-
1
-
-
84909953328
-
Reversible Behavioral Phenotypes in a Conditional Mouse Model of TDP-43 Proteinopathies
-
PID: 25392493
-
Alfieri JA, Pino NS, Igaz LM (2014) Reversible Behavioral Phenotypes in a Conditional Mouse Model of TDP-43 Proteinopathies. J Neurosci 34:15244–15259. doi:10.1523/jneurosci.1918-14.2014
-
(2014)
J Neurosci
, vol.34
, pp. 15244-15259
-
-
Alfieri, J.A.1
Pino, N.S.2
Igaz, L.M.3
-
2
-
-
84874262984
-
ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43
-
COI: 1:CAS:528:DC%2BC3sXjvFShu7o%3D, PID: 23382207
-
Arnold ES, Ling SC, Huelga SC, Lagier-Tourenne C, Polymenidou M, Ditsworth D et al (2013) ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43. Proc Natl Acad Sci 110:E736–E745. doi:10.1073/pnas.1222809110
-
(2013)
Proc Natl Acad Sci
, vol.110
, pp. 736-745
-
-
Arnold, E.S.1
Ling, S.C.2
Huelga, S.C.3
Lagier-Tourenne, C.4
Polymenidou, M.5
Ditsworth, D.6
-
3
-
-
78751616191
-
TDP-43 regulates its mRNA levels through a negative feedback loop
-
COI: 1:CAS:528:DC%2BC3cXhsFSku7jI, PID: 21131904
-
Ayala YM, De Conti L, Avendano-Vazquez SE, Dhir A, Romano M, D’Ambrogio A et al (2011) TDP-43 regulates its mRNA levels through a negative feedback loop. EMBO J 30:277–288. doi:10.1038/emboj.2010.310
-
(2011)
EMBO J
, vol.30
, pp. 277-288
-
-
Ayala, Y.M.1
De Conti, L.2
Avendano-Vazquez, S.E.3
Dhir, A.4
Romano, M.5
D’Ambrogio, A.6
-
4
-
-
59549094064
-
Structural determinants of the cellular localization and shuttling of TDP-43
-
COI: 1:CAS:528:DC%2BD1cXhsFaktLjM, PID: 18957508
-
Ayala YM, Zago P, D’Ambrogio A, Xu YF, Petrucelli L, Buratti E et al (2008) Structural determinants of the cellular localization and shuttling of TDP-43. J Cell Sci 121:3778–3785. doi:10.1242/jcs.038950
-
(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
-
5
-
-
0025788760
-
Neurofilament reassembly in vitro: biochemical, morphological and immuno-electron microscopic studies employing monoclonal antibodies to defined epitopes
-
COI: 1:CAS:528:DyaK3MXmtVWmtbo%3D, PID: 1718561
-
Balin BJ, Clark EA, Trojanowski JQ, Lee VM (1991) Neurofilament reassembly in vitro: biochemical, morphological and immuno-electron microscopic studies employing monoclonal antibodies to defined epitopes. Brain Res 556:181–195
-
(1991)
Brain Res
, vol.556
, pp. 181-195
-
-
Balin, B.J.1
Clark, E.A.2
Trojanowski, J.Q.3
Lee, V.M.4
-
6
-
-
84904729990
-
Autophagy induction enhances TDP43 turnover and survival in neuronal ALS models
-
COI: 1:CAS:528:DC%2BC2cXhtVKlsrbI, PID: 24974230
-
Barmada SJ, Serio A, Arjun A, Bilican B, Daub A, Ando DM et al (2014) Autophagy induction enhances TDP43 turnover and survival in neuronal ALS models. Nat Chem Biol 10:677–685. doi:10.1038/nchembio.1563
-
(2014)
Nat Chem Biol
, vol.10
, pp. 677-685
-
-
Barmada, S.J.1
Serio, A.2
Arjun, A.3
Bilican, B.4
Daub, A.5
Ando, D.M.6
-
7
-
-
84890121734
-
Amyotrophic lateral sclerosis–a model of corticofugal axonal spread
-
COI: 1:CAS:528:DC%2BC3sXhslygurrK, PID: 24217521
-
Braak H, Brettschneider J, Ludolph AC, Lee VM, Trojanowski JQ, Del Tredici K (2013) Amyotrophic lateral sclerosis–a model of corticofugal axonal spread. Nat Rev Neurol 9:708–714. doi:10.1038/nrneurol.2013.221
