-
1
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
Lefebvre, S. et al. (1995) Identification and characterization of a spinal muscular atrophy-determining gene. Cell 80, 155-165
-
(1995)
Cell
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
-
2
-
-
0027401203
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
DOI 10.1038/362059a0
-
Rosen, D.R. et al. (1993) Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 362, 59-62 (Pubitemid 23087289)
-
(1993)
Nature
, vol.362
, Issue.6415
, pp. 59-62
-
-
Rosen, D.R.1
Siddique, T.2
Patterson, D.3
Figlewicz, D.A.4
Sapp, P.5
Hentati, A.6
Donaldson, D.7
Goto, J.8
O'Regan, J.P.9
Deng, H.-X.10
Rahmani, Z.11
Krizus, A.12
McKenna-Yasek, D.13
Cayabyab, A.14
Gaston, S.M.15
Berger, R.16
Tanzi, R.E.17
Halperin, J.J.18
Herzfeldt, B.19
-
3
-
-
42249102078
-
Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS
-
Turner, B.J. and Talbot, K. (2008) Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS. Progress in Neurobiology 85, 94-134
-
(2008)
Progress in Neurobiology
, vol.85
, pp. 94-134
-
-
Turner, B.J.1
Talbot, K.2
-
4
-
-
0035516124
-
From Charcot to Lou Gehrig: Deciphering selective motor neuron death in ALS
-
DOI 10.1038/35097565
-
Cleveland, D.W. and Rothstein, J.D. (2001) From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS. Nature Reviews Neuroscience 2, 806-819 (Pubitemid 33674062)
-
(2001)
Nature Reviews Neuroscience
, vol.2
, Issue.11
, pp. 806-819
-
-
Cleveland, D.W.1
Rothstein, J.D.2
-
5
-
-
23144448320
-
Molecular and cellular pathways of neurodegeneration in motor neurone disease
-
Shaw, P.J. (2005) Molecular and cellular pathways of neurodegeneration in motor neurone disease. Journal of Neurology Neurosurgeryand Psychiatry 76, 1046-1057
-
(2005)
Journal of Neurology Neurosurgeryand Psychiatry
, vol.76
, pp. 1046-1057
-
-
Shaw, P.J.1
-
6
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
DOI 10.1126/science.1134108
-
Neumann, M. et al. (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314, 130-133 (Pubitemid 44547757)
-
(2006)
Science
, vol.314
, Issue.5796
, 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.-Y.19
-
7
-
-
34249946466
-
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
-
DOI 10.1002/ana.21147
-
Mackenzie, I.R. et al. (2007) Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations. Annals of Neurology 61, 427-434 (Pubitemid 46878770)
-
(2007)
Annals of Neurology
, vol.61
, Issue.5
, pp. 427-434
-
-
Mackenzie, I.R.A.1
Bigio, E.H.2
Ince, P.G.3
Geser, F.4
Neumann, M.5
Cairns, N.J.6
Kwong, L.K.7
Forman, M.S.8
Ravits, J.9
Stewart, H.10
Eisen, A.11
McClusky, L.12
Kretzschmar, H.A.13
Monoranu, C.M.14
Highley, J.R.15
Kirby, J.16
Siddique, T.17
Shaw, P.J.18
Lee, V.M.-Y.19
Trojanowski, J.Q.20
more..
-
8
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
DOI 10.1126/science.1154584
-
Sreedharan, J. et al. (2008) TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis. Science 319, 1668-1672 (Pubitemid 351432505)
-
(2008)
Science
, vol.319
, Issue.5870
, 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
-
9
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
Vance, C. et al. (2009) Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 323, 1208-1211
-
(2009)
Science
, vol.323
, pp. 1208-1211
-
-
Vance, C.1
-
10
-
-
72849106592
-
RNA processing and its regulation: Global insights into biological networks
-
Licatalosi, D.D. and Darnell, R.B (2010) RNA processing and its regulation: global insights into biological networks. Nature Reviews Genetics 11, 75-87
-
(2010)
Nature Reviews Genetics
, vol.11
, pp. 75-87
-
-
Licatalosi, D.D.1
Darnell, R.B.2
-
11
-
-
0019815917
-
A quantitative light microscopic study of the dendrites of cat spinal alpha-motoneurons after intracellular staining with horseradish peroxidase
-
Ulfhake, B. and Kellerth, J.O. (1981) A quantitative light microscopic study of the dendrites of cat spinal alpha-motoneurons after intracellular staining with horseradish peroxidase. Journal of Comparative Neurology 202, 571-583 (Pubitemid 12216132)
-
(1981)
Journal of Comparative Neurology
, vol.202
, Issue.4
, pp. 571-583
-
-
Ulfhake, B.1
Kellerth, J.-O.2
-
12
-
-
46149116992
-
Descending pathways in motor control
-
Lemon, R.N. (2008) Descending pathways in motor control. Annual Review of Neuroscience 31, 195-218
-
(2008)
Annual Review of Neuroscience
, vol.31
, pp. 195-218
-
-
Lemon, R.N.1
-
13
-
-
67749084497
-
Amyotrophic lateral sclerosis-Evolutionary and other perspectives
-
Eisen, A. (2009) Amyotrophic lateral sclerosis-Evolutionary and other perspectives. Muscle and Nerve 40, 297-304
-
(2009)
Muscle and Nerve
, vol.40
, pp. 297-304
-
-
Eisen, A.1
-
14
-
-
0018238065
-
Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy
-
Pearn, J. (1978) Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy. Journal of Medical Genetics 15, 409-413
-
(1978)
Journal of Medical Genetics
, vol.15
, pp. 409-413
-
-
Pearn, J.1
-
15
-
-
0030981541
-
Correlation between severity and SMN protein level in spinal muscular atrophy
-
DOI 10.1038/ng0797-265
-
Lefebvre, S. et al. (1997) Correlation between severity and SMN protein level in spinal muscular atrophy. Nature Genetics 16, 265-269 (Pubitemid 27280210)
-
(1997)
Nature Genetics
, vol.16
, Issue.3
, pp. 265-269
-
-
Lefebvre, S.1
Burlet, P.2
Liu, Q.3
Bertrandy, S.4
Clermont, O.5
Munnich, A.6
Dreyfuss, G.7
Melki, J.8
-
16
-
-
0030931720
-
Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos
-
DOI 10.1073/pnas.94.18.9920
-
Schrank, B. et al. (1997) Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos. Proceedings of the National Academy of Sciences of the United States of America 94, 9920-9925 (Pubitemid 27408166)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.18
, pp. 9920-9925
-
-
Schrank, B.1
Gotz, R.2
Gunnersen, J.M.3
Ure, J.M.4
Toyka, K.V.5
Smith, A.G.6
Sendtner, M.7
-
17
-
-
0036207384
-
Listening to silence and understanding nonsense: Exonic mutations that affect splicing
-
DOI 10.1038/nrg775
-
Cartegni, L., Chew, S.L. and Krainer, A.R. (2002) Listening to silence and understanding nonsense: exonic mutations that affect splicing. Nature Reviews Genetics 3, 285-298 (Pubitemid 34279797)
-
(2002)
Nature Reviews Genetics
, vol.3
, Issue.4
, pp. 285-298
-
-
Cartegni, L.1
Chew, S.L.2
Krainer, A.R.3
-
18
-
-
0041665176
-
A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy
-
DOI 10.1038/ng1207
-
Kashima, T. and Manley, J.L. (2003) A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy. Nature Genetics 34, 460-463 (Pubitemid 36935342)
-
(2003)
Nature Genetics
, vol.34
, Issue.4
, pp. 460-463
-
-
Kashima, T.1
Manley, J.L.2
-
19
-
-
0032799998
-
A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2
-
DOI 10.1093/hmg/8.7.1177
-
Monani, U.R. et al. (1999) A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2. Human Molecular Genetics 8, 1177-1183 (Pubitemid 29328985)
-
(1999)
Human Molecular Genetics
, vol.8
, Issue.7
, pp. 1177-1183
-
-
Monani, U.R.1
Lorson, C.L.2
Parsons, D.W.3
Prior, T.W.4
Androphy, E.J.5
Burghes, A.H.M.6
McPherson, J.D.7
-
21
-
-
0031420149
-
Different entities of proximal spinal muscular atrophy within one family
-
DOI 10.1007/s004390050572
-
Wirth, B. et al. (1997) Different entities of proximal spinal muscular atrophy within one family. Human Genetics 100, 676-680 (Pubitemid 28072375)
-
(1997)
Human Genetics
, vol.100
, Issue.5-6
, pp. 676-680
-
-
Wirth, B.1
Tessarolo, D.2
Hahnen, E.3
Rudnik-Schoneborn, S.4
Raschke, H.5
Liguori, M.6
Giacanelli, M.7
Zerres, K.8
-
22
-
-
42549088649
-
Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy
-
DOI 10.1126/science.1155085
-
Oprea, G.E. et al. (2008) Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy. Science 320, 524-527 (Pubitemid 351590664)
-
(2008)
Science
, vol.320
, Issue.5875
, pp. 524-527
-
-
Oprea, G.E.1
Krober, S.2
McWhorter, M.L.3
Rossoll, W.4
Muller, S.5
Krawczak, M.6
Bassell, G.J.7
Beattie, C.E.8
Wirth, B.9
-
23
-
-
41449118875
-
Diagnosis and management of motor neurone disease
-
DOI 10.1136/bmj.39493.511759.BE
-
McDermott, C.J. and Shaw, P.J. (2008) Diagnosis and management of motor neurone disease. British Medical Journal 336, 658-662 (Pubitemid 351481237)
-
(2008)
BMJ
, vol.336
, Issue.7645
, pp. 658-662
-
-
McDermott, C.J.1
Shaw, P.J.2
-
25
-
-
54049140363
-
The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis
-
Strong, M.J. (2008) The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis 9, 323-338
-
(2008)
Amyotrophic Lateral Sclerosis
, vol.9
, pp. 323-338
-
-
Strong, M.J.1
-
26
-
-
23844441835
-
Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum
-
Mackenzie, I.R. and Feldman, H.H. (2005) Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum. Journal of Neuropathology and Experimental Neurology 64, 730-739 (Pubitemid 41177114)
-
(2005)
Journal of Neuropathology and Experimental Neurology
, vol.64
, Issue.8
, pp. 730-739
-
-
Mackenzie, I.R.A.1
Feldman, H.H.2
-
27
-
-
0034326242
-
Cognitive change in motor neurone disease/amyotrophic lateral sclerosis (MND/ALS)
-
Neary, D., Snowden, J.S. and Mann, D.M. (2000) Cognitive change in motor neurone disease/amyotrophic lateral sclerosis (MND/ALS). Journal of the Neurological Sciences 180, 15-20
-
(2000)
Journal of the Neurological Sciences
, vol.180
, pp. 15-20
-
-
Neary, D.1
Snowden, J.S.2
Mann, D.M.3
-
28
-
-
33750716074
-
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
DOI 10.1016/j.bbrc.2006.10.093, PII S0006291X06023187
-
Arai, T. et al. (2006) TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochemical and Biophysical Research Communications 351, 602-611 (Pubitemid 44708852)
-
(2006)
Biochemical and Biophysical Research Communications
, vol.351
, Issue.3
, 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
-
29
-
-
41949119043
-
TDP-43 A315T mutation in familial motor neuron disease
-
DOI 10.1002/ana.21344
-
Gitcho, M.A. et al. (2008) TDP-43 A315T mutation in familial motor neuron disease. Annals of Neurology 63, 535-538 (Pubitemid 351614720)
-
(2008)
Annals of Neurology
, vol.63
, Issue.4
, 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 III, 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
-
30
-
-
70350721803
-
Mutation within TARDBP leads to Frontotemporal Dementia without motor neuron disease
-
Borroni, B. et al. (2009) Mutation within TARDBP leads to Frontotemporal Dementia without motor neuron disease. Human Mutation 30, E974-983
-
(2009)
Human Mutation
, vol.30
-
-
Borroni, B.1
-
31
-
-
40349102131
-
Prevalence of SOD1 mutations in the Italian ALS population
-
DOI 10.1212/01.wnl.0000299187.90432.3f, PII 0000611420080212000008
-
Chiò, A et al. (2008) Prevalence of SOD1 mutations in the Italian ALS population. Neurology. 70, 533-7 (Pubitemid 351653378)
-
(2008)
Neurology
, vol.70
, Issue.7
, pp. 533-537
-
-
Chio, A.1
Traynor, B.J.2
Lombardo, F.3
Fimognari, M.4
Calvo, A.5
Ghiglione, P.6
Mutani, R.7
Restagno, G.8
-
32
-
-
37749032923
-
Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004
-
O'Toole, O. et al. (2008) Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004. Journal of Neurology Neurosurgery and Psychiatry 79, 30-32
-
(2008)
Journal of Neurology Neurosurgery and Psychiatry
, vol.79
