-
1
-
-
84865843186
-
The genetics and neuropathology of amyotrophic lateral sclerosis
-
Al-Chalabi A., Jones A., Troakes C., King A., Al-Sarraj S., van den Berg L.H. The genetics and neuropathology of amyotrophic lateral sclerosis. Acta Neuropathol. 2012, 124:339-352.
-
(2012)
Acta Neuropathol.
, vol.124
, pp. 339-352
-
-
Al-Chalabi, A.1
Jones, A.2
Troakes, C.3
King, A.4
Al-Sarraj, S.5
van den Berg, L.H.6
-
2
-
-
70349991886
-
LRRK2 regulates autophagic activity and localizes to specific membrane microdomains in a novel human genomic reporter cellular model
-
Alegre-Abarrategui J., Christian H., Lufino M.M., Mutihac R., Venda L.L., Ansorge O., Wade-Martins R. LRRK2 regulates autophagic activity and localizes to specific membrane microdomains in a novel human genomic reporter cellular model. Hum. Mol. Genet. 2009, 18:4022-4034.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 4022-4034
-
-
Alegre-Abarrategui, J.1
Christian, H.2
Lufino, M.M.3
Mutihac, R.4
Venda, L.L.5
Ansorge, O.6
Wade-Martins, R.7
-
3
-
-
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
-
4
-
-
43649100018
-
Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis
-
Atkin J.D., Farg M.A., Walker A.K., McLean C., Tomas D., Horne M.K. Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis. Neurobiol. Dis. 2008, 30:400-407.
-
(2008)
Neurobiol. Dis.
, vol.30
, pp. 400-407
-
-
Atkin, J.D.1
Farg, M.A.2
Walker, A.K.3
McLean, C.4
Tomas, D.5
Horne, M.K.6
-
5
-
-
74949135753
-
Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis
-
Barmada S.J., Skibinski G., Korb E., Rao E.J., Wu J.Y., Finkbeiner S. Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis. J. Neurosci. Off. J. Soc. Neurosci. 2010, 30:639-649.
-
(2010)
J. Neurosci. Off. J. Soc. 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
-
6
-
-
0025326163
-
Calcium-dependent regulation of protein synthesis in intact mammalian cells
-
Brostrom C.O., Brostrom M.A. Calcium-dependent regulation of protein synthesis in intact mammalian cells. Annu. Rev. Physiol. 1990, 52:577-590.
-
(1990)
Annu. Rev. Physiol.
, vol.52
, pp. 577-590
-
-
Brostrom, C.O.1
Brostrom, M.A.2
-
7
-
-
0035794665
-
Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping
-
Buratti E., Dork T., Zuccato E., Pagani F., Romano M., Baralle F.E. Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping. EMBO J. 2001, 20:1774-1784.
-
(2001)
EMBO J.
, vol.20
, pp. 1774-1784
-
-
Buratti, E.1
Dork, T.2
Zuccato, E.3
Pagani, F.4
Romano, M.5
Baralle, F.E.6
-
8
-
-
84887686626
-
Heat-shock protein dysregulation is associated with functional and pathological TDP-43 aggregation
-
Chang H.Y., Hou S.C., Way T.D., Wong C.H., Wang I.F. Heat-shock protein dysregulation is associated with functional and pathological TDP-43 aggregation. Nat. Commun. 2013, 4:2757.
-
(2013)
Nat. Commun.
, vol.4
, pp. 2757
-
-
Chang, H.Y.1
Hou, S.C.2
Way, T.D.3
Wong, C.H.4
Wang, I.F.5
-
9
-
-
80051613693
-
A comparison of exogenous promoter activity at the ROSA26 locus using a ΦiC31 integrase mediated cassette exchange approach in mouse ES cells
-
Chen C.M., Krohn J., Bhattacharya S., Davies B. A comparison of exogenous promoter activity at the ROSA26 locus using a ΦiC31 integrase mediated cassette exchange approach in mouse ES cells. PLoS ONE 2011, 6:e23376.