-
(2013)
Nat Rev Neurol
, vol.9
, pp. 708-714
-
-
Braak, H.1
Brettschneider, J.2
Ludolph, A.C.3
Lee, V.M.4
Trojanowski, J.Q.5
Del Tredici, K.6
-
8
-
-
84906314307
-
Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD)
-
COI: 1:CAS:528:DC%2BC2cXptFOnsQ%3D%3D, PID: 24407427
-
Brettschneider J, Del Tredici K, Irwin DJ, Grossman M, Robinson JL, Toledo JB et al (2014) Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD). Acta Neuropathol 127:423–439. doi:10.1007/s00401-013-1238-y
-
(2014)
Acta Neuropathol
, vol.127
, pp. 423-439
-
-
Brettschneider, J.1
Del Tredici, K.2
Irwin, D.J.3
Grossman, M.4
Robinson, J.L.5
Toledo, J.B.6
-
9
-
-
84883292041
-
Stages of pTDP-43 pathology in amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC3sXhtlKku7jE, PID: 23686809
-
Brettschneider J, Del Tredici K, Toledo JB, Robinson JL, Irwin DJ, Grossman M et al (2013) Stages of pTDP-43 pathology in amyotrophic lateral sclerosis. Ann Neurol 74:20–38. doi:10.1002/ana.23937
-
(2013)
Ann Neurol
, vol.74
, pp. 20-38
-
-
Brettschneider, J.1
Del Tredici, K.2
Toledo, J.B.3
Robinson, J.L.4
Irwin, D.J.5
Grossman, M.6
-
10
-
-
77950867149
-
TAR DNA-binding protein 43 in neurodegenerative disease
-
COI: 1:CAS:528:DC%2BC3cXksVehurc%3D, PID: 20234357
-
Chen-Plotkin AS, Lee VM, Trojanowski JQ (2010) TAR DNA-binding protein 43 in neurodegenerative disease. Nat Rev Neurol 6:211–220. doi:10.1038/nrneurol.2010.18
-
(2010)
Nat Rev Neurol
, vol.6
, pp. 211-220
-
-
Chen-Plotkin, A.S.1
Lee, V.M.2
Trojanowski, J.Q.3
-
11
-
-
77958012134
-
Deletion of TDP-43 down-regulates Tbc1d1, a gene linked to obesity, and alters body fat metabolism
-
COI: 1:CAS:528:DC%2BC3cXhtF2gtrnK, PID: 20660762
-
Chiang PM, Ling J, Jeong YH, Price DL, Aja SM, Wong PC (2010) Deletion of TDP-43 down-regulates Tbc1d1, a gene linked to obesity, and alters body fat metabolism. Proc Natl Acad Sci 107:16320–16324. doi:10.1073/pnas.1002176107
-
(2010)
Proc Natl Acad Sci
, vol.107
, pp. 16320-16324
-
-
Chiang, P.M.1
Ling, J.2
Jeong, Y.H.3
Price, D.L.4
Aja, S.M.5
Wong, P.C.6
-
12
-
-
43549091368
-
Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis
-
PID: 18474740
-
Geser F, Brandmeir NJ, Kwong LK, Martinez-Lage M, Elman L, McCluskey L et al (2008) Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis. Arch Neurol 65:636–641. doi:10.1001/archneur.65.5.636
-
(2008)
Arch Neurol
, vol.65
, pp. 636-641
-
-
Geser, F.1
Brandmeir, N.J.2
Kwong, L.K.3
Martinez-Lage, M.4
Elman, L.5
McCluskey, L.6
-
13
-
-
60549117972
-
Clinical and pathological continuum of multisystem TDP-43 proteinopathies
-
PID: 19204154
-
Geser F, Martinez-Lage M, Robinson J, Uryu K, Neumann M, Brandmeir NJ et al (2009) Clinical and pathological continuum of multisystem TDP-43 proteinopathies. Arch Neurol 66:180–189. doi:10.1001/archneurol.2008.558
-
(2009)
Arch Neurol
, vol.66
, pp. 180-189
-
-
Geser, F.1
Martinez-Lage, M.2
Robinson, J.3
Uryu, K.4
Neumann, M.5
Brandmeir, N.J.6
-
14
-
-
80755189921
-
How can we improve clinical trials in amyotrophic lateral sclerosis?