, pp. 30-32
-
-
O'Toole, O.1
-
33
-
-
33645422711
-
ANG mutations segregate with familial and 'sporadic'amyotrophic lateral sclerosis
-
Greenway, M.J. et al. (2006) ANG mutations segregate with familial and 'sporadic'amyotrophic lateral sclerosis. Nature Genetics 38, 411-413
-
(2006)
Nature Genetics
, vol.38
, pp. 411-413
-
-
Greenway, M.J.1
-
35
-
-
70349581626
-
ALS motor phenotype heterogeneity, focality, and spread: Deconstructing motor neuron degeneration
-
Ravits, J.M. and La Spada, A.R. (2009) ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration. Neurology 73, 805-811
-
(2009)
Neurology
, vol.73
, pp. 805-811
-
-
Ravits, J.M.1
La Spada, A.R.2
-
36
-
-
33750992481
-
The molecular genetics of non-ALS motor neuron diseases
-
DOI 10.1016/j.bbadis.2006.04.003, PII S092544390600072X
-
James, P.A. and Talbot, K. (2006) The molecular genetics of non-ALS motor neuron diseases. Biochimica et Biophysica Acta 1762, 986-1000 (Pubitemid 44750576)
-
(2006)
Biochimica et Biophysica Acta - Molecular Basis of Disease
, vol.1762
, Issue.11-12
, pp. 986-1000
-
-
James, P.A.1
Talbot, K.2
-
37
-
-
0141560434
-
Alternative splicing in the nervous system: An emerging source of diversity and regulation
-
DOI 10.1016/S0006-3223(03)00375-5
-
Lee, C.J. and Irizarry, K. (2003) Alternative splicing in the nervous system: an emerging source of diversity and regulation. Biological Psychiatry 54, 771-776 (Pubitemid 37205128)
-
(2003)
Biological Psychiatry
, vol.54
, Issue.8
, pp. 771-776
-
-
Lee, C.J.1
Irizarry, K.2
-
38
-
-
35548940665
-
Neuronal regulation of alternative pre-mRNA splicing
-
DOI 10.1038/nrn2237, PII NRN2237
-
Li, Q., Lee, J.A. and Black, D.L. (2007) Neuronal regulation of alternative pre-mRNA splicing. Nature Reviews Neuroscience 8, 819-831 (Pubitemid 350006218)
-
(2007)
Nature Reviews Neuroscience
, vol.8
, Issue.11
, pp. 819-831
-
-
Li, Q.1
Lee, J.-A.2
Black, D.L.3
-
39
-
-
4444318773
-
Alternative splicing of Drosophila Dscam generates axon guidance receptors that exhibit isoform-specific homophilic binding
-
DOI 10.1016/j.cell.2004.08.021, PII S0092867404007962
-
Wojtowicz, W.M. et al. (2004) Alternative splicing of Drosophila Dscam generates axon guidance receptors that exhibit isoform-specific homophilic binding. Cell 118, 619-633 (Pubitemid 39179714)
-
(2004)
Cell
, vol.118
, Issue.5
, pp. 619-633
-
-
Wojtowicz, W.M.1
Flanagan, J.J.2
Millard, S.S.3
Zipursky, S.L.4
Clemens, J.C.5
-
40
-
-
34247536245
-
Dendrite Self-Avoidance Is Controlled by Dscam
-
DOI 10.1016/j.cell.2007.04.013, PII S0092867407004709
-
Matthews, B.J. et al. (2007) Dendrite self-avoidance is controlled by Dscam. Cell 129, 593-604 (Pubitemid 46660975)
-
(2007)
Cell
, vol.129
, Issue.3
, pp. 593-604
-
-
Matthews, B.J.1
Kim, M.E.2
Flanagan, J.J.3
Hattori, D.4
Clemens, J.C.5
Zipursky, S.6
Grueber, W.B.7
-
41
-
-
26944444692
-
A splice code for trans-synaptic cell adhesion mediated by binding of neuroligin 1 to alpha- and beta-neurexins
-
DOI 10.1016/j.neuron.2005.08.026, PII S0896627305007014
-
Boucard, A.A. et al. (2005) A splice code for transsynaptic cell adhesion mediated by binding of neuroligin 1 to alpha- and beta-neurexins. Neuron 48, 229-236 (Pubitemid 41476357)
-
(2005)
Neuron
, vol.48
, Issue.2
, pp. 229-236
-
-
Boucard, A.A.1
Chubykin, A.A.2
Comoletti, D.3
Taylor, P.4
Sudhof, T.C.5
-
42
-
-
13544269142
-
Control of excitatory and inhibitory synapse formation by neuroligins
-
DOI 10.1126/science.1107470
-
Chih, B., Engelman, H. and Scheiffele, P. (2005) Control of excitatory and inhibitory synapse formation by neuroligins. Science 307, 1324-1328 (Pubitemid 40299984)
-
(2005)
Science
, vol.307
, Issue.5713
, pp. 1324-1328
-
-
Chih, B.1
Engelman, H.2
Scheiffele, P.3
-
43
-
-
33745994650
-
Alternative Splicing Controls Selective Trans-Synaptic Interactions of the Neuroligin-Neurexin Complex
-
DOI 10.1016/j.neuron.2006.06.005, PII S0896627306004582
-
Chih, B., Gollan, L. and Scheiffele, P. (2006) Alternative splicing controls selective transsynaptic interactions of the neuroligin-neurexin complex. Neuron 51, 171-178 (Pubitemid 44063616)
-
(2006)
Neuron
, vol.51
, Issue.2
, pp. 171-178
-
-
Chih, B.1
Gollan, L.2
Scheiffele, P.3
-
44
-
-
33847198227
-
Alternative splicing controls G protein-dependent inhibition of N-type calcium channels in nociceptors
-
Raingo, J., Castiglioni, A.J. and Lipscombe, D. (2007) Alternative splicing controls G protein-dependent inhibition of N-type calcium channels in nociceptors. Nature Neuroscience 10, 285-292
-
(2007)
Nature Neuroscience
, vol.10
, pp. 285-292
-
-
Raingo, J.1
Castiglioni, A.J.2
Lipscombe, D.3
-
45
-
-
60349104299
-
The spliceosome: Design principles of a dynamic RNP machine
-
Wahl, M.C., Will, C.L. and Luhrmann, R. (2009) The spliceosome: design principles of a dynamic RNP machine. Cell 136, 701-718
-
(2009)
Cell
, vol.136
, pp. 701-718
-
-
Wahl, M.C.1
Will, C.L.2
Luhrmann, R.3
-
46
-
-
26844431946
-
Splicing of a rare class of introns by the U12-dependent spliceosome
-
DOI 10.1515/BC.2005.084
-
Will, C.L. and Luhrmann, R. (2005) Splicing of a rare class of introns by the U12-dependent spliceosome. Biological Chemistry 386, 713-724 (Pubitemid 41448152)
-
(2005)
Biological Chemistry
, vol.386
, Issue.8
, pp. 713-724
-
-
Will, C.L.1
Luhrmann, R.2
-
47
-
-
0035735484
-
A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs
-
DOI 10.1038/ncb1101-945
-
Meister, G. et al. (2001) A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs. Nature Cell Biology 3, 945-949 (Pubitemid 34428738)
-
(2001)
Nature Cell Biology
, vol.3
, Issue.11
, pp. 945-949
-
-
Meister, G.1
Buhler, D.2
Pillai, R.3
Lottspeich, F.4
Fischer, U.5
-
48
-
-
2242443509
-
Essential role for the SMN complex in the specificity of snRNP assembly
-
DOI 10.1126/science.1074962
-
Pellizzoni, L., Yong, J. and Dreyfuss, G. (2002) Essential role for the SMN complex in the specificity of snRNP assembly. Science 298, 1775-1779 (Pubitemid 35404118)
-
(2002)
Science
, vol.298
, Issue.5599
, pp. 1775-1779
-
-
Pellizzoni, L.1
Yong, J.2
Dreyfuss, G.3
-
49
-
-
13144293035
-
The neuronal RNA-binding protein Nova-2 is implicated as the autoantigen targeted in POMA patients with dementia
-
DOI 10.1073/pnas.95.22.13254
-
Yang, Y.Y., Yin, G.L. and Darnell, R.B. (1998) The neuronal RNA-binding protein Nova-2 is implicated as the autoantigen targeted in POMA patients with dementia. Proceedings of the National Academy of Sciences of the United States of America 95, 13254-13259 (Pubitemid 28509558)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.22
, pp. 13254-13259
-
-
Yang, Y.Y.L.1
Yin, G.L.2
Darnell, R.B.3
-
50
-
-
0033757702
-
Nova-1 regulates neuronspecific alternative splicing and is essential for neuronal viability
-
Jensen, K.B. et al. (2000) Nova-1 regulates neuronspecific alternative splicing and is essential for neuronal viability. Neuron 25, 359-371
-
(2000)
Neuron
, vol.25
, pp. 359-371
-
-
Jensen, K.B.1
-
51
-
-
33749056769
-
An RNA map predicting Nova-dependent splicing regulation
-
DOI 10.1038/nature05304, PII NATURE05304
-
Ule, J. et al. (2006) An RNA map predicting Nova-dependent splicing regulation. Nature 444, 580-586 (Pubitemid 44864431)
-
(2006)
Nature
, vol.444
, Issue.7119
, pp. 580-586
-
-
Ule, J.1
Stefani, G.2
Mele, A.3
Ruggiu, M.4
Wang, X.5
Taneri, B.6
Gaasterland, T.7
Blencowe, B.J.8
Darnell, R.B.9
-
52
-
-
23044431574
-
Nova regulates brain-specific splicing to shape the synapse
-
DOI 10.1038/ng1610
-
Ule, J. et al. (2005) Nova regulates brain-specific splicing to shape the synapse. Nature Genetics 37, 844-852 (Pubitemid 41077110)
-
(2005)
Nature Genetics
, vol.37
, Issue.8
, pp. 844-852
-
-
Ule, J.1
Ule, A.2
Spencer, J.3
Williams, A.4
Hu, J.-S.5
Cline, M.6
Wang, H.7
Clark, T.8
Fraser, C.9
Ruggiu, M.10
Zeeberg, B.R.11
Kane, D.12
Weinstein, J.N.13
Blume, J.14
Darnell, R.B.15
-
53
-
-
62549111005
-
Rescuing Z+ agrin splicing in Nova null mice restores synapse formation and unmasks a physiologic defect in motor neuron firing
-
Ruggiu, M. et al. (2009) Rescuing Z+ agrin splicing in Nova null mice restores synapse formation and unmasks a physiologic defect in motor neuron firing. Proceedings of the National Academy of Sciences of the United States of America 106, 3513-3518
-
(2009)
Proceedings of the National Academy of Sciences of the United States of America
, vol.106
, pp. 3513-3518
-
-
Ruggiu, M.1
-
54
-
-
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. and Baralle, F.E. (2001) Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9. Journal of Biological Chemistry 276, 36337-36343
-
(2001)
Journal of Biological Chemistry
, vol.276
, pp. 36337-36343
-
-
Buratti, E.1
Baralle, F.E.2
-
55
-
-
0035794665
-
Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping
-
DOI 10.1093/emboj/20.7.1774
-
Buratti, E. et al. (2001) Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping. EMBO Journal 20, 1774-1784 (Pubitemid 32299413)
-
(2001)
EMBO Journal
, vol.20
, Issue.7
, pp. 1774-1784
-
-
Buratti, E.1
Dork, T.2
Zuccato, E.3
Pagani, F.4
Romano, M.5
Baralle, F.E.6
-
56
-
-
2442676753
-
Nuclear factor TDP-43 binds to the polymorphic TG repeats in CFTR intron 8 and causes skipping of exon 9: A functional link with disease penetrance [2]
-
DOI 10.1086/420978
-
Buratti, E. et al. (2004) Nuclear factor TDP-43 binds to the polymorphicTGrepeats inCFTR intron 8 and causes skipping of exon 9: a functional link with disease penetrance. American Journal of Human Genetics 74, 1322-1325 (Pubitemid 38669335)
-
(2004)
American Journal of Human Genetics
, vol.74
, Issue.6
, pp. 1322-1325
-
-
Buratti, E.1
Brindisi, A.2
Pagani, F.3
Baralle, F.E.4
-
57
-
-
32344435621
-
TDP43 depletion rescues aberrant CFTR exon 9 skipping
-
DOI 10.1016/j.febslet.2006.01.052, PII S0014579306001050
-
Ayala, Y.M., Pagani, F. and Baralle, F.E. (2006) TDP43 depletion rescues aberrant CFTR exon 9 skipping. FEBS Letters 580, 1339-1344 (Pubitemid 43221997)
-
(2006)
FEBS Letters
, vol.580
, Issue.5
, pp. 1339-1344
-
-
Ayala, Y.M.1
Pagani, F.2
Baralle, F.E.3
-
58
-
-
27744554553
-
Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene
-
DOI 10.1093/nar/gki897
-
Mercado, P.A. et al. (2005) Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene. Nucleic Acids Research 33, 6000-6010 (Pubitemid 41742619)
-
(2005)
Nucleic Acids Research
, vol.33
, Issue.18
, pp. 6000-6010
-
-
Mercado, P.A.1
Ayala, Y.M.2
Romano, M.3
Buratti, E.4
Baralle, F.E.5
-
59
-
-
67651151305
-
Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo
-
D'Ambrogio, A. et al. (2009) Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo. Nucleic Acids Res 37, 4116-4126
-
(2009)
Nucleic Acids Res
, vol.37
, pp. 4116-4126
-
-
D'Ambrogio, A.1
-
60
-
-
41649106307
-
TDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expression
-
DOI 10.1073/pnas.0800546105
-
Ayala, Y.M., Misteli, T. and Baralle, F.E. (2008) TDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expression. Proceedings of the National Academy of Sciences of the United States of America 105, 3785-3789 (Pubitemid 351723476)
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.10
, pp. 3785-3789
-
-
Ayala, Y.M.1
Misteli, T.2
Baralle, F.E.3
-
61
-
-
