-
1
-
-
84893508018
-
Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations
-
Alami NH, Smith RB, Carrasco MA, Williams LA, Winborn CS, Han SS, Kiskinis E, Winborn B, Freibaum BD, Kanagaraj A, Clare AJ, Badders NM, Bilican B, Chaum E, Chandran S, Shaw CE, Eggan KC, Maniatis T, Taylor JP (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
Clare, A.J.11
Badders, N.M.12
Bilican, B.13
Chaum, E.14
Chandran, S.15
Shaw, C.E.16
Eggan, K.C.17
Maniatis, T.18
Taylor, J.P.19
-
2
-
-
78751616191
-
TDP-43 regulates its mRNA levels through a negative feedback loop
-
Ayala YM, De Conti L, Avendaño-Vázquez SE, Dhir A, Romano M, D’Ambrogio A, Tollervey J, Ule J, Baralle M, Buratti E, Baralle FE (2011) TDP-43 regulates its mRNA levels through a negative feedback loop. EMBO J 30:277–288.
-
(2011)
EMBO J
, vol.30
, pp. 277-288
-
-
Ayala, Y.M.1
De Conti, L.2
Avendaño-Vázquez, S.E.3
Dhir, A.4
Romano, M.5
D’Ambrogio, A.6
Tollervey, J.7
Ule, J.8
Baralle, M.9
Buratti, E.10
Baralle, F.E.11
-
3
-
-
84879349589
-
Eukaryotic stress granules are cleared by autophagy and Cdc48/VCP function
-
Buchan JR, Kolaitis RM, Taylor JP, Parker R (2013) Eukaryotic stress granules are cleared by autophagy and Cdc48/VCP function. Cell 153:1461–1474.
-
(2013)
Cell
, vol.153
, pp. 1474
-
-
Buchan, J.R.1
Kolaitis, R.M.2
Taylor, J.P.3
Parker, R.4
-
4
-
-
0035965309
-
Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9
-
Buratti E, Baralle FE (2001) Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9. J Biol Chem 276:36337–36343.
-
(2001)
J Biol Chem
, vol.276
, pp. 36337-36343
-
-
Buratti, E.1
Baralle, F.E.2
-
5
-
-
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, 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
-
6
-
-
65249107203
-
Microtubule assembly, organization and dynamics in axons and dendrites
-
Conde C, Cáceres A (2009) Microtubule assembly, organization and dynamics in axons and dendrites. Nat Rev Neurosci 10:319–332.
-
(2009)
Nat Rev Neurosci
, vol.10
, pp. 319-332
-
-
Conde, C.1
Cáceres, A.2
-
7
-
-
77951183978
-
Prion-like disorders: Blurring the divide between transmissibility and infectivity
-
Cushman M, Johnson BS, King OD, Gitler AD, 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
-
8
-
-
79952268025
-
TDP-43 is directed to stress granules by sorbi-tol, a novel physiological osmotic and oxidative stressor
-
Dewey CM, Cenik B, Sephton CF, Dries DR, Mayer P 3rd, Good SK, Johnson BA, Herz J, Yu G (2011) TDP-43 is directed to stress granules by sorbi-tol, 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
-
9
-
-
34047175919
-
Histone deacetylase 6 inhibition compensates for the transport deficit in Huntington’s disease by increasing tubulin acetyla-tion
-
Dompierre JP, Godin JD, Charrin BC, Cordeliéres FP, King SJ, Humbert S, Saudou F (2007) Histone deacetylase 6 inhibition compensates for the transport deficit in Huntington’s disease by increasing tubulin acetyla-tion. J Neurosci 27:3571–3583.
