-
1
-
-
33747605320
-
Molecular biology of amyotrophic lateral sclerosis: insights from genetics
-
Pasinelli P, Brown RH, (2006) Molecular biology of amyotrophic lateral sclerosis: insights from genetics. Nat Rev Neurosci 7: 710-723.
-
(2006)
Nat Rev Neurosci
, vol.7
, pp. 710-723
-
-
Pasinelli, P.1
Brown, R.H.2
-
3
-
-
77953739234
-
The neurobiology of amyotrophic lateral sclerosis
-
Bento-Abreu A, Van Damme P, Van Den Bosch L, Robberecht W, (2010) The neurobiology of amyotrophic lateral sclerosis. Eur J Neurosci 31: 2247-2265.
-
(2010)
Eur J Neurosci
, vol.31
, pp. 2247-2265
-
-
Bento-Abreu, A.1
Van Damme, P.2
Van Den Bosch, L.3
Robberecht, W.4
-
4
-
-
79952840023
-
Genetics of familial Amyotrophic lateral sclerosis
-
Ticozzi N, Tiloca C, Morelli C, Colombrita C, Poletti B, et al. (2011) Genetics of familial Amyotrophic lateral sclerosis. Arch Ital Biol 149: 65-82.
-
(2011)
Arch Ital Biol
, vol.149
, pp. 65-82
-
-
Ticozzi, N.1
Tiloca, C.2
Morelli, C.3
Colombrita, C.4
Poletti, B.5
-
5
-
-
61349156118
-
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
-
Kwiatkowski TJ Jr, Bosco DA, LeClerc AL, Tamrazian E, Vanderburg CR, 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
Bosco, D.A.2
LeClerc, A.L.3
Tamrazian, E.4
Vanderburg, C.R.5
-
6
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
Vance C, Rogelj B, Hortobágyi T, De Vos KJ, Nishimura AL, 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
Rogelj, B.2
Hortobágyi, T.3
De Vos, K.J.4
Nishimura, A.L.5
-
7
-
-
33645422711
-
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
-
Greenway MJ, Andersen PM, Russ C, Ennis S, Cashman S, et al. (2006) ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis. Nat Genet 38: 411-413.
-
(2006)
Nat Genet
, vol.38
, pp. 411-413
-
-
Greenway, M.J.1
Andersen, P.M.2
Russ, C.3
Ennis, S.4
Cashman, S.5
-
8
-
-
41949119043
-
TDP-43 A315T mutation in familial motor neuron disease
-
Gitcho MA, Baloh RH, Chakraverty S, Mayo K, Norton JB, et al. (2008) TDP-43 A315T mutation in familial motor neuron disease. Ann Neurol 63: 535-538.
-
(2008)
Ann Neurol
, vol.63
, pp. 535-538
-
-
Gitcho, M.A.1
Baloh, R.H.2
Chakraverty, S.3
Mayo, K.4
Norton, J.B.5
-
9
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, et al. (2008) TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat Genet 40: 572-574.
-
(2008)
Nat Genet
, vol.40
, pp. 572-574
-
-
Kabashi, E.1
Valdmanis, P.N.2
Dion, P.3
Spiegelman, D.4
McConkey, B.J.5
-
10
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
Sreedharan J, Blair IP, Tripathi VB, Hu X, Vance C, et al. (2008) TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319: 1668-1672.
-
(2008)
Science
, vol.319
, pp. 1668-1672
-
-
Sreedharan, J.1
Blair, I.P.2
Tripathi, V.B.3
Hu, X.4
Vance, C.5
-
11
-
-
42949094584
-
TDP-43 mutation in familial amyotrophic lateral sclerosis
-
Yokoseki A, Shiga A, Tan CF, Tagawa A, Kaneko H, et al. (2008) TDP-43 mutation in familial amyotrophic lateral sclerosis. Ann Neurol 63: 538-542.
-
(2008)
Ann Neurol
, vol.63
, pp. 538-542
-
-
Yokoseki, A.1
Shiga, A.2
Tan, C.F.3
Tagawa, A.4
Kaneko, H.5
-
12
-
-
77953890823
-
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
-
Lagier-Tourenne C, Polymenidou M, Cleveland DW, (2010) TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration. Hum Mol Genet 19: R46-64.
-
(2010)
Hum Mol Genet
, vol.19
-
-
Lagier-Tourenne, C.1
Polymenidou, M.2
Cleveland, D.W.3
-
13
-
-
84863527997
-
RNA-binding proteins in neurodegenerative disease: TDP-43 and beyond
-
Hanson KA, Kim SH, Tibbetts RS, (2012) RNA-binding proteins in neurodegenerative disease: TDP-43 and beyond. Wiley Interdiscip Rev RNA 3: 265-285.
