-
1
-
-
32344435621
-
TDP43 depletion rescues aberrant CFTR exon 9 skipping
-
Ayala YM, Pagani F, Baralle FE. TDP43 depletion rescues aberrant CFTR exon 9 skipping. FEBS Lett 2006; 580: 1339-1344
-
(2006)
FEBS Lett
, vol.580
, pp. 1339-1344
-
-
Ayala, Y.M.1
Pagani, F.2
Baralle, F.E.3
-
2
-
-
59549094064
-
Structural determinants of the cellular localization and shuttling of TDP-43
-
Ayala YM, Zago P, D'Ambrogio A, Xu YF, Petrucelli L, Buratti E, et al. Structural determinants of the cellular localization and shuttling of TDP-43. J Cell Sci 2008; 121: 3778-3785
-
(2008)
J Cell Sci
, vol.121
, pp. 3778-3785
-
-
Ayala, Y.M.1
Zago, P.2
D'Ambrogio, A.3
Xu, Y.F.4
Petrucelli, L.5
Buratti, E.6
-
3
-
-
74949135753
-
Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis
-
Barmada SJ, Skibinski G, Korb E, Rao EJ, Wu JY, Finkbeiner S. Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis. J Neurosci 2010; 30: 639-649
-
(2010)
J Neurosci
, vol.30
, pp. 639-649
-
-
Barmada, S.J.1
Skibinski, G.2
Korb, E.3
Rao, E.J.4
Wu, J.Y.5
Finkbeiner, S.6
-
4
-
-
65649112431
-
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration
-
Benajiba L, Le Ber I, Camuzat A, Lacoste M, Thomas-Anterion C, Couratier P, et al. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Ann Neurol 2009; 65: 470-473
-
(2009)
Ann Neurol
, vol.65
, pp. 470-473
-
-
Benajiba, L.1
Le Ber, I.2
Camuzat, A.3
Lacoste, M.4
Thomas-Anterion, C.5
Couratier, P.6
-
5
-
-
38449102667
-
Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease
-
Buratti E, Baralle FE. Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease. Front Biosci 2008; 13: 867-878
-
(2008)
Front Biosci
, vol.13
, pp. 867-878
-
-
Buratti, E.1
Baralle, F.E.2
-
6
-
-
34447096691
-
Neuropathologic diagnostic and nosologic criteria for frontotem-poral lobar degeneration: Consensus of the Consortium for Frontotemporal Lobar Degeneration
-
Cairns NJ, Bigio EH, Mackenzie IR, Neumann M, Lee VM, Hatanpaa KJ, et al. Neuropathologic diagnostic and nosologic criteria for frontotem-poral lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration. Acta Neuropathol 2007; 114: 5-22.
-
(2007)
Acta Neuropathol
, vol.114
, pp. 5-22
-
-
Cairns, N.J.1
Bigio, E.H.2
MacKenzie, I.R.3
Neumann, M.4
Lee, V.M.5
Hatanpaa, K.J.6
-
7
-
-
0003774114
-
Isolation of the heterogeneous nuclear RNA-ribo-nucleoprotein complex (hnRNP): A unique supramolecular assembly
-
Choi YD, Dreyfuss G. Isolation of the heterogeneous nuclear RNA-ribo-nucleoprotein complex (hnRNP): a unique supramolecular assembly. Proc Natl Acad Sci USA 1984; 81: 7471-7475
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 7471-7475
-
-
Choi, Y.D.1
Dreyfuss, G.2
-
8
-
-
58249089343
-
Age-dependent deterioration of nuclear pore complexes causes a loss of nuclear integrity in postmitotic cells
-
D'Angelo MA, Raices M, Panowski SH, Hetzer MW. Age-dependent deterioration of nuclear pore complexes causes a loss of nuclear integrity in postmitotic cells. Cell 2009; 136: 284-295
-
(2009)
Cell
, vol.136
, pp. 284-295
-
-
D'Angelo, M.A.1
Raices, M.2
Panowski, S.H.3
Hetzer, M.W.4
-
9
-
-
60849103086
-
