-
1
-
-
84928136247
-
Cytoplasmic hGle1A regulates stress granules by modulation of translation
-
Aditi, Folkmann, A.W., Wente, S.R., Cytoplasmic hGle1A regulates stress granules by modulation of translation. Mol. Biol. Cell 26 (2015), 1476–1490.
-
(2015)
Mol. Biol. Cell
, vol.26
, pp. 1476-1490
-
-
Aditi1
Folkmann, A.W.2
Wente, S.R.3
-
2
-
-
84893508018
-
Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations
-
Alami, N.H., Smith, R.B., Carrasco, M.A., Williams, L.A., Winborn, C.S., Han, S.S., Kiskinis, E., Winborn, B., Freibaum, B.D., Kanagaraj, A., Clare, A.J., Badders, N.M., Bilican, B., Chaum, E., Chandran, S., Shaw, C.E., Eggan, K.C., Maniatis, T., Taylor, J.P., Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations. Neuron 81 (2014), 536–543.
-
(2014)
Neuron
, vol.81
, pp. 536-543
-
-
Alami, N.H.1
Smith, R.B.2
Carrasco, M.A.3
Williams, L.A.4
Winborn, C.S.5
Han, S.S.6
Kiskinis, E.7
Winborn, B.8
Freibaum, B.D.9
Kanagaraj, A.10
Clare, A.J.11
Badders, N.M.12
Bilican, B.13
Chaum, E.14
Chandran, S.15
Shaw, C.E.16
Eggan, K.C.17
Maniatis, T.18
Taylor, J.P.19
-
3
-
-
33745736445
-
Inositol hexakisphosphate and Gle1 activate the DEAD-box protein Dbp5 for nuclear mRNA export
-
Alcázar-Román, A.R., Tran, E.J., Guo, S., Wente, S.R., Inositol hexakisphosphate and Gle1 activate the DEAD-box protein Dbp5 for nuclear mRNA export. Nat. Cell Biol. 8 (2006), 711–716.
-
(2006)
Nat. Cell Biol.
, vol.8
, pp. 711-716
-
-
Alcázar-Román, A.R.1
Tran, E.J.2
Guo, S.3
Wente, S.R.4
-
4
-
-
77952776550
-
Control of mRNA export and translation termination by inositol hexakisphosphate requires specific interaction with Gle1
-
Alcázar-Román, A.R., Bolger, T.A., Wente, S.R., Control of mRNA export and translation termination by inositol hexakisphosphate requires specific interaction with Gle1. J. Biol. Chem. 285 (2010), 16683–16692.
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 16683-16692
-
-
Alcázar-Román, A.R.1
Bolger, T.A.2
Wente, S.R.3
-
5
-
-
78651356190
-
Phytic acid as a potential treatment for alzheimer's pathology: evidence from animal and in vitro models
-
Anekonda, T.S., Wadsworth, T.L., Sabin, R., Frahler, K., Harris, C., Petriko, B., Ralle, M., Woltjer, R., Quinn, J.F., Phytic acid as a potential treatment for alzheimer's pathology: evidence from animal and in vitro models. J. Alzheimers Dis. 23 (2011), 21–35.
-
(2011)
J. Alzheimers Dis.
, vol.23
, pp. 21-35
-
-
Anekonda, T.S.1
Wadsworth, T.L.2
Sabin, R.3
Frahler, K.4
Harris, C.5
Petriko, B.6
Ralle, M.7
Woltjer, R.8
Quinn, J.F.9
-
6
-
-
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. 351 (2006), 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
-
7
-
-
84870572714
-
Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models
-
Armakola, M., Higgins, M.J., Figley, M.D., Barmada, S.J., Scarborough, E.A., Diaz, Z., Fang, X., Shorter, J., Krogan, N.J., Finkbeiner, S., Farese, R.V. Jr., Gitler, A.D., Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models. Nat. Genet. 44 (2012), 1302–1309.
-
(2012)
Nat. Genet.
, vol.44
, pp. 1302-1309
-
-
Armakola, M.1
Higgins, M.J.2
Figley, M.D.3
Barmada, S.J.4
Scarborough, E.A.5
Diaz, Z.6
Fang, X.7
Shorter, J.8
Krogan, N.J.9
Finkbeiner, S.10
Farese, R.V.11
Gitler, A.D.12
-
8
-
-
84883149037
-
Amyotrophic lateral sclerosis-linked FUS/TLS alters stress granule assembly and dynamics
-
Baron, D.M., Kaushansky, L.J., Ward, C.L., Sama, R.R., Chian, R.J., Boggio, K.J., Quaresma, A.J., Nickerson, J.A., Bosco, D.A., Amyotrophic lateral sclerosis-linked FUS/TLS alters stress granule assembly and dynamics. Mol. Neurodegener., 8, 2013, 30.
-
(2013)
Mol. Neurodegener.
, vol.8
, pp. 30
-
-
Baron, D.M.1
Kaushansky, L.J.2
Ward, C.L.3
Sama, R.R.4
Chian, R.J.5
Boggio, K.J.6
Quaresma, A.J.7
Nickerson, J.A.8
Bosco, D.A.9
-
9
-
-
84883446343
-
Stress granules in neurodegeneration – lessons learnt from TAR DNA binding protein of 43 kDa and fused in sarcoma
-
Bentmann, E., Haass, C., Dormann, D., Stress granules in neurodegeneration – lessons learnt from TAR DNA binding protein of 43 kDa and fused in sarcoma. FEBS J. 280 (2013), 4348–4370.
-
(2013)
FEBS J.