-
COI: 1:CAS:528:DC%2BC3MXhsVahur3J, PID: 21947135
-
Gordon PH, Meininger V (2011) How can we improve clinical trials in amyotrophic lateral sclerosis? Nat Rev Neurol 7:650–654. doi:10.1038/nrneurol.2011.147
-
(2011)
Nat Rev Neurol
, vol.7
, pp. 650-654
-
-
Gordon, P.H.1
Meininger, V.2
-
15
-
-
84879895467
-
Distinct alpha-synuclein strains differentially promote tau inclusions in neurons
-
COI: 1:CAS:528:DC%2BC3sXhtVGktbzE, PID: 23827677
-
Guo JL, Covell DJ, Daniels JP, Iba M, Stieber A, Zhang B et al (2013) Distinct alpha-synuclein strains differentially promote tau inclusions in neurons. Cell 154:103–117. doi:10.1016/j.cell.2013.05.057
-
(2013)
Cell
, vol.154
, pp. 103-117
-
-
Guo, J.L.1
Covell, D.J.2
Daniels, J.P.3
Iba, M.4
Stieber, A.5
Zhang, B.6
-
16
-
-
84893642253
-
Cell-to-cell transmission of pathogenic proteins in neurodegenerative diseases
-
COI: 1:CAS:528:DC%2BC2cXitVenu7s%3D, PID: 24504409
-
Guo JL, Lee VM (2014) Cell-to-cell transmission of pathogenic proteins in neurodegenerative diseases. Nat Med 20:130–138. doi:10.1038/nm.3457
-
(2014)
Nat Med
, vol.20
, pp. 130-138
-
-
Guo, J.L.1
Lee, V.M.2
-
17
-
-
0028284779
-
Motor neuron degeneration in mice that express a human Cu, Zn superoxide dismutase mutation
-
COI: 1:CAS:528:DyaK2cXksFGisbk%3D, PID: 8209258
-
Gurney ME, Pu H, Chiu AY, Dal Canto MC, Polchow CY, Alexander DD et al (1994) Motor neuron degeneration in mice that express a human Cu, Zn superoxide dismutase mutation. Science 264:1772–1775
-
(1994)
Science
, vol.264
, pp. 1772-1775
-
-
Gurney, M.E.1
Pu, H.2
Chiu, A.Y.3
Dal Canto, M.C.4
Polchow, C.Y.5
Alexander, D.D.6
-
18
-
-
0034982656
-
Neuron-specific expression of Cre recombinase during the late phase of brain development
-
COI: 1:CAS:528:DC%2BD3MXjsleiur0%3D, PID: 11377750
-
Hirasawa M, Cho A, Sreenath T, Sauer B, Julien JP, Kulkarni AB (2001) Neuron-specific expression of Cre recombinase during the late phase of brain development. Neurosci Res 40:125–132
-
(2001)
Neurosci Res
, vol.40
, pp. 125-132
-
-
Hirasawa, M.1
Cho, A.2
Sreenath, T.3
Sauer, B.4
Julien, J.P.5
Kulkarni, A.B.6
-
19
-
-
84907894705
-
Proteopathic tau seeding predicts tauopathy in vivo
-
COI: 1:CAS:528:DC%2BC2cXhs1Wqs7bO, PID: 25261551
-
Holmes BB, Furman JL, Mahan TE, Yamasaki TR, Mirbaha H, Eades WC et al (2014) Proteopathic tau seeding predicts tauopathy in vivo. Proc Natl Acad Sci 111:E4376–E4385. doi:10.1073/pnas.1411649111
-
(2014)
Proc Natl Acad Sci
, vol.111
, pp. 4376-4385
-
-
Holmes, B.B.1
Furman, J.L.2
Mahan, T.E.3
Yamasaki, T.R.4
Mirbaha, H.5
Eades, W.C.6
-
20
-
-
84855472423
-
Mutant TDP-43 in motor neurons promotes the onset and progression of ALS in rats
-
COI: 1:CAS:528:DC%2BC38XkvFClsw%3D%3D, PID: 22156203
-
Huang C, Tong J, Bi F, Zhou H, Xia XG (2012) Mutant TDP-43 in motor neurons promotes the onset and progression of ALS in rats. J Clin Invest 122:107–118. doi:10.1172/jci59130
-
(2012)
J Clin Invest
, vol.122
, pp. 107-118
-
-
Huang, C.1
Tong, J.2
Bi, F.3
Zhou, H.4
Xia, X.G.5
-
21
-
-
84872346089
-
Synthetic tau fibrils mediate transmission of neurofibrillary tangles in a transgenic mouse model of Alzheimer’s-like tauopathy