-
(2011)
PLoS ONE
, vol.6
, pp. e23376
-
-
Chen, C.M.1
Krohn, J.2
Bhattacharya, S.3
Davies, B.4
-
10
-
-
80755153025
-
TDP-43 functions and pathogenic mechanisms implicated in TDP-43 proteinopathies
-
Cohen T.J., Lee V.M., Trojanowski J.Q. TDP-43 functions and pathogenic mechanisms implicated in TDP-43 proteinopathies. Trends Mol. Med. 2011, 17:659-667.
-
(2011)
Trends Mol. Med.
, vol.17
, pp. 659-667
-
-
Cohen, T.J.1
Lee, V.M.2
Trojanowski, J.Q.3
-
11
-
-
62149146109
-
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis
-
Daoud H., Valdmanis P.N., Kabashi E., Dion P., Dupre N., Camu W., Meininger V., Rouleau G.A. Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis. J. Med. Genet. 2009, 46:112-114.
-
(2009)
J. Med. Genet.
, vol.46
, pp. 112-114
-
-
Daoud, H.1
Valdmanis, P.N.2
Kabashi, E.3
Dion, P.4
Dupre, N.5
Camu, W.6
Meininger, V.7
Rouleau, G.A.8
-
12
-
-
0030813067
-
Evidence of increased oxidative damage in both sporadic and familial amyotrophic lateral sclerosis
-
Ferrante R.J., Browne S.E., Shinobu L.A., Bowling A.C., Baik M.J., MacGarvey U., Kowall N.W., Brown R.H., Beal M.F. Evidence of increased oxidative damage in both sporadic and familial amyotrophic lateral sclerosis. J. Neurochem. 1997, 69:2064-2074.
-
(1997)
J. Neurochem.
, vol.69
, pp. 2064-2074
-
-
Ferrante, R.J.1
Browne, S.E.2
Shinobu, L.A.3
Bowling, A.C.4
Baik, M.J.5
MacGarvey, U.6
Kowall, N.W.7
Brown, R.H.8
Beal, M.F.9
-
13
-
-
0034705141
-
Bcl-2 decreases the free Ca2+ concentration within the endoplasmic reticulum
-
Foyouzi-Youssefi R., Arnaudeau S., Borner C., Kelley W.L., Tschopp J., Lew D.P., Demaurex N., Krause K.H. Bcl-2 decreases the free Ca2+ concentration within the endoplasmic reticulum. Proc. Natl. Acad. Sci. U. S. A. 2000, 97:5723-5728.
-
(2000)
Proc. Natl. Acad. Sci. U. S. A.
, vol.97
, pp. 5723-5728
-
-
Foyouzi-Youssefi, R.1
Arnaudeau, S.2
Borner, C.3
Kelley, W.L.4
Tschopp, J.5
Lew, D.P.6
Demaurex, N.7
Krause, K.H.8
-
14
-
-
41949119043
-
TDP-43 A315T mutation in familial motor neuron disease
-
Gitcho M.A., Baloh R.H., Chakraverty S., Mayo K., Norton J.B., Levitch D., Hatanpaa K.J., White C.L., Bigio E.H., Caselli R., Baker M., Al-Lozi M.T., Morris J.C., Pestronk A., Rademakers R., Goate A.M., Cairns N.J. TDP-43 A315T mutation in familial motor neuron disease. Ann. Neurol. 2008, 63:535-538.
-
(2008)
Ann. Neurol.
, vol.63
, pp. 535-538
-
-
Gitcho, M.A.1
Baloh, R.H.2
Chakraverty, S.3
Mayo, K.4
Norton, J.B.5
Levitch, D.6
Hatanpaa, K.J.7
White, C.L.8
Bigio, E.H.9
Caselli, R.10
Baker, M.11
Al-Lozi, M.T.12
Morris, J.C.13
Pestronk, A.14
Rademakers, R.15
Goate, A.M.16
Cairns, N.J.17
-
15
-
-
0028851245
-
Depletion of calcium from the lumen of endoplasmic reticulum reversibly inhibits passive diffusion and signal-mediated transport into the nucleus
-
Greber U.F., Gerace L. Depletion of calcium from the lumen of endoplasmic reticulum reversibly inhibits passive diffusion and signal-mediated transport into the nucleus. J. Cell Biol. 1995, 128:5-14.