, vol.280
, pp. 4348-4370
-
-
Bentmann, E.1
Haass, C.2
Dormann, D.3
-
10
-
-
49549099576
-
The mRNA export factor Gle1 and inositol hexakisphosphate regulate distinct stages of translation
-
Bolger, T.A., Folkmann, A.W., Tran, E.J., Wente, S.R., The mRNA export factor Gle1 and inositol hexakisphosphate regulate distinct stages of translation. Cell 134 (2008), 624–633.
-
(2008)
Cell
, vol.134
, pp. 624-633
-
-
Bolger, T.A.1
Folkmann, A.W.2
Tran, E.J.3
Wente, S.R.4
-
11
-
-
81155154337
-
Gle1 is a multifunctional DEAD-box protein regulator that modulates Ded1 in translation initiation
-
Bolger, T.A., Wente, S.R., Gle1 is a multifunctional DEAD-box protein regulator that modulates Ded1 in translation initiation. J. Biol. Chem. 286 (2011), 39750–39759.
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 39750-39759
-
-
Bolger, T.A.1
Wente, S.R.2
-
12
-
-
37549032751
-
Intracellular localization of human Ins(1,3,4,5,6)P5 2-kinase
-
Brehm, M.A., Schenk, T.M., Zhou, X., Fanick, W., Lin, H., Windhorst, S., Nalaskowski, M.M., Kobras, M., Shears, S.B., Mayr, G.W., Intracellular localization of human Ins(1,3,4,5,6)P5 2-kinase. Biochem. J. 408 (2007), 335–345.
-
(2007)
Biochem. J.
, vol.408
, pp. 335-345
-
-
Brehm, M.A.1
Schenk, T.M.2
Zhou, X.3
Fanick, W.4
Lin, H.5
Windhorst, S.6
Nalaskowski, M.M.7
Kobras, M.8
Shears, S.B.9
Mayr, G.W.10
-
13
-
-
84861978013
-
Structural basis for polyadenosine-RNA binding by Nab2 Zn fingers and its function in mRNA nuclear export
-
Brockmann, C., Soucek, S., Kuhlmann, S.I., Mills-Lujan, K., Kelly, S.M., Yang, J.C., Iglesias, N., Stutz, F., Corbett, A.H., Neuhaus, D., Stewart, M., Structural basis for polyadenosine-RNA binding by Nab2 Zn fingers and its function in mRNA nuclear export. Structure 20 (2012), 1007–1018.
-
(2012)
Structure
, vol.20
, pp. 1007-1018
-
-
Brockmann, C.1
Soucek, S.2
Kuhlmann, S.I.3
Mills-Lujan, K.4
Kelly, S.M.5
Yang, J.C.6
Iglesias, N.7
Stutz, F.8
Corbett, A.H.9
Neuhaus, D.10
Stewart, M.11
-
14
-
-
84879349589
-
Eukaryotic stress granules are cleared by autophagy and Cdc48/VCP functions
-
Buchan, J.R., Kolaitis, R.M., Taylor, J.P., Parker, R., Eukaryotic stress granules are cleared by autophagy and Cdc48/VCP functions. Cell 153 (2013), 1461–1474.
-
(2013)
Cell
, vol.153
, pp. 1461-1474
-
-
Buchan, J.R.1
Kolaitis, R.M.2
Taylor, J.P.3
Parker, R.4
-
15
-
-
77957829719
-
The mitogen-activated protein kinase Slt2 regulates nuclear retention of non-heat shock mRNAs during heat shock-induced stress
-
Carmody, S.R., Tran, E.J., Apponi, L.H., Corbett, A.H., Wente, S.R., The mitogen-activated protein kinase Slt2 regulates nuclear retention of non-heat shock mRNAs during heat shock-induced stress. Mol. Cell Biol. 30 (2010), 5168–5179.
-
(2010)
Mol. Cell Biol.
, vol.30
, pp. 5168-5179
-
-
Carmody, S.R.1
Tran, E.J.2
Apponi, L.H.3
Corbett, A.H.4
Wente, S.R.5
-
16
-
-
70350135049
-
TDP-43 is recruited to stress granules in conditions of oxidative insult
-
Colombrita, C., Zennaro, E., Fallini, C., Weber, M., Sommacal, A., Buratti, E., Silani, V., Ratti, A., TDP-43 is recruited to stress granules in conditions of oxidative insult. J. Neurochem. 111 (2009), 1051–1061.
-
(2009)
J. Neurochem.
, vol.111
, pp. 1051-1061
-
-
Colombrita, C.1
Zennaro, E.2
Fallini, C.3
Weber, M.4
Sommacal, A.5
Buratti, E.6
Silani, V.7
Ratti, A.8
-
17
-
-
79959865166
-
TDP-43 and FUS: a nuclear affair
-
Dormann, D., Haass, C., TDP-43 and FUS: a nuclear affair. Trends Neurosci. 34 (2011), 339–348.
-
(2011)
Trends Neurosci.
, vol.34
, pp. 339-348
-
-
Dormann, D.1
Haass, C.2
-
18
-
-
77955792022
-
ALS-associated fused in sarcoma (FUS) mutations disrupt transportin-mediated nuclear import
-
Dormann, D., Rodde, R., Edbauer, D., Bentmann, E., Fischer, I., Hruscha, A., Than, M.E., Mackenzie, I.R., Capell, A., Schmid, B., Neumann, M., Haass, C., ALS-associated fused in sarcoma (FUS) mutations disrupt transportin-mediated nuclear import. EMBO J. 29 (2010), 2841–2857.
-
(2010)
EMBO J.