-
COI: 1:CAS:528:DC%2BC3sXhsVems70%3D, PID: 23325240
-
Iba M, Guo JL, McBride JD, Zhang B, Trojanowski JQ, Lee VM (2013) Synthetic tau fibrils mediate transmission of neurofibrillary tangles in a transgenic mouse model of Alzheimer’s-like tauopathy. J Neurosci 33:1024–1037. doi:10.1523/jneurosci.2642-12.2013
-
(2013)
J Neurosci
, vol.33
, pp. 1024-1037
-
-
Iba, M.1
Guo, J.L.2
McBride, J.D.3
Zhang, B.4
Trojanowski, J.Q.5
Lee, V.M.6
-
22
-
-
79551523377
-
Dysregulation of the ALS-associated gene TDP-43 leads to neuronal death and degeneration in mice
-
COI: 1:CAS:528:DC%2BC3MXhsl2qsrs%3D, PID: 21206091
-
Igaz LM, Kwong LK, Lee EB, Chen-Plotkin A, Swanson E, Unger T et al (2011) Dysregulation of the ALS-associated gene TDP-43 leads to neuronal death and degeneration in mice. J Clin Invest 121:726–738. doi:10.1172/jci44867
-
(2011)
J Clin Invest
, vol.121
, pp. 726-738
-
-
Igaz, L.M.1
Kwong, L.K.2
Lee, E.B.3
Chen-Plotkin, A.4
Swanson, E.5
Unger, T.6
-
23
-
-
46749138739
-
Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BD1cXptVGqu7o%3D, PID: 18535185
-
Igaz LM, Kwong LK, Xu Y, Truax AC, Uryu K, Neumann M et al (2008) Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Am J Pathol 173:182–194. doi:10.2353/ajpath.2008.080003
-
(2008)
Am J Pathol
, vol.173
, pp. 182-194
-
-
Igaz, L.M.1
Kwong, L.K.2
Xu, Y.3
Truax, A.C.4
Uryu, K.5
Neumann, M.6
-
24
-
-
77953026500
-
Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis
-
COI: 1:CAS:528:DC%2BC3cXjs1aisr4%3D, PID: 20198480
-
Kraemer BC, Schuck T, Wheeler JM, Robinson LC, Trojanowski JQ, Lee VM et al (2010) Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis. Acta Neuropathol 119:409–419. doi:10.1007/s00401-010-0659-0
-
(2010)
Acta Neuropathol
, vol.119
, pp. 409-419
-
-
Kraemer, B.C.1
Schuck, T.2
Wheeler, J.M.3
Robinson, L.C.4
Trojanowski, J.Q.5
Lee, V.M.6
-
25
-
-
84921918540
-
Novel monoclonal antibodies to normal and pathologically altered human TDP-43 proteins
-
PID: 24690345
-
Kwong LK, Irwin DJ, Walker AK, Xu Y, Riddle DM, Trojanowski JQ et al (2014) Novel monoclonal antibodies to normal and pathologically altered human TDP-43 proteins. Acta Neuropathol Commun 2:33. doi:10.1186/2051-5960-2-33
-
(2014)
Acta Neuropathol Commun
, vol.2
, pp. 33
-
-
Kwong, L.K.1
Irwin, D.J.2
Walker, A.K.3
Xu, Y.4
Riddle, D.M.5
Trojanowski, J.Q.6
-
26
-
-
84155167265
-
Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration
-
COI: 1:CAS:528:DC%2BC3MXhsFeqt7fP
-
Lee EB, Lee VM, Trojanowski JQ (2012) Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration. Nat Rev Neurosci 13:38–50. doi:10.1038/nrn3121
-
(2012)
Nat Rev Neurosci
, vol.13
, pp. 38-50
-
-
Lee, E.B.1
Lee, V.M.2
Trojanowski, J.Q.3
-
27
-
-
0023520075
-
Monoclonal antibodies distinguish several differentially phosphorylated states of the two largest rat neurofilament subunits (NF-H and NF-M) and demonstrate their existence in the normal nervous system of adult rats
-
COI: 1:CAS:528:DyaL1cXjvVCn, PID: 3119789
-