-
(1995)
J. Cell Biol.
, vol.128
, pp. 5-14
-
-
Greber, U.F.1
Gerace, L.2
-
16
-
-
36749067790
-
Oxidative and endoplasmic reticulum stress interplay in sporadic amyotrophic lateral sclerosis
-
Ilieva E.V., Ayala V., Jove M., Dalfo E., Cacabelos D., Povedano M., Bellmunt M.J., Ferrer I., Pamplona R., Portero-Otin M. Oxidative and endoplasmic reticulum stress interplay in sporadic amyotrophic lateral sclerosis. Brain 2007, 130:3111-3123.
-
(2007)
Brain
, vol.130
, pp. 3111-3123
-
-
Ilieva, E.V.1
Ayala, V.2
Jove, M.3
Dalfo, E.4
Cacabelos, D.5
Povedano, M.6
Bellmunt, M.J.7
Ferrer, I.8
Pamplona, R.9
Portero-Otin, M.10
-
17
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
Kabashi E., Valdmanis P.N., Dion P., Spiegelman D., McConkey B.J., Vande Velde C., Bouchard J.P., Lacomblez L., Pochigaeva K., Salachas F., Pradat P.F., Camu W., Meininger V., Dupre N., Rouleau G.A. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat. Genet. 2008, 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
-
18
-
-
84868088848
-
High-content RNAi screening identifies the Type 1 inositol triphosphate receptor as a modifier of TDP-43 localization and neurotoxicity
-
Kim S.H., Zhan L., Hanson K.A., Tibbetts R.S. High-content RNAi screening identifies the Type 1 inositol triphosphate receptor as a modifier of TDP-43 localization and neurotoxicity. Hum. Mol. Genet. 2012, 21(22):4845-4856.
-
(2012)
Hum. Mol. Genet.
, vol.21
, Issue.22
, pp. 4845-4856
-
-
Kim, S.H.1
Zhan, L.2
Hanson, K.A.3
Tibbetts, R.S.4
-
19
-
-
77953026500
-
Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis
-
Kraemer B.C., Schuck T., Wheeler J.M., Robinson L.C., Trojanowski J.Q., Lee V.M.Y., Schellenberg G.D. Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis. Acta Neuropathol. 2010, 119:409-419.
-
(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.Y.6
Schellenberg, G.D.7
-
20
-
-
77953890823
-
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
-
Lagier-Tourenne C., Polymenidou M., Cleveland D.W. TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration. Hum. Mol. Genet. 2010, 19:R46-R64.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. R46-R64
-
-
Lagier-Tourenne, C.1
Polymenidou, M.2
Cleveland, D.W.3
-
22
-
-
0025729489
-
Ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis. Morphology, distribution, and specificity
-
Leigh P.N., Whitwell H., Garofalo O., Buller J., Swash M., Martin J.E., Gallo J.M., Weller R.O., Anderton B.H. Ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis. Morphology, distribution, and specificity. Brain 1991, 114(Pt 2):775-788.
-
(1991)
Brain
, vol.114
, pp. 775-788
-
-
Leigh, P.N.1
Whitwell, H.2
Garofalo, O.3
Buller, J.4
Swash, M.5
Martin, J.E.6
Gallo, J.M.7
Weller, R.O.8
Anderton, B.H.9
-
23
-
-
79952589652
-
TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1
-
McDonald K.K., Aulas A., Destroismaisons L., Pickles S., Beleac E., Camu W., Rouleau G.A., Vande Velde C. TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1. Hum. Mol. Genet. 2011, 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
-
24
-
-
27744554553
-
Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene
-
Mercado P.A., Ayala Y.M., Romano M., Buratti E., Baralle F.E. Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene. Nucleic Acids Res. 2005, 33:6000-6010.
-
(2005)
Nucleic Acids Res.
, vol.33
, pp. 6000-6010
-
-
Mercado, P.A.1
Ayala, Y.M.2
Romano, M.3
Buratti, E.4
Baralle, F.E.5
-
25
-
-
84861860140
-
Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject
-
1846.e
-
Mosca L., Lunetta C., Tarlarini C., Avemaria F., Maestri E., Melazzini M., Corbo M., Penco S. Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject. Neurobiol. Aging 2012, 33(1846.e):1841-1844.