57649174592
-
TDP-43 overexpression enhances exon 7 inclusion during the survival of motor neuron pre-mRNA splicing
-
Bose, J.K. et al. (2008) TDP-43 overexpression enhances exon 7 inclusion during the survival of motor neuron pre-mRNA splicing. Journal of Biological Chemistry 283, 28852-28859
-
(2008)
Journal of Biological Chemistry
, vol.283
, pp. 28852-28859
-
-
Bose, J.K.1
-
62
-
-
7244242399
-
Domain architectures and characterization of an RNA-binding protein, TLS
-
DOI 10.1074/jbc.M408552200
-
Iko, Y. et al. (2004) Domain architectures and characterization of an RNA-binding protein, TLS. Journal of Biological Chemistry 279, 44834-44840 (Pubitemid 39430895)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.43
, pp. 44834-44840
-
-
Iko, Y.1
Kodama, T.S.2
Kasai, N.3
Oyama, T.4
Morita, E.H.5
Muto, T.6
Okumura, M.7
Fujii, R.8
Takumi, T.9
Tate, S.-I.10
Morikawa, K.11
-
63
-
-
0032561190
-
Oncoprotein TLS interacts with serine-arginine proteins involved in RNA splicing
-
DOI 10.1074/jbc.273.43.27761
-
Yang, L. et al. (1998) Oncoprotein TLS interacts with serine-arginine proteins involved in RNA splicing. Journal of Biological Chemistry 273, 27761-27764 (Pubitemid 28496059)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.43
, pp. 27761-27764
-
-
Yang, L.1
Embree, L.J.2
Tsai, S.3
Hickstein, D.D.4
-
64
-
-
0344407006
-
Proto-oncoprotein TLS/FUS is associated to the nuclear matrix and complexed with splicing factors PTB, SRm160, and SR proteins
-
DOI 10.1016/S0014-4827(02)00046-0
-
Meissner, M. et al. (2003) Proto-oncoprotein TLS/FUS is associated to the nuclear matrix and complexed with splicing factors PTB, SRm160, and SR proteins. Experimental Cell Research 283, 184-195 (Pubitemid 36269024)
-
(2003)
Experimental Cell Research
, vol.283
, Issue.2
, pp. 184-195
-
-
Meissner, M.1
Lopato, S.2
Gotzmann, J.3
Sauermann, G.4
Barta, A.5
-
65
-
-
26844516084
-
beta-Catenin interacts with the FUS proto-oncogene product and regulates pre-mRNA splicing
-
DOI 10.1053/j.gastro.2005.07.025, PII S0016508505013892
-
Sato, S. et al. (2005) beta-catenin interacts with the FUS proto-oncogene product and regulates pre-mRNA splicing. Gastroenterology 129, 1225-1236 (Pubitemid 41446862)
-
(2005)
Gastroenterology
, vol.129
, Issue.4
, pp. 1225-1236
-
-
Sato, S.1
Idogawa, M.2
Honda, K.3
Fujii, G.4
Kawashima, H.5
Takekuma, K.6
Hoshika, A.7
Hirohashi, S.8
Yamada, T.9
-
66
-
-
0034053964
-
TLS-ERG leukemia fusion protein inhibits RNA splicing mediated by serine-arginine proteins
-
DOI 10.1128/MCB.20.10.3345-3354.2000
-
Yang, L., Embree, L.J. and Hickstein, D.D. (2000) TLS-ERG leukemia fusion protein inhibits RNA splicing mediated by serine-arginine proteins. Molecular and Cellular Biology 20, 3345-3354 (Pubitemid 30243880)
-
(2000)
Molecular and Cellular Biology
, vol.20
, Issue.10
, pp. 3345-3354
-
-
Yang, L.1
Embree, L.J.2
Hickstein, D.D.3
-
67
-
-
0035794162
-
Identification of an RNA binding specificity for the potential splicing factor TLS
-
Lerga, A. et al. (2001) Identification of an RNA binding specificity for the potential splicing factor TLS. Journal of Biological Chemistry 276, 6807-6816
-
(2001)
Journal of Biological Chemistry
, vol.276
, pp. 6807-6816
-
-
Lerga, A.1
-
68
-
-
34247625005
-
Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43
-
DOI 10.1007/s00401-006-0189-y
-
Davidson, Y. et al. (2007) Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43. Acta Neuropathologica 113, 521-533 (Pubitemid 46672598)
-
(2007)
Acta Neuropathologica
, vol.113
, Issue.5
, pp. 521-533
-
-
Davidson, Y.1
Kelley, T.2
Mackenzie, I.R.A.3
Pickering-Brown, S.4
Du, P.D.5
Neary, D.6
Snowden, J.S.7
Mann, D.M.A.8
-
69
-
-
34547663747
-
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions
-
DOI 10.2353/ajpath.2007.070182
-
Cairns, N.J. et al. (2007) TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. American Journal of Pathology 171, 227-240 (Pubitemid 47342406)
-
(2007)
American Journal of Pathology
, vol.171
, Issue.1
, pp. 227-240
-
-
Cairns, N.J.1
Neumann, M.2
Bigio, E.H.3
Holm, I.E.4
Troost, D.5
Hatanpaa, K.J.6
Foong, C.7
White III, C.L.8
Schneider, J.A.9
Kretzschmar, H.A.10
Carter, D.11
Taylor-Reinwald, L.12
Paulsmeyer, K.13
Strider, J.14
Gitcho, M.15
Goate, A.M.16
Morris, J.C.17
Mishra, M.18
Kwong, L.K.19
Stieber, A.20
Xu, Y.21
Forman, M.S.22
Trojanowski, J.Q.23
Lee, V.M.-Y.24
Mackenzie, I.R.A.25
more..
-
70
-
-
61349156118
-
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
-
Kwiatkowski, T.J., Jr. et al. (2009) Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323, 1205-1208
-
(2009)
Science
, vol.323
, pp. 1205-1208
-
-
Kwiatkowski Jr., T.J.1
-
71
-
-
70350673956
-
A new sub-type of frontotemporal lobar degeneration with FUS pathology
-
Neumann, M. et al. (2009) A new sub-type of frontotemporal lobar degeneration with FUS pathology. Brain 132, 2922-2931
-
(2009)
Brain
, vol.132
, pp. 2922-2931
-
-
Neumann, M.1
-
72
-
-
67349271683
-
Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior
-
Feiguin, F. et al. (2009) Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior. FEBS Lett 583, 1586-1592
-
(2009)
FEBS Lett
, vol.583
, pp. 1586-1592
-
-
Feiguin, F.1
-
73
-
-
48249083430
-
The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response
-
Andersson, M.K. et al. (2008) The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response. BMC Cell Biology 9, 37
-
(2008)
BMC Cell Biology
, vol.9
, pp. 37
-
-
Andersson, M.K.1
-
74
-
-
0030272143
-
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS
-
DOI 10.1006/geno.1996.0513
-
Aman, P. et al. (1996) Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS. Genomics 37, 1-8 (Pubitemid 26341827)
-
(1996)
Genomics
, vol.37
, Issue.1
, pp. 1-8
-
-
Aman, P.1
Panagopoulos, I.2
Lassen, C.3
Fioretos, T.4
Mencinger, M.5
Toresson, H.6
Hoglund, M.7
Forster, A.8
Rabbitts, T.H.9
Ron, D.10
Mandahl, N.11
Mitelman, F.12
-
75
-
-
28744434333
-
The activity of the spinal muscular atrophy protein is regulated during development and cellular differentiation
-
DOI 10.1093/hmg/ddi390
-
Gabanella, F. et al. (2005) The activity of the spinal muscular atrophy protein is regulated during development and cellular differentiation. Human Molecular Genetics 14, 3629-3642 (Pubitemid 41754664)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.23
, pp. 3629-3642
-
-
Gabanella, F.1
Carissimi, C.2
Usiello, A.3
Pellizzoni, L.4
-
76
-
-
41549119007
-
Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severityand preferentiallyaffect a subset of spliceosomal snRNPs
-
Gabanella, F. et al. (2007) Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severityand preferentiallyaffect a subset of spliceosomal snRNPs. PLoS One 2, e921
-
(2007)
PLoS One
, vol.2
-
-
Gabanella, F.1
-
77
-
-
43049168361
-
SMN Deficiency Causes Tissue-Specific Perturbations in the Repertoire of snRNAs and Widespread Defects in Splicing
-
DOI 10.1016/j.cell.2008.03.031, PII S0092867408004601
-
Zhang, Z. et al. (2008) SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing. Cell 133, 585-600 (Pubitemid 351636302)
-
(2008)
Cell
, vol.133
, Issue.4
, pp. 585-600
-
-
Zhang, Z.1
Lotti, F.2
Dittmar, K.3
Younis, I.4
Wan, L.5
Kasim, M.6
Dreyfuss, G.7
-
78
-
-
74249094999
-
Alternative splicing events are alte feature of pathology ina mouse model of spinal muscular atrophy
-
Baumer, D. et al. (2009) Alternative splicing events are alte feature of pathology ina mouse model of spinal muscular atrophy. PLoS Genetics 5, e1000773.
-
(2009)
PLoS Genetics
, vol.5
-
-
Baumer, D.1
-
79
-
-
39749188127
-
An aggregate-inducing peripherin isoform generated through intron retention is upregulated in amyotrophic lateral sclerosis and associated with disease pathology
-
DOI 10.1523/JNEUROSCI.3222-07.2008
-
Xiao, S. et al. (2008) An aggregate-inducing peripherin isoform generated through intron retention is upregulated in amyotrophic lateral sclerosis and associated with disease pathology. Journal of Neuroscience 28, 1833-1840 (Pubitemid 351302676)
-
(2008)
Journal of Neuroscience
, vol.28
, Issue.8
, pp. 1833-1840
-
-
Xiao, S.1
Tjostheim, S.2
Sanelli, T.3
McLean, J.R.4
Horne, P.5
Fan, Y.6
Ravits, J.7
Strong, M.J.8
Robertson, J.9
-
80
-
-
77949477815
-
Sporadic ALS has compartment-specific aberrant exon splicing and altered cell-matrix adhesion biology
-
Rabin, S. et al. (2010) Sporadic ALS has compartment-specific aberrant exon splicing and altered cell-matrix adhesion biology. Human Molecular Genetics 19, 313-328
-
(2010)
Human Molecular Genetics
, vol.19
, pp. 313-328
-
-
Rabin, S.1
-
81
-
-
33746206334
-
RNA trafficking and local protein synthesis in dendrites: An overview
-
Martin, K.C. and Zukin, R.S. (2006) RNA trafficking and local protein synthesis in dendrites: an overview. Journal of Neuroscience 26, 7131-7134
-
(2006)
Journal of Neuroscience
, vol.26
, pp. 7131-7134
-
-
Martin, K.C.1
Zukin, R.S.2
-
82
-
-
34248585758
-
The nuclear nurture and cytoplasmic nature of localized mRNPs
-
DOI 10.1016/j.semcdb.2007.01.002, PII S1084952107000249, Mechanisms and biological significance of RNA localization AND Development of ectodermal appendages
-
Giorgi, C. and Moore, M.J. (2007) The nuclear nurture and cytoplasmic nature of localized mRNPs. Seminars in Cell and Developmental Biology 18, 186-193 (Pubitemid 46756360)
-
(2007)
Seminars in Cell and Developmental Biology
, vol.18
, Issue.2
, pp. 186-193
-
-
Giorgi, C.1
Moore, M.J.2
-
83
-
-
0037314639
-
Real-time visualization of ZBP1 association with beta-actin mRNA during transcription and localization
-
DOI 10.1016/S0960-9822(03)00044-7, PII S0960982203000447
-
Oleynikov, Y. and Singer, R.H. (2003) Real-time visualization of ZBP1 association with beta-actin mRNA during transcription and localization. Current Biology 13, 199-207 (Pubitemid 36178297)
-
(2003)
Current Biology
, vol.13
, Issue.3
, pp. 199-207
-
-
Oleynikov, Y.1
Singer, R.H.2
-
84
-
-
63349085410
-
Dendritic LSm1/CBP80-mRNPs mark the early steps of transport commitment and translational control
-
di Penta, A. et al. (2009) Dendritic LSm1/CBP80-mRNPs mark the early steps of transport commitment and translational control. Journal of Cell Biology 184, 423-435
-
(2009)
Journal of Cell Biology
, vol.184
, pp. 423-435
-
-
Di Penta, A.1
-
85
-
-
0037033786
-
A predominantly nuclear protein affecting cytoplasmic localization of beta-actin mRNA in fibroblasts and neurons
-
DOI 10.1083/jcb.200105133
-
Gu, W. et al. (2002) A predominantly nuclear protein affecting cytoplasmic localization of betaactin mRNA in fibroblasts and neurons. Journal of Cell Biology 156, 41-51 (Pubitemid 34846934)
-
(2002)
Journal of Cell Biology
, vol.156
, Issue.1
, pp. 41-51
-
-
Gu, W.1
Pan, F.2
Zhang, H.3
Bassell, G.J.4
Singer, R.H.5
-
86
-
-
0030934410
-
Characterization of a beta-actin mRNA zipcode-binding protein
-
Ross, A.F. et al. (1997) Characterization of a beta-actin mRNA zipcode-binding protein. Molecular and Cellular Biology 17, 2158-2165 (Pubitemid 27133302)
-
(1997)
Molecular and Cellular Biology
, vol.17
, Issue.4
, pp. 2158-2165
-
-
Ross, A.F.1
Oleynikov, Y.2
Kislauskis, E.H.3
Taneja, K.L.4
Singer, R.H.5
-
87
-
-
13544257399
-
How and why does beta-actin mRNA target?