Lee VM, Carden MJ, Schlaepfer WW, Trojanowski JQ (1987) Monoclonal antibodies distinguish several differentially phosphorylated states of the two largest rat neurofilament subunits (NF-H and NF-M) and demonstrate their existence in the normal nervous system of adult rats. J Neurosci 7:3474–3488
-
(1987)
J Neurosci
, vol.7
, pp. 3474-3488
-
-
Lee, V.M.1
Carden, M.J.2
Schlaepfer, W.W.3
Trojanowski, J.Q.4
-
28
-
-
0021330771
-
Monoclonal antibodies to gel-excised glial filament protein and their reactivities with other intermediate filament proteins
-
COI: 1:CAS:528:DyaL2cXms1eksg%3D%3D, PID: 6358415
-
Lee VM, Page CD, Wu HL, Schlaepfer WW (1984) Monoclonal antibodies to gel-excised glial filament protein and their reactivities with other intermediate filament proteins. J Neurochem 42:25–32
-
(1984)
J Neurochem
, vol.42
, pp. 25-32
-
-
Lee, V.M.1
Page, C.D.2
Wu, H.L.3
Schlaepfer, W.W.4
-
29
-
-
84881490873
-
Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis
-
COI: 1:CAS:528:DC%2BC3sXht1eksbbN, PID: 23931993
-
Ling SC, Polymenidou M, Cleveland DW (2013) Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis. Neuron 79:416–438. doi:10.1016/j.neuron.2013.07.033
-
(2013)
Neuron
, vol.79
, pp. 416-438
-
-
Ling, S.C.1
Polymenidou, M.2
Cleveland, D.W.3
-
30
-
-
59249085091
-
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies
-
COI: 1:CAS:528:DC%2BD1MXhtVCltLw%3D, PID: 19125255
-
Neumann M, Kwong LK, Lee EB, Kremmer E, Flatley A, Xu Y et al (2009) Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies. Acta Neuropathol 117:137–149. doi:10.1007/s00401-008-0477-9
-
(2009)
Acta Neuropathol
, vol.117
, pp. 137-149
-
-
Neumann, M.1
Kwong, L.K.2
Lee, E.B.3
Kremmer, E.4
Flatley, A.5
Xu, Y.6
-
31
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BD28XhtVCiurrL, PID: 17023659
-
Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT et al (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314:130–133. doi:10.1126/science.1134108
-
(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
-
32
-
-
84885484356
-
Prion-like properties of pathological TDP-43 aggregates from diseased brains
-
COI: 1:CAS:528:DC%2BC3sXhtVKntbjM, PID: 23831027
-
Nonaka T, Masuda-Suzukake M, Arai T, Hasegawa Y, Akatsu H, Obi T et al (2013) Prion-like properties of pathological TDP-43 aggregates from diseased brains. Cell Rep 4:124–134. doi:10.1016/j.celrep.2013.06.007
-
(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
-
34
-
-
79956304001
-
A “two-hit” hypothesis for inclusion formation by carboxyl-terminal fragments of TDP-43 protein linked to RNA depletion and impaired microtubule-dependent transport
-
COI: 1:CAS:528:DC%2BC3MXmtlGltbw%3D, PID: 21454607
-
Pesiridis GS, Tripathy K, Tanik S, Trojanowski JQ, Lee VM (2011) A “two-hit” hypothesis for inclusion formation by carboxyl-terminal fragments of TDP-43 protein linked to RNA depletion and impaired microtubule-dependent transport. J Biol Chem 286:18845–18855. doi:10.1074/jbc.M111.231118
-
(2011)
J Biol Chem
, vol.286
, pp. 18845-18855
-
-
Pesiridis, G.S.1
Tripathy, K.2
Tanik, S.3
Trojanowski, J.Q.4
Lee, V.M.5
-
35
-
-
79953185674
-
Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43
-
COI: 1:CAS:528:DC%2BC3MXisFensb0%3D, PID: 21358643
-
Polymenidou M, Lagier-Tourenne C, Hutt KR, Huelga SC, Moran J, Liang TY et al (2011) Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. Nat Neurosci 14:459–468. doi:10.1038/nn.2779
-
(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
-
36
-
-
34249313704
-
Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS
-
COI: 1:CAS:528:DC%2BD2sXmtVKjurg%3D, PID: 17543992
-
Robertson J, Sanelli T, Xiao S, Yang W, Horne P, Hammond R et al (2007) Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS. Neurosci Lett 420:128–132. doi:10.1016/j.neulet.2007.03.066
-
(2007)
Neurosci Lett
, vol.420
, pp. 128-132
-
-
Robertson, J.1
Sanelli, T.2
Xiao, S.3
Yang, W.4
Horne, P.5
Hammond, R.6
-
37
-
-
33846076379
-
Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies
-
COI: 1:CAS:528:DC%2BD28XhtFeitLbJ, PID: 17003490
-
Sampathu DM, Neumann M, Kwong LK, Chou TT, Micsenyi M, Truax A et al (2006) Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies. Am J Pathol 169:1343–1352. doi:10.2353/ajpath.2006.060438
-
(2006)
Am J Pathol
, vol.169
, pp. 1343-1352
-
-
Sampathu, D.M.1
Neumann, M.2
Kwong, L.K.3
Chou, T.T.4
Micsenyi, M.5
Truax, A.6
-
38
-
-
84902486430
-
Distinct tau prion strains propagate in cells and mice and define different tauopathies
-
COI: 1:CAS:528:DC%2BC2cXoslClsrY%3D, PID: 24857020
-
Sanders DW, Kaufman SK, DeVos SL, Sharma AM, Mirbaha H, Li A et al (2014) Distinct tau prion strains propagate in cells and mice and define different tauopathies. Neuron 82:1271–1288. doi:10.1016/j.neuron.2014.04.047
-
(2014)
Neuron
, vol.82
, pp. 1271-1288
-
-
Sanders, D.W.1
Kaufman, S.K.2
DeVos, S.L.3
Sharma, A.M.4
Mirbaha, H.5
Li, A.6
-
39
-
-
84903362511
-
Differential roles of the ubiquitin proteasome system and autophagy in the clearance of soluble and aggregated TDP-43 species
-
COI: 1:CAS:528:DC%2BC2cXmvFSgt7k%3D, PID: 24424030
-
Scotter EL, Vance C, Nishimura AL, Lee YB, Chen HJ, Urwin H et al (2014) Differential roles of the ubiquitin proteasome system and autophagy in the clearance of soluble and aggregated TDP-43 species. J Cell Sci 127:1263–1278. doi:10.1242/jcs.140087
-
(2014)
J Cell Sci
, vol.127
, pp. 1263-1278
-
-
Scotter, E.L.1
Vance, C.2
Nishimura, A.L.3
Lee, Y.B.4
Chen, H.J.5
Urwin, H.6
-
40
-
-
77949878273
-
TDP-43 is a developmentally regulated protein essential for early embryonic development
-
COI: 1:CAS:528:DC%2BC3cXit1ait7k%3D, PID: 20040602
-
Sephton CF, Good SK, Atkin S, Dewey CM, Mayer P 3rd, Herz J et al (2010) TDP-43 is a developmentally regulated protein essential for early embryonic development. J Biol Chem 285:6826–6834. doi:10.1074/jbc.M109.061846
-
(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
-
41
-
-
65149101697
-
Mislocalization of TDP-43 in the G93A mutant SOD1 transgenic mouse model of ALS
-
COI: 1:CAS:528:DC%2BD1MXmtVShsLs%3D, PID: 19379791
-
Shan X, Vocadlo D, Krieger C (2009) Mislocalization of TDP-43 in the G93A mutant SOD1 transgenic mouse model of ALS. Neurosci Lett 458:70–74. doi:10.1016/j.neulet.2009.04.031
-
(2009)
Neurosci Lett
, vol.458
, pp. 70-74
-
-
Shan, X.1
Vocadlo, D.2
Krieger, C.3
-
42
-
-
0025165101
-
Phosphorylated high molecular weight neurofilament protein in lower motor neurons in amyotrophic lateral sclerosis and other neurodegenerative diseases involving ventral horn cells
-
COI: 1:STN:280:DyaK3c3lt1GmtQ%3D%3D, PID: 2111074
-
Sobue G, Hashizume Y, Yasuda T, Mukai E, Kumagai T, Mitsuma T et al (1990) Phosphorylated high molecular weight neurofilament protein in lower motor neurons in amyotrophic lateral sclerosis and other neurodegenerative diseases involving ventral horn cells. Acta Neuropathol 79:402–408
-
(1990)
Acta Neuropathol
, vol.79
, pp. 402-408
-
-
Sobue, G.1
Hashizume, Y.2
Yasuda, T.3
Mukai, E.4
Kumagai, T.5
Mitsuma, T.6
-
43
-
-
84903689436
-
A platform for discovery: the University of Pennsylvania Integrated Neurodegenerative Disease Biobank
-
Toledo JB, Van Deerlin VM, Lee EB, Suh E, Baek Y, Robinson JL et al (2014) A platform for discovery: the University of Pennsylvania Integrated Neurodegenerative Disease Biobank. Alzheimers Dement 10(477–484):e471. doi:10.1016/j.jalz.2013.06.003
-
(2014)
Alzheimers Dement
, vol.10
, Issue.477-484
, pp. 471
-
-
Toledo, J.B.1
Van Deerlin, V.M.2
Lee, E.B.3
Suh, E.4
Baek, Y.5
Robinson, J.L.6
-
44
-
-
77955395385
-
Elevated expression of TDP-43 in the forebrain of mice is sufficient to cause neurological and pathological phenotypes mimicking FTLD-U
-
COI: 1:CAS:528:DC%2BC3cXhtVejt7bI, PID: 20660618
-
Tsai KJ, Yang CH, Fang YH, Cho KH, Chien WL, Wang WT et al (2010) Elevated expression of TDP-43 in the forebrain of mice is sufficient to cause neurological and pathological phenotypes mimicking FTLD-U. J Exp Med 207:1661–1673. doi:10.1084/jem.20092164
-
(2010)
J Exp Med
, vol.207
, pp. 1661-1673
-
-
Tsai, K.J.1
Yang, C.H.2
Fang, Y.H.3
Cho, K.H.4
Chien, W.L.5
Wang, W.T.6
-
45
-
-
56449116386
-
TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy
-
PID: 18957104
-
Turner BJ, Baumer D, Parkinson NJ, Scaber J, Ansorge O, Talbot K (2008) TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy. BMC Neurosci 9:104. doi:10.1186/1471-2202-9-104
-
(2008)
BMC Neurosci
, vol.9
, pp. 104
-
-
Turner, B.J.1
Baumer, D.2
Parkinson, N.J.3
Scaber, J.4
Ansorge, O.5
Talbot, K.6
-
46
-
-
84866289381
-
Autophagy activators rescue and alleviate pathogenesis of a mouse model with proteinopathies of the TAR DNA-binding protein 43
-
COI: 1:CAS:528:DC%2BC38XhsVels77N, PID: 22932872
-
Wang IF, Guo BS, Liu YC, Wu CC, Yang CH, Tsai KJ et al (2012) Autophagy activators rescue and alleviate pathogenesis of a mouse model with proteinopathies of the TAR DNA-binding protein 43. Proc Natl Acad Sci 109:15024–15029. doi:10.1073/pnas.1206362109
-
(2012)
Proc Natl Acad Sci
, vol.109
, pp. 15024-15029
-
-
Wang, I.F.1
Guo, B.S.2
Liu, Y.C.3
Wu, C.C.4
Yang, C.H.5
Tsai, K.J.6
-
47
-
-
0037108967
-
Higher order arrangement of the eukaryotic nuclear bodies
-
COI: 1:CAS:528:DC%2BD38XotVKmsb4%3D, PID: 12361981
-
Wang IF, Reddy NM, Shen CK (2002) Higher order arrangement of the eukaryotic nuclear bodies. Proc Natl Acad Sci 99:13583–13588. doi:10.1073/pnas.212483099
-
(2002)
Proc Natl Acad Sci
, vol.99
, pp. 13583-13588
-
-
Wang, I.F.1
Reddy, N.M.2
Shen, C.K.3
-
48
-
-
73249152831
-
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration
-
COI: 1:CAS:528:DC%2BD1MXhsVKmsLzJ, PID: 19833869
-
Wegorzewska I, Bell S, Cairns NJ, Miller TM, Baloh RH (2009) TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration. Proc Natl Acad Sci 106:18809–18814. doi:10.1073/pnas.0908767106
-
(2009)
Proc Natl Acad Sci
, vol.106
, pp. 18809-18814
-
-
Wegorzewska, I.1
Bell, S.2
Cairns, N.J.3
Miller, T.M.4
Baloh, R.H.5
-
49
-
-
77649269011
-
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration
-
COI: 1:CAS:528:DC%2BC3cXjtFyls78%3D, PID: 20133711
-
Wils H, Kleinberger G, Janssens J, Pereson S, Joris G, Cuijt I et al (2010) TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration. Proc Natl Acad Sci 107:3858–3863. doi:10.1073/pnas.0912417107
-
(2010)
Proc Natl Acad Sci
, vol.107
, pp. 3858-3863
-
-
Wils, H.1
Kleinberger, G.2
Janssens, J.3
Pereson, S.4
Joris, G.5
Cuijt, I.6
-
50
-
-
74749107048
-
TDP-43, a neuro-pathosignature factor, is essential for early mouse embryogenesis
-
COI: 1:CAS:528:DC%2BC3cXitFGjt7Y%3D, PID: 20014337
-
Wu LS, Cheng WC, Hou SC, Yan YT, Jiang ST, Shen CK (2010) TDP-43, a neuro-pathosignature factor, is essential for early mouse embryogenesis. Genesis 48:56–62. doi:10.1002/dvg.20584
-
(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
-
51
-
-
84865028374
-
Targeted depletion of TDP-43 expression in the spinal cord motor neurons leads to the development of amyotrophic lateral sclerosis-like phenotypes in mice
-
COI: 1:CAS:528:DC%2BC38XhtFOksLzJ, PID: 22718760
-
Wu LS, Cheng WC, Shen CK (2012) Targeted depletion of TDP-43 expression in the spinal cord motor neurons leads to the development of amyotrophic lateral sclerosis-like phenotypes in mice. J Biol Chem 287:27335–27344. doi:10.1074/jbc.M112.359000
-
(2012)
J Biol Chem
, vol.287
, pp. 27335-27344
-
-
Wu, L.S.1
Cheng, W.C.2
Shen, C.K.3
-
52
-
-
33846538660
-
Synapse loss and microglial activation precede tangles in a P301S tauopathy mouse model
-
COI: 1:CAS:528:DC%2BD2sXitVektbk%3D, PID: 17270732
-
Yoshiyama Y, Higuchi M, Zhang B, Huang SM, Iwata N, Saido TC et al (2007) Synapse loss and microglial activation precede tangles in a P301S tauopathy mouse model. Neuron 53:337–351. doi:10.1016/j.neuron.2007.01.010
-
(2007)
Neuron
, vol.53
, pp. 337-351
-
-
Yoshiyama, Y.1
Higuchi, M.2
Zhang, B.3
Huang, S.M.4
Iwata, N.5
Saido, T.C.6
-
53
-
-
85040709233
-
Phosphorylation regulates proteasomal-mediated degradation and solubility of TAR DNA binding protein-43 C-terminal fragments
-
PID: 20804554
-
Zhang YJ, Gendron TF, Xu YF, Ko LW, Yen SH, Petrucelli L (2010) Phosphorylation regulates proteasomal-mediated degradation and solubility of TAR DNA binding protein-43 C-terminal fragments. Mol Neurodegener 5:33. doi:10.1186/1750-1326-5-33
-
(2010)
Mol Neurodegener
, vol.5
, pp. 33
-
-
Zhang, Y.J.1
Gendron, T.F.2
Xu, Y.F.3
Ko, L.W.4
Yen, S.H.5
Petrucelli, L.6
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