., Oristano, R., Liu, A.X., Ramos, D., Jethava, N., Hosangadi, D. et al. (2011) A yeast functional screen predicts new candidate ALS disease genes. Proc. Natl. Acad. Sci. USA, 108, 20881-20890.
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 20881-20890
-
-
Couthouis, J.1
Hart, M.P.2
Shorter, J.3
DeJesus-Hernandez, M.4
Erion, R.5
Oristano, R.6
Liu, A.X.7
Ramos, D.8
Jethava, N.9
Hosangadi, D.10
-
14
-
-
79957488875
-
Wild-type and A315T mutant TDP-43 exert differential neurotoxicity in a Drosophila model of ALS
-
Estes, P.S., Boehringer, A., Zwick, R., Tang, J.E., Grigsby, B. and Zarnescu, D.C. (2011) Wild-type and A315T mutant TDP-43 exert differential neurotoxicity in a Drosophila model of ALS. Hum. Mol. Genet., 20, 2308-2321.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 2308-2321
-
-
Estes, P.S.1
Boehringer, A.2
Zwick, R.3
Tang, J.E.4
Grigsby, B.5
Zarnescu, D.C.6
-
15
-
-
80052374038
-
FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis
-
Kabashi, E., Bercier, V., Lissouba, A., Liao, M., Brustein, E., Rouleau, G.A. and Drapeau, P. (2011) FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis. PLoS Genet., 7, e1002214.
-
(2011)
PLoS Genet.
, vol.7
, pp. e1002214
-
-
Kabashi, E.1
Bercier, V.2
Lissouba, A.3
Liao, M.4
Brustein, E.5
Rouleau, G.A.6
Drapeau, P.7
-
16
-
-
78149429744
-
Progranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathy
-
Laird, A.S., Van Hoecke, A., De Muynck, L., Timmers, M., Van den Bosch, L., Van Damme, P. and Robberecht, W. (2010) Progranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathy. PLoS ONE, 5, e13368.
-
(2010)
PLoS ONE
, vol.5
, pp. e13368
-
-
Laird, A.S.1
Van Hoecke, A.2
De Muynck, L.3
Timmers, M.4
Van den Bosch, L.5
Van Damme, P.6
Robberecht, W.7
-
17
-
-
77649258646
-
A Drosophilamodel for TDP-43 proteinopathy
-
Li, Y., Ray, P., Rao, E.J., Shi, C., Guo, W., Chen, X., Woodruff, E.A. III, Fushimi, K. andWu, J.Y. (2010) A Drosophilamodel for TDP-43 proteinopathy. Proc. Natl. Acad. Sci. USA, 107, 3169-3174.
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 3169-3174
-
-
Li, Y.1
Ray, P.2
Rao, E.J.3
Shi, C.4
Guo, W.5
Chen, X.6
Woodruff, E.A.7
Fushimi, K.8
Wu, J.Y.9
-
18
-
-
78649750391
-
Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy
-
Liachko, N.F., Guthrie, C.R. and Kraemer, B.C. (2010) Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy. J. Neurosci., 30, 16208-16219.
-
(2010)
J. Neurosci.
, vol.30
, pp. 16208-16219
-
-
Liachko, N.F.1
Guthrie, C.R.2
Kraemer, B.C.3
-
19
-
-
70350356317
-
Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching
-
Lu, Y., Ferris, J. and Gao, F.B. (2009) Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching. Mol. Brain, 2, 30.
-
(2009)
Mol. Brain
, vol.2
, pp. 30
-
-
Lu, Y.1
Ferris, J.2
Gao, F.B.3
-
20
-
-
73249152831
-
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration
-
Wegorzewska, I., Bell, S., Cairns, N.J., Miller, T.M. and Baloh, R.H. (2009) TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration. Proc. Natl. Acad. Sci. USA, 106, 18809-18814.
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 18809-18814
-
-
Wegorzewska, I.1
Bell, S.2
Cairns, N.J.3
Miller, T.M.4
Baloh, R.H.5
-
21
-
-
84893508018
-
Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations
-
Alami, N.H., Smith, R.B., Carrasco, M.A., Williams, L.A., Winborn, C.S., Han, S.S., Kiskinis, E., Winborn, B., Freibaum, B.D., Kanagaraj, A. et al. (2014) Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations. Neuron, 81, 536-543.