-
(2012)
Neurobiol. Aging
, vol.33
, pp. 1841-1844
-
-
Mosca, L.1
Lunetta, C.2
Tarlarini, C.3
Avemaria, F.4
Maestri, E.5
Melazzini, M.6
Corbo, M.7
Penco, S.8
-
26
-
-
0034698838
-
Changes in endoplasmic reticulum luminal environment affect cell sensitivity to apoptosis
-
Nakamura K., Bossy-Wetzel E., Burns K., Fadel M.P., Lozyk M., Goping I.S., Opas M., Bleackley R.C., Green D.R., Michalak M. Changes in endoplasmic reticulum luminal environment affect cell sensitivity to apoptosis. J. Cell Biol. 2000, 150:731-740.
-
(2000)
J. Cell Biol.
, vol.150
, pp. 731-740
-
-
Nakamura, K.1
Bossy-Wetzel, E.2
Burns, K.3
Fadel, M.P.4
Lozyk, M.5
Goping, I.S.6
Opas, M.7
Bleackley, R.C.8
Green, D.R.9
Michalak, M.10
-
27
-
-
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., McCluskey L.F., Miller B.L., Masliah E., Mackenzie I.R., Feldman H., Feiden W., Kretzschmar H.A., Trojanowski J.Q., Lee V.M. 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
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
Trojanowski, J.Q.18
Lee, V.M.19
-
29
-
-
0029066110
-
Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs
-
Ou S.H., Wu F., Harrich D., Garcia-Martinez L.F., Gaynor R.B. Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs. J. Virol. 1995, 69:3584-3596.
-
(1995)
J. Virol.
, vol.69
, pp. 3584-3596
-
-
Ou, S.H.1
Wu, F.2
Harrich, D.3
Garcia-Martinez, L.F.4
Gaynor, R.B.5
-
30
-
-
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:R156-R162.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. R156-R162
-
-
Pesiridis, G.S.1
Lee, V.M.2
Trojanowski, J.Q.3
-
31
-
-
47349089719
-
Targeting Bcl-2-IP3 receptor interaction to reverse Bcl-2's inhibition of apoptotic calcium signals
-
Rong Y.P., Aromolaran A.S., Bultynck G., Zhong F., Li X., McColl K., Matsuyama S., Herlitze S., Roderick H.L., Bootman M.D., Mignery G.A., Parys J.B., De Smedt H., Distelhorst C.W. Targeting Bcl-2-IP3 receptor interaction to reverse Bcl-2's inhibition of apoptotic calcium signals. Mol. Cell 2008, 31:255-265.
-
(2008)
Mol. Cell
, vol.31
, pp. 255-265
-
-
Rong, Y.P.1
Aromolaran, A.S.2
Bultynck, G.3
Zhong, F.4
Li, X.5
McColl, K.6
Matsuyama, S.7
Herlitze, S.8
Roderick, H.L.9
Bootman, M.D.10
Mignery, G.A.11
Parys, J.B.12
De Smedt, H.13
Distelhorst, C.W.14
-
32
-
-
0025361036
-
The involvement of calcium in transport of secretory proteins from the endoplasmic reticulum
-
Sambrook J.F. The involvement of calcium in transport of secretory proteins from the endoplasmic reticulum. Cell 1990, 61:197-199.
-
(1990)
Cell
, vol.61
, pp. 197-199
-
-
Sambrook, J.F.1
-
33
-
-
0037418843
-
2+: a control point for apoptosis
-
2+: a control point for apoptosis. Science 2003, 300:135-139.
-
(2003)
Science
, vol.300
, pp. 135-139
-
-
Scorrano, L.1
Oakes, S.A.2
Opferman, J.T.3
Cheng, E.H.4
Sorcinelli, M.D.5
Pozzan, T.6
Korsmeyer, S.J.7
-
34
-
-
78651408754
-
Identification of neuronal RNA targets of TDP-43-containing ribonucleoprotein complexes
-
Sephton C.F., Cenik C., Kucukural A., Dammer E.B., Cenik B., Han Y., Dewey C.M., Roth F.P., Herz J., Peng J., Moore M.J., Yu G. Identification of neuronal RNA targets of TDP-43-containing ribonucleoprotein complexes. J. Biol. Chem. 2011, 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
-
35
-
-
1442335318
-
Control of mitochondrial permeability by Bcl-2 family members
-
Sharpe J.C., Arnoult D., Youle R.J. Control of mitochondrial permeability by Bcl-2 family members. Biochim. Biophys. Acta 2004, 1644:107-113.