-
DOI 10.1042/BC20040063
-
Condeelis, J. and Singer, R.H. (2005) Howand why does beta-actin mRNA target? Biology of the Cell 97, 97-110 (Pubitemid 40220716)
-
(2005)
Biology of the Cell
, vol.97
, Issue.1
, pp. 97-110
-
-
Condeelis, J.1
Singer, R.H.2
-
88
-
-
0037996871
-
Activity-dependent trafficking and dynamic localization of zipcode binding protein 1 and beta-actin mRNA in dendrites and spines of hippocampal neurons
-
Tiruchinapalli, D.M. et al. (2003) Activity-dependent trafficking and dynamic localization of zipcode binding protein 1 and beta-actin mRNA in dendrites and spines of hippocampal neurons. Journal of Neuroscience 23, 3251-3261 (Pubitemid 36531966)
-
(2003)
Journal of Neuroscience
, vol.23
, Issue.8
, pp. 3251-3261
-
-
Tiruchinapalli, D.M.1
Oleynikov, Y.2
Kelic, S.3
Shenoy, S.M.4
Hartley, A.5
Stanton, P.K.6
Singer, R.H.7
Bassell, G.J.8
-
89
-
-
0035797518
-
Neurotrophin-induced transport of a beta-actin mRNP complex increases beta-actin levels and stimulates growth cone motility
-
DOI 10.1016/S0896-6273(01)00357-9
-
Zhang, H.L. et al. (2001) Neurotrophin-induced transport of a beta-actin mRNP complex increases beta-actin levels and stimulates growth cone motility. Neuron 31, 261-275 (Pubitemid 32762979)
-
(2001)
Neuron
, vol.31
, Issue.2
, pp. 261-275
-
-
Zhang, H.L.1
Eom, T.2
Oleynikov, Y.3
Shenoy, S.M.4
Liebelt, D.A.5
Dictenberg, J.B.6
Singer, R.H.7
Bassell, G.J.8
-
90
-
-
0029808910
-
Translocation of RNA granules in living neurons
-
Knowles, R.B. et al. (1996) Translocation of RNA granules in living neurons. Journal of Neuroscience 16, 7812-7820 (Pubitemid 26405044)
-
(1996)
Journal of Neuroscience
, vol.16
, Issue.24
, pp. 7812-7820
-
-
Knowles, R.B.1
Sabry, J.H.2
Martone, M.E.3
Deerinck, T.J.4
Ellisman, M.H.5
Bassell, G.J.6
Kosik, K.S.7
-
91
-
-
0035923735
-
Neuronal RNA granules: A link between RNA localization and stimulation-dependent translation
-
DOI 10.1016/S0896-6273(01)00508-6
-
Krichevsky, A.M. and Kosik, K.S. (2001) Neuronal RNA granules: a link between RNA localization and stimulation-dependent translation. Neuron 32, 683-696 (Pubitemid 33145201)
-
(2001)
Neuron
, vol.32
, Issue.4
, pp. 683-696
-
-
Krichevsky, A.M.1
Kosik, K.S.2
-
92
-
-
33748526877
-
NeuronalRNA granules: Movers and makers
-
Kiebler, M.A. and Bassell, G.J. (2006)NeuronalRNA granules: movers and makers. Neuron 51, 685-690
-
(2006)
Neuron
, vol.51
, pp. 685-690
-
-
Kiebler, M.A.1
Bassell, G.J.2
-
93
-
-
60149086205
-
MRNA localization: Gene expression in the spatial dimension
-
Martin, K.C. and Ephrussi, A. (2009) mRNA localization: gene expression in the spatial dimension. Cell 136, 719-730
-
(2009)
Cell
, vol.136
, pp. 719-730
-
-
Martin, K.C.1
Ephrussi, A.2
-
94
-
-
33645727310
-
Characterization of an RNA granule from developing brain
-
Elvira, G. et al. (2006) Characterization of an RNA granule from developing brain. Molecular and Cellular Proteomics 5, 635-651
-
(2006)
Molecular and Cellular Proteomics
, vol.5
, pp. 635-651
-
-
Elvira, G.1
-
95
-
-
0032952380
-
The mammalian Staufen protein localizes to the somatodendritic domain of cultured hippocampal neurons: Implications for its involvement in mRNA transport
-
Kiebler, M.A. et al. (1999) The mammalian staufen protein localizes to the somatodendritic domain of cultured hippocampal neurons: implications for its involvement in mRNA transport. Journal of Neuroscience 19, 288-297 (Pubitemid 29028969)
-
(1999)
Journal of Neuroscience
, vol.19
, Issue.1
, pp. 288-297
-
-
Kiebler, M.A.1
Hemraj, I.2
Verkade, P.3
Kohrmann, M.4
Fortes, P.5
Marion, R.M.6
Ortin, J.7
Dotti, C.G.8
-
96
-
-
4143088149
-
Kinesin transports RNA: Isolation and characterization of an RNA-transporting granule
-
DOI 10.1016/j.neuron.2004.07.022, PII S0896627304004635
-
Kanai, Y., Dohmae, N. and Hirokawa, N. (2004) Kinesin transports RNA: isolation and characterization of an RNA-transporting granule. Neuron 43, 513-525 (Pubitemid 39094678)
-
(2004)
Neuron
, vol.43
, Issue.4
, pp. 513-525
-
-
Kanai, Y.1
Dohmae, N.2
Hirokawa, N.3
-
97
-
-
67049155508
-
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis
-
Landers, J.E. et al. (2009) Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences of the United States of America 106, 9004-9009
-
(2009)
Proceedings of the National Academy of Sciences of the United States of America
, vol.106
, pp. 9004-9009
-
-
Landers, J.E.1
-
98
-
-
4143084861
-
Point mutations of the p150 subunit of dynactin (DCTN1) gene ALS
-
Munch, C. et al. (2004) Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS. Neurology 63, 724-726 (Pubitemid 39100836)
-
(2004)
Neurology
, vol.63
, Issue.4
, pp. 724-726
-
-
Munch, C.1
Sedlmeier, R.2
Meyer, T.3
Homberg, V.4
Sperfeld, A.D.5
Kurt, A.6
Prudlo, J.7
Peraus, G.8
Hanemann, C.O.9
Stumm, G.10
Ludolph, A.C.11
-
99
-
-
27644558934
-
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD
-
DOI 10.1002/ana.20631
-
Munch, C. et al. (2005) Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD. Annals of Neurology 58, 777-780 (Pubitemid 41552554)
-
(2005)
Annals of Neurology
, vol.58
, Issue.5
, pp. 777-780
-
-
Munch, C.1
Rosenbohm, A.2
Sperfeld, A.-D.3
Uttner, I.4
Reske, S.5
Krause, B.J.6
Sedlmeier, R.7
Meyer, T.8
Hanemann, C.O.9
Stumm, G.10
Ludolph, A.C.11
-
100
-
-
0037382240
-
Mutant dynactin in motor neuron disease
-
DOI 10.1038/ng1123
-
Puls, I. et al. (2003) Mutant dynactin in motor neuron disease. Nature Genetics 33, 455-456 (Pubitemid 36390002)
-
(2003)
Nature Genetics
, vol.33
, Issue.4
, pp. 455-456
-
-
Puls, I.1
Jonnakuty, C.2
LaMonte, B.H.3
Holzbaur, E.L.F.4
Tokito, M.5
Mann, E.6
Floeter, M.K.7
Bidus, K.8
Drayna, D.9
Oh, S.J.10
Brown Jr., R.H.11
Ludlow, C.L.12
Fischbeck, K.H.13
-
101
-
-
15744378126
-
The RNA binding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology
-
DOI 10.1016/j.cub.2005.01.058
-
Fujii, R. et al. (2005) TheRNAbinding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology. Current Biology 15, 587-593 (Pubitemid 40413401)
-
(2005)
Current Biology
, vol.15
, Issue.6
, pp. 587-593
-
-
Fujii, R.1
Okabe, S.2
Urushido, T.3
Inoue, K.4
Yoshimura, A.5
Tachibana, T.6
Nishikawa, T.7
Hicks, G.G.8
Takumi, T.9
-
102
-
-
30544448358
-
TLS facilitates transport of mRNA encoding an actin-stabilizing protein to dendritic spines
-
DOI 10.1242/jcs.02692
-
Fujii, R. and Takumi, T. (2005) TLS facilitates transport of mRNA encoding an actin-stabilizing protein to dendritic spines. Journal of Cell Science 118, 5755-5765 (Pubitemid 43079269)
-
(2005)
Journal of Cell Science
, vol.118
, Issue.24
, pp. 5755-5765
-
-
Fujii, R.1
Takumi, T.2
-
103
-
-
33751428390
-
Myosin-Va Facilitates the Accumulation of mRNA/Protein Complex in Dendritic Spines
-
DOI 10.1016/j.cub.2006.10.024, PII S0960982206023608
-
Yoshimura, A. et al. (2006) Myosin-Va facilitates the accumulation of mRNA/protein complex in dendritic spines. Current Biology 16, 2345-2351 (Pubitemid 44821840)
-
(2006)
Current Biology
, vol.16
, Issue.23
, pp. 2345-2351
-
-
Yoshimura, A.1
Fujii, R.2
Watanabe, Y.3
Okabe, S.4
Fukui, K.5
Takumi, T.6
-
104
-
-
0036647269
-
Survival motor neuron (SMN) protein: Role in neurite outgrowth and neuromuscular maturation during neuronal differentiation and development
-
Fan, L. and Simard, L.R. (2002) Survival motor neuron (SMN) protein: role in neurite outgrowth and neuromuscular maturation during neuronal differentiation and development. Human Molecular Genetics 11, 1605-1614 (Pubitemid 34812256)
-
(2002)
Human Molecular Genetics
, vol.11
, Issue.14
, pp. 1605-1614
-
-
Fan, L.1
Simard, L.R.2
-
105
-
-
0036154096
-
Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: A role for Smn in RNA processing in motor axons?