, vol.29
, pp. 2841-2857
-
-
Dormann, D.1
Rodde, R.2
Edbauer, D.3
Bentmann, E.4
Fischer, I.5
Hruscha, A.6
Than, M.E.7
Mackenzie, I.R.8
Capell, A.9
Schmid, B.10
Neumann, M.11
Haass, C.12
-
19
-
-
82655173728
-
Disease progression in a mouse model of amyotrophic lateral sclerosis: the influence of chronic stress and corticosterone
-
Fidler, J.A., Treleaven, C.M., Frakes, A., Tamsett, T.J., McCrate, M., Cheng, S.H., Shihabuddin, L.S., Kaspar, B.K., Dodge, J.C., Disease progression in a mouse model of amyotrophic lateral sclerosis: the influence of chronic stress and corticosterone. FASEB J 25 (2011), 4369–4377.
-
(2011)
FASEB J
, vol.25
, pp. 4369-4377
-
-
Fidler, J.A.1
Treleaven, C.M.2
Frakes, A.3
Tamsett, T.J.4
McCrate, M.5
Cheng, S.H.6
Shihabuddin, L.S.7
Kaspar, B.K.8
Dodge, J.C.9
-
20
-
-
84886796260
-
Gle1 functions during mRNA export in an oligomeric complex that is altered in human disease
-
Folkmann, A.W., Collier, S.E., Zhan, X., Aditi, Ohi, M.D., Wente, S.R., Gle1 functions during mRNA export in an oligomeric complex that is altered in human disease. Cell 155 (2013), 582–593.
-
(2013)
Cell
, vol.155
, pp. 582-593
-
-
Folkmann, A.W.1
Collier, S.E.2
Zhan, X.3
Aditi4
Ohi, M.D.5
Wente, S.R.6
-
21
-
-
84857590342
-
Dbp5, Gle1-IP6 and Nup159: a working model for mRNP export
-
Folkmann, A.W., Noble, K.N., Cole, C.N., Wente, S.R., Dbp5, Gle1-IP6 and Nup159: a working model for mRNP export. Nucleus 2 (2011), 540–548.
-
(2011)
Nucleus
, vol.2
, pp. 540-548
-
-
Folkmann, A.W.1
Noble, K.N.2
Cole, C.N.3
Wente, S.R.4
-
22
-
-
84893385652
-
Insights into mRNA export-linked molecular mechanisms of human disease through a Gle1 structure-function analysis
-
Folkmann, A.W., Dawson, T.R., Wente, S.R., Insights into mRNA export-linked molecular mechanisms of human disease through a Gle1 structure-function analysis. Adv. Biol. Regul. 54 (2014), 74–91.
-
(2014)
Adv. Biol. Regul.
, vol.54
, pp. 74-91
-
-
Folkmann, A.W.1
Dawson, T.R.2
Wente, S.R.3
-
23
-
-
84940938959
-
Neurodegeneration: problems at the nuclear pore
-
Fox, B.W., Tibbetts, R.S., Neurodegeneration: problems at the nuclear pore. Nature 525 (2015), 36–37.
-
(2015)
Nature
, vol.525
, pp. 36-37
-
-
Fox, B.W.1
Tibbetts, R.S.2
-
24
-
-
84940925534
-
GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport
-
Freibaum, B.D., Lu, Y., Lopez-Gonzalez, R., Kim, N.C., Almeida, S., Lee, K.H., Badders, N., Valentine, M., Miller, B.L., Wong, P.C., Petrucelli, L., Kim, H.J., Gao, F.B., Taylor, J.P., GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport. Nature 525 (2015), 129–133.
-
(2015)
Nature
, vol.525
, pp. 129-133
-
-
Freibaum, B.D.1
Lu, Y.2
Lopez-Gonzalez, R.3
Kim, N.C.4
Almeida, S.5
Lee, K.H.6
Badders, N.7
Valentine, M.8
Miller, B.L.9
Wong, P.C.10
Petrucelli, L.11
Kim, H.J.12
Gao, F.B.13
Taylor, J.P.14
-
25
-
-
84890803688
-
Autophagy and apoptosis dysfunction in neurodegenerative disorders
-
Ghavami, S., Shojaei, S., Yeganeh, B., Ande, S.R., Jangamreddy, J.R., Mehrpour, M., Christoffersson, J., Chaabane, W., Moghadam, A.R., Kashani, H.H., Hashemi, M., Owji, A.A., Łos, M.J., Autophagy and apoptosis dysfunction in neurodegenerative disorders. Prog. Neurobiol. 112 (2014), 24–49.
-
(2014)
Prog. Neurobiol.
, vol.112
, pp. 24-49
-
-
Ghavami, S.1
Shojaei, S.2
Yeganeh, B.3
Ande, S.R.4
Jangamreddy, J.R.5
Mehrpour, M.6
Christoffersson, J.7
Chaabane, W.8
Moghadam, A.R.9
Kashani, H.H.10
Hashemi, M.11
Owji, A.A.12
Łos, M.J.13
-
26
-
-
84920755855
-
Unmasking the messenger
-
Hutten, S., Sharangdhar, T., Kiebler, M., Unmasking the messenger. RNA Biol. 11 (2014), 992–997.
-
(2014)
RNA Biol.
, vol.11
, pp. 992-997
-
-
Hutten, S.1
Sharangdhar, T.2
Kiebler, M.3
-
27
-
-
77956277960
-
Ubiquitin-mediated mRNP dynamics and surveillance prior to budding yeast mRNA export
-
Iglesias, N., Tutucci, E., Gwizdek, C., Vinciguerra, P., Von Dach, E., Corbett, A.H., Dargemont, C., Stutz, F., Ubiquitin-mediated mRNP dynamics and surveillance prior to budding yeast mRNA export. Genes Dev. 24 (2010), 1927–1938.