-
(2012)
Wiley Interdiscip Rev RNA
, vol.3
, pp. 265-285
-
-
Hanson, K.A.1
Kim, S.H.2
Tibbetts, R.S.3
-
14
-
-
77449136874
-
The TET family of proteins: functions and roles in disease
-
Tan AY, Manley JL, (2009) The TET family of proteins: functions and roles in disease. J Mol Cell Biol 1: 82-92.
-
(2009)
J Mol Cell Biol
, vol.1
, pp. 82-92
-
-
Tan, A.Y.1
Manley, J.L.2
-
15
-
-
0030272143
-
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS
-
Aman P, Panagopoulos I, Lassen C, Fioretos T, Mencinger M, et al. (1996) Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS. Genomics 37: 1-8.
-
(1996)
Genomics
, vol.37
, pp. 1-8
-
-
Aman, P.1
Panagopoulos, I.2
Lassen, C.3
Fioretos, T.4
Mencinger, M.5
-
16
-
-
77957867303
-
Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules
-
Bosco DA, Lemay N, Ko HK, Zhou H, Burke C, et al. (2010) Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules. Hum Mol Genet 19: 4160-4175.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 4160-4175
-
-
Bosco, D.A.1
Lemay, N.2
Ko, H.K.3
Zhou, H.4
Burke, C.5
-
17
-
-
79551472601
-
Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS
-
Ito D, Seki M, Tsunoda Y, Uchiyama H, Suzuki N, (2011) Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS. Ann Neurol 69: 152-162.
-
(2011)
Ann Neurol
, vol.69
, pp. 152-162
-
-
Ito, D.1
Seki, M.2
Tsunoda, Y.3
Uchiyama, H.4
Suzuki, N.5
-
18
-
-
79954616116
-
Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations
-
Kino Y, Washizu C, Aquilanti E, Okuno M, Kurosawa M, et al. (2011) Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations. Nucleic Acids Res 39: 2781-2798.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. 2781-2798
-
-
Kino, Y.1
Washizu, C.2
Aquilanti, E.3
Okuno, M.4
Kurosawa, M.5
-
19
-
-
84874531814
-
RNA-binding ability of FUS regulates neurodegeneration, cytoplasmic mislocalization and incorporation into stress granules associated with FUS carrying ALS-linked mutations
-
Daigle JG, Lanson NA Jr, Smith RB, Casci I, Maltare A, et al. (2013) RNA-binding ability of FUS regulates neurodegeneration, cytoplasmic mislocalization and incorporation into stress granules associated with FUS carrying ALS-linked mutations. Hum Mol Genet.
-
(2013)
Hum Mol Genet
-
-
Daigle, J.G.1
Lanson Jr., N.A.2
Smith, R.B.3
Casci, I.4
Maltare, A.5
-
20
-
-
79958720175
-
A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43
-
Lanson NA Jr, Maltare A, King H, Smith R, Kim JH, et al. (2011) A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43. Hum Mol Genet 20: 2510-2523.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2510-2523
-
-
Lanson Jr., N.A.1
Maltare, A.2
King, H.3
Smith, R.4
Kim, J.H.5
-
21
-
-
27944460430
-
Protein arginine methyltransferases: guardians of the Arg?
-
Fackelmayer FO, (2005) Protein arginine methyltransferases: guardians of the Arg? Trends Biochem Sci 30: 666-671.
-
(2005)
Trends Biochem Sci
, vol.30
, pp. 666-671
-
-
Fackelmayer, F.O.1
-
22
-
-
58149295717
-
Protein arginine methylation in mammals: who, what, and why
-
Bedford MT, Clarke SG, (2009) Protein arginine methylation in mammals: who, what, and why. Mol Cell 33: 1-13.
-
(2009)
Mol Cell
, vol.33
, pp. 1-13
-
-
Bedford, M.T.1
Clarke, S.G.2
-
23
-
-
64749109224
-
Minireview: protein arginine methylation of nonhistone proteins in transcriptional regulation
-
Lee YH, Stallcup MR, (2009) Minireview: protein arginine methylation of nonhistone proteins in transcriptional regulation. Mol Endocrinol 23: 425-433.
-
(2009)
Mol Endocrinol
, vol.23
, pp. 425-433
-
-
Lee, Y.H.1
Stallcup, M.R.2
-
24
-
-
67649968054
-
The protein arginine methyltransferase family: an update about function, new perspectives and the physiological role in humans
-
Wolf SS, (2009) The protein arginine methyltransferase family: an update about function, new perspectives and the physiological role in humans. Cell Mol Life Sci 66: 2109-2121.