-
Rossoll, W. et al. (2002) Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons? Human Molecular Genetics 11, 93-105 (Pubitemid 34100772)
-
(2002)
Human Molecular Genetics
, vol.11
, Issue.1
, pp. 93-105
-
-
Rossoll, W.1
Kroning, A.-K.2
Ohndorf, U.-M.3
Steegborn, C.4
Jablonka, S.5
Sendtner, M.6
-
106
-
-
0035282740
-
Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy
-
Jablonka, S. et al. (2001) Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy. Human Molecular Genetics 10, 497-505 (Pubitemid 32181672)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.5
, pp. 497-505
-
-
Jablonka, S.1
Bandilla, M.2
Wiese, S.3
Buhler, D.4
Wirth, B.5
Sendtner, M.6
Fischer, U.7
-
107
-
-
0032921750
-
Subcellular distribution of survival motor neuron (SMN) protein: Possible involvement in nucleocytoplasmic and dendritic transport
-
DOI 10.1046/j.1460-9568.1999.00428.x
-
Bechade, C. et al. (1999) Subcellular distribution of survival motor neuron (SMN) protein: possible involvement in nucleocytoplasmic and dendritic transport. European Journal of Neuroscience 11, 293-304 (Pubitemid 29012332)
-
(1999)
European Journal of Neuroscience
, vol.11
, Issue.1
, pp. 293-304
-
-
Bechade, C.1
-
108
-
-
0034096078
-
Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cord
-
Pagliardini, S. et al. (2000) Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cord. Human Molecular Genetics 9, 47-56 (Pubitemid 30145287)
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.1
, pp. 47-56
-
-
Pagliardini, S.1
Giavazzi, A.2
Setola, V.3
Lizier, C.4
Di, L.M.5
DeBiasi, S.6
Battaglia, G.7
-
109
-
-
33745597622
-
SMN, the product of the spinal muscular atrophy-determining gene, is expressed widely but selectively in the developing human forebrain
-
DOI 10.1002/cne.21010
-
Briese, M. et al. (2006) SMN, the product of the spinal muscular atrophy-determining gene, is expressed widely but selectively in the developing human forebrain. Journal of Comparative Neurology 497, 808-816 (Pubitemid 43993444)
-
(2006)
Journal of Comparative Neurology
, vol.497
, Issue.5
, pp. 808-816
-
-
Briese, M.1
Richter, D.-U.2
Sattelle, D.B.3
Ulfig, N.4
-
110
-
-
33646810505
-
Neuronal-specific roles of the survival motor neuron protein: Evidence from survival motor neuron expression patterns in the developing human central nervous system
-
Giavazzi, A. et al. (2006) Neuronal-specific roles of the survival motor neuron protein: evidence from survival motor neuron expression patterns in the developing human central nervous system. Journal of Neuropathology and Experimental Neurology 65, 267-277
-
(2006)
Journal of Neuropathology and Experimental Neurology
, vol.65
, pp. 267-277
-
-
Giavazzi, A.1
-
111
-
-
70249095607
-
Spinal muscular atrophy and a model for survival of motor neuron protein function in axonal ribonucleoprotein complexes
-
Rossoll, W. and Bassell, GJ (2009) Spinal muscular atrophy and a model for survival of motor neuron protein function in axonal ribonucleoprotein complexes. Results and Problems in Cell Differentiation. 48, 289-326
-
(2009)
Results and Problems in Cell Differentiation
, vol.48
, pp. 289-326
-
-
Rossoll, W.1
Bassell, G.J.2
-
112
-
-
0042887389
-
Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding
-
DOI 10.1083/jcb.200303168
-
McWhorter, M.L. et al. (2003) Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding. Journal of Cell Biology 162, 919-931 (Pubitemid 37087731)
-
(2003)
Journal of Cell Biology
, vol.162
, Issue.5
, pp. 919-931
-
-
McWhorter, M.L.1
Monani, U.R.2
Burghes, A.H.M.3
Beattie, C.E.4
-
113
-
-
0345599021
-
Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons
-
DOI 10.1083/jcb.200304128
-
Rossoll, W. et al. (2003) Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons. Journal of Cell Biology 163, 801-812 (Pubitemid 37517887)
-
(2003)
Journal of Cell Biology
, vol.163
, Issue.4
, pp. 801-812
-
-
Rossoll, W.1
Jablonka, S.2
Andreassi, C.3
Kroning, A.-K.4
Karle, K.5
Monani, U.R.6
Sendtner, M.7
-
114
-
-
33748186105
-
Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons
-
DOI 10.1523/JNEUROSCI.3967-05.2006
-
Zhang, H. et al. (2006) Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons. Journal of Neuroscience 26, 8622-8632 (Pubitemid 44316191)
-
(2006)
Journal of Neuroscience
, vol.26
, Issue.33
, pp. 8622-8632
-
-
Zhang, H.1
Xing, L.2
Rossoll, W.3
Wichterle, H.4
Singer, R.H.5
Bassell, G.J.6
-
115
-
-
0036809734
-
SMN-mediated assembly of RNPs: A complex story
-
DOI 10.1016/S0962-8924(02)02371-1, PII S0962892402023711
-
Meister, G., Eggert, C. and Fischer, U. (2002) SMN-mediated assembly of RNPs: a complex story. Trends in Cell Biology 12, 472-478 (Pubitemid 35346518)
-
(2002)
Trends in Cell Biology
, vol.12
, Issue.10
, pp. 472-478
-
-
Meister, G.1
Eggert, C.2
Fischer, U.3
-
116
-
-
0036441201
-
Actin cytoskeleton regulation in neuronal morphogenesis and structural plasticity
-
Luo, L. (2002) Actin cytoskeleton regulation in neuronal morphogenesis and structural plasticity. Annual Reviewof Cell and Developmental Biology 18, 601-635
-
(2002)
Annual Reviewof Cell and Developmental Biology
, vol.18
, pp. 601-635
-
-
Luo, L.1
-
117
-
-
34249751076
-
TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein
-
DOI 10.1016/j.mcn.2007.03.007, PII S1044743107000784
-
Strong, M.J. et al. (2007) TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein. Molecular and Cellular Neurosciences 35, 320-327 (Pubitemid 46843567)
-
(2007)
Molecular and Cellular Neuroscience
, vol.35
, Issue.2
, 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
-
118
-
-
42449163952
-
TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive factor
-
Wang, I.F. et al. (2008) TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive factor. Journal of Neurochemistry 105, 797-806
-
(2008)
Journal of Neurochemistry
, vol.105
, pp. 797-806
-
-
Wang, I.F.1
-
119
-
-
34547476995
-
Mutant Cu/Zn-superoxide dismutase associated with amyotrophic lateral sclerosis destabilizes vascular endothelial growth factor mRNA and downregulates its expression
-
DOI 10.1523/JNEUROSCI.1877-07.2007
-
Lu, L. et al. (2007) Mutant Cu/Zn-superoxide dismutase associated with amyotrophic lateral sclerosis destabilizes vascular endothelial growth factor mRNA and downregulates its expression. Journal of Neuroscience 27, 7929-7938 (Pubitemid 47173324)
-
(2007)
Journal of Neuroscience
, vol.27
, Issue.30
, pp. 7929-7938
-
-
Lu, L.1
Zheng, L.2
Viera, L.3
Suswam, E.4
Li, Y.5
Li, X.6
Estevez, A.G.7
King, P.H.8
-
120
-
-
58549102138
-
Mutant copper-zinc superoxide dismutase associated with amyotrophic lateral sclerosis binds to adenine/uridine-rich stability elements in the vascular endothelial growth factor 3′-untranslated region
-
Li, X. et al. (2009) Mutant copper-zinc superoxide dismutase associated with amyotrophic lateral sclerosis binds to adenine/uridine-rich stability elements in the vascular endothelial growth factor 3′-untranslated region. Journal of Neurochemistry 108, 1032-1044
-
(2009)
Journal of Neurochemistry
, vol.108
, pp. 1032-1044
-
-
Li, X.1
-
121
-
-
12844269876
-
Mutant copper-zinc superoxide dismutase binds to and destabilizes human low molecular weight neurofilament mRNA
-
Ge, W.W. et al. (2005) Mutant copper-zinc superoxide dismutase binds to and destabilizes human low molecular weight neurofilament mRNA. Journal of Biological Chemistry 280, 118-124
-
(2005)
Journal of Biological Chemistry
, vol.280
, pp. 118-124
-
-
Ge, W.W.1
-
122
-
-
73949134014
-
TarDNAbinding protein of 43 kDa (TDP-43), 14-3-3 proteins and copper/zinc superoxide dismutase (SOD1) interact to modulate NFL mRNA stability. Implications for altered RNA processing in amyotrophic lateral sclerosis (ALS)
-
Volkening, K. et al. (2009) TarDNAbinding protein of 43 kDa (TDP-43), 14-3-3 proteins and copper/zinc superoxide dismutase (SOD1) interact to modulate NFL mRNA stability. Implications for altered RNA processing in amyotrophic lateral sclerosis (ALS). Brain Research 1305, 168-182
-
(2009)
Brain Research
, vol.1305
, pp. 168-182
-
-
Volkening, K.1
-
123
-
-
56749096054
-
Translational control of localized mRNAs: Restricting protein synthesis in space and time
-
Besse, F. and Ephrussi, A. (2008) Translational control of localized mRNAs: restricting protein synthesis in space and time. Nature Reviews Molecular Cell Biology 9, 971-980
-
(2008)
Nature Reviews Molecular Cell Biology
, vol.9
, pp. 971-980
-
-
Besse, F.1
Ephrussi, A.2
-
124
-
-
51549108502
-
The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP
-
Napoli, I. et al. (2008) The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. Cell 134, 1042-1054
-
(2008)
Cell
, vol.134
, pp. 1042-1054
-
-
Napoli, I.1
-
125
-
-
28544443162
-
Spatial regulation of beta-actin translation by Src-dependent phosphorylation of ZBP1
-
DOI 10.1038/nature04115, PII N04115
-
Huttelmaier, S. et al. (2005) Spatial regulation of beta-actin translation by Src-dependent phosphorylation of ZBP1. Nature 438, 512-515 (Pubitemid 41742024)
-
(2005)
Nature
, vol.438
, Issue.7067
, pp. 512-515
-
-
Huttelmaier, S.1
Zenklusen, D.2
Lederer, M.3
Dictenberg, J.4
Lorenz, M.5
Meng, X.6
Bassell, G.J.7
Condeelis, J.8
Singer, R.H.9
-
126
-
-
0036565678
-
N-methyl-D-aspartate receptor signaling results in Aurora kinase-catalyzed CPEB phosphorylation and alpha CaMKII mRNA polyadenylation at synapses
-
Huang, Y.S. et al. (2002) N-methyl-D-aspartate receptor signaling results in Aurora kinase-catalyzed CPEB phosphorylation and alpha CaMKII mRNA polyadenylation at synapses. EMBO Journal 21, 2139-2148
-
(2002)
EMBO Journal
, vol.21
, pp. 2139-2148
-
-
Huang, Y.S.1
-
127
-
-
0029865777
-
Cortical plaque-like structures identify ribosome-containing domains in the Mauthner cell axon
-
Koenig, E. and Martin, R. (1996) Cortical plaque-like structures identify ribosome-containing domains in the Mauthner cell axon. Journal of Neuroscience 16, 1400-1411 (Pubitemid 26145920)
-
(1996)
Journal of Neuroscience
, vol.16
, Issue.4
, pp. 1400-1411
-
-
Koenig, E.1
Martin, R.2
-
128
-
-
0034668948
-
Cryptic peripheral ribosomal domains distributed intermittently along mammalian myelinated axons
-
Koenig, E. et al. (2000) Cryptic peripheral ribosomal domains distributed intermittently along mammalian myelinated axons. Journal of Neuroscience 20, 8390-8400
-
(2000)
Journal of Neuroscience
, vol.20
, pp. 8390-8400
-
-
Koenig, E.1
-
129
-
-
59049099831
-
A functional equivalent of endoplasmic reticulum and Golgi in axons for secretion of locally synthesized proteins
-
Merianda, T.T. et al. (2009) A functional equivalent of endoplasmic reticulum and Golgi in axons for secretion of locally synthesized proteins. Molecular and Cellular Neurosciences 40, 128-142
-
(2009)
Molecular and Cellular Neurosciences
, vol.40
, pp. 128-142
-
-
Merianda, T.T.1
-
130
-
-
46549085203
-
Function and regulation of local axonal translation
-
Lin, A.C. and Holt, C.E. (2008) Function and regulation of local axonal translation. Current Opinion in Neurobiology 18, 60-68
-
(2008)
Current Opinion in Neurobiology
, vol.18
, pp. 60-68
-
-
Lin, A.C.1
Holt, C.E.2
-
131
-
-
42049103212
-
Local gene expression in axons and nerve endings: The glia-neuron unit
-
DOI 10.1152/physrev.00051.2006
-
Giuditta, A. et al. (2008) Local gene expression in axons and nerve endings: the glia-neuron unit. Physiological Reviews 88, 515-555 (Pubitemid 351520087)
-
(2008)
Physiological Reviews
, vol.88
, Issue.2
, pp. 515-555
-
-
Giuditta, A.1
Jong, T.C.2
Eyman, M.3
Cefaliello, C.4
Bruno, A.P.5
Crispino, M.6
-
132
-
-
33749031843
-
Asymmetrical beta-actin mRNA translation in growth cones mediates attractive turning to netrin-1
-
Leung, K.M. et al. (2006) Asymmetrical beta-actin mRNA translation in growth cones mediates attractive turning to netrin-1. Nature Neuroscience 9, 1247-1256
-
(2006)
Nature Neuroscience
, vol.9
, pp. 1247-1256
-
-
Leung, K.M.1
-
133
-
-
34548056140
-
Local translation and directional steering in axons
-
DOI 10.1038/sj.emboj.7601808, PII 7601808
-
Lin, A.C. and Holt, C.E. (2007) Local translation and directional steering in axons. EMBO Journal 26, 3729-3736 (Pubitemid 47295875)
-
(2007)
EMBO Journal
, vol.26
, Issue.16
, pp. 3729-3736
-
-
Lin, A.C.1
Holt, C.E.2
-
134
-
-
9144273965
-
Axoplasmic importins enable retrograde injury signaling in lesioned nerve
-
DOI 10.1016/S0896-6273(03)00770-0
-
Hanz, S. et al. (2003) Axoplasmic importins enable retrograde injury signaling in lesioned nerve. Neuron 40, 1095-1104 (Pubitemid 38032787)
-
(2003)
Neuron
, vol.40
, Issue.6
, pp. 1095-1104
-
-
Hanz, S.1
Perlson, E.2
Willis, D.3
Zheng, J.-Q.4
Massarwa, R.5
Huerta, J.J.6
Koltzenburg, M.7
Kohler, M.8
Van-Minnen, J.9
Twiss, J.L.10
Fainzilber, M.11
-
135
-
-
47749146105
-
Localized Regulation of Axonal RanGTPase Controls Retrograde Injury Signaling in Peripheral Nerve
-
DOI 10.1016/j.neuron.2008.05.029, PII S0896627308004923
-
Yudin, D. et al. (2008) Localized regulation of axonal RanGTPase controls retrograde injury signaling in peripheral nerve. Neuron 59, 241-252 (Pubitemid 352033684)
-
(2008)
Neuron
, vol.59
, Issue.2
, pp. 241-252
-
-
Yudin, D.1
Hanz, S.2
Yoo, S.3
Iavnilovitch, E.4
Willis, D.5
Gradus, T.6
Vuppalanchi, D.7
Segal-Ruder, Y.8
Ben-Yaakov, K.9
Hieda, M.10
Yoneda, Y.11
Twiss, J.L.12
Fainzilber, M.13
-
136
-
-
65549139891
-
Axonal mRNA in uninjured and regenerating cortical mammalian axons
-
Taylor, A.M. et al. (2009) Axonal mRNA in uninjured and regenerating cortical mammalian axons. Journal of Neuroscience 29, 4697-4707
-
(2009)
Journal of Neuroscience
, vol.29
, pp. 4697-4707
-
-
Taylor, A.M.1
-
137
-
-
19944432196
-
Differential transport and local translation of cytoskeletal, injury-response, and neurodegeneration protein mRNAs in axons
-
DOI 10.1523/JNEUROSCI.4235-04.2005
-
Willis, D. et al. (2005) Differential transport and local translation of cytoskeletal, injury-response, and neurodegeneration protein mRNAs in axons. Journal of Neuroscience 25, 778-791 (Pubitemid 40170992)
-
(2005)
Journal of Neuroscience
, vol.25
, Issue.4
, pp. 778-791
-
-
Willis, D.1
Ka, W.L.2
Zheng, J.-Q.3
Chang, J.H.4
Smit, A.5
Kelly, T.6
Merianda, T.T.7
Sylvester, J.8
Van Minnen, J.9
Twiss, J.L.10
-
138
-
-
44849127752
-
Local translation in primary afferent fibers regulates nociception
-
Jimenez-Diaz, L. et al. (2008) Local translation in primary afferent fibers regulates nociception. PLoS One 3, e1961
-
(2008)
PLoS One
, vol.3
-
-
Jimenez-Diaz, L.1
-
139
-
-
77950864433
-
Dynamics of axonal mRNA transport and implications for peripheral nerve regeneration
-
Yoo, S. et al. (2010) Dynamics of axonal mRNA transport and implications for peripheral nerve regeneration. Experimental Neurology 223, 19-27
-
(2010)
Experimental Neurology
, vol.223
, pp. 19-27
-
-
Yoo, S.1
-
140
-
-
0038067742
-
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V
-
DOI 10.1086/375039
-
Antonellis, A. et al. (2003) Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. American Journal of HumanGenetics 72, 1293-1299 (Pubitemid 36530017)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.5
, pp. 1293-1299
-
-
Antonellis, A.1
Ellsworth, R.E.2
Sambuughin, N.3
Puls, I.4
Abel, A.5
Lee-Lin, S.-Q.6
Jordanova, A.7
Kremensky, I.8
Christodoulou, K.9
Middleton, L.T.10
Sivakumar, K.11
Ionasescu, V.12
Funalot, B.13
Vance, J.M.14
Goldfarb, L.G.15
Fischbeck, K.H.16
Green, E.D.17
-
141
-
-
31744448271
-
Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy
-
DOI 10.1038/ng1727, PII NG1727
-
Jordanova, A. et al. (2006) Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy. Nature Genetics 38, 197-202 (Pubitemid 43177233)
-
(2006)
Nature Genetics
, vol.38
, Issue.2
, pp. 197-202
-
-
Jordanova, A.1
Irobi, J.2
Thomas, F.P.3
Van Dijck, P.4
Meerschaert, K.5
Dewil, M.6
Dierick, I.7
Jacobs, A.8
De Vriendt, E.9
Guergueltcheva, V.10
Rao, C.V.11
Tournev, I.12
Gondim, F.A.A.13
D'Hooghe, M.14
Van Gerwen, V.15
Callaerts, P.16
Van Den, B.L.17
Timmermans, J.-P.18
Robberecht, W.19
Gettemans, J.20
Thevelein, J.M.21
De Jonghe, P.22
Kremensky, I.23
Timmerman, V.24
more..