-
(2010)
Genes Dev.
, vol.24
, pp. 1927-1938
-
-
Iglesias, N.1
Tutucci, E.2
Gwizdek, C.3
Vinciguerra, P.4
Von Dach, E.5
Corbett, A.H.6
Dargemont, C.7
Stutz, F.8
-
28
-
-
84902185820
-
RNA helicase proteins as chaperones and remodelers
-
Jarmoskaite, I., Russell, R., RNA helicase proteins as chaperones and remodelers. Annu. Rev. Biochem. 83 (2014), 697–725.
-
(2014)
Annu. Rev. Biochem.
, vol.83
, pp. 697-725
-
-
Jarmoskaite, I.1
Russell, R.2
-
29
-
-
44049097065
-
A yeast TDP-43 proteinopathy model: exploring the molecular determinants of TDP-43 aggregation and cellular toxicity
-
Johnson, B.S., McCaffery, J.M., Lindquist, S., Gitler, A.D., A yeast TDP-43 proteinopathy model: exploring the molecular determinants of TDP-43 aggregation and cellular toxicity. Proc. Natl. Acad. Sci. U. S. A. 105 (2008), 6439–6444.
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 6439-6444
-
-
Johnson, B.S.1
McCaffery, J.M.2
Lindquist, S.3
Gitler, A.D.4
-
30
-
-
78649941297
-
Exome sequencing reveals VCP mutations as a cause of familial ALS
-
Johnson, J.O., Mandrioli, J., Benatar, M., Abramzon, Y., Van Deerlin, V.M., Trojanowski, J.Q., Gibbs, J.R., Brunetti, M., Gronka, S., Wuu, J., Ding, J., McCluskey, L., Martinez-Lage, M., Falcone, D., Hernandez, D.G., Arepalli, S., Chong, S., Schymick, J.C., Rothstein, J., Landi, F., Wang, Y.D., Calvo, A., Mora, G., Sabatelli, M., Monsurrò, M.R., Battistini, S., Salvi, F., Spataro, R., Sola, P., Borghero, G., ITALSGEN Consortium, Galassi, G., Scholz, S.W., Taylor, J.P., Restagno, G., Chiò, A., Traynor, B.J., Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 68 (2010), 857–864.
-
(2010)
Neuron
, vol.68
, pp. 857-864
-
-
Johnson, J.O.1
Mandrioli, J.2
Benatar, M.3
Abramzon, Y.4
Van Deerlin, V.M.5
Trojanowski, J.Q.6
Gibbs, J.R.7
Brunetti, M.8
Gronka, S.9
Wuu, J.10
Ding, J.11
McCluskey, L.12
Martinez-Lage, M.13
Falcone, D.14
Hernandez, D.G.15
Arepalli, S.16
Chong, S.17
Schymick, J.C.18
Rothstein, J.19
Landi, F.20
Wang, Y.D.21
Calvo, A.22
Mora, G.23
Sabatelli, M.24
Monsurrò, M.R.25
Battistini, S.26
Salvi, F.27
Spataro, R.28
Sola, P.29
Borghero, G.30
ITALSGEN Consortium31
Galassi, G.32
Scholz, S.W.33
Taylor, J.P.34
Restagno, G.35
Chiò, A.36
Traynor, B.J.37
more..
-
31
-
-
84940426318
-
Modifiers of C9orf72 dipeptide repeat toxicity connect nucleocytoplasmic transport defects to FTD/ALS
-
Jovičić, A., Mertens, J., Boeynaems, S., Bogaert, E., Chai, N., Yamada, S.B., Paul, J.W. 3rd, Sun, S., Herdy, J.R., Bieri, G., Kramer, N.J., Gage, F.H., Van Den Bosch, L., Robberecht, W., Gitler, A.D., Modifiers of C9orf72 dipeptide repeat toxicity connect nucleocytoplasmic transport defects to FTD/ALS. Neurosci 18 (2015), 1226–1229.
-
(2015)
Neurosci
, vol.18
, pp. 1226-1229
-
-
Jovičić, A.1
Mertens, J.2
Boeynaems, S.3
Bogaert, E.4
Chai, N.5
Yamada, S.B.6
Paul, J.W.7
Sun, S.8
Herdy, J.R.9
Bieri, G.10
Kramer, N.J.11
Gage, F.H.12
Van Den Bosch, L.13
Robberecht, W.14
Gitler, A.D.15
-
32
-
-
84924489696
-
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
-
Kaneb, H.M., Folkmann, A.W., Belzil, V.V., Jao, L.E., Leblond, C.S., Girard, S.L., Daoud, H., Noreau, A., Rochefort, D., Hince, P., Szuto, A., Levert, A., Vidal, S., André-Guimont, C., Camu, W., Bouchard, J.P., Dupré, N., Rouleau, G.A., Wente, S.R., Dion, P.A., Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis. Hum. Mol. Genet. 24 (2015), 1363–1373.
-
(2015)
Hum. Mol. Genet.
, vol.24
, pp. 1363-1373
-
-
Kaneb, H.M.1
Folkmann, A.W.2
Belzil, V.V.3
Jao, L.E.4
Leblond, C.S.5
Girard, S.L.6
Daoud, H.7
Noreau, A.8
Rochefort, D.9
Hince, P.10
Szuto, A.11
Levert, A.12
Vidal, S.13
André-Guimont, C.14
Camu, W.15
Bouchard, J.P.16
Dupré, N.17
Rouleau, G.A.18
Wente, S.R.19
Dion, P.A.20
more..