-
(2007)
J Neurosci
, vol.27
, pp. 3571-3583
-
-
Dompierre, J.P.1
Godin, J.D.2
Charrin, B.C.3
Cordeliéres, F.P.4
King, S.J.5
Humbert, S.6
Saudou, F.7
-
10
-
-
77956155218
-
Ataxin-2 intermediate-length poly-glutamine expansions are associated with increased risk for ALS
-
Elden AC, Kim HJ, Hart MP, Chen-Plotkin AS, Johnson BS, Fang X, Arma-kola M, Geser F, Greene R, Lu MM, Padmanabhan A, Clay-Falcone D, McCluskey L, Elman L, Juhr D, Gruber PJ, Rüb U, Auburger G, Tro-janowski JQ, Lee VM, et al. (2010) Ataxin-2 intermediate-length poly-glutamine 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
Arma-Kola, M.7
Geser, F.8
Greene, R.9
Lu, M.M.10
Padmanabhan, A.11
Clay-Falcone, D.12
McCluskey, L.13
Elman, L.14
Juhr, D.15
Gruber, P.J.16
Rüb, U.17
Auburger, G.18
Tro-Janowski, J.Q.19
Lee, V.M.20
more..
-
11
-
-
79957488875
-
Wild-type and A315T mutant TDP-43 exert differential neurotoxicityina Drosophila model of ALS
-
Estes PS, Boehringer A, Zwick R, Tang JE, Grigsby B, Zarnescu DC (2011) Wild-type and A315T mutant TDP-43 exert differential neurotoxicityina 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
-
12
-
-
84877832189
-
Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyo-trophic lateral sclerosis
-
Estes PS, Daniel SG, McCallum AP, Boehringer AV, Sukhina AS, Zwick RA, Zarnescu DC (2013) Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyo-trophic 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
-
13
-
-
84865063851
-
The ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth
-
Fallini C, Bassell GJ, 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
-
14
-
-
80052136588
-
TDP-43 knockdown impairs neurite outgrowth dependent on its target histone deacetylase 6
-
Fiesel FC, Schurr C, Weber SS, Kahle PJ (2011) TDP-43 knockdown impairsneurite outgrowth dependent on its target histone deacetylase 6. Mol Neurodegener 6:64.
-
(2011)
Mol Neurodegener
, vol.6
-
-
Fiesel, F.C.1
Schurr, C.2
Weber, S.S.3
Kahle, P.J.4
-
15
-
-
76149120427
-
Global analysis of TDP-43 interacting proteins reveals strong association with RNA splicing and translation machinery
-
Freibaum BD, Chitta RK, High AA, Taylor JP (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
-
16
-
-
79952585752
-
TDP-43 regulates Drosophila neuromuscular junctions growth by modulating Futsch/MAP1B levels and synaptic mi-crotubules organization
-
Godena VK, Romano G, Romano M, Appocher C, Klima R, Buratti E, Baralle FE, Feiguin F (2011) TDP-43 regulates Drosophila neuromuscular junctions growth by modulating Futsch/MAP1B levels and synaptic mi-crotubules organization. PLoS One 6:e17808.
-
(2011)
Plos One
, vol.6
-
-
Godena, V.K.1
Romano, G.2
Romano, M.3
Appocher, C.4
Klima, R.5
Buratti, E.6
Baralle, F.E.7
Feiguin, F.8
-
17
-
-
0030087911
-
Distinct expression patterns detected within individual tissues by the GAL4 enhancer trap technique
-
Gustafson K, Boulianne GL (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
-
18
-
-
0033680949
-
Drosophila Futsch/22C10 is a MAP1B-like protein required for dendritic and axonal development
-
Hummel T, Krukkert K, Roos J, Davis G, Klämbt C (2000) Drosophila Futsch/22C10 is a MAP1B-like protein required for dendritic and axonal development. Neuron 26:357–370.