-
143
-
-
75749132024
-
GARS axonopathy - Not every neuron's cup of tRNA
-
Motley, W., Talbot, K. and Fischbeck, K. (2010) GARS axonopathy - not every neuron's cup of tRNA Trends in Neuroscience 33, 59-66
-
(2010)
Trends in Neuroscience
, vol.33
, pp. 59-66
-
-
Motley, W.1
Talbot, K.2
Fischbeck, K.3
-
144
-
-
34347348110
-
Cytoplasmic and mitochondrial protein translation in axonal and dendritic terminal arborization
-
DOI 10.1038/nn1910, PII NN1910
-
Chihara, T., Luginbuhl, D. and Luo, L. (2007) Cytoplasmic and mitochondrial protein translation in axonal and dendritic terminal arborization. Nature Neuroscience 10, 828-837 (Pubitemid 47013428)
-
(2007)
Nature Neuroscience
, vol.10
, Issue.7
, pp. 828-837
-
-
Chihara, T.1
Luginbuhl, D.2
Luo, L.3
-
145
-
-
17944374029
-
Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1
-
DOI 10.1038/ng703
-
Grohmann, K. et al. (2001) Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1. Nature Genetics 29, 75-77 (Pubitemid 32801813)
-
(2001)
Nature Genetics
, vol.29
, Issue.1
, pp. 75-77
-
-
Grohmann, K.1
Schuelke, M.2
Diers, A.3
Hoffmann, K.4
Lucke, B.5
Adams, C.6
Bertini, E.7
Leonhardt-Horti, H.8
Muntoni, F.9
Ouvrier, R.10
Pfeufer, A.11
Rossi, R.12
Van Maldergem, L.13
Wilmshurst, J.M.14
Wienker, T.F.15
Sendtner, M.16
Rudnik-Schoneborn, S.17
Zerres, K.18
Hubner, C.19
-
146
-
-
5744242172
-
Characterization of lghmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1)
-
DOI 10.1093/hmg/ddh222
-
Grohmann, K. et al. (2004) Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1). Human Molecular Genetics 13, 2031-2042 (Pubitemid 39377827)
-
(2004)
Human Molecular Genetics
, vol.13
, Issue.18
, pp. 2031-2042
-
-
Grohmann, K.1
Rossoll, W.2
Kobsar, I.3
Holtmann, B.4
Jablonka, S.5
Wessig, C.6
Stoltenburg-Didinger, G.7
Fischer, U.8
Hubner, C.9
Martini, R.10
Sendtner, M.11
-
147
-
-
63149150048
-
IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1)
-
Guenther, U.P. et al. (2009) IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1). Human Molecular Genetics 18, 1288-1300
-
(2009)
Human Molecular Genetics
, vol.18
, pp. 1288-1300
-
-
Guenther, U.P.1
-
148
-
-
2442658908
-
DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)
-
Chen, Y.Z. et al. (2004) DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). American Journal of Human Genetics 74, 1128-1135
-
(2004)
American Journal of Human Genetics
, vol.74
, pp. 1128-1135
-
-
Chen, Y.Z.1
-
149
-
-
34250775522
-
Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage
-
DOI 10.1083/jcb.200701042
-
Suraweera, A. et al. (2007) Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage. Journal of Cell Biology 177, 969-979 (Pubitemid 46955702)
-
(2007)
Journal of Cell Biology
, vol.177
, Issue.6
, pp. 969-979
-
-
Suraweera, A.1
Becherel, O.J.2
Chen, P.3
Rundle, N.4
Woods, R.5
Nakamura, J.6
Gatei, M.7
Criscuolo, C.8
Filla, A.9
Chessa, L.10
Fusser, M.11
Epe, B.12
Gueven, N.13
Lavin, M.F.14
-
150
-
-
69449101422
-
Functional role for senataxin, defective in ataxia oculomotor apraxia type 2, in transcriptional regulation
-
Suraweera, A. et al. (2009) Functional role for senataxin, defective in ataxia oculomotor apraxia type 2, in transcriptional regulation. Human Molecular Genetics 18, 3384-3396
-
(2009)
Human Molecular Genetics
, vol.18
, pp. 3384-3396
-
-
Suraweera, A.1
-
151
-
-
33745131439
-
Senataxin, the yeast Sen1p orthologue: Characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease
-
Chen, Y.Z. et al. (2006) Senataxin, the yeast Sen1p orthologue: characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease. Neurobiology of Disease 23, 97-108
-
(2006)
Neurobiology of Disease
, vol.23
, pp. 97-108
-
-
Chen, Y.Z.1
-
152
-
-
60849118924
-
Dynein motor contributes to stress granule dynamics in primary neurons
-
Tsai, N.P., Tsui, Y.C. and Wei, L.N. (2009) Dynein motor contributes to stress granule dynamics in primary neurons. Neuroscience 159, 647-656
-
(2009)
Neuroscience
, vol.159
, pp. 647-656
-
-
Tsai, N.P.1
Tsui, Y.C.2
Wei, L.N.3
-
153
-
-
34247252415
-
Convergence of stress granules and protein aggregates in hippocampal cornu ammonis 1 at later reperfusion following global brain ischemia
-
DOI 10.1016/j.neuroscience.2007.01.050, PII S0306452207001029
-
DeGracia, D.J. et al. (2007) Convergence of stress granules and protein aggregates in hippocampal cornu ammonis 1 at later reperfusion following global brain ischemia. Neuroscience 146, 562-572 (Pubitemid 46621138)
-
(2007)
Neuroscience
, vol.146
, Issue.2
, pp. 562-572
-
-
DeGracia, D.J.1
Rudolph, J.2
Roberts, G.G.3
Rafols, J.A.4
Wang, J.5
-
156
-
-
3242699557
-
Global mRNA stabilization preferentially linked to translational repression during the endoplasmic reticulum stress response
-
DOI 10.1128/MCB.24.15.6773-6787.2004
-
Kawai, T. et al. (2004) Global mRNA stabilization preferentially linked to translational repression during the endoplasmic reticulum stress response. Molecular and Cellular Biology 24, 6773-6787 (Pubitemid 38944356)
-
(2004)
Molecular and Cellular Biology
, vol.24
, Issue.15
, pp. 6773-6787
-
-
Kawai, T.1
Fan, J.2
Mazan-Mamczarz, K.3
Gorospe, M.4
-
158
-
-
0037353039
-
An integrated stress response regulates amino acid metabolism and resistance to oxidative stress
-
DOI 10.1016/S1097-2765(03)00105-9
-
Harding, H.P. et al. (2003) An integrated stress response regulates amino acid metabolism and resistance to oxidative stress. Molecular Cell 11, 619-633 (Pubitemid 36385118)
-
(2003)
Molecular Cell
, vol.11
, Issue.3
, pp. 619-633
-
-
Harding, H.P.1
Zhang, Y.2
Zeng, H.3
Novoa, I.4
Lu, P.D.5
Calfon, M.6
Sadri, N.7
Yun, C.8
Popko, B.9
Paules, R.10
Stojdl, D.F.11
Bell, J.C.12
Hettmann, T.13
Leiden, J.M.14
Ron, D.15
-
159
-
-
0036154218
-
Met)-Deficient preinitiation complexes are core constituents of mammalian stress granules
-
DOI 10.1091/mbc.01-05-0221
-
Kedersha, N. et al. (2002) Evidence that ternary complex (eIF2-GTP-tRNA(i)(Met))-deficient preinitiation complexes are core constituents
-
(2002)
Molecular Biology of the Cell
, vol.13
, Issue.1
, pp. 195-210
-
-
Kedersha, N.1
Chen, S.2
Gilks, N.3
Li, W.4
Miller, I.J.5
Stahl, J.6
Anderson, P.7
-
160
-
-
59549094064
-
Structural determinants of the cellular localization and shuttling of TDP-43
-
Ayala, Y.M. et al. (2008) Structural determinants of the cellular localization and shuttling of TDP-43. Journal of Cell Science 121, 3778-3785
-
(2008)
Journal of Cell Science
, vol.121
, pp. 3778-3785
-
-
Ayala, Y.M.1
-
161
-
-
0030746523
-
TLS (FUS) binds RNA in vivo and engages in nucleo-cytoplasmic shuttling
-
Zinszner, H. et al. (1997) TLS (FUS) binds RNA in vivo and engages in nucleo-cytoplasmic shuttling. Journal of Cell Science 110, 1741-1750 (Pubitemid 27352853)
-
(1997)
Journal of Cell Science
, vol.110
, Issue.15
, pp. 1741-1750
-
-
Zinszner, H.1
Sok, J.2
Immanuel, D.3
Yin, Y.4
Ron, D.5
-
162
-
-
0034638837
-
Dynamic shuttling of TIA-1 accompanies the recruitment of mRNA to mammalian stress granules
-
Kedersha, N. et al. (2000) Dynamic shuttling of TIA-1 accompanies the recruitment of mRNA to mammalian stress granules. Journal of Cell Biology 151, 1257-1268
-
(2000)
Journal of Cell Biology
, vol.151
, pp. 1257-1268
-
-
Kedersha, N.1
-
163
-
-
0028928016
-
The RNA-binding protein TIAR is translocated from the nucleus to the cytoplasm during Fas-mediated apoptotic cell death
-
Taupin, J.L. et al. (1995) The RNA-binding protein TIAR is translocated from the nucleus to the cytoplasm during Fas-mediated apoptotic cell death. Proceedings of the National Academy of Sciences of the United States of America 92, 1629-1633
-
(1995)
Proceedings of the National Academy of Sciences of the United States of America
, vol.92
, pp. 1629-1633
-
-
Taupin, J.L.1
-
165
-
-
58049221032
-
Divergent patterns of cytosolic TDP-43 and neuronal progranulin expression following axotomy: Implications for TDP-43 in the physiological response to neuronal injury
-
Moisse, K. et al. (2009) Divergent patterns of cytosolic TDP-43 and neuronal progranulin expression following axotomy: implications for TDP-43 in the physiological response to neuronal injury. Brain Res 1249, 202-211
-
(2009)
Brain Res
, vol.1249
, pp. 202-211
-
-
Moisse, K.1
-
166
-
-
70349292075
-
Cytosolic TDP-43 expression following axotomy is associated with caspase 3 activation in NFL(-/-) mice: Support for a role for TDP-43 in the physiological response to neuronal injury
-
Moisse, K. et al. (2009) Cytosolic TDP-43 expression following axotomy is associated with caspase 3 activation in NFL(-/-) mice: Support for a role for TDP-43 in the physiological response to neuronal injury. Brain Res 1296, 176-86
-
(2009)
Brain Res
, vol.1296
, pp. 176-186
-
-
Moisse, K.1
-
167
-
-
70350135049
-
TDP-43 is recruited to stress granules in conditions of oxidative insult
-
Colombrita, C. et al. (2009) TDP-43 is recruited to stress granules in conditions of oxidative insult. Journal of Neurochemistry 111, 1051-61
-
(2009)
Journal of Neurochemistry
, vol.111
, pp. 1051-1061
-
-
Colombrita, C.1
-
168
-
-
51849117597
-
Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease
-
Fujita, K. et al. (2008) Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease. Acta Neuropathol 116, 439-445
-
(2008)
Acta Neuropathol
, vol.116
, pp. 439-445
-
-
Fujita, K.1
-
169
-
-
70449517359
-
FUS pathology in basophilic inclusion body disease
-
Munoz, D.G. et al. (2009) FUS pathology in basophilic inclusion body disease. Acta Neuropathol 118, 617-627
-
(2009)
Acta Neuropathol
, vol.118
, pp. 617-627
-
-
Munoz, D.G.1
-
170
-
-
20144378698
-
Heme-regulated inhibitor kinase-mediated phosphorylation of eukaryotic translation initiation factor 2 inhibits translation, induces stress granule formation, and mediates survival upon arsenite exposure
-
DOI 10.1074/jbc.M412882200
-