-
33
-
-
0034638837
-
Dynamic shuttling of TIA-1 accompanies the recruitment of mRNA to mammalian stress granules
-
Kedersha, N., Cho, M.R., Li, W., Yacono, P.W., Chen, S., Gilks, N., Golan, D.E., Anderson, P., Dynamic shuttling of TIA-1 accompanies the recruitment of mRNA to mammalian stress granules. J. Cell Biol. 151 (2000), 1257–1268.
-
(2000)
J. Cell Biol.
, vol.151
, pp. 1257-1268
-
-
Kedersha, N.1
Cho, M.R.2
Li, W.3
Yacono, P.W.4
Chen, S.5
Gilks, N.6
Golan, D.E.7
Anderson, P.8
-
34
-
-
0037417412
-
An essential role for hGle1 nucleocytoplasmic shuttling in mRNA export
-
Kendirgi, F., Barry, D.M., Griffis, E.R., Powers, M.A., Wente, S.R., An essential role for hGle1 nucleocytoplasmic shuttling in mRNA export. J. Cell Biol. 160 (2003), 1029–1040.
-
(2003)
J. Cell Biol.
, vol.160
, pp. 1029-1040
-
-
Kendirgi, F.1
Barry, D.M.2
Griffis, E.R.3
Powers, M.A.4
Wente, S.R.5
-
35
-
-
24344457631
-
Interaction between the shuttling mRNA export factor Gle1 and the nucleoporin hCG1: a conserved mechanism in the export of Hsp70 mRNA
-
Kendirgi, F., Rexer, D.J., Alcázar-Román, A.R., Onishko, H.M., Wente, S.R., Interaction between the shuttling mRNA export factor Gle1 and the nucleoporin hCG1: a conserved mechanism in the export of Hsp70 mRNA. Mol. Biol. Cell 16 (2005), 4304–4315.
-
(2005)
Mol. Biol. Cell
, vol.16
, pp. 4304-4315
-
-
Kendirgi, F.1
Rexer, D.J.2
Alcázar-Román, A.R.3
Onishko, H.M.4
Wente, S.R.5
-
36
-
-
84875605133
-
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
-
Kim, H.J., Kim, N.C., Wang, Y.D., Scarborough, E.A., Moore, J., Diaz, Z., MacLea, K.S., Freibaum, B., Li, S., Molliex, A., Kanagaraj, A.P., Carter, R., Boylan, K.B., Wojtas, A.M., Rademakers, R., Pinkus, J.L., Greenberg, S.A., Trojanowski, J.Q., Traynor, B.J., Smith, B.N., Topp, S., Gkazi, A.S., Miller, J., Shaw, C.E., Kottlors, M., Kirschner, J., Pestronk, A., Li, Y.R., Ford, A.F., Gitler, A.D., Benatar, M., King, O.D., Kimonis, V.E., Ross, E.D., Weihl, C.C., Shorter, J., Taylor, J.P., Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS. Nature 495 (2013), 467–473.
-
(2013)
Nature
, vol.495
, pp. 467-473
-
-
Kim, H.J.1
Kim, N.C.2
Wang, Y.D.3
Scarborough, E.A.4
Moore, J.5
Diaz, Z.6
MacLea, K.S.7
Freibaum, B.8
Li, S.9
Molliex, A.10
Kanagaraj, A.P.11
Carter, R.12
Boylan, K.B.13
Wojtas, A.M.14
Rademakers, R.15
Pinkus, J.L.16
Greenberg, S.A.17
Trojanowski, J.Q.18
Traynor, B.J.19
Smith, B.N.20
Topp, S.21
Gkazi, A.S.22
Miller, J.23
Shaw, C.E.24
Kottlors, M.25
Kirschner, J.26
Pestronk, A.27
Li, Y.R.28
Ford, A.F.29
Gitler, A.D.30
Benatar, M.31
King, O.D.32
Kimonis, V.E.33
Ross, E.D.34
Weihl, C.C.35
Shorter, J.36
Taylor, J.P.37
more..
-
37
-
-
84895822652
-
Therapeutic modulation of eIF2α phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models
-
Kim, H.J., Raphael, A.R., LaDow, E.S., McGurk, L., Weber, R.A., Trojanowski, J.Q., Lee, V.M., Finkbeiner, S., Gitler, A.D., Bonini, N.M., Therapeutic modulation of eIF2α phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models. Nat. Genet. 46 (2014), 152–160.
-
(2014)
Nat. Genet.
, vol.46
, pp. 152-160
-
-
Kim, H.J.1
Raphael, A.R.2
LaDow, E.S.3
McGurk, L.4
Weber, R.A.5
Trojanowski, J.Q.6
Lee, V.M.7
Finkbeiner, S.8
Gitler, A.D.9
Bonini, N.M.10
-
38
-
-
84862151933
-
The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease
-
King, O.D., Gitler, A.D., Shorter, J., The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease. Brain Res. 1462 (2012), 61–80.
-
(2012)
Brain Res.