-
(2000)
Neuron
, vol.26
, pp. 357-370
-
-
Hummel, T.1
Krukkert, K.2
Roos, J.3
Davis, G.4
Klämbt, C.5
-
19
-
-
84884777626
-
Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders
-
Janssens J, 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
-
20
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, Vande Velde C, Bouchard JP, Lacomblez L, Pochigaeva K, Salachas F, Pradat PF, Camu W, Meininger V, Dupre N, Rouleau GA (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
Pradat, P.F.11
Camu, W.12
Meininger, V.13
Dupre, N.14
Rouleau, G.A.15
-
21
-
-
84862151933
-
The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease
-
King OD, Gitler AD, 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
-
22
-
-
62149141328
-
Rethinking ALS: The FUS about TDP-43
-
Lagier-Tourenne C, Cleveland DW (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
-
23
-
-
84881490873
-
Converging mechanisms in ALS and FTD: Disrupted RNA and protein homeostasis
-
Ling SC, Polymenidou M, Cleveland DW (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
-
24
-
-
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 YJ, Vanderweyde T, Citro A, Mehta T, Zaarur N, McKee A, Bowser R, Sherman M, Petrucelli L, Wolozin B (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
-
-
Liu-Yesucevitz, L.1
Bilgutay, A.2
Zhang, Y.J.3
Vanderweyde, T.4
Citro, A.5
Mehta, T.6
Zaarur, N.7
McKee, A.8
Bowser, R.9
Sherman, M.10
Petrucelli, L.11
Wolozin, B.12
-
25
-
-
84877909895
-
Autophagy and microtubules–new story, old players
-
Mackeh R, Perdiz D, Lorin S, Codogno P, Poüs C (2013) Autophagy and microtubules–new story, old players. J Cell Sci 126:1071–1080.
-
(2013)
J Cell Sci
, vol.126
, pp. 1071-1080
-
-
Mackeh, R.1
Perdiz, D.2
Lorin, S.3
Codogno, P.4
Poüs, C.5
-
26
-
-
84894387057
-
Abnormal mitochondrial transport and morphology are common pathological denominators in SOD1 and TDP43 ALS mouse models
-
Magrane J, Cortez C, Gan WB, Manfredi G (2013) Abnormal mitochondrial transport and morphology are common pathological denominators in SOD1 and TDP43 ALS mouse models. Hum Mol Genet 23:1413–1424.
-
(2013)
Hum Mol Genet
, vol.23
, pp. 1413-1424
-
-
Magrane, J.1
Cortez, C.2
Gan, W.B.3
Manfredi, G.4
-
27
-
-
79952589652
-
TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1
-
McDonald KK, Aulas A, Destroismaisons L, Pickles S, Beleac E, Camu W, Rouleau GA, 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
-
28
-
-
77249160149
-
Microtubules govern stress granule mobility and dynamics
-
Nadezhdina ES, Lomakin AJ, Shpilman AA, Chudinova EM, Ivanov PA (2010) Microtubules govern stress granule mobility and dynamics. Biochim Biophys Acta 1803:361–371.
-
(2010)
Biochim Biophys Acta
, vol.1803
, pp. 361-371
-
-
Nadezhdina, E.S.1
Lomakin, A.J.2
Shpilman, A.A.3
Chudinova, E.M.4
Ivanov, P.A.5
-
29
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, Bruce J, Schuck T, Grossman M, Clark CM, McCluskey LF, Miller BL, Masliah E, Mackenzie IR, Feldman H, Feiden W, Kretzschmar HA, Tro-janowski JQ, Lee VM (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
McCluskey, L.F.11
Miller, B.L.12
Masliah, E.13
Mackenzie, I.R.14
Feldman, H.15
Feiden, W.16
Kretzschmar, H.A.17
Tro-Janowski, J.Q.18
Lee, V.M.19
-
30
-
-
84882254367
-
The role of autophagy in neurodegenerative disease
-
Nixon RA (2013) The role of autophagy in neurodegenerative disease. Nat Med 19:983–997.
-
(2013)
Nat Med
, vol.19
, pp. 983-997
-
-
Nixon, R.A.1
-
31
-
-
0029066110
-
Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs
-
Ou SH, Wu F, Harrich D, García-Martínez LF, Gaynor RB (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. 3596
-
-
Ou, S.H.1
Wu, F.2
Harrich, D.3
García-Martínez, L.F.4
Gaynor, R.B.5
-
32
-
-
84857124994
-
Endogenous TDP-43 localized to stress granules can subsequently form protein aggregates
-
Parker SJ, Meyerowitz J, James JL, Liddell JR, Crouch PJ, Kanninen KM, White AR (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
-
33
-
-
17344392308
-
A new mathematical model for relative quantification in real-time RT-PCR
-
Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29:e45.