-
(2004)
Biochim. Biophys. Acta
, vol.1644
, pp. 107-113
-
-
Sharpe, J.C.1
Arnoult, D.2
Youle, R.J.3
-
36
-
-
0029082389
-
Oxidative damage to protein in sporadic motor neuron disease spinal cord
-
Shaw P.J., Ince P.G., Falkous G., Mantle D. Oxidative damage to protein in sporadic motor neuron disease spinal cord. Ann. Neurol. 1995, 38:691-695.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 691-695
-
-
Shaw, P.J.1
Ince, P.G.2
Falkous, G.3
Mantle, D.4
-
37
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
Sreedharan J., Blair I.P., Tripathi V.B., Hu X., Vance C., Rogelj B., Ackerley S., Durnall J.C., Williams K.L., Buratti E., Baralle F., de Belleroche J., Mitchell J.D., Leigh P.N., Al-Chalabi A., Miller C.C., Nicholson G., Shaw C.E. 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
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
-
38
-
-
34249751076
-
TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein
-
Strong M.J., Volkening K., Hammond R., Yang W., Strong W., Leystra-Lantz C., Shoesmith C. TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein. Mol. Cell. Neurosci. 2007, 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
-
39
-
-
77957558614
-
Calpastatin reduces toxicity of SOD1G93A in a culture model of amyotrophic lateral sclerosis
-
Tradewell M.L., Durham H.D. Calpastatin reduces toxicity of SOD1G93A in a culture model of amyotrophic lateral sclerosis. Neuroreport 2010, 21:976-979.
-
(2010)
Neuroreport
, vol.21
, pp. 976-979
-
-
Tradewell, M.L.1
Durham, H.D.2
-
40
-
-
79954633016
-
Calcium dysregulation, mitochondrial pathology and protein aggregation in a culture model of amyotrophic lateral sclerosis: mechanistic relationship and differential sensitivity to intervention
-
Tradewell M.L., Cooper L.A., Minotti S., Durham H.D. Calcium dysregulation, mitochondrial pathology and protein aggregation in a culture model of amyotrophic lateral sclerosis: mechanistic relationship and differential sensitivity to intervention. Neurobiol. Dis. 2011, 42:265-275.
-
(2011)
Neurobiol. Dis.
, vol.42
, pp. 265-275
-
-
Tradewell, M.L.1
Cooper, L.A.2
Minotti, S.3
Durham, H.D.4
-
41
-
-
41949100148
-
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
-
Van Deerlin V.M., Leverenz J.B., Bekris L.M., Bird T.D., Yuan W., Elman L.B., Clay D., Wood E.M., Chen-Plotkin A.S., Martinez-Lage M., Steinbart E., McCluskey L., Grossman M., Neumann M., Wu I.L., Yang W.S., Kalb R., Galasko D.R., Montine T.J., Trojanowski J.Q., Lee V.M., Schellenberg G.D., Yu C.E. TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. Lancet Neurol. 2008, 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
McCluskey, 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
Lee, V.M.21
Schellenberg, G.D.22
Yu, C.E.23
more..