McEwen, E. et al. (2005) Heme-regulated inhibitor kinase-mediated phosphorylation of eukaryotic translation initiation factor 2 inhibits translation, induces stress granule formation, and mediates survival upon arsenite exposure. Journal of Biological Chemistry 280, 16925-16933 (Pubitemid 41389152)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.17
, pp. 16925-16933
-
-
McEwen, E.1
Kedersha, N.2
Song, B.3
Scheuner, D.4
Gilks, N.5
Han, A.6
Chen, J.-J.7
Anderson, P.8
Kaufman, R.J.9
-
171
-
-
33749493493
-
Inhibition of ribosome recruitment induces stress granule formation independently of eukaryotic initiation factor 2alpha phosphorylation
-
DOI 10.1091/mbc.E06-04-0318
-
Mazroui, R. et al. (2006) Inhibition of ribosome recruitment induces stress granule formation independently of eukaryotic initiation factor 2alpha phosphorylation. Molecular Biology of the Cell 17, 4212-4219 (Pubitemid 44522042)
-
(2006)
Molecular Biology of the Cell
, vol.17
, Issue.10
, pp. 4212-4219
-
-
Mazroui, R.1
Sukarieh, R.2
Bordeleau, M.-E.3
Kaufman, R.J.4
Northcote, P.5
Tanaka, J.6
Gallouzi, I.7
Pelletier, J.8
-
172
-
-
65249129859
-
Angiogenin cleaves tRNA and promotes stress-induced translational repression
-
Yamasaki, S. et al. (2009) Angiogenin cleaves tRNA and promotes stress-induced translational repression. Journal of Cell Biology 185, 35-42
-
(2009)
Journal of Cell Biology
, vol.185
, pp. 35-42
-
-
Yamasaki, S.1
-
173
-
-
38649105800
-
Identification of new ANG gene mutations in a large cohort of Italian patients withamyotrophic lateral sclerosis
-
Gellera, C. et al. (2008) Identification of new ANG gene mutations in a large cohort of Italian patients withamyotrophic lateral sclerosis. Neurogenetics 9, 33-40
-
(2008)
Neurogenetics
, vol.9
, pp. 33-40
-
-
Gellera, C.1
-
174
-
-
35448983646
-
Characterization of human angiogenin variants implicated in amyotrophic lateral sclerosis
-
DOI 10.1021/bi701333h
-
Crabtree, B. et al. (2007) Characterization of human angiogenin variants implicated in amyotrophic lateral sclerosis. Biochemistry 46, 11810-11818 (Pubitemid 47623749)
-
(2007)
Biochemistry
, vol.46
, Issue.42
, pp. 11810-11818
-
-
Crabtree, B.1
Thiyagarajan, N.2
Prior, S.H.3
Wilson, P.4
Iyer, S.5
Ferns, T.6
Shapiro, R.7
Brew, K.8
Subramanian, V.9
Acharya, K.R.10
-
175
-
-
37549019664
-
Human angiogenin is a neuroprotective factor and amyotrophic lateral sclerosis associated angiogenin variants affect neurite extension/pathfinding and survival of motor neurons
-
Subramanian, V., Crabtree, B. and Acharya, K.R. (2008) Human angiogenin is a neuroprotective factor and amyotrophic lateral sclerosis associated angiogenin variants affect neurite extension/pathfinding and survival of motor neurons.Human Molecular Genetics 17, 130-149
-
(2008)
Human Molecular Genetics
, vol.17
, pp. 130-149
-
-
Subramanian, V.1
Crabtree, B.2
Acharya, K.R.3
-
176
-
-
0346095163
-
Rpp20 interacts with SMN and is re-distributed into SMN granules in response to stress
-
DOI 10.1016/j.bbrc.2003.12.084
-
Hua, Y. and Zhou, J. (2004) Rpp20 interacts with SMN and is re-distributed into SMN granules in response to stress. Biochemical and Biophysical Research Communications 314, 268-276 (Pubitemid 38058396)
-
(2004)
Biochemical and Biophysical Research Communications
, vol.314
, Issue.1
, pp. 268-276
-
-
Hua, Y.1
Zhou, J.2
-
177
-
-
4143097170
-
Survival motor neuron protein facilitates assembly of stress granules
-
DOI 10.1016/j.febslet.2004.07.010, PII S0014579304008671
-
Hua, Y. and Zhou, J. (2004) Survival motor neuron protein facilitates assembly of stress granules. FEBS Lett 572, 69-74 (Pubitemid 39092515)
-
(2004)
FEBS Letters
, vol.572
, Issue.1-3
, pp. 69-74
-
-
Hua, Y.1
Zhou, J.2
-
178
-
-
58149401820
-
Dendrites of mammalian neurons contain specialized P-body-like structures that respond to neuronal activation
-
Cougot, N. et al. (2008) Dendrites of mammalian neurons contain specialized P-body-like structures that respond to neuronal activation. Journal of Neuroscience 28, 13793-13804
-
(2008)
Journal of Neuroscience
, vol.28
, pp. 13793-13804
-
-
Cougot, N.1
-
179
-
-
57349185922
-
Perplexing bodies: The putative roles of P-bodies in neurons
-
Zeitelhofer, M., Macchi, P. and Dahm, R. (2008) Perplexing bodies: The putative roles of P-bodies in neurons. RNA Biol 5, 244-248
-
(2008)
RNA Biol
, vol.5
, pp. 244-248
-
-
Zeitelhofer, M.1
Macchi, P.2
Dahm, R.3
-
180
-
-
50549094555
-
Dynamic interaction between P-bodies and transport ribonucleoprotein particles in dendrites of mature hippocampal neurons
-
Zeitelhofer, M. et al. (2008) Dynamic interaction between P-bodies and transport ribonucleoprotein particles in dendrites of mature hippocampal neurons. Journal of Neuroscience 28, 7555-7562
-
(2008)
Journal of Neuroscience
, vol.28
, pp. 7555-7562
-
-
Zeitelhofer, M.1
-
181
-
-
27144515901
-
Cell biology: Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies
-
DOI 10.1126/science.1115791
-
Brengues, M., Teixeira, D. and Parker, R. (2005) Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies. Science 310, 486-489 (Pubitemid 41507961)
-
(2005)
Science
, vol.310
, Issue.5747
, pp. 486-489
-
-
Brengues, M.1
Teixeira, D.2
Parker, R.3
-
182
-
-
2442566370
-
Cytoplasmic foci are sites of mRNA decay in human cells
-
DOI 10.1083/jcb.200309008
-
Cougot, N., Babajko, S. and Seraphin, B. (2004) Cytoplasmic foci are sites of mRNA decay in human cells. Journal of Cell Biology 165, 31-40 (Pubitemid 38649174)
-
(2004)
Journal of Cell Biology
, vol.165
, Issue.1
, pp. 31-40
-
-
Cougot, N.1
Babajko, S.2
Seraphin, B.3
-
183
-
-
33744977432
-
Targeting of Aberrant mRNAs to Cytoplasmic Processing Bodies
-
DOI 10.1016/j.cell.2006.04.037, PII S0092867406006192
-
Sheth, U. and Parker, R. (2006) Targeting of aberrant mRNAsto cytoplasmic processing bodies. Cell 125, 1095-1109 (Pubitemid 43866203)
-
(2006)
Cell
, vol.125
, Issue.6
, pp. 1095-1109
-
-
Sheth, U.1
Parker, R.2
-
184
-
-
66249103703
-
RNA granules: Post-transcriptional and epigenetic modulators of gene expression
-
Anderson, P. and Kedersha, N. (2009) RNA granules: post-transcriptional and epigenetic modulators of gene expression. Nature Reviews Molecular Cell Biology 10, 430-436
-
(2009)
Nature Reviews Molecular Cell Biology
, vol.10
, pp. 430-436
-
-
Anderson, P.1
Kedersha, N.2
-
185
-
-
33847417585
-
P Bodies and the Control of mRNA Translation and Degradation
-
DOI 10.1016/j.molcel.2007.02.011, PII S1097276507001116
-
Parker, R. and Sheth, U. (2007) P bodies and the control of mRNA translation and degradation. Molecular Cell 25, 635-646 (Pubitemid 46341926)
-
(2007)
Molecular Cell
, vol.25
, Issue.5
, pp. 635-646
-
-
Parker, R.1
Sheth, U.2
-
186
-
-
9144225636
-
The Microprocessor complex mediates the genesis of microRNAs
-
DOI 10.1038/nature03120
-
Gregory, R.I. et al. (2004) The Microprocessor complex mediates the genesis of microRNAs. Nature 432, 235-240 (Pubitemid 39545855)
-
(2004)
Nature
, vol.432
, Issue.7014
, pp. 235-240
-
-
Gregory, R.I.1
Yan, K.-P.2
Amuthan, G.3
Chendrimada, T.4
Doratotaj, B.5
Cooch, N.6
Shiekhattar, R.7
-
187
-
-
54049150793
-
MicroRNAs: Tiny regulators of synapse function in development and disease
-
Bicker, S. and Schratt, G. (2008) microRNAs: tiny regulators of synapse function in development and disease. Journal of Cellular and Molecular Medicine 12, 1466-1476
-
(2008)
Journal of Cellular and Molecular Medicine
, vol.12
, pp. 1466-1476
-
-
Bicker, S.1
Schratt, G.2
-
188
-
-
60149088848
-
Origins and Mechanisms of miRNAs and siRNAs
-
Carthew, R.W. and Sontheimer, E.J. (2009) Origins and Mechanisms of miRNAs and siRNAs. Cell 136, 642-655
-
(2009)
Cell
, vol.136
, pp. 642-655
-
-
Carthew, R.W.1
Sontheimer, E.J.2
-
189
-
-
33751254116
-
The neuronal microRNA system
-
Kosik, K.S. (2006) The neuronal microRNA system. Nature Reviews Neuroscience 7, 911-920
-
(2006)
Nature Reviews Neuroscience
, vol.7
, pp. 911-920
-
-
Kosik, K.S.1
-
190
-
-
34447261382
-
Cerebellar neurodegeneration in the absence of microRNAs
-
DOI 10.1084/jem.20070823
-
Schaefer, A. et al. (2007) Cerebellar neurodegeneration in the absence of microRNAs. Journal of Experimental Medicine 204, 1553-1558 (Pubitemid 47048023)
-
(2007)
Journal of Experimental Medicine
, vol.204
, Issue.7
, pp. 1553-1558
-
-
Schaefer, A.1
O'Carroll, D.2
Chan, L.T.3
Hillman, D.4
Sugimori, M.5
Llinas, R.6
Greengard, P.7
-
191
-
-
44949139634
-
Dicer inactivation leads to progressive functional and structural degeneration of the mouse retina
-
Damiani, D. et al. (2008) Dicer inactivation leads to progressive functional and structural degeneration of the mouse retina. Journal of Neuroscience 28, 4878-4887
-
(2008)
Journal of Neuroscience
, vol.28
, pp. 4878-4887
-
-
Damiani, D.1
-
192
-
-
34548537573
-
A MicroRNA feedback circuit in midbraindopamine neurons
-
Kim, J. et al. (2007) A MicroRNA feedback circuit in midbraindopamine neurons. Science 317, 1220-1224
-
(2007)
Science
, vol.317
, pp. 1220-1224
-
-
Kim, J.1
-
193
-
-
77955865880
-
Macro role(s) of microRNAs in fragile X syndrome?
-
Li, X. and Jin, P. (2009) Macro role(s) of microRNAs in fragile X syndrome? Neuromolecular Medicine 11, 200-207
-
(2009)
Neuromolecular Medicine
, vol.11
, pp. 200-207
-
-
Li, X.1
Jin, P.2
-
194
-
-
26844498125
-
Medicine: Sequence variants in SLITRK1 are associated with Tourette's syndrome
-
DOI 10.1126/science.1116502
-
Abelson, J.F. et al. (2005) Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science 310, 317-320 (Pubitemid 41457198)
-
(2005)
Science
, vol.310
, Issue.5746
, pp. 317-320
-
-
Abelson, J.F.1
Kwan, K.Y.2
O'Roak, B.J.3
Baek, D.Y.4
Stillman, A.A.5
Morgan, T.M.6
Mathews, C.A.7
Pauls, D.L.8
Rasin, M.-R.9
Gunel, M.10
Davis, N.R.11
Ercan-Sencicek, A.G.12
Guez, D.H.13
Spertus, J.A.14
Leckman, J.F.15
Dure IV, L.S.16
Kurlan, R.17
Singer, H.S.18
Gilbert, D.L.19
Farhi, A.20
Louvi, A.21
Lifton, R.P.22
Sestan, N.23
State, M.W.24
more..