Irie K. hnRNP K interacts with RNA binding motif protein 42 and functions in the maintenance of cellular ATP level during stress conditions
-
Fukuda T, Naiki T, Saito M, Irie K. hnRNP K interacts with RNA binding motif protein 42 and functions in the maintenance of cellular ATP level during stress conditions. Genes Cells 2009; 14: 113-128
-
(2009)
Genes Cells
, vol.14
, pp. 113-128
-
-
Fukuda, T.1
Naiki, T.2
Saito, M.3
-
10
-
-
0035126176
-
P35/cdk5 binds and phosphorylates beta-catenin and regulates beta-catenin/presenilin-1 interaction
-
Kesavapany S, Lau KF, McLoughlin DM, Brownlees J, Ackerley S, Leigh PN, et al. p35/cdk5 binds and phosphorylates beta-catenin and regulates beta-catenin/presenilin-1 interaction. Eur J Neurosci 2001; 13: 241-247
-
(2001)
Eur J Neurosci
, vol.13
, pp. 241-247
-
-
Kesavapany, S.1
Lau, K.F.2
McLoughlin, D.M.3
Brownlees, J.4
Ackerley, S.5
Leigh, P.N.6
-
11
-
-
70449393271
-
Nuclear contour irregularity and abnormal transporter protein distribution in anterior horn cells in amyotrophic lateral sclerosis
-
Kinoshita Y, Ito H, Hirano A, Fujita K, Wate R, Nakamura M, et al. Nuclear contour irregularity and abnormal transporter protein distribution in anterior horn cells in amyotrophic lateral sclerosis. J Neuropathol Exp Neurol 2009; 68: 1184-1192
-
(2009)
J Neuropathol Exp Neurol
, vol.68
, pp. 1184-1192
-
-
Kinoshita, Y.1
Ito, H.2
Hirano, A.3
Fujita, K.4
Wate, R.5
Nakamura, M.6
-
12
-
-
39149111609
-
Oxidative stress mislocalizes and retains transport factor importin-alpha and nucleoporins Nup153 and Nup88 in nuclei where they generate high molecular mass complexes
-
Kodiha M, Tran D, Qian C, Morogan A, Presley JF, Brown CM, et al. Oxidative stress mislocalizes and retains transport factor importin-alpha and nucleoporins Nup153 and Nup88 in nuclei where they generate high molecular mass complexes. Biochim Biophys Acta 2008; 1783: 405-418
-
(2008)
Biochim Biophys Acta
, vol.1783
, pp. 405-418
-
-
Kodiha, M.1
Tran, D.2
Qian, C.3
Morogan, A.4
Presley, J.F.5
Brown, C.M.6
-
13
-
-
0039612732
-
Evidence for distinct substrate specificities of importin alpha family members in nuclear protein import
-
Kohler M, Speck C, Christiansen M, Bischoff FR, Prehn S, Haller H, et al. Evidence for distinct substrate specificities of importin alpha family members in nuclear protein import. Mol Cell Biol 1999; 19: 7782-7791
-
(1999)
Mol Cell Biol
, vol.19
, pp. 7782-7791
-
-
Kohler, M.1
Speck, C.2
Christiansen, M.3
Bischoff, F.R.4
Prehn, S.5
Haller, H.6
-
14
-
-
0342276108
-
Export of importin alpha from the nucleus is mediated by a specific nuclear transport factor
-
Kutay U, Bischoff FR, Kostka S, Kraft R, Gorlich D. Export of importin alpha from the nucleus is mediated by a specific nuclear transport factor. Cell 1997; 90: 1061-1071
-
(1997)
Cell
, vol.90
, pp. 1061-1071
-
-
Kutay, U.1
Bischoff, F.R.2
Kostka, S.3
Kraft, R.4
Gorlich, D.5
-
15
-
-
37349039461
-
TDP-43 proteinopathies: Neurodegenerative protein misfolding diseases without amyloidosis
-
Kwong LK, Uryu K, Trojanowski JQ, Lee VM. TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis. Neurosignals 2008; 16: 41-51.
-
(2008)
Neurosignals
, vol.16
, pp. 41-51
-
-
Kwong, L.K.1
Uryu, K.2
Trojanowski, J.Q.3
Lee, V.M.4
-
16
-
-
62149141328
-
Rethinking ALS: The FUS about TDP-43
-
Lagier-Tourenne C, Cleveland DW. Rethinking ALS: the FUS about TDP-43. Cell 2009; 136: 1001-1004
-
(2009)
Cell
, vol.136
, pp. 1001-1004
-
-
Lagier-Tourenne, C.1
Cleveland, D.W.2
-
17
-
-
34247135913
-
Classical nuclear localization signals: Definition, function, and interaction with importin alpha
-
Lange A, Mills RE, Lange CJ, Stewart M, Devine SE, Corbett AH. Classical nuclear localization signals: definition, function, and interaction with importin alpha. J Biol Chem 2007; 282: 5101-5105
-
(2007)
J Biol Chem
, vol.282
, pp. 5101-5105
-
-
Lange, A.1
Mills, R.E.2
Lange, C.J.3
Stewart, M.4
Devine, S.E.5
Corbett, A.H.6
-
18
-
-
33746776838
-
Rules for nuclear localization sequence recognition by karyopherin beta 2
-
Lee BJ, Cansizoglu AE, Suel KE, Louis TH, Zhang Z, Chook YM. Rules for nuclear localization sequence recognition by karyopherin beta 2. Cell 2006; 126: 543-558
-
(2006)
Cell
, vol.126
, pp. 543-558
-
-
Lee, B.J.1
Cansizoglu, A.E.2
Suel, K.E.3
Louis, T.H.4
Zhang, Z.5
Chook, Y.M.6
-
19
-
-
33646365075
-
Regulation of Stat3 nuclear import by importin alpha5 and importin alpha7 via two different functional sequence elements
-
Ma J, Cao X. Regulation of Stat3 nuclear import by importin alpha5 and importin alpha7 via two different functional sequence elements. Cell Signal 2006; 18: 1117-1126
-
(2006)
Cell Signal
, vol.18
, pp. 1117-1126
-
-
Ma, J.1
Cao, X.2
-
20
-
-
57049105123
-
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: Consensus recommendations
-
Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, et al. Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations. Acta Neuropathol 2009; 117: 15-18
-
(2009)
Acta Neuropathol
, vol.117
, pp. 15-18
-
-
MacKenzie, I.R.1
Neumann, M.2
Bigio, E.H.3
Cairns, N.J.4
Alafuzoff, I.5
Kril, J.6
-
21
-
-
2942532727
-
Cortical selective vulnerability in motor neuron disease: A mor-phometric study
-
Maekawa S, al-Sarraj S, Kibble M, Landau S, Parnavelas J, Cotter D, et al. Cortical selective vulnerability in motor neuron disease: a mor-phometric study. Brain 2004; 127: 1237-1251
-
(2004)
Brain
, vol.127
, pp. 1237-1251
-
-
Maekawa, S.1
Al-Sarraj, S.2
Kibble, M.3
Landau, S.4
Parnavelas, J.5
Cotter, D.6
-
22
-
-
75949083202
-
Protein targets of oxidative damage in human neurodegenerative diseases with abnormal protein aggregates
-
Martinez A, Portero-Otin M, Pamplona R, Ferrer I. Protein targets of oxidative damage in human neurodegenerative diseases with abnormal protein aggregates. Brain Pathol 2009; 20: 281-297
-
(2009)
Brain Pathol
, vol.20
, pp. 281-297
-
-
Martinez, A.1
Portero-Otin, M.2
Pamplona, R.3
Ferrer, I.4
-
23
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 2006; 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
-
24
-
-
58149498300
-
Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells
-
Nonaka T, Arai T, Buratti E, Baralle FE, Akiyama H, Hasegawa M. Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells. FEBS Lett 2009; 583: 394-400.
-
(2009)
FEBS Lett
, vol.583
, pp. 394-400
-
-
Nonaka, T.1
Arai, T.2
Buratti, E.3
Baralle, F.E.4
Akiyama, H.5
Hasegawa, M.6
-
25
-
-
0036290393
-
Age-associated reduction of nuclear protein import in human fibroblasts
-
Pujol G, Soderqvist H, Radu A. Age-associated reduction of nuclear protein import in human fibroblasts. Biochem Biophys Res Commun 2002; 294: 354-358
-
(2002)
Biochem Biophys Res Commun
, vol.294
, pp. 354-358
-
-
Pujol, G.1
Soderqvist, H.2
Radu, A.3
-
27
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
Sreedharan J, Blair IP, Tripathi VB, Hu X, Vance C, Rogelj B, et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 2008; 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
-
28
-
-
36749081534
-
Crossing the nuclear envelope: Hierarchical regulation of nucleocytoplasmic transport
-
Terry LJ, Shows EB, Wente SR. Crossing the nuclear envelope: hierarchical regulation of nucleocytoplasmic transport. Science 2007; 318: 1412-1416
-
(2007)
Science
, vol.318
, pp. 1412-1416
-
-
Terry, L.J.1
Shows, E.B.2
Wente, S.R.3
-
29
-
-
0344256486
-
Structural diversity and functional implications of the eukaryotic TDP gene family
-
Wang HY, Wang IF, Bose J, Shen CK. Structural diversity and functional implications of the eukaryotic TDP gene family. Genomics 2004; 83: 130-139
-
(2004)
Genomics
, vol.83
, pp. 130-139
-
-
Wang, H.Y.1
Wang, I.F.2
Bose, J.3
Shen, C.K.4
-
30
-
-
43249114144
-
Membrane-bound beta-amyloid oligomers are recruited into lipid rafts by a fyn-depen-dent mechanism
-
Williamson R, Usardi A, Hanger DP, Anderton BH. Membrane-bound beta-amyloid oligomers are recruited into lipid rafts by a fyn-depen-dent mechanism. FASEB J 2008; 22: 1552-1559
-
(2008)
FASEB J
, vol.22
, pp. 1552-1559
-
-
Williamson, R.1
Usardi, A.2
Hanger, D.P.3
Anderton, B.H.4
-
31
-
-
77649269011
-
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration
-
Wils H, Kleinberger G, Janssens J, Pereson S, Joris G, Cuijt I, et al. TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration. Proc Natl Acad Sci USA 2010; 107: 3858-3863
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 3858-3863
-
-
Wils, H.1
Kleinberger, G.2
Janssens, J.3
Pereson, S.4
Joris, G.5
Cuijt, I.6
-
32
-
-
44749091997
-
Disturbance of nuclear and cytoplasmic TAR DNA-binding protein (TDP-43) induces disease-like redistribution, sequestration, and aggregate formation
-
Winton MJ, Igaz LM, Wong MM, Kwong LK, Trojanowski JQ, Lee VM. Disturbance of nuclear and cytoplasmic TAR DNA-binding protein (TDP-43) induces disease-like redistribution, sequestration, and aggregate formation. J Biol Chem 2008a; 283: 13302-13309
-
(2008)
J Biol Chem
, vol.283
, pp. 13302-13309
-
-
Winton, M.J.1
Igaz, L.M.2
Wong, M.M.3
Kwong, L.K.4
Trojanowski, J.Q.5
Lee, V.M.6
-
33
-
-
44749093657
-
A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro
-
Winton MJ, Van Deerlin VM, Kwong LK, Yuan W, Wood EM, Yu CE, et al. A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro. FEBS Lett 2008b; 582: 2252-2256
-
(2008)
FEBS Lett
, vol.582
, pp. 2252-2256
-
-
Winton, M.J.1
Van Deerlin, V.M.2
Kwong, L.K.3
Yuan, W.4
Wood, E.M.5
Yu, C.E.6
|