-
42
-
-
0035895505
-
The sequence of the human genome
-
Venter J.C., Adams M.D., Myers E.W., Li P.W., Mural R.J., Sutton G.G., Smith H.O., Yandell M., Evans C.A., Holt R.A., Gocayne J.D., Amanatides P., Ballew R.M., Huson D.H., Wortman J.R., Zhang Q., Kodira C.D., Zheng X.H., Chen L., Skupski M., Subramanian G., Thomas P.D., Zhang J., Gabor Miklos G.L., Nelson C., Broder S., Clark A.G., Nadeau J., McKusick V.A., Zinder N., Levine A.J., Roberts R.J., Simon M., Slayman C., Hunkapiller M., Bolanos R., Delcher A., Dew I., Fasulo D., Flanigan M., Florea L., Halpern A., Hannenhalli S., Kravitz S., Levy S., Mobarry C., Reinert K., Remington K., Abu-Threideh J., Beasley E., Biddick K., Bonazzi V., Brandon R., Cargill M., Chandramouliswaran I., Charlab R., Chaturvedi K., Deng Z., Di Francesco V., Dunn P., Eilbeck K., Evangelista C., Gabrielian A.E., Gan W., Ge W., Gong F., Gu Z., Guan P., Heiman T.J., Higgins M.E., Ji R.R., Ke Z., Ketchum K.A., Lai Z., Lei Y., Li Z., Li J., Liang Y., Lin X., Lu F., Merkulov G.V., Milshina N., Moore H.M., Naik A.K., Narayan V.A., Neelam B., Nusskern D., Rusch D.B., Salzberg S., Shao W., Shue B., Sun J., Wang Z., Wang A., Wang X., Wang J., Wei M., Wides R., Xiao C., Yan C., Yao A., Ye J., Zhan M., Zhang W., Zhang H., Zhao Q., Zheng L., Zhong F., Zhong W., Zhu S., Zhao S., Gilbert D., Baumhueter S., Spier G., Carter C., Cravchik A., Woodage T., Ali F., An H., Awe A., Baldwin D., Baden H., Barnstead M., Barrow I., Beeson K., Busam D., Carver A., Center A., Cheng M.L., Curry L., Danaher S., Davenport L., Desilets R., Dietz S., Dodson K., Doup L., Ferriera S., Garg N., Gluecksmann A., Hart B., Haynes J., Haynes C., Heiner C., Hladun S., Hostin D., Houck J., Howland T., Ibegwam C., Johnson J., Kalush F., Kline L., Koduru S., Love A., Mann F., May D., McCawley S., McIntosh T., McMullen I., Moy M., Moy L., Murphy B., Nelson K., Pfannkoch C., Pratts E., Puri V., Qureshi H., Reardon M., Rodriguez R., Rogers Y.H., Romblad D., Ruhfel B., Scott R., Sitter C., Smallwood M., Stewart E., Strong R., Suh E., Thomas R., Tint N.N., Tse S., Vech C., Wang G., Wetter J., Williams S., Williams M., Windsor S., Winn-Deen E., Wolfe K., Zaveri J., Zaveri K., Abril J.F., Guigó R., Campbell M.J., Sjolander K.V., Karlak B., Kejariwal A., Mi H., Lazareva B., Hatton T., Narechania A., Diemer K., Muruganujan A., Guo N., Sato S., Bafna V., Istrail S., Lippert R., Schwartz R., Walenz B., Yooseph S., Allen D., Basu A., Baxendale J., Blick L., Caminha M., Carnes-Stine J., Caulk P., Chiang Y.H., Coyne M., Dahlke C., Mays A., Dombroski M., Donnelly M., Ely D., Esparham S., Fosler C., Gire H., Glanowski S., Glasser K., Glodek A., Gorokhov M., Graham K., Gropman B., Harris M., Heil J., Henderson S., Hoover J., Jennings D., Jordan C., Jordan J., Kasha J., Kagan L., Kraft C., Levitsky A., Lewis M., Liu X., Lopez J., Ma D., Majoros W., McDaniel J., Murphy S., Newman M., Nguyen T., Nguyen N., Nodell M., Pan S., Peck J., Peterson M., Rowe W., Sanders R., Scott J., Simpson M., Smith T., Sprague A., Stockwell T., Turner R., Venter E., Wang M., Wen M., Wu D., Wu M., Xia A., Zandieh A., Zhu X. The sequence of the human genome. Science 2001, 291:1304-1351.