-
(2014)
Neuron
, vol.81
, pp. 536-543
-
-
Alami, N.H.1
Smith, R.B.2
Carrasco, M.A.3
Williams, L.A.4
Winborn, C.S.5
Han, S.S.6
Kiskinis, E.7
Winborn, B.8
Freibaum, B.D.9
Kanagaraj, A.10
-
22
-
-
84911877805
-
Futsch/MAP1B mRNA Is a translational target of TDP-43 and is neuroprotective in a Drosophila model of amyotrophic lateral sclerosis
-
Coyne, A.N., Siddegowda, B.B., Estes, P.S., Johannesmeyer, J., Kovalik, T., Daniel, S.G., Pearson, A., Bowser, R. and Zarnescu, D.C. (2014) Futsch/MAP1B mRNA Is a translational target of TDP-43 and is neuroprotective in a Drosophila model of amyotrophic lateral sclerosis. J. Neurosci., 34, 15962-15974.
-
(2014)
J. Neurosci.
, vol.34
, pp. 15962-15974
-
-
Coyne, A.N.1
Siddegowda, B.B.2
Estes, P.S.3
Johannesmeyer, J.4
Kovalik, T.5
Daniel, S.G.6
Pearson, A.7
Bowser, R.8
Zarnescu, D.C.9
-
23
-
-
77951183978
-
Prion-like disorders: blurring the divide between transmissibility and infectivity
-
Cushman, M., Johnson, B.S., King, O.D., Gitler, A.D. and Shorter, J. (2010) Prion-like disorders: blurring the divide between transmissibility and infectivity. J. Cell Sci., 123, 1191-1201.
-
(2010)
J. Cell Sci.
, vol.123
, pp. 1191-1201
-
-
Cushman, M.1
Johnson, B.S.2
King, O.D.3
Gitler, A.D.4
Shorter, J.5
-
24
-
-
84862151933
-
The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease
-
King, O.D., Gitler, A.D. and Shorter, J. (2012) The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease. Brain Res., 1462, 61-80.
-
(2012)
Brain Res.
, vol.1462
, pp. 61-80
-
-
King, O.D.1
Gitler, A.D.2
Shorter, J.3
-
25
-
-
0029066110
-
Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs
-
Ou, S.H., Wu, F., Harrich, D., Garcia-Martinez, L.F. and Gaynor, R.B. (1995) Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs. J. Virol., 69, 3584-3596.
-
(1995)
J. Virol.
, vol.69
, pp. 3584-3596
-
-
Ou, S.H.1
Wu, F.2
Harrich, D.3
Garcia-Martinez, L.F.4
Gaynor, R.B.5
-
26
-
-
77957918535
-
TDP-43-mediated neuron loss in vivo requires RNA-binding activity
-
Voigt, A., Herholz, D., Fiesel, F.C., Kaur, K., Muller, D., Karsten, P., Weber, S.S., Kahle, P.J., Marquardt, T. and Schulz, J.B. (2010) TDP-43-mediated neuron loss in vivo requires RNA-binding activity. PLoS One, 5, e12247.
-
(2010)
PLoS One
, vol.5
, pp. e12247
-
-
Voigt, A.1
Herholz, D.2
Fiesel, F.C.3
Kaur, K.4
Muller, D.5
Karsten, P.6
Weber, S.S.7
Kahle, P.J.8
Marquardt, T.9
Schulz, J.B.10
-
27
-
-
84887011964
-
RNA binding mediates neurotoxicity in the transgenic Drosophila model of TDP-43 proteinopathy
-
Ihara, R., Matsukawa, K., Nagata, Y., Kunugi, H., Tsuji, S., Chihara, T., Kuranaga, E., Miura, M., Wakabayashi, T., Hashimoto, T. et al. (2013) RNA binding mediates neurotoxicity in the transgenic Drosophila model of TDP-43 proteinopathy. Hum. Mol. Genet., 22, 4474-4484.
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 4474-4484
-
-
Ihara, R.1
Matsukawa, K.2
Nagata, Y.3
Kunugi, H.4
Tsuji, S.5
Chihara, T.6
Kuranaga, E.7
Miura, M.8
Wakabayashi, T.9
Hashimoto, T.10
-
28
-
-
76149120427
-
Global analysis of TDP-43 interacting proteins reveals strong association with RNA splicing and translation machinery
-
Freibaum, B.D., Chitta, R.K., High, A.A. and Taylor, J.P. (2010) Global analysis of TDP-43 interacting proteins reveals strong association with RNA splicing and translation machinery. J. Proteome Res., 9, 1104-1120.
-
(2010)
J. Proteome Res.
, vol.9
, pp. 1104-1120
-
-
Freibaum, B.D.1
Chitta, R.K.2
High, A.A.3
Taylor, J.P.4
-
29
-
-
84865063851
-
The ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth
-
Fallini, C., Bassell, G.J. and Rossoll, W. (2012) The ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth. Hum. Mol. Genet., 21, 3703- 3718.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 3703- 3718
-
-
Fallini, C.1
Bassell, G.J.2
Rossoll, W.3
-
30
-
-
42449163952
-
TDP-43, the signature protein of FTLD-U, is a neuronal activityresponsive factor
-
Wang, I.F., Wu, L.S., Chang, H.Y. and Shen, C.K. (2008) TDP-43, the signature protein of FTLD-U, is a neuronal activityresponsive factor. J. Neurochem., 105, 797-806.
-
(2008)
J. Neurochem.
, vol.105
, pp. 797-806
-
-
Wang, I.F.1
Wu, L.S.2
Chang, H.Y.3
Shen, C.K.4
-
31
-
-
84863307704
-
Neurodegeneration-associated TDP-43 interacts with fragile X mental retardation protein (FMRP)/Staufen (STAU1) and regulates SIRT1 expression in neuronal cells
-
Yu, Z., Fan, D., Gui, B., Shi, L., Xuan, C., Shan, L., Wang, Q., Shang, Y. andWang, Y. (2012) Neurodegeneration-associated TDP-43 interacts with fragile X mental retardation protein (FMRP)/Staufen (STAU1) and regulates SIRT1 expression in neuronal cells. J. Biol. Chem., 287, 22560-22572.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 22560-22572
-
-
Yu, Z.1
Fan, D.2
Gui, B.3
Shi, L.4
Xuan, C.5
Shan, L.6
Wang, Q.7
Shang, Y.8
Wang, Y.9
-
32
-
-
70350135049
-
TDP-43 is recruited to stress granules in conditions of oxidative insult
-
Colombrita, C., Zennaro, E., Fallini, C., Weber, M., Sommacal, A., Buratti, E., Silani, V. and Ratti, A. (2009) TDP-43 is recruited to stress granules in conditions of oxidative insult. J. Neurochem., 111, 1051-1061.
-
(2009)
J. Neurochem.
, vol.111
, pp. 1051-1061
-
-
Colombrita, C.1
Zennaro, E.2
Fallini, C.3
Weber, M.4
Sommacal, A.5
Buratti, E.6
Silani, V.7
Ratti, A.8
-
33
-
-
79952268025
-
TDP-43 is directed to stress granules by sorbitol, a novel physiological osmotic and oxidative stressor
-
Dewey, C.M., Cenik, B., Sephton, C.F., Dries, D.R., Mayer, P. III, Good, S.K., Johnson, B.A., Herz, J. and Yu, G. (2011) TDP-43 is directed to stress granules by sorbitol, a novel physiological osmotic and oxidative stressor. Mol. Cell. Biol., 31, 1098-1108.
-
(2011)
Mol. Cell. Biol.
, vol.31
, pp. 1098-1108
-
-
Dewey, C.M.1
Cenik, B.2
Sephton, C.F.3
Dries, D.R.4
Mayer, P.5
Good, S.K.6
Johnson, B.A.7
Herz, J.8
Yu, G.9
-
34
-
-
79952589652
-
TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1
-
McDonald, K.K., Aulas, A., Destroismaisons, L., Pickles, S., Beleac, E., Camu, W., Rouleau, G.A. and Vande Velde, C. (2011) TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1. Hum. Mol. Genet., 20, 1400-1410.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 1400-1410
-
-
McDonald, K.K.1
Aulas, A.2
Destroismaisons, L.3
Pickles, S.4
Beleac, E.5
Camu, W.6
Rouleau, G.A.7
Vande Velde, C.8
-
35
-
-
78149461229
-
Tar DNA binding protein-43 (TDP- 43) associates with stress granules: analysis of cultured cells and pathological brain tissue
-
Liu-Yesucevitz, L., Bilgutay, A., Zhang, Y.J., Vanderwyde, T., Citro, A., Mehta, T., Zaarur, N., McKee, A., Bowser, R., Sherman, M. et al. (2010) Tar DNA binding protein-43 (TDP- 43) associates with stress granules: analysis of cultured cells and pathological brain tissue. PLoS ONE, 5, e13250.
-
(2010)
PLoS ONE
, vol.5
, pp. e13250
-
-
Liu-Yesucevitz, L.1
Bilgutay, A.2
Zhang, Y.J.3
Vanderwyde, T.4
Citro, A.5
Mehta, T.6
Zaarur, N.7
McKee, A.8
Bowser, R.9
Sherman, M.10
-
36
-
-
84877832189
-
Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyotrophic lateral sclerosis
-
Estes, P.S., Daniel, S.G., McCallum, A.P., Boehringer, A.V., Sukhina, A.S., Zwick, R.A. and Zarnescu, D.C. (2013) Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyotrophic lateral sclerosis. Dis. Model. Mech., 6, 721-733.
-
(2013)
Dis. Model. Mech.
, vol.6
, pp. 721-733
-
-
Estes, P.S.1
Daniel, S.G.2
McCallum, A.P.3
Boehringer, A.V.4
Sukhina, A.S.5
Zwick, R.A.6
Zarnescu, D.C.7
-
37
-
-
84857124994
-
Endogenous TDP-43 localized to stress granules can subsequently form protein aggregates
-
Parker, S.J., Meyerowitz, J., James, J.L., Liddell, J.R., Crouch, P.J., Kanninen, K.M. and White, A.R. (2012) Endogenous TDP-43 localized to stress granules can subsequently form protein aggregates. Neurochem. Int., 60, 415-424.
-
(2012)
Neurochem. Int.
, vol.60
, pp. 415-424
-
-
Parker, S.J.1
Meyerowitz, J.2
James, J.L.3
Liddell, J.R.4
Crouch, P.J.5
Kanninen, K.M.6
White, A.R.7
-
38
-
-
84882801549
-
Altered ribostasis: RNA-protein granules in degenerative disorders
-
Ramaswami, M., Taylor, J.P. and Parker, R. (2013) Altered ribostasis: RNA-protein granules in degenerative disorders. Cell, 154, 727-736.
-
(2013)
Cell
, vol.154
, pp. 727-736
-
-
Ramaswami, M.1
Taylor, J.P.2
Parker, R.3
-
39
-
-
84869192353
-
Regulated protein aggregation: stress granules and neurodegeneration
-
Wolozin, B. (2012) Regulated protein aggregation: stress granules and neurodegeneration. Mol. Neurodegener., 7, 56.
-
(2012)
Mol. Neurodegener.
, vol.7
, pp. 56
-
-
Wolozin, B.1
-
40
-
-
84878661360
-
Stress granules as crucibles of ALS pathogenesis
-
Li, Y.R., King, O.D., Shorter, J. and Gitler, A.D. (2013) Stress granules as crucibles of ALS pathogenesis. J. Cell Biol., 201, 361-372.
-
(2013)
J. Cell Biol.
, vol.201
, pp. 361-372
-
-
Li, Y.R.1
King, O.D.2
Shorter, J.3
Gitler, A.D.4
-
41
-
-
80755143679
-
Local RNA translation at the synapse and in disease
-
Liu-Yesucevitz, L., Bassell, G.J., Gitler, A.D., Hart, A.C., Klann, E., Richter, J.D., Warren, S.T. andWolozin, B. (2011) Local RNA translation at the synapse and in disease. J. Neurosci., 31, 16086-16093.
-
(2011)
J. Neurosci.
, vol.31
, pp. 16086-16093
-
-
Liu-Yesucevitz, L.1
Bassell, G.J.2
Gitler, A.D.3
Hart, A.C.4
Klann, E.5
Richter, J.D.6
Warren, S.T.7
Wolozin, B.8
-
42
-
-
84862124493
-
Fragile X Protein is required for inhibition of insulin signaling and regulates glial-dependent neuroblast reactivation in the developing brain
-
Callan, M.A., Clements, N., Ahrendt, N. and Zarnescu, D.C. (2012) Fragile X Protein is required for inhibition of insulin signaling and regulates glial-dependent neuroblast reactivation in the developing brain. Brain Res., 1462, 151-161.
-
(2012)
Brain Res.
, vol.1462
, pp. 151-161
-
-
Callan, M.A.1
Clements, N.2
Ahrendt, N.3
Zarnescu, D.C.4
-
43
-
-
77956155218
-
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
-
Elden, A.C., Kim, H.J., Hart, M.P., Chen-Plotkin, A.S., Johnson, B.S., Fang, X., Armakola, M., Geser, F., Greene, R., Lu, M.M. et al. (2010) Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS. Nature, 466, 1069-1075.
-
(2010)
Nature
, vol.466
, pp. 1069-1075
-
-
Elden, A.C.1
Kim, H.J.2
Hart, M.P.3
Chen-Plotkin, A.S.4
Johnson, B.S.5
Fang, X.6
Armakola, M.7
Geser, F.8
Greene, R.9
Lu, M.M.10
-
44
-
-
84885484356
-
Prion-like properties of pathological TDP-43 aggregates from diseased brains
-
Nonaka, T., Masuda-Suzukake, M., Arai, T., Hasegawa, Y., Akatsu, H., Obi, T., Yoshida, M., Murayama, S., Mann, D.M., Akiyama, H. et al. (2013) Prion-like properties of pathological TDP-43 aggregates from diseased brains. Cell Rep., 4, 124-134.
-
(2013)
Cell Rep.
, vol.4
, pp. 124-134
-
-
Nonaka, T.1
Masuda-Suzukake, M.2
Arai, T.3
Hasegawa, Y.4
Akatsu, H.5
Obi, T.6
Yoshida, M.7
Murayama, S.8
Mann, D.M.9
Akiyama, H.10
-
45
-
-
0035977134
-
Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function
-
Zhang, Y.Q., Bailey, A.M., Matthies, H.J., Renden, R.B., Smith, M.A., Speese, S.D., Rubin, G.M. and Broadie, K. (2001) Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function. Cell, 107, 591-603.
-
(2001)
Cell
, vol.107
, pp. 591-603
-
-
Zhang, Y.Q.1
Bailey, A.M.2
Matthies, H.J.3
Renden, R.B.4
Smith, M.A.5
Speese, S.D.6
Rubin, G.M.7
Broadie, K.8
-
46
-
-
84895822652
-
Therapeutic modulation of eIF2alpha phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models
-
Kim, H.J., Raphael, A.R., Ladow, E.S., McGurk, L., Weber, R.A., Trojanowski, J.Q., Lee, V.M., Finkbeiner, S., Gitler, A.D. and Bonini, N.M. (2014) Therapeutic modulation of eIF2alpha phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models. Nat. Genet., 46, 152-160.
-
(2014)
Nat. Genet.
, vol.46
, pp. 152-160
-
-
Kim, H.J.1
Raphael, A.R.2
Ladow, E.S.3
McGurk, L.4
Weber, R.A.5
Trojanowski, J.Q.6
Lee, V.M.7
Finkbeiner, S.8
Gitler, A.D.9
Bonini, N.M.10
-
47
-
-
84908224269
-
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
-
Smith, B.N., Ticozzi, N., Fallini, C., Gkazi, A.S., Topp, S., Kenna, K.P., Scotter, E.L., Kost, J., Keagle, P., Miller, J.W. et al. (2014) Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. Neuron, 84, 324-331.