-
(2009)
Cell Mol Life Sci
, vol.66
, pp. 2109-2121
-
-
Wolf, S.S.1
-
25
-
-
0038000050
-
Detection of arginine dimethylated peptides by parallel precursor ion scanning mass spectrometry in positive ion mode
-
Rappsilber J, Friesen WJ, Paushkin S, Dreyfuss G, Mann M, (2003) Detection of arginine dimethylated peptides by parallel precursor ion scanning mass spectrometry in positive ion mode. Anal Chem 75: 3107-3114.
-
(2003)
Anal Chem
, vol.75
, pp. 3107-3114
-
-
Rappsilber, J.1
Friesen, W.J.2
Paushkin, S.3
Dreyfuss, G.4
Mann, M.5
-
26
-
-
79151471350
-
TLS and PRMT1 synergistically coactivate transcription at the survivin promoter through TLS arginine methylation
-
Du K, Arai S, Kawamura T, Matsushita A, Kurokawa R, (2011) TLS and PRMT1 synergistically coactivate transcription at the survivin promoter through TLS arginine methylation. Biochem Biophys Res Commun 404: 991-996.
-
(2011)
Biochem Biophys Res Commun
, vol.404
, pp. 991-996
-
-
Du, K.1
Arai, S.2
Kawamura, T.3
Matsushita, A.4
Kurokawa, R.5
-
27
-
-
84869005887
-
The Effect of PRMT1-Mediated Arginine Methylation on the Subcellular Localization, Stress Granules, and Detergent-Insoluble Aggregates of FUS/TLS
-
Yamaguchi A, Kitajo K, (2012) The Effect of PRMT1-Mediated Arginine Methylation on the Subcellular Localization, Stress Granules, and Detergent-Insoluble Aggregates of FUS/TLS. PLoS One 7: e49267.
-
(2012)
PLoS One
, vol.7
-
-
Yamaguchi, A.1
Kitajo, K.2
-
28
-
-
84869237956
-
Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS
-
Dormann D, Madl T, Valori CF, Bentmann E, Tahirovic S, et al. (2012) Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS. EMBO J 31: 4258-4275.
-
(2012)
EMBO J
, vol.31
, pp. 4258-4275
-
-
Dormann, D.1
Madl, T.2
Valori, C.F.3
Bentmann, E.4
Tahirovic, S.5
-
29
-
-
83455162720
-
Arginine methylation by PRMT1 regulates nuclear-cytoplasmic localization and toxicity of FUS/TLS harbouring ALS-linked mutations
-
Tradewell ML, Yu Z, Tibshirani M, Boulanger MC, Durham HD, et al. (2012) Arginine methylation by PRMT1 regulates nuclear-cytoplasmic localization and toxicity of FUS/TLS harbouring ALS-linked mutations. Hum Mol Genet 21: 136-149.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 136-149
-
-
Tradewell, M.L.1
Yu, Z.2
Tibshirani, M.3
Boulanger, M.C.4
Durham, H.D.5
-
30
-
-
25444463928
-
PRMT8, a new membrane-bound tissue-specific member of the protein arginine methyltransferase family
-
Lee J, Sayegh J, Daniel J, Clarke S, Bedford MT, (2005) PRMT8, a new membrane-bound tissue-specific member of the protein arginine methyltransferase family. J Biol Chem 280: 32890-32896.
-
(2005)
J Biol Chem
, vol.280
, pp. 32890-32896
-
-
Lee, J.1
Sayegh, J.2
Daniel, J.3
Clarke, S.4
Bedford, M.T.5
-
31
-
-
34250004658
-
Specific regional distribution of protein arginine methyltransferase 8 (PRMT8) in the mouse brain
-
Taneda T, Miyata S, Kousaka A, Inoue K, Koyama Y, et al. (2007) Specific regional distribution of protein arginine methyltransferase 8 (PRMT8) in the mouse brain. Brain Res 1155: 1-9.
-
(2007)
Brain Res
, vol.1155
, pp. 1-9
-
-
Taneda, T.1
Miyata, S.2
Kousaka, A.3
Inoue, K.4
Koyama, Y.5
-
32
-
-
76249125981
-
The distribution and characterization of endogenous protein arginine N-methyltransferase 8 in mouse CNS
-
Kousaka A, Mori Y, Koyama Y, Taneda T, Miyata S, et al. (2009) The distribution and characterization of endogenous protein arginine N-methyltransferase 8 in mouse CNS. Neuroscience 163: 1146-1157.
-
(2009)
Neuroscience
, vol.163
, pp. 1146-1157
-
-
Kousaka, A.1
Mori, Y.2
Koyama, Y.3
Taneda, T.4
Miyata, S.5
-
33
-
-
0025909235
-
Embryonic mouse spinal cord motor neuron hybrid cells
-
Salazar-Grueso EF, Kim S, Kim H, (1991) Embryonic mouse spinal cord motor neuron hybrid cells. Neuroreport 2: 505-508.