-
(2001)
Nucleic Acids Res
, vol.29
-
-
Pfaffl, M.W.1
-
34
-
-
79953185674
-
Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43
-
Polymenidou M, Lagier-Tourenne C, Hutt KR, Huelga SC, Moran J, Liang TY, Ling SC, Sun E, Wancewicz E, Mazur C, Kordasiewicz H, Sedaghat Y, Donohue JP, Shiue L, Bennett CF, Yeo GW, Cleveland DW (2011) Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. Nat Neurosci 14:459–468.
-
(2011)
Nat Neurosci
, vol.14
, pp. 459-468
-
-
Polymenidou, M.1
Lagier-Tourenne, C.2
Hutt, K.R.3
Huelga, S.C.4
Moran, J.5
Liang, T.Y.6
Ling, S.C.7
Sun, E.8
Wancewicz, E.9
Mazur, C.10
Kordasiewicz, H.11
Sedaghat, Y.12
Donohue, J.P.13
Shiue, L.14
Bennett, C.F.15
Yeo, G.W.16
Cleveland, D.W.17
-
35
-
-
84882801549
-
Altered ribostasis: RNA-protein granules in degenerative disorders
-
Ramaswami M, Taylor JP, 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
-
36
-
-
84875441083
-
The changing scene of amyotrophic lateral sclerosis
-
Robberecht W, 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
-
37
-
-
0033710887
-
Drosophila Futsch regulates synaptic microtubule organization and is necessary for synaptic growth
-
Roos J, Hummel T, Ng N, Klämbt C, Davis GW (2000) Drosophila Futsch regulates synaptic microtubule organization and is necessary for synaptic growth. Neuron 26:371–382.
-
(2000)
Neuron
, vol.26
, pp. 371-382
-
-
Roos, J.1
Hummel, T.2
Ng, N.3
Klämbt, C.4
Davis, G.W.5
-
38
-
-
2442477424
-
New synaptic bouton formation is disrupted by misregulation of micro-tubule stability in aPKC mutants
-
Ruiz-Canada C, Ashley J, Moeckel-Cole S, Drier E, Yin J, Budnik V (2004) New synaptic bouton formation is disrupted by misregulation of micro-tubule stability in aPKC mutants. Neuron 42:567–580.
-
(2004)
Neuron
, vol.42
, pp. 567-580
-
-
Ruiz-Canada, C.1
Ashley, J.2
Moeckel-Cole, S.3
Drier, E.4
Yin, J.5
Budnik, V.6
-
39
-
-
78651408754
-
Identification of neu-ronal RNA targets of TDP-43-containing ribonucleoprotein complexes
-
Sephton CF, Cenik C, Kucukural A, Dammer EB, Cenik B, Han Y, Dewey CM, Roth FP, Herz J, Peng J, Moore MJ, Yu G (2011) Identification of neu-ronal RNA targets of TDP-43-containing ribonucleoprotein complexes. J Biol Chem 286:1204–1215.
-
(2011)
J Biol Chem
, vol.286
, pp. 1204-1215
-
-
Sephton, C.F.1
Cenik, C.2
Kucukural, A.3
Dammer, E.B.4
Cenik, B.5
Han, Y.6
Dewey, C.M.7
Roth, F.P.8
Herz, J.9
Peng, J.10
Moore, M.J.11
Yu, G.12
-
40
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
Sreedharan J, Blair IP, Tripathi VB, Hu X, Vance C, Rogelj B, Ackerley S, Durnall JC, Williams KL, Buratti E, Baralle F, de Belleroche J, Mitchell JD, Leigh PN, Al-Chalabi A, Miller CC, Nicholson G, Shaw CE (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
Baralle, F.11
De Belleroche, J.12
Mitchell, J.D.13
Leigh, P.N.14
Al-Chalabi, A.15
Miller, C.C.16
Nicholson, G.17
Shaw, C.E.18
-
41
-
-
34249751076
-
TDP43 isa human low molecular weight neurofila-ment (hNFL) mRNA-binding protein
-
Strong MJ, Volkening K, Hammond R, Yang W, Strong W, Leystra-Lantz C, Shoesmith C (2007) TDP43 isa human low molecular weight neurofila-ment (hNFL) mRNA-binding protein. Mol Cell Neurosci 35:320–327.
