-
1
-
-
33750716074
-
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Arai T., Hasegawa M., Akiyama H., Ikeda K., Nonaka T., Mori H., Mann D., Tsuchiya K., Yoshida M., Hashizume Y., Oda T. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem. Biophys. Res. Commun. 2006, 351:602-611.
-
(2006)
Biochem. Biophys. Res. Commun.
, vol.351
, pp. 602-611
-
-
Arai, T.1
Hasegawa, M.2
Akiyama, H.3
Ikeda, K.4
Nonaka, T.5
Mori, H.6
Mann, D.7
Tsuchiya, K.8
Yoshida, M.9
Hashizume, Y.10
Oda, T.11
-
2
-
-
77949908515
-
Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathy
-
Arai T., Hasegawa M., Nonoka T., Kametani F., Yamashita M., Hosokawa M., Niizato K., Tsuchiya K., Kobayashi Z., Ikeda K., et al. Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathy. Neuropathology 2010, 30:170-181.
-
(2010)
Neuropathology
, vol.30
, pp. 170-181
-
-
Arai, T.1
Hasegawa, M.2
Nonoka, T.3
Kametani, F.4
Yamashita, M.5
Hosokawa, M.6
Niizato, K.7
Tsuchiya, K.8
Kobayashi, Z.9
Ikeda, K.10
-
3
-
-
0035947372
-
Impairment of the ubiquitin-proteasome system by protein aggregation
-
Bence N.F., Sampat R.M., Kopito R.R. Impairment of the ubiquitin-proteasome system by protein aggregation. Science 2001, 292:1552-1555.
-
(2001)
Science
, vol.292
, pp. 1552-1555
-
-
Bence, N.F.1
Sampat, R.M.2
Kopito, R.R.3
-
4
-
-
84878873344
-
Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid
-
Bigio E.H., Wu J.Y., Deng H.X., Bit-Ivan E.N., Mao Q., Ganti R., Peterson M., Siddique N., Geula C., Siddique T., Mesulam M. Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid. Acta Neuropathol. 2013, 125:463-465.
-
(2013)
Acta Neuropathol.
, vol.125
, pp. 463-465
-
-
Bigio, E.H.1
Wu, J.Y.2
Deng, H.X.3
Bit-Ivan, E.N.4
Mao, Q.5
Ganti, R.6
Peterson, M.7
Siddique, N.8
Geula, C.9
Siddique, T.10
Mesulam, M.11
-
5
-
-
0025863618
-
Neuropathological stageing of Alzheimer-related changes
-
Braak H., Braak E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol. 1991, 82:239-259.
-
(1991)
Acta Neuropathol.
, vol.82
, pp. 239-259
-
-
Braak, H.1
Braak, E.2
-
6
-
-
0037333666
-
Staging of brain pathology related to sporadic Parkinson's disease
-
Braak H., Del Tredici K., Rüb U., de Vos R.A., Jansen Steur E.N., Braak E. Staging of brain pathology related to sporadic Parkinson's disease. Neurobiol. Aging 2003, 24:197-211.
-
(2003)
Neurobiol. Aging
, vol.24
, pp. 197-211
-
-
Braak, H.1
Del Tredici, K.2
Rüb, U.3
de Vos, R.A.4
Jansen Steur, E.N.5
Braak, E.6
-
7
-
-
0028142392
-
El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial "Clinical Limits of Amyotrophic Lateral Sclerosis" workshop contributors
-
Brooks B.R. El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial "Clinical Limits of Amyotrophic Lateral Sclerosis" workshop contributors. J.Neurol. Sci. 1994, 124(Suppl):96-107.
-
(1994)
J.Neurol. Sci.
, vol.124
, Issue.SUPPL
, pp. 96-107
-
-
Brooks, B.R.1
-
8
-
-
84857768992
-
Cellular model of TAR DNA binding protein 43 (TDP-43) aggregation based on its C-terminal Q/N rich region
-
Budini M., Buratti E., Stuani C., Guarnaccia C., Romano V., De Conti L., Baralle F.E. Cellular model of TAR DNA binding protein 43 (TDP-43) aggregation based on its C-terminal Q/N rich region. J.Biol. Chem. 2012, 287:7512-7525.
-
(2012)
J.Biol. Chem.
, vol.287
, pp. 7512-7525
-
-
Budini, M.1
Buratti, E.2
Stuani, C.3
Guarnaccia, C.4
Romano, V.5
De Conti, L.6
Baralle, F.E.7
-
9
-
-
69549114542
-
The molecular links between TDP-43 dysfunction and neurodegeneration
-
Buratti E., Baralle F.E. The molecular links between TDP-43 dysfunction and neurodegeneration. Adv. Genet. 2009, 66:1-34.
-
(2009)
Adv. Genet.
, vol.66
, pp. 1-34
-
-
Buratti, E.1
Baralle, F.E.2
-
10
-
-
0035794665
-
Nuclear factor TDP-43 and SR proteins promote invitro and invivo CFTR exon 9 skipping
-
Buratti E., Dörk T., Zuccato E., Pagani F., Romano M., Baralle F.E. Nuclear factor TDP-43 and SR proteins promote invitro and invivo CFTR exon 9 skipping. EMBO J. 2001, 20:1774-1784.
-
(2001)
EMBO J.
, vol.20
, pp. 1774-1784
-
-
Buratti, E.1
Dörk, T.2
Zuccato, E.3
Pagani, F.4
Romano, M.5
Baralle, F.E.6
-
11
-
-
67650077008
-
Transmission and spreading of tauopathy in transgenic mouse brain
-
Clavaguera F., Bolmont T., Crowther R.A., Abramowski D., Frank S., Probst A., Fraser G., Stalder A.K., Beibel M., Staufenbiel M., et al. Transmission and spreading of tauopathy in transgenic mouse brain. Nat. Cell Biol. 2009, 11:909-913.
-
(2009)
Nat. Cell Biol.
, vol.11
, pp. 909-913
-
-
Clavaguera, F.1
Bolmont, T.2
Crowther, R.A.3
Abramowski, D.4
Frank, S.5
Probst, A.6
Fraser, G.7
Stalder, A.K.8
Beibel, M.9
Staufenbiel, M.10
-
12
-
-
84857275902
-
Propagation of tau pathology in a model of early Alzheimer's disease
-
de Calignon A., Polydoro M., Suárez-Calvet M., William C., Adamowicz D.H., Kopeikina K.J., Pitstick R., Sahara N., Ashe K.H., Carlson G.A., et al. Propagation of tau pathology in a model of early Alzheimer's disease. Neuron 2012, 73:685-697.
-
(2012)
Neuron
, vol.73
, pp. 685-697
-
-
de Calignon, A.1
Polydoro, M.2
Suárez-Calvet, M.3
William, C.4
Adamowicz, D.H.5
Kopeikina, K.J.6
Pitstick, R.7
Sahara, N.8
Ashe, K.H.9
Carlson, G.A.10
-
13
-
-
69149089854
-
Inclusion formation and neuronal cell death through neuron-to-neuron transmission of alpha-synuclein
-
Desplats P., Lee H.J., Bae E.J., Patrick C., Rockenstein E., Crews L., Spencer B., Masliah E., Lee S.J. Inclusion formation and neuronal cell death through neuron-to-neuron transmission of alpha-synuclein. Proc. Natl. Acad. Sci. USA 2009, 106:13010-13015.
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 13010-13015
-
-
Desplats, P.1
Lee, H.J.2
Bae, E.J.3
Patrick, C.4
Rockenstein, E.5
Crews, L.6
Spencer, B.7
Masliah, E.8
Lee, S.J.9
-
14
-
-
3042788972
-
Cells release prions in association with exosomes
-
Fevrier B., Vilette D., Archer F., Loew D., Faigle W., Vidal M., Laude H., Raposo G. Cells release prions in association with exosomes. Proc. Natl. Acad. Sci. USA 2004, 101:9683-9688.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 9683-9688
-
-
Fevrier, B.1
Vilette, D.2
Archer, F.3
Loew, D.4
Faigle, W.5
Vidal, M.6
Laude, H.7
Raposo, G.8
-
15
-
-
67649273927
-
Propagation of tau misfolding from the outside to the inside of a cell
-
Frost B., Jacks R.L., Diamond M.I. Propagation of tau misfolding from the outside to the inside of a cell. J.Biol. Chem. 2009, 284:12845-12852.
-
(2009)
J.Biol. Chem.
, vol.284
, pp. 12845-12852
-
-
Frost, B.1
Jacks, R.L.2
Diamond, M.I.3
-
16
-
-
79956311051
-
A seeding reaction recapitulates intracellular formation of Sarkosyl-insoluble transactivation response element (TAR) DNA-binding protein-43 inclusions
-
Furukawa Y., Kaneko K., Watanabe S., Yamanaka K., Nukina N. A seeding reaction recapitulates intracellular formation of Sarkosyl-insoluble transactivation response element (TAR) DNA-binding protein-43 inclusions. J.Biol. Chem. 2011, 286:18664-18672.
-
(2011)
J.Biol. Chem.
, vol.286
, pp. 18664-18672
-
-
Furukawa, Y.1
Kaneko, K.2
Watanabe, S.3
Yamanaka, K.4
Nukina, N.5
-
17
-
-
77954385676
-
The propagation of prion-like protein inclusions in neurodegenerative diseases
-
Goedert M., Clavaguera F., Tolnay M. The propagation of prion-like protein inclusions in neurodegenerative diseases. Trends Neurosci. 2010, 33:317-325.
-
(2010)
Trends Neurosci.
, vol.33
, pp. 317-325
-
-
Goedert, M.1
Clavaguera, F.2
Tolnay, M.3
-
18
-
-
61849178720
-
Prions hijack tunnelling nanotubes for intercellular spread
-
Gousset K., Schiff E., Langevin C., Marijanovic Z., Caputo A., Browman D.T., Chenouard N., de Chaumont F., Martino A., Enninga J., et al. Prions hijack tunnelling nanotubes for intercellular spread. Nat. Cell Biol. 2009, 11:328-336.
-
(2009)
Nat. Cell Biol.
, vol.11
, pp. 328-336
-
-
Gousset, K.1
Schiff, E.2
Langevin, C.3
Marijanovic, Z.4
Caputo, A.5
Browman, D.T.6
Chenouard, N.7
de Chaumont, F.8
Martino, A.9
Enninga, J.10
-
19
-
-
79960040173
-
An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity
-
Guo W., Chen Y., Zhou X., Kar A., Ray P., Chen X., Rao E.J., Yang M., Ye H., Zhu L., et al. An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity. Nat. Struct. Mol. Biol. 2011, 18:822-830.
-
(2011)
Nat. Struct. Mol. Biol.
, vol.18
, pp. 822-830
-
-
Guo, W.1
Chen, Y.2
Zhou, X.3
Kar, A.4
Ray, P.5
Chen, X.6
Rao, E.J.7
Yang, M.8
Ye, H.9
Zhu, L.10
-
20
-
-
47949086625
-
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Hasegawa M., Arai T., Nonaka T., Kametani F., Yoshida M., Hashizume Y., Beach T.G., Buratti E., Baralle F., Morita M., et al. Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Ann. Neurol. 2008, 64:60-70.
-
(2008)
Ann. Neurol.
, vol.64
, pp. 60-70
-
-
Hasegawa, M.1
Arai, T.2
Nonaka, T.3
Kametani, F.4
Yoshida, M.5
Hashizume, Y.6
Beach, T.G.7
Buratti, E.8
Baralle, F.9
Morita, M.10
-
21
-
-
80855138744
-
Molecular dissection of TDP-43 proteinopathies
-
Hasegawa M., Nonaka T., Tsuji H., Tamaoka A., Yamashita M., Kametani F., Yoshida M., Arai T., Akiyama H. Molecular dissection of TDP-43 proteinopathies. J.Mol. Neurosci. 2011, 45:480-485.
-
(2011)
J.Mol. Neurosci.
, vol.45
, pp. 480-485
-
-
Hasegawa, M.1
Nonaka, T.2
Tsuji, H.3
Tamaoka, A.4
Yamashita, M.5
Kametani, F.6
Yoshida, M.7
Arai, T.8
Akiyama, H.9
-
22
-
-
67649797399
-
Expression of TDP-43 C-terminal fragments invitro recapitulates pathological features of TDP-43 proteinopathies
-
Igaz L.M., Kwong L.K., Chen-Plotkin A., Winton M.J., Unger T.L., Xu Y., Neumann M., Trojanowski J.Q., Lee V.M. Expression of TDP-43 C-terminal fragments invitro recapitulates pathological features of TDP-43 proteinopathies. J.Biol. Chem. 2009, 284:8516-8524.
-
(2009)
J.Biol. Chem.
, vol.284
, pp. 8516-8524
-
-
Igaz, L.M.1
Kwong, L.K.2
Chen-Plotkin, A.3
Winton, M.J.4
Unger, T.L.5
Xu, Y.6
Neumann, M.7
Trojanowski, J.Q.8
Lee, V.M.9
-
23
-
-
43249114934
-
Lewy body-like pathology in long-term embryonic nigral transplants in Parkinson's disease
-
Kordower J.H., Chu Y., Hauser R.A., Freeman T.B., Olanow C.W. Lewy body-like pathology in long-term embryonic nigral transplants in Parkinson's disease. Nat. Med. 2008, 14:504-506.
-
(2008)
Nat. Med.
, vol.14
, pp. 504-506
-
-
Kordower, J.H.1
Chu, Y.2
Hauser, R.A.3
Freeman, T.B.4
Olanow, C.W.5
-
24
-
-
43249110200
-
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation
-
Li J.Y., Englund E., Holton J.L., Soulet D., Hagell P., Lees A.J., Lashley T., Quinn N.P., Rehncrona S., Björklund A., et al. Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation. Nat. Med. 2008, 14:501-503.
-
(2008)
Nat. Med.
, vol.14
, pp. 501-503
-
-
Li, J.Y.1
Englund, E.2
Holton, J.L.3
Soulet, D.4
Hagell, P.5
Lees, A.J.6
Lashley, T.7
Quinn, N.P.8
Rehncrona, S.9
Björklund, A.10
-
25
-
-
84856454190
-
Trans-synaptic spread of tau pathology invivo
-
Liu L., Drouet V., Wu J.W., Witter M.P., Small S.A., Clelland C., Duff K. Trans-synaptic spread of tau pathology invivo. PLoS ONE 2012, 7:e31302.
-
(2012)
PLoS ONE
, vol.7
-
-
Liu, L.1
Drouet, V.2
Wu, J.W.3
Witter, M.P.4
Small, S.A.5
Clelland, C.6
Duff, K.7
-
26
-
-
72149119358
-
Exogenous alpha-synuclein fibrils seed the formation of Lewy body-like intracellular inclusions in cultured cells
-
Luk K.C., Song C., O'Brien P., Stieber A., Branch J.R., Brunden K.R., Trojanowski J.Q., Lee V.M. Exogenous alpha-synuclein fibrils seed the formation of Lewy body-like intracellular inclusions in cultured cells. Proc. Natl. Acad. Sci. USA 2009, 106:20051-20056.
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 20051-20056
-
-
Luk, K.C.1
Song, C.2
O'Brien, P.3
Stieber, A.4
Branch, J.R.5
Brunden, K.R.6
Trojanowski, J.Q.7
Lee, V.M.8
-
27
-
-
84869109864
-
Pathological α-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice
-
Luk K.C., Kehm V., Carroll J., Zhang B., O'Brien P., Trojanowski J.Q., Lee V.M. Pathological α-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice. Science 2012, 338:949-953.
-
(2012)
Science
, vol.338
, pp. 949-953
-
-
Luk, K.C.1
Kehm, V.2
Carroll, J.3
Zhang, B.4
O'Brien, P.5
Trojanowski, J.Q.6
Lee, V.M.7
-
28
-
-
84862609075
-
Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in mice
-
Luk K.C., Kehm V.M., Zhang B., O'Brien P., Trojanowski J.Q., Lee V.M. Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in mice. J.Exp. Med. 2012, 209:975-986.
-
(2012)
J.Exp. Med.
, vol.209
, pp. 975-986
-
-
Luk, K.C.1
Kehm, V.M.2
Zhang, B.3
O'Brien, P.4
Trojanowski, J.Q.5
Lee, V.M.6
-
29
-
-
79959599081
-
A harmonized classification system for FTLD-TDP pathology
-
Mackenzie I.R., Neumann M., Baborie A., Sampathu D.M., Du Plessis D., Jaros E., Perry R.H., Trojanowski J.Q., Mann D.M., Lee V.M. A harmonized classification system for FTLD-TDP pathology. Acta Neuropathol. 2011, 122:111-113.
-
(2011)
Acta Neuropathol.
, vol.122
, pp. 111-113
-
-
Mackenzie, I.R.1
Neumann, M.2
Baborie, A.3
Sampathu, D.M.4
Du Plessis, D.5
Jaros, E.6
Perry, R.H.7
Trojanowski, J.Q.8
Mann, D.M.9
Lee, V.M.10
-
30
-
-
84876057762
-
Prion-like spreading of pathological α-synuclein in brain
-
Masuda-Suzukake M., Nonaka T., Hosokawa M., Oikawa T., Arai T., Akiyama H., Mann D.M.A., Hasegawa M. Prion-like spreading of pathological α-synuclein in brain. Brain 2013, 136:1128-1138.
-
(2013)
Brain
, vol.136
, pp. 1128-1138
-
-
Masuda-Suzukake, M.1
Nonaka, T.2
Hosokawa, M.3
Oikawa, T.4
Arai, T.5
Akiyama, H.6
Mann, D.M.A.7
Hasegawa, M.8
-
31
-
-
0031672540
-
Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria
-
Neary D., Snowden J.S., Gustafson L., Passant U., Stuss D., Black S., Freedman M., Kertesz A., Robert P.H., Albert M., et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 1998, 51:1546-1554.
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
Passant, U.4
Stuss, D.5
Black, S.6
Freedman, M.7
Kertesz, A.8
Robert, P.H.9
Albert, M.10
-
32
-
-
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. 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
Bruce, J.7
Schuck, T.8
Grossman, M.9
Clark, C.M.10
-
33
-
-
69049084725
-
A cellular model to monitor proteasome dysfunction by alpha-synuclein
-
Nonaka T., Hasegawa M. A cellular model to monitor proteasome dysfunction by alpha-synuclein. Biochemistry 2009, 48:8014-8022.
-
(2009)
Biochemistry
, vol.48
, pp. 8014-8022
-
-
Nonaka, T.1
Hasegawa, M.2
-
34
-
-
67650113333
-
Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43
-
Nonaka T., Kametani F., Arai T., Akiyama H., Hasegawa M. Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43. Hum. Mol. Genet. 2009, 18:3353-3364.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3353-3364
-
-
Nonaka, T.1
Kametani, F.2
Arai, T.3
Akiyama, H.4
Hasegawa, M.5
-
35
-
-
78049376559
-
Seeded aggregation and toxicity of alpha-synuclein and tau: cellular models of neurodegenerative diseases
-
Nonaka T., Watanabe S.T., Iwatsubo T., Hasegawa M. Seeded aggregation and toxicity of alpha-synuclein and tau: cellular models of neurodegenerative diseases. J.Biol. Chem. 2010, 285:34885-34898.
-
(2010)
J.Biol. Chem.
, vol.285
, pp. 34885-34898
-
-
Nonaka, T.1
Watanabe, S.T.2
Iwatsubo, T.3
Hasegawa, M.4
-
36
-
-
77649252528
-
Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis
-
Pesiridis G.S., Lee V.M., Trojanowski J.Q. Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis. Hum. Mol. Genet. 2009, 18(R2):R156-R162.
-
(2009)
Hum. Mol. Genet.
, vol.18
, Issue.R2
-
-
Pesiridis, G.S.1
Lee, V.M.2
Trojanowski, J.Q.3
-
37
-
-
80155157847
-
The seeds of neurodegeneration: prion-like spreading in ALS
-
Polymenidou M., Cleveland D.W. The seeds of neurodegeneration: prion-like spreading in ALS. Cell 2011, 147:498-508.
-
(2011)
Cell
, vol.147
, pp. 498-508
-
-
Polymenidou, M.1
Cleveland, D.W.2
-
38
-
-
59649095699
-
Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregates
-
Ren P.H., Lauckner J.E., Kachirskaia I., Heuser J.E., Melki R., Kopito R.R. Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregates. Nat. Cell Biol. 2009, 11:219-225.
-
(2009)
Nat. Cell Biol.
, vol.11
, pp. 219-225
-
-
Ren, P.H.1
Lauckner, J.E.2
Kachirskaia, I.3
Heuser, J.E.4
Melki, R.5
Kopito, R.R.6
-
39
-
-
77949878273
-
TDP-43 is a developmentally regulated protein essential for early embryonic development
-
Sephton C.F., Good S.K., Atkin S., Dewey C.M., Mayer P., Herz J., Yu G. TDP-43 is a developmentally regulated protein essential for early embryonic development. J.Biol. Chem. 2010, 285:6826-6834.
-
(2010)
J.Biol. Chem.
, vol.285
, pp. 6826-6834
-
-
Sephton, C.F.1
Good, S.K.2
Atkin, S.3
Dewey, C.M.4
Mayer, P.5
Herz, J.6
Yu, G.7
-
41
-
-
84870188303
-
Molecular analysis and biochemical classification of TDP-43 proteinopathy
-
Tsuji H., Arai T., Kametani F., Nonaka T., Yamashita M., Suzukake M., Hosokawa M., Yoshida M., Hatsuta H., Takao M., et al. Molecular analysis and biochemical classification of TDP-43 proteinopathy. Brain 2012, 135:3380-3391.
-
(2012)
Brain
, vol.135
, pp. 3380-3391
-
-
Tsuji, H.1
Arai, T.2
Kametani, F.3
Nonaka, T.4
Yamashita, M.5
Suzukake, M.6
Hosokawa, M.7
Yoshida, M.8
Hatsuta, H.9
Takao, M.10
-
42
-
-
74749107048
-
TDP-43, a neuro-pathosignature factor, is essential for early mouse embryogenesis
-
Wu L.S., Cheng W.C., Hou S.C., Yan Y.T., Jiang S.T., Shen C.K. TDP-43, a neuro-pathosignature factor, is essential for early mouse embryogenesis. Genesis 2010, 48:56-62.
-
(2010)
Genesis
, vol.48
, pp. 56-62
-
-
Wu, L.S.1
Cheng, W.C.2
Hou, S.C.3
Yan, Y.T.4
Jiang, S.T.5
Shen, C.K.6
-
43
-
-
66149114101
-
Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity
-
Zhang Y.J., Xu Y.F., Cook C., Gendron T.F., Roettges P., Link C.D., Lin W.L., Tong J., Castanedes-Casey M., Ash P., et al. Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity. Proc. Natl. Acad. Sci. USA 2009, 106:7607-7612.
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 7607-7612
-
-
Zhang, Y.J.1
Xu, Y.F.2
Cook, C.3
Gendron, T.F.4
Roettges, P.5
Link, C.D.6
Lin, W.L.7
Tong, J.8
Castanedes-Casey, M.9
Ash, P.10
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