-
(1991)
Neuroreport
, vol.2
, pp. 505-508
-
-
Salazar-Grueso, E.F.1
Kim, S.2
Kim, H.3
-
34
-
-
34447309577
-
Akt blocks ligand binding and protects against expanded polyglutamine androgen receptor toxicity
-
Palazzolo I, Burnett BG, Young JE, Brenne PL, La Spada AR, et al. (2007) Akt blocks ligand binding and protects against expanded polyglutamine androgen receptor toxicity. Hum Mol Genet 16: 1593-1603.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 1593-1603
-
-
Palazzolo, I.1
Burnett, B.G.2
Young, J.E.3
Brenne, P.L.4
La Spada, A.R.5
-
35
-
-
77953648932
-
B2 attenuates polyglutamine-expanded androgen receptor toxicity in cell and fly models of spinal and bulbar muscular atrophy
-
Palazzolo I, Nedelsky NB, Askew CE, Harmison GG, Kasantsev AG, et al. (2010) B2 attenuates polyglutamine-expanded androgen receptor toxicity in cell and fly models of spinal and bulbar muscular atrophy. J Neurosci Res 88: 2207-2216.
-
(2010)
J Neurosci Res
, vol.88
, pp. 2207-2216
-
-
Palazzolo, I.1
Nedelsky, N.B.2
Askew, C.E.3
Harmison, G.G.4
Kasantsev, A.G.5
-
36
-
-
34250183177
-
HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS
-
Pandey UB, Nie Z, Batlevi Y, McCray BA, Ritson GP, et al. (2007) HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS. Nature 447: 859-863.
-
(2007)
Nature
, vol.447
, pp. 859-863
-
-
Pandey, U.B.1
Nie, Z.2
Batlevi, Y.3
McCray, B.A.4
Ritson, G.P.5
-
37
-
-
66149108467
-
Human protein arginine methyltransferases in vivo-distinct properties of eight canonical members of the PRMT family
-
Herrmann F, Pably P, Eckerich C, Bedford MT, Fackelmayer FO, (2009) Human protein arginine methyltransferases in vivo-distinct properties of eight canonical members of the PRMT family. J Cell Sci 122: 667-677.
-
(2009)
J Cell Sci
, vol.122
, pp. 667-677
-
-
Herrmann, F.1
Pably, P.2
Eckerich, C.3
Bedford, M.T.4
Fackelmayer, F.O.5
-
38
-
-
24744432516
-
Arginine methylation of yeast mRNA-binding protein Npl3 directly affects its function, nuclear export, and intranuclear protein interactions
-
McBride AE, Cook JT, Stemmler EA, Rutledge KL, McGrath KA, et al. (2005) Arginine methylation of yeast mRNA-binding protein Npl3 directly affects its function, nuclear export, and intranuclear protein interactions. J Biol Chem 280: 30888-30898.
-
(2005)
J Biol Chem
, vol.280
, pp. 30888-30898
-
-
McBride, A.E.1
Cook, J.T.2
Stemmler, E.A.3
Rutledge, K.L.4
McGrath, K.A.5
-
39
-
-
34447560908
-
Protein arginine methylation in Candida albicans: role in nuclear transport
-
McBride AE, Zurita-Lopez C, Regis A, Blum E, Conboy A, et al. (2007) Protein arginine methylation in Candida albicans: role in nuclear transport. Eukaryot Cell 6: 1119-1129.
-
(2007)
Eukaryot Cell
, vol.6
, pp. 1119-1129
-
-
McBride, A.E.1
Zurita-Lopez, C.2
Regis, A.3
Blum, E.4
Conboy, A.5
-
40
-
-
0037077040
-
Toxic proteins in neurodegenerative disease
-
Taylor JP, Hardy J, Fischbeck KH, (2002) Toxic proteins in neurodegenerative disease. Science 296: 1991-1995.
-
(2002)
Science
, vol.296
, pp. 1991-1995
-
-
Taylor, J.P.1
Hardy, J.2
Fischbeck, K.H.3
-
41
-
-
20444504698
-
The genetic epidemiology of neurodegenerative disease
-
Bertram L, Tanzi RE, (2005) The genetic epidemiology of neurodegenerative disease. J Clin Invest 115: 1449-1457.
-
(2005)
J Clin Invest
, vol.115
, pp. 1449-1457
-
-
Bertram, L.1
Tanzi, R.E.2
-
42
-
-
7244236320
-
Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
-
Arrasate M, Mitra S, Schweitzer ES, Segal MR, Finkbeiner S, (2004) Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death. Nature 431: 805-810.
-
(2004)
Nature
, vol.431
, pp. