-
1
-
-
34250209501
-
Amyotrophic lateral sclerosis
-
Mitchell JD, Borasio GD. Amyotrophic lateral sclerosis. Lancet. 2007;369:2031-41.
-
(2007)
Lancet
, vol.369
, pp. 2031-2041
-
-
Mitchell, J.D.1
Borasio, G.D.2
-
2
-
-
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;314:130-3.
-
(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
-
3
-
-
47949096734
-
Sporadic amyotrophic lateral sclerosis: Two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions
-
Nishihira Y, Tan C-F, Onodera O, Toyoshima Y, Yamada M, Morita T, et al. Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions. Acta Neuropathol. 2008;116:169-82.
-
(2008)
Acta Neuropathol
, vol.116
, pp. 169-182
-
-
Nishihira, Y.1
Tan, C.-F.2
Onodera, O.3
Toyoshima, Y.4
Yamada, M.5
Morita, T.6
-
4
-
-
34247625005
-
Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNAbinding protein TDP-43
-
Davidson Y, Kelley T, Mackenzie IR, Pickering-Brown S, Du Plessis D, Neary D, et al. Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNAbinding protein, TDP-43. Acta Neuropathol. 2007;113:521-33.
-
(2007)
Acta Neuropathol
, vol.113
, pp. 521-533
-
-
Davidson, Y.1
Kelley, T.2
MacKenzie, I.R.3
Pickering-Brown, S.4
Du Plessis, D.5
Neary, D.6
-
5
-
-
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. 2008;283:13302-9.
-
(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
-
6
-
-
41949100148
-
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: A genetic and histopathological analysis
-
van Deerlin VM, Leverenz JB, Bekris LM, Bird TD, Yuan W, Elman LB, et al. TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. Lancet Neurol. 2008;7:409-16.
-
(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
-
7
-
-
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;319:1668-72.
-
(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
-
8
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, van de Velde C, et al. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat Genet. 2008;40:572-4.
-
(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
Van De Velde, C.6
-
9
-
-
42949094584
-
TDP-43 mutations in familial amyotrophic lateral sclerosis
-
Yokoseki A, Shiga A, Tan CF, Tagawa A, Kaneko H, Koyama A, et al. TDP-43 mutations in familial amyotrophic lateral sclerosis. Ann Neurol. 2008;63:538-42.
-
(2008)
Ann Neurol
, vol.63
, pp. 538-542
-
-
Yokoseki, A.1
Shiga, A.2
Tan, C.F.3
Tagawa, A.4
Kaneko, H.5
Koyama, A.6
-
10
-
-
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. 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. 2001;276:36337-43.
-
(2001)
J Biol Chem
, vol.276
, pp. 36337-36343
-
-
Buratti, E.1
Baralle, F.E.2
-
11
-
-
0033917463
-
Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis
-
Vielhaber S, Kunz D, Winkler K, Wiedemann FR, Kirches E, Feistner H, et al. Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis. Brain. 2000;123:1339-48.
-
(2000)
Brain
, vol.123
, pp. 1339-1348
-
-
Vielhaber, S.1
Kunz, D.2
Winkler, K.3
Wiedemann, F.R.4
Kirches, E.5
Feistner, H.6
-
12
-
-
33847767167
-
Activities of mitochondrial complexes correlate with nNOS amount in muscle from ALS patients
-
Soraru' G, Vergani L, Fedrizzi L, D'Ascenzo C, Polo A, Bernazzi B, et al. Activities of mitochondrial complexes correlate with nNOS amount in muscle from ALS patients. Neuropathol Appl Neurobiol. 2007;33:204-11.
-
(2007)
Neuropathol Appl Neurobiol
, vol.33
, pp. 204-211
-
-
Soraru, G.1
Vergani, L.2
Fedrizzi, L.3
D'Ascenzo, C.4
Polo, A.5
Bernazzi, B.6
-
13
-
-
53149138951
-
TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia
-
Weihl C, Temiz PP, Miller S, Watts G, Smith C, Forman M, et al. TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia. J Neurol Neurosurg Psychiatry. 2008;79:1186-9.
-
(2008)
J Neurol Neurosurg Psychiatry
, vol.79
, pp. 1186-1189
-
-
Weihl, C.1
Temiz, P.P.2
Miller, S.3
Watts, G.4
Smith, C.5
Forman, M.6
-
16
-
-
34848921202
-
Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43
-
Zhang YJ, Xu Y, Dickey CA, Baralle F, Bailey R, Pickering-Brown S, et al. Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43. J Neurosci. 2007;27:10530-4.
-
(2007)
J Neurosci
, vol.27
, pp. 10530-10534
-
-
Zhang, Y.J.1
Xu, Y.2
Dickey, C.A.3
Baralle, F.4
Bailey, R.5
Pickering-Brown, S.6
-
17
-
-
33749568019
-
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
-
DOI 10.1093/hmg/ddl241
-
Gass J, Cannon A, Mackenzie IR, Boeve B, Baker M, Adamson J, et al. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum Mol Genet. 2006;15:2988-3001. (Pubitemid 44530703)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.20
, pp. 2988-3001
-
-
Gass, J.1
Cannon, A.2
Mackenzie, I.R.3
Boeve, B.4
Baker, M.5
Adamson, J.6
Crook, R.7
Melquist, S.8
Kuntz, K.9
Petersen, R.10
Josephs, K.11
Pickering-Brown, S.M.12
Graff-Radford, N.13
Uitti, R.14
Dickson, D.15
Wszolek, Z.16
Gonzalez, J.17
Beach, T.G.18
Bigio, E.19
Johnson, N.20
Weintraub, S.21
Mesulam, M.22
White III, C.L.23
Woodruff, B.24
Caselli, R.25
Hsiung, G.-Y.26
Feldman, H.27
Knopman, D.28
Hutton, M.29
Rademakers, R.30
more..
-
18
-
-
55949089475
-
TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Steinacker P, Hendrich C, Sperfeld AD, Jesse S, von Arnim CA, Lehnert S, et al. TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Arch Neurol. 2008;65:1481-7.
-
(2008)
Arch Neurol
, vol.65
, pp. 1481-1487
-
-
Steinacker, P.1
Hendrich, C.2
Sperfeld, A.D.3
Jesse, S.4
Von Arnim, C.A.5
Lehnert, S.6
-
19
-
-
44649137415
-
Concomitant TAR-DNAbinding protein 43 is present in Alzheimer's disease and cortical-basal degeneration but not in other tauopathies
-
Uryu K, Nakashima-Yasuda H, Forman MS, Forman MS, Kwong LK, Clark CM, et al. Concomitant TAR-DNAbinding protein 43 is present in Alzheimer's disease and cortical-basal degeneration but not in other tauopathies. Neuropathol Exp Neurol. 2008;67:555-64.
-
(2008)
Neuropathol Exp Neurol
, vol.67
, pp. 555-564
-
-
Uryu, K.1
Nakashima-Yasuda, H.2
Forman, M.S.3
Forman, M.S.4
Kwong, L.K.5
Clark, C.M.6
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