, vol.1462
, pp. 61-80
-
-
King, O.D.1
Gitler, A.D.2
Shorter, J.3
-
39
-
-
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., Kaneko, S., Nakano, S., Kusaka, H., Nuclear contour irregularity and abnormal transporter protein distribution in anterior horn cells in amyotrophic lateral sclerosis. J. Neuropathol. Exp. Neurol. 68 (2009), 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
Kaneko, S.7
Nakano, S.8
Kusaka, H.9
-
40
-
-
61349156118
-
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
-
Kwiatkowski, T.J. Jr., Bosco, D.A., Leclerc, A.L., Tamrazian, E., Vanderburg, C.R., Russ, C., Davis, A., Gilchrist, J., Kasarskis, E.J., Munsat, T., Valdmanis, P., Rouleau, G.A., Hosler, B.A., Cortelli, P., de Jong, P.J., Yoshinaga, Y., Haines, J.L., Pericak-Vance, M.A., Yan, J., Ticozzi, N., Siddique, T., McKenna-Yasek, D., Sapp, P.C., Horvitz, H.R., Landers, J.E., Brown, R.H. Jr., Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323 (2009), 1205–1208.
-
(2009)
Science
, vol.323
, pp. 1205-1208
-
-
Kwiatkowski, T.J.1
Bosco, D.A.2
Leclerc, A.L.3
Tamrazian, E.4
Vanderburg, C.R.5
Russ, C.6
Davis, A.7
Gilchrist, J.8
Kasarskis, E.J.9
Munsat, T.10
Valdmanis, P.11
Rouleau, G.A.12
Hosler, B.A.13
Cortelli, P.14
de Jong, P.J.15
Yoshinaga, Y.16
Haines, J.L.17
Pericak-Vance, M.A.18
Yan, J.19
Ticozzi, N.20
Siddique, T.21
McKenna-Yasek, D.22
Sapp, P.C.23
Horvitz, H.R.24
Landers, J.E.25
Brown, R.H.26
more..
-
41
-
-
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 114 (1991), 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
-
42
-
-
78149461229
-
Tar DNA binding protein-43 (TDP-43) associates with stress granules: analysis of cultured cells and pathological brain tissue
-
Liu-Yesucevitz, L., Bilgutay, A., Zhang, Y.J., Vanderweyde, T., Citro, A., Mehta, T., Zaarur, N., McKee, A., Bowser, R., Sherman, M., Perucelli, L., Wolozin, B., Tar DNA binding protein-43 (TDP-43) associates with stress granules: analysis of cultured cells and pathological brain tissue. PLoS One, 5, 2010, e13250.
-
(2010)
PLoS One
, vol.5
, pp. e13250
-
-
Liu-Yesucevitz, L.1
Bilgutay, A.2
Zhang, Y.J.3
Vanderweyde, T.4
Citro, A.5
Mehta, T.6
Zaarur, N.7
McKee, A.8
Bowser, R.9
Sherman, M.10
Perucelli, L.11
Wolozin, B.12
-
43
-
-
84896298823
-
ALS-linked mutations enlarge TDP-43-enriched neuronal RNA granules in the dendritic arbor
-
Liu-Yesucevitz, L., Lin, A.Y., Ebata, A., Boon, J.Y., Reid, W., Xu, Y.F., Kobrin, K., Murphy, G.J., Petrucelli, L., Wolozin, B., ALS-linked mutations enlarge TDP-43-enriched neuronal RNA granules in the dendritic arbor. J. Neurosci. 34 (2014), 4167–4174.
-
(2014)
J. Neurosci.
, vol.34
, pp. 4167-4174
-
-
Liu-Yesucevitz, L.1
Lin, A.Y.2
Ebata, A.3
Boon, J.Y.4
Reid, W.5
Xu, Y.F.6
Kobrin, K.7
Murphy, G.J.8
Petrucelli, L.9
Wolozin, B.10
-
44
-
-
77953012604
-
Heat shock protein 90 in neurodegenerative diseases
-
Luo, W., Sun, W., Taldone, T., Rodina, A., Chiosis, G., Heat shock protein 90 in neurodegenerative diseases. Mol. Neurodegener., 5, 2010, 24.
-
(2010)
Mol. Neurodegener.
, vol.5
, pp. 24
-
-
Luo, W.1
Sun, W.2
Taldone, T.3
Rodina, A.4
Chiosis, G.5
-
45
-
-
84925379504
-
Altering nuclear pore complex function impacts longevity and mitochondrial function in S. cerevisiae
-
Lord, C.L., Timney, B.L., Rout, M.P., Wente, S.R., Altering nuclear pore complex function impacts longevity and mitochondrial function in S. cerevisiae. J. Cell Biol. 208 (2015), 729–744.
-
(2015)
J. Cell Biol.
, vol.208
, pp. 729-744
-
-
Lord, C.L.1
Timney, B.L.2
Rout, M.P.3
Wente, S.R.4
-
46
-
-
27944474017
-
The DEAD-box protein Dbp5p is required to dissociate Mex67p from exported mRNPs at the nuclear rim
-
Lund, M.K., Guthrie, C., The DEAD-box protein Dbp5p is required to dissociate Mex67p from exported mRNPs at the nuclear rim. Mol. Cell 20 (2005), 645–651.
-
(2005)
Mol. Cell
, vol.20
, pp. 645-651
-
-
Lund, M.K.1
Guthrie, C.2
-
47
-
-
84929660745
-
Phytic acid attenuates inflammatory responses and the levels of NF-κB and p-ERK in MPTP-induced Parkinson's disease model of mice
-
Lv, Y., Zhang, Z., Hou, L., Zhang, L., Zhang, J., Wang, Y., Liu, C., Xu, P., Liu, L., Gai, X., Lu, T., Phytic acid attenuates inflammatory responses and the levels of NF-κB and p-ERK in MPTP-induced Parkinson's disease model of mice. Neurosci. Lett. 597 (2015), 132–136.
-
(2015)
Neurosci. Lett.
, vol.597
, pp. 132-136
-
-
Lv, Y.1
Zhang, Z.2
Hou, L.3
Zhang, L.4
Zhang, J.5
Wang, Y.6
Liu, C.7
Xu, P.8
Liu, L.9
Gai, X.10
Lu, T.11
-
48
-
-
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. 20 (2011), 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
-
49
-
-
84901033525
-
Principles and properties of eukaryotic mRNPs
-
Mitchell, S.F., Parker, R., Principles and properties of eukaryotic mRNPs. Mol. Cell 54 (2014), 547–558.
-
(2014)
Mol. Cell
, vol.54
, pp. 547-558
-
-
Mitchell, S.F.1
Parker, R.2
-
50
-
-
0029745374
-
An RNA-export mediator with an essential nuclear export signal
-
Murphy, R., Wente, S.R., An RNA-export mediator with an essential nuclear export signal. Nature 383 (1996), 357–360.
-
(1996)
Nature
, vol.383
, pp. 357-360
-
-
Murphy, R.1
Wente, S.R.2
-
51
-
-
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 314 (2006), 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
-
52
-
-
38649121433
-
Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease
-
Nousiainen, H.O., Kestilä, M., Pakkasjärvi, N., Honkala, H., Kuure, S., Tallila, J., Vuopala, K., Ignatius, J., Herva, R., Peltonen, L., Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease. Nat. Genet. 40 (2008), 155–157.
-
(2008)
Nat. Genet.
, vol.40
, pp. 155-157
-
-
Nousiainen, H.O.1
Kestilä, M.2
Pakkasjärvi, N.3
Honkala, H.4
Kuure, S.5
Tallila, J.6
Vuopala, K.7
Ignatius, J.8
Herva, R.9
Peltonen, L.10
-
53
-
-
84926076573
-
RNA-binding proteins in neurodegeneration: seq and you shall receive
-
Nussbacher, J.K., Batra, R., Lagier-Tourenne, C., Yeo, G.W., RNA-binding proteins in neurodegeneration: seq and you shall receive. Trends Neurosci. 38 (2015), 226–236.
-
(2015)
Trends Neurosci.
, vol.38
, pp. 226-236
-
-
Nussbacher, J.K.1
Batra, R.2
Lagier-Tourenne, C.3
Yeo, G.W.4
-
54
-
-
84857124994
-
Endogenous TDP-43 localized to stress granules can subsequently form protein aggregates
-
Parker, S.J., Meyerowitz, J., James, J.L., Liddell, J.R., Crouch, P.J., Kanninen, K.M., White, A.R., Endogenous TDP-43 localized to stress granules can subsequently form protein aggregates. Neurochem. Int. 60 (2012), 415–424.
-
(2012)
Neurochem. Int.
, vol.60
, pp. 415-424
-
-
Parker, S.J.1
Meyerowitz, J.2
James, J.L.3
Liddell, J.R.4
Crouch, P.J.5
Kanninen, K.M.6
White, A.R.7
-
55
-
-
80051632945
-
Nuclear transport, oxidative stress, and neurodegeneration
-
Patel, V.P., Chu, C.T., Nuclear transport, oxidative stress, and neurodegeneration. Int. J. Clin. Exp. Pathol. 4 (2011), 215–229.
-
(2011)
Int. J. Clin. Exp. Pathol.
, vol.4
, pp. 215-229
-
-
Patel, V.P.1
Chu, C.T.2
-
56
-
-
84949228570
-
Rodent models of amyotrophic lateral sclerosis
-
Philips, T., Rothstein, J.D., Rodent models of amyotrophic lateral sclerosis. Curr. Protoc. Pharmacol. 69 (2015), 5.67.1–5.67.21.
-
(2015)
Curr. Protoc. Pharmacol.
, vol.69
, pp. 5.67.1-5.67.21
-
-
Philips, T.1
Rothstein, J.D.2
-
57
-
-
84882801549
-
Altered ribostasis: RNA-protein granules in degenerative disorders
-
Ramaswami, M., Taylor, J.P., Parker, R., Altered ribostasis: RNA-protein granules in degenerative disorders. Cell 154 (2013), 727–736.
-
(2013)
Cell
, vol.154
, pp. 727-736
-
-
Ramaswami, M.1
Taylor, J.P.2
Parker, R.3
-
58
-
-
1842571608
-
The mRNA export factor human Gle1 interacts with the nuclear pore complex protein Nup155
-
Rayala, H.J., Kendirgi, F., Barry, D.M., Majerus, P.W., Wente, S.R., The mRNA export factor human Gle1 interacts with the nuclear pore complex protein Nup155. Mol. Cell Proteomics 3 (2004), 145–155.
-
(2004)
Mol. Cell Proteomics
, vol.3
, pp. 145-155
-
-
Rayala, H.J.1
Kendirgi, F.2
Barry, D.M.3
Majerus, P.W.4
Wente, S.R.5
-
59
-
-
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 319 (2008), 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
-
60
-
-
79955502687
-
Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLS
-
Sun, Z., Diaz, Z., Fang, X., Hart, M.P., Chesi, A., Shorter, J., Gitler, A.D., Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLS. PLoS Biol., 9, 2011, e1000614.
-
(2011)
PLoS Biol.
, vol.9
, pp. e1000614
-
-
Sun, Z.1
Diaz, Z.2
Fang, X.3
Hart, M.P.4
Chesi, A.5
Shorter, J.6
Gitler, A.D.7
-
61
-
-
0037451173
-
The RasGAP-associated endoribonuclease G3BP assembles stress granules
-
Tourrière, H., Chebli, K., Zekri, L., Courselaud, B., Blanchard, J.M., Bertrand, E., Tazi, J., The RasGAP-associated endoribonuclease G3BP assembles stress granules. J. Cell Biol. 160 (2003), 823–831.
-
(2003)
J. Cell Biol.
, vol.160
, pp. 823-831
-
-
Tourrière, H.1
Chebli, K.2
Zekri, L.3
Courselaud, B.4
Blanchard, J.M.5
Bertrand, E.6
Tazi, J.7
-
62
-
-
36749016233
-
The DEAD-box protein Dbp5 controls mRNA export by triggering specific RNA:protein remodeling events
-
Tran, E.J., Zhou, Y., Corbett, A.H., Wente, S.R., The DEAD-box protein Dbp5 controls mRNA export by triggering specific RNA:protein remodeling events. Mol. Cell 28 (2007), 850–859.
-
(2007)
Mol. Cell
, vol.28
, pp. 850-859
-
-
Tran, E.J.1
Zhou, Y.2
Corbett, A.H.3
Wente, S.R.4
-
63
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
Vance, C., Rogelj, B., Hortobágyi, T., De Vos, K.J., Nishimura, A.L., Sreedharan, J., Hu, X., Smith, B., Ruddy, D., Wright, P., Ganesalingam, J., Williams, K.L., Tripathi, V., Al-Saraj, S., Al-Chalabi, A., Leigh, P.N., Blair, I.P., Nicholson, G., de Belleroche, J., Gallo, J.M., Miller, C.C., Shaw, C.E., Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 323 (2009), 1208–1211.
-
(2009)
Science
, vol.323
, pp. 1208-1211
-
-
Vance, C.1
Rogelj, B.2
Hortobágyi, T.3
De Vos, K.J.4
Nishimura, A.L.5
Sreedharan, J.6
Hu, X.7
Smith, B.8
Ruddy, D.9
Wright, P.10
Ganesalingam, J.11
Williams, K.L.12
Tripathi, V.13
Al-Saraj, S.14
Al-Chalabi, A.15
Leigh, P.N.16
Blair, I.P.17
Nicholson, G.18
de Belleroche, J.19
Gallo, J.M.20
Miller, C.C.21
Shaw, C.E.22
more..
-
64
-
-
84878565260
-
ALS mutant FUS disrupts nuclear localization and sequesters wild-type FUS within cytoplasmic stress granules
-
Vance, C., Scotter, E.L., Nishimura, A.L., Troakes, C., Mitchell, J.C., Kathe, C., Urwin, H., Manser, C., Miller, C.C., Hortobágyi, T., Dragunow, M., Rogelj, B., Shaw, C.E., ALS mutant FUS disrupts nuclear localization and sequesters wild-type FUS within cytoplasmic stress granules. Hum. Mol. Genet. 22 (2013), 2676–2688.
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 2676-2688
-
-
Vance, C.1
Scotter, E.L.2
Nishimura, A.L.3
Troakes, C.4
Mitchell, J.C.5
Kathe, C.6
Urwin, H.7
Manser, C.8
Miller, C.C.9
Hortobágyi, T.10
Dragunow, M.11
Rogelj, B.12
Shaw, C.E.13
-
65
-
-
39549115452
-
Neuroprotective effect of the natural iron chelator, phytic acid in a cell culture model of Parkinson's disease
-
Xu, Q., Kanthasamy, A.G., Reddy, M.B., Neuroprotective effect of the natural iron chelator, phytic acid in a cell culture model of Parkinson's disease. Toxicology 245 (2008), 101–108.
-
(2008)
Toxicology
, vol.245
, pp. 101-108
-
-
Xu, Q.1
Kanthasamy, A.G.2
Reddy, M.B.3
-
66
-
-
84940923271
-
The C9orf72 repeat expansion disrupts nucleocytoplasmic transport
-
Zhang, K., Donnelly, C.J., Haeusler, A.R., Grima, J.C., Machamer, J.B., Steinwald, P., Daley, E.L., Miller, S.J., Cunningham, K.M., Vidensky, S., Gupta, S., Thomas, M.A., Hong, I., Chiu, S.L., Huganir, R.L., Ostrow, L.W., Matunis, M.J., Wang, Sattler, Lloyd, T.E., Rothstein, J.D., The C9orf72 repeat expansion disrupts nucleocytoplasmic transport. Nature 525 (2015), 56–61.
-
(2015)
Nature
, vol.525
, pp. 56-61
-
-
Zhang, K.1
Donnelly, C.J.2
Haeusler, A.R.3
Grima, J.C.4
Machamer, J.B.5
Steinwald, P.6
Daley, E.L.7
Miller, S.J.8
Cunningham, K.M.9
Vidensky, S.10
Gupta, S.11
Thomas, M.A.12
Hong, I.13
Chiu, S.L.14
Huganir, R.L.15
Ostrow, L.W.16
Matunis, M.J.17
Wang18
Sattler19
Lloyd, T.E.20
Rothstein, J.D.21
more..
-
67
-
-
33750288443
-
Altered distributions of nucleocytoplasmic transport-related proteins in the spinal cord of a mouse model of amyotrophic lateral sclerosis
-
Zhang, J., Ito, H., Wate, R., Ohnishi, S., Nakano, S., Kusaka, H., Altered distributions of nucleocytoplasmic transport-related proteins in the spinal cord of a mouse model of amyotrophic lateral sclerosis. Acta Neuropathol. 112 (2006), 673–680.
-
(2006)
Acta Neuropathol.
, vol.112
, pp. 673-680
-
-
Zhang, J.1
Ito, H.2
Wate, R.3
Ohnishi, S.4
Nakano, S.5
Kusaka, H.6
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