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
Sutton, G.G.6
Smith, H.O.7
Yandell, M.8
Evans, C.A.9
Holt, R.A.10
Gocayne, J.D.11
Amanatides, P.12
Ballew, R.M.13
Huson, D.H.14
Wortman, J.R.15
Zhang, Q.16
Kodira, C.D.17
Zheng, X.H.18
Chen, L.19
Skupski, M.20
Subramanian, G.21
Thomas, P.D.22
Zhang, J.23
Gabor Miklos, G.L.24
Nelson, C.25
Broder, S.26
Clark, A.G.27
Nadeau, J.28
McKusick, V.A.29
Zinder, N.30
Levine, A.J.31
Roberts, R.J.32
Simon, M.33
Slayman, C.34
Hunkapiller, M.35
Bolanos, R.36
Delcher, A.37
Dew, I.38
Fasulo, D.39
Flanigan, M.40
Florea, L.41
Halpern, A.42
Hannenhalli, S.43
Kravitz, S.44
Levy, S.45
Mobarry, C.46
Reinert, K.47
Remington, K.48
Abu-Threideh, J.49
Beasley, E.50
Biddick, K.51
Bonazzi, V.52
Brandon, R.53
Cargill, M.54
Chandramouliswaran, I.55
Charlab, R.56
Chaturvedi, K.57
Deng, Z.58
Di Francesco, V.59
Dunn, P.60
Eilbeck, K.61
Evangelista, C.62
Gabrielian, A.E.63
Gan, W.64
Ge, W.65
Gong, F.66
Gu, Z.67
Guan, P.68
Heiman, T.J.69
Higgins, M.E.70
Ji, R.R.71
Ke, Z.72
Ketchum, K.A.73
Lai, Z.74
Lei, Y.75
Li, Z.76
Li, J.77
Liang, Y.78
Lin, X.79
Lu, F.80
Merkulov, G.V.81
Milshina, N.82
Moore, H.M.83
Naik, A.K.84
Narayan, V.A.85
Neelam, B.86
Nusskern, D.87
Rusch, D.B.88
Salzberg, S.89
Shao, W.90
Shue, B.91
Sun, J.92
Wang, Z.93
Wang, A.94
Wang, X.95
Wang, J.96
Wei, M.97
Wides, R.98
Xiao, C.99
more..
-
43
-
-
79955812764
-
TDP-43-based animal models of neurodegeneration: new insights into ALS pathology and pathophysiology
-
Wegorzewska I., Baloh R.H. TDP-43-based animal models of neurodegeneration: new insights into ALS pathology and pathophysiology. Neurodegener. Dis. 2011, 8:262-274.
-
(2011)
Neurodegener. Dis.
, vol.8
, pp. 262-274
-
-
Wegorzewska, I.1
Baloh, R.H.2
-
44
-
-
75149138783
-
Isolation and enrichment of embryonic mouse motoneurons from the lumbar spinal cord of individual mouse embryos
-
Wiese S., Herrmann T., Drepper C., Jablonka S., Funk N., Klausmeyer A., Rogers M.L., Rush R., Sendtner M. Isolation and enrichment of embryonic mouse motoneurons from the lumbar spinal cord of individual mouse embryos. Nat. Protoc. 2010, 5:31-38.
-
(2010)
Nat. Protoc.
, vol.5
, pp. 31-38
-
-
Wiese, S.1
Herrmann, T.2
Drepper, C.3
Jablonka, S.4
Funk, N.5
Klausmeyer, A.6
Rogers, M.L.7
Rush, R.8
Sendtner, M.9
-
45
-
-
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.J. TDP-43, a neuro-pathosignature factor, is essential for early mouse embryogenesis. Genesis (New York, N Y: 2000) 2010, 48:56-62.
-
(2010)
Genesis (New York, N Y: 2000)
, 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.J.6
-
46
-
-
42949094584
-
TDP-43 mutation in familial amyotrophic lateral sclerosis
-
Yokoseki A., Shiga A., Tan C.F., Tagawa A., Kaneko H., Koyama A., Eguchi H., Tsujino A., Ikeuchi T., Kakita A., Okamoto K., Nishizawa M., Takahashi H., Onodera O. TDP-43 mutation in familial amyotrophic lateral sclerosis. Ann. Neurol. 2008, 63:538-542.
-
(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
Eguchi, H.7
Tsujino, A.8
Ikeuchi, T.9
Kakita, A.10
Okamoto, K.11
Nishizawa, M.12
Takahashi, H.13
Onodera, O.14
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