-
(2014)
Neuron
, vol.84
, pp. 324-331
-
-
Smith, B.N.1
Ticozzi, N.2
Fallini, C.3
Gkazi, A.S.4
Topp, S.5
Kenna, K.P.6
Scotter, E.L.7
Kost, J.8
Keagle, P.9
Miller, J.W.10
-
48
-
-
84908323798
-
TDP-43 suppresses CGG repeat-induced neurotoxicity through interactions with HnRNP A2/B1
-
He, F., Krans, A., Freibaum, B.D., Taylor, J.P. and Todd, P.K. (2014) TDP-43 suppresses CGG repeat-induced neurotoxicity through interactions with HnRNP A2/B1. Hum. Mol. Genet., 23, 5036-5051.
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. 5036-5051
-
-
He, F.1
Krans, A.2
Freibaum, B.D.3
Taylor, J.P.4
Todd, P.K.5
-
49
-
-
84908313138
-
CGG repeats in RNA modulate expression of TDP-43 in mouse and fly models of fragile X tremor ataxia syndrome
-
Galloway, J.N., Shaw, C., Yu, P., Parghi, D., Poidevin, M., Jin, P. and Nelson, D.L. (2014) CGG repeats in RNA modulate expression of TDP-43 in mouse and fly models of fragile X tremor ataxia syndrome. Hum. Mol. Genet., 23, 5906-5915.
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. 5906-5915
-
-
Galloway, J.N.1
Shaw, C.2
Yu, P.3
Parghi, D.4
Poidevin, M.5
Jin, P.6
Nelson, D.L.7
-
50
-
-
0030087911
-
Distinct expression patterns detected within individual tissues by the GAL4 enhancer trap technique
-
Gustafson, K. and Boulianne, G.L. (1996) Distinct expression patterns detected within individual tissues by the GAL4 enhancer trap technique. Genome, 39, 174-182.
-
(1996)
Genome
, vol.39
, pp. 174-182
-
-
Gustafson, K.1
Boulianne, G.L.2
-
51
-
-
52049096606
-
Fragile X protein controls the efficacy of mRNA transport in Drosophila neurons
-
Estes, P.S., O'Shea, M., Clasen, S. and Zarnescu, D.C. (2008) Fragile X protein controls the efficacy of mRNA transport in Drosophila neurons. Mol. Cell. Neurosci., 39, 170-179.
-
(2008)
Mol. Cell. Neurosci.
, vol.39
, pp. 170-179
-
-
Estes, P.S.1
O'Shea, M.2
Clasen, S.3
Zarnescu, D.C.4
-
52
-
-
78650083095
-
Development of a novel nonradiometric assay for nucleic acid binding to TDP-43 suitable for high-throughput screening using AlphaScreen technology
-
Cassel, J.A., Blass, B.E., Reitz, A.B. and Pawlyk, A.C. (2010) Development of a novel nonradiometric assay for nucleic acid binding to TDP-43 suitable for high-throughput screening using AlphaScreen technology. J. Biomol. Screen., 15, 1099- 1106.
-
(2010)
J. Biomol. Screen.
, vol.15
, pp. 1099- 1106
-
-
Cassel, J.A.1
Blass, B.E.2
Reitz, A.B.3
Pawlyk, A.C.4
-
53
-
-
84864279352
-
Characterization of a series of 4-aminoquinolines that stimulate caspase-7 mediated cleavage of TDP-43 and inhibit its function
-
Cassel, J.A., McDonnell, M.E., Velvadapu, V., Andrianov, V. and Reitz, A.B. (2012) Characterization of a series of 4-aminoquinolines that stimulate caspase-7 mediated cleavage of TDP-43 and inhibit its function. Biochimie, 94, 1974-1981.
-
(2012)
Biochimie
, vol.94
, pp. 1974-1981
-
-
Cassel, J.A.1
McDonnell, M.E.2
Velvadapu, V.3
Andrianov, V.4
Reitz, A.B.5
-
54
-
-
17344392308
-
A new mathematical model for relative quantification in real-time RT-PCR
-
Pfaffl, M.W. (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res., 29, e45.
-
(2001)
Nucleic Acids Res.
, vol.29
, pp. e45
-
-
Pfaffl, M.W.1
|