-
195
-
-
33847203593
-
Micro-RNA speciation in fetal, adult and Alzheimer's disease hippocampus
-
Lukiw, W.J. (2007) Micro-RNA speciation in fetal, adult and Alzheimer's disease hippocampus. Neuroreport 18, 297-300
-
(2007)
Neuroreport
, vol.18
, pp. 297-300
-
-
Lukiw, W.J.1
-
196
-
-
33845609985
-
A new role for microRNA pathways: Modulation of degeneration induced by pathogenic human disease proteins
-
Bilen, J., Liu, N. and Bonini, N.M. (2006)A new role for microRNA pathways: modulation of degeneration induced by pathogenic human disease proteins. Cell Cycle 5, 2835-2838 (Pubitemid 44953931)
-
(2006)
Cell Cycle
, vol.5
, Issue.24
, pp. 2835-2838
-
-
Bilen, J.1
Liu, N.2
Bonini, N.M.3
-
197
-
-
33749078547
-
MicroRNA Pathways Modulate Polyglutamine-Induced Neurodegeneration
-
DOI 10.1016/j.molcel.2006.07.030, PII S1097276506005326
-
Bilen, J. et al. (2006) MicroRNA pathways modulate polyglutamine-induced neurodegeneration. Molecular Cell 24, 157-163 (Pubitemid 44466675)
-
(2006)
Molecular Cell
, vol.24
, Issue.1
, pp. 157-163
-
-
Bilen, J.1
Liu, N.2
Burnett, B.G.3
Pittman, R.N.4
Bonini, N.M.5
-
198
-
-
33749568019
-
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
-
DOI 10.1093/hmg/ddl241
-
Gass, J. et al. (2006) Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Human Molecular Genetics 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..
-
199
-
-
56049083010
-
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
-
Rademakers, R. et al. (2008) Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia. Human Molecular Genetics 17, 3631-3642
-
(2008)
Human Molecular Genetics
, vol.17
, pp. 3631-3642
-
-
Rademakers, R.1
-
200
-
-
0035997389
-
RNA editing by adenosine deaminases that act on RNA
-
Bass, B.L. (2002) RNA editing by adenosine deaminases that act on RNA. Annual Review of Biochemistry 71, 817-846
-
(2002)
Annual Review of Biochemistry
, vol.71
, pp. 817-846
-
-
Bass, B.L.1
-
201
-
-
0242573188
-
AMPA receptor tetramerization is mediated by Q/R editing
-
DOI 10.1016/S0896-6273(03)00668-8
-
Greger, I.H. et al. (2003) AMPA receptor tetramerization is mediated by Q/R editing. Neuron 40, 763-774 (Pubitemid 37431036)
-
(2003)
Neuron
, vol.40
, Issue.4
, pp. 763-774
-
-
Greger, I.H.1
Khatri, L.2
Kong, X.3
Ziff, E.B.4
-
202
-
-
0026543243
-
Divalent ion permeability of AMPA receptor channels is dominated by the edited form of a single subunit
-
Burnashev, N. et al. (1992) Divalent ion permeability of AMPA receptor channels is dominated by the edited form of a single subunit. Neuron 8, 189-198
-
(1992)
Neuron
, vol.8
, pp. 189-198
-
-
Burnashev, N.1
-
203
-
-
1542378930
-
Glutamate receptors: RNA editing and death ofmotor neurons
-
Kawahara, Y. et al. (2004) Glutamate receptors: RNA editing and death ofmotor neurons. Nature 427, 801
-
(2004)
Nature
, vol.427
, pp. 801
-
-
Kawahara, Y.1
-
204
-
-
15044346521
-
Deficient RNA editing of GluR2 and neuronal death in amyotropic lateral sclerosis
-
DOI 10.1007/s00109-004-0599-z
-
Kwak, S. and Kawahara, Y. (2005) Deficient RNA editing of GluR2 and neuronal death in amyotropic lateral sclerosis. Journal of Molecular Medicine 83, 110-120 (Pubitemid 40379299)
-
(2005)
Journal of Molecular Medicine
, vol.83
, Issue.2
, pp. 110-120
-
-
Kwak, S.1
Kawahara, Y.2
-
205
-
-
0030808439
-
Oxidative damage to nucleic acids photosensitized by titanium dioxide
-
DOI 10.1016/S0891-5849(97)00068-3, PII S0891584997000683
-
Wamer, W.G., Yin, J.J. and Wei, R.R. (1997) Oxidative damage to nucleic acids photosensitized by titanium dioxide. Free Radical Biology and Medicine 23, 851-858 (Pubitemid 27402610)
-
(1997)
Free Radical Biology and Medicine
, vol.23
, Issue.6
, pp. 851-858
-
-
Wamer, W.G.1
Yin, J.-J.2
Wei, R.R.3
-
206
-
-
33846090651
-
Oxidized messenger RNA induces translation errors
-
DOI 10.1073/pnas.0609737104
-
Tanaka, M., Chock, P.B. and Stadtman, E.R. (2007) Oxidized messenger RNA induces translation errors. Proceedings of the National Academy of Sciences of the United States of America 104, 66-71 (Pubitemid 46067985)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.1
, pp. 66-71
-
-
Tanaka, M.1
Chock, P.B.2
Stadtman, E.R.3
-
207
-
-
34548476954
-
Messenger RNA oxidation is an early event preceding cell death and causes reduced protein expression
-
DOI 10.1096/fj.07-8200com
-
Shan, X., Chang, Y. and Lin, C.L. (2007) Messenger RNA oxidation is an early event preceding cell death and causes reduced protein expression. FASEB Journal 21, 2753-2764 (Pubitemid 47372743)
-
(2007)
FASEB Journal
, vol.21
, Issue.11
, pp. 2753-2764
-
-
Shan, X.1
Chang, Y.2
Lin, C.-L.G.3
-
208
-
-
67349251839
-
RNA oxidation in Alzheimer disease and related neurodegenerative disorders
-
Nunomura, A. et al. (2009) RNA oxidation in Alzheimer disease and related neurodegenerative disorders. Acta Neuropathol 118, 151-166
-
(2009)
Acta Neuropathol
, vol.118
, pp. 151-166
-
-
Nunomura, A.1
-
209
-
-
51349120583
-
Messenger RNA oxidation occurs early in disease pathogenesis and promotes motorneurondegenerationinALS
-
Chang, Y. et al. (2008) Messenger RNA oxidation occurs early in disease pathogenesis and promotes motorneurondegenerationinALS.PLoSOne3, e2849
-
(2008)
PLoSOne
, vol.3
-
-
Chang, Y.1
-
210
-
-
0032771012
-
Identification of survival motor neuron as a transcriptional activator-binding protein
-
DOI 10.1093/hmg/8.7.1219
-
Strasswimmer, J. et al. (1999) Identification of survival motor neuron as a transcriptional activator-binding protein. Human Molecular Genetics 8, 1219-1226 (Pubitemid 29328990)
-
(1999)
Human Molecular Genetics
, vol.8
, Issue.7
, pp. 1219-1226
-
-
Strasswimmer, J.1
Lorson, C.L.2
Breiding, D.E.3
Chen, J.J.4
Le, T.5
Burghes, A.H.M.6
Androphy, E.J.7
-
211
-
-
0035825155
-
A functional interaction between the survival motor neuron complex and RNA polymerase II
-
DOI 10.1083/jcb.152.1.75
-
Pellizzoni, L. et al. (2001) A functional interaction between the survival motor neuron complex and RNA polymerase II. Journal of Cell Biology 152, 75-85 (Pubitemid 32102438)
-
(2001)
Journal of Cell Biology
, vol.152
, Issue.1
, pp. 75-85
-
-
Pellizzoni, L.1
Charroux, B.2
Rappsilber, J.3
Mann, M.4
Dreyfuss, G.5
-
212
-
-
25844461744
-
Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy
-
DOI 10.1101/gad.342005
-
Winkler, C. et al. (2005) Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy. Genes and Development 19, 2320-2330 (Pubitemid 41396909)
-
(2005)
Genes and Development
, vol.19
, Issue.19
, pp. 2320-2330
-
-
Winkler, C.1
Eggert, C.2
Gradl, D.3
Meister, G.4
Giegerich, M.5
Wedlich, D.6
Laggerbauer, B.7
Fischer, U.8
-
213
-
-
33749853624
-
Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons
-
DOI 10.1523/JNEUROSCI.1671-06.2006
-
Antonellis, A. et al. (2006) Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons. Journal of Neuroscience 26, 10397-10406 (Pubitemid 44564590)
-
(2006)
Journal of Neuroscience
, vol.26
, Issue.41
, pp. 10397-10406
-
-
Antonellis, A.1
Lee-Lin, S.-Q.2
Wasterlain, A.3
Leo, P.4
Quezado, M.5
Goldfarb, L.G.6
Myung, K.7
Burgess, S.8
Fischbeck, K.H.9
Green, E.D.10
-
214
-
-
38649121433
-
Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease
-
DOI 10.1038/ng.2007.65, PII NG200765
-
Nousiainen, H.O. et al. (2008) Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease. Nature Genetics 40, 155-157 (Pubitemid 351171396)
-
(2008)
Nature Genetics
, vol.40
, Issue.2
, pp. 155-157
-
-
Nousiainen, H.O.1
Kestila, M.2
Pakkasjarvi, N.3
Honkala, H.4
Kuure, S.5
Tallila, J.6
Vuopala, K.7
Ignatius, J.8
Herva, R.9
Peltonen, L.10
-
215
-
-
49549099576
-
The mRNA export factor Gle1 and inositol hexakisphosphate regulate distinct stages of translation
-
Bolger, T.A. et al. (2008) The mRNA export factor Gle1 and inositol hexakisphosphate regulate distinct stages of translation. Cell 134, 624-633
-
(2008)
Cell
, vol.134
, pp. 624-633
-
-
Bolger, T.A.1
-
216
-
-
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. et al. (1995) Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs. Journal of Virology 69, 3584-3596
-
(1995)
Journal of Virology
, vol.69
, pp. 3584-3596
-
-
Ou, S.H.1
-
217
-
-
37549025044
-
A novel CpG-free vertebrate insulator silences the testis-specific SP-10 gene in somatic tissues: Role for TDP-43 in insulator function
-
Abhyankar, M.M., Urekar, C. and Reddi, P.P. (2007) A novel CpG-free vertebrate insulator silences the testis-specific SP-10 gene in somatic tissues: role for TDP-43 in insulator function. Journal of Biological Chemistry 282, 36143-36154
-
(2007)
Journal of Biological Chemistry
, vol.282
, pp. 36143-36154
-
-
Abhyankar, M.M.1
Urekar, C.2
Reddi, P.P.3
-
218
-
-
46649093597
-
Induced ncRNAs allosterically modify RNA-binding proteins in cis to inhibit transcription
-
DOI 10.1038/nature06992, PII NATURE06992
-
Wang, X. et al. (2008) Induced ncRNAs allosterically modify RNA-binding proteins in cis to inhibit transcription. Nature 454, 126-130 (Pubitemid 351934270)
-
(2008)
Nature
, vol.454
, Issue.7200
, pp. 126-130
-
-
Wang, X.1
Arai, S.2
Song, X.3
Reichart, D.4
Du, K.5
Pascual, G.6
Tempst, P.7
Rosenfeld, M.G.8
Glass, C.K.9
Kurokawa, R.10
-
219
-
-
0037435587
-
Identification and characterization of an angiogenin-binding DNA sequence that stimulates luciferase reporter gene expression
-
Xu, Z.P. et al. (2003) Identification and characterization of an angiogenin-binding DNA sequence that stimulates luciferase reporter gene expression. Biochemistry 42, 121-128
-
(2003)
Biochemistry
, vol.42
, pp. 121-128
-
-
Xu, Z.P.1
-
220
-
-
0036293389
-
The nuclear function of angiogenin in endothelial cells is related to rRNA production
-
Xu, Z.P. et al. (2002) The nuclear function of angiogenin in endothelial cells is related to rRNA production. Biochemical and Biophysical Research Communications 294, 287-292
-
(2002)
Biochemical and Biophysical Research Communications
, vol.294
, pp. 287-292
-
-
Xu, Z.P.1
-
221
-
-
13944277097
-
Angiogenin is translocated to the nucleus of HeLa cells and is involved in ribosomal RNA transcription and cell proliferation
-
DOI 10.1158/0008-5472.CAN-04-2058
-
Tsuji, T. et al. (2005) Angiogenin is translocated to the nucleus of HeLa cells and is involved in ribosomalRNAtranscription and cell proliferation. Cancer Research 65, 1352-1360 (Pubitemid 40270162)
-
(2005)
Cancer Research
, vol.65
, Issue.4
, pp. 1352-1360
-
-
Tsuji, T.1
Sun, Y.2
Kishimoto, K.3
Olson, K.A.4
Liu, S.5
Hirukawa, S.6
Hu, G.-F.7
-
222
-
-
0026794004
-
Angiogenin is a cytotoxic, tRNA-specific ribonuclease in the RNase A superfamily
-
Saxena, S.K. et al. (1992) Angiogenin is a cytotoxic, tRNA-specific ribonuclease in the RNase A superfamily. Journal of Biological Chemistry 267, 21982-21986666
-
(1992)
Journal of Biological Chemistry
, vol.267
, pp. 21982-21986666
-
-
Saxena, S.K.1
|