-
(2007)
Mol Cell Neurosci
, vol.35
, pp. 320-327
-
-
Strong, M.J.1
Volkening, K.2
Hammond, R.3
Yang, W.4
Strong, W.5
Leystra-Lantz, C.6
Shoesmith, C.7
-
42
-
-
79953180492
-
Characterizing the RNA targets and position-dependent splicing regulation byTDP-43
-
Tollervey JR, Curk T, Rogelj B, Briese M, Cereda M, Kayikci M, König J, Hortobágyi T, Nishimura AL, Zupunski V, Patani R, Chandran S, Rot G, Zupan B, Shaw CE, Ule J (2011) Characterizing the RNA targets and position-dependent splicing regulation byTDP-43. Nat Neurosci 14:452–458.
-
(2011)
Nat Neurosci
, vol.14
, pp. 458
-
-
Tollervey, J.R.1
Curk, T.2
Rogelj, B.3
Briese, M.4
Cereda, M.5
Kayikci, M.6
König, J.7
Hortobágyi, T.8
Nishimura, A.L.9
Zupunski, V.10
Patani, R.11
Chandran, S.12
Rot, G.13
Zupan, B.14
Shaw, C.E.15
Ule, J.16
-
43
-
-
41949100148
-
TARDBP mutationsin amyo-trophic lateral sclerosis with TDP-43 neuropathology: A genetic and his-topathological analysis
-
Van Deerlin VM, Leverenz JB, Bekris LM, Bird TD, Yuan W, Elman LB, Clay D, Wood EM, Chen-Plotkin AS, Martinez-Lage M, Steinbart E, McClus-key L, Grossman M, Neumann M, Wu IL, Yang WS, Kalb R, Galasko DR, Montine TJ, Trojanowski JQ, et al. (2008) TARDBP mutationsin amyo-trophic lateral sclerosis with TDP-43 neuropathology: a genetic and his-topathological 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
Steinbart, E.11
McClus-Key, L.12
Grossman, M.13
Neumann, M.14
Wu, I.L.15
Yang, W.S.16
Kalb, R.17
Galasko, D.R.18
Montine, T.J.19
Trojanowski, J.Q.20
more..
-
44
-
-
73949134014
-
Tar DNA binding protein of 43 kDa (TDP-43), 14-3-3 proteins and copper/ zinc superoxide dismutase (SOD1) interact to modulate NFL mRNA stability. Implications for altered RNA processing in amyotrophic lateral sclerosis (ALS)
-
Volkening K, Leystra-Lantz C, Yang W, Jaffee H, Strong MJ (2009) Tar DNA binding protein of 43 kDa (TDP-43), 14-3-3 proteins and copper/ zinc superoxide dismutase (SOD1) interact to modulate NFL mRNA stability. Implications for altered RNA processing in amyotrophic lateral sclerosis (ALS). Brain Res 1305:168–182.
-
(2009)
Brain Res
, vol.1305
, pp. 168-182
-
-
Volkening, K.1
Leystra-Lantz, C.2
Yang, W.3
Jaffee, H.4
Strong, M.J.5
-
45
-
-
42449163952
-
TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive factor
-
Wang IF, Wu LS, Chang HY, Shen CK (2008) TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive 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
-
46
-
-
84896914639
-
Partial loss of TDP-43 function causes phenotypes of amyotrophic lateral sclerosis
-
Yang C, Wang H, Qiao T, Yang B, Aliaga L, Qiu L, Tan W, Salameh J, McKenna-Yasek DM, Smith T, Peng L, Moore MJ, Brown RH Jr, Cai H, Xu Z (2014) Partial loss of TDP-43 function causes phenotypes of amyotrophic lateral sclerosis. Proc Natl Acad Sci U S A111:E1121–E1129.
-
(2014)
Proc Natl Acad Sci U S
, vol.A111
, pp. E1121-E1129
-
-
Yang, C.1
Wang, H.2
Qiao, T.3
Yang, B.4
Aliaga, L.5
Qiu, L.6
Tan, W.7
Salameh, J.8
McKenna-Yasek, D.M.9
Smith, T.10
Peng, L.11
Moore, M.J.12
Brown, R.H.13
Cai, H.14
Xu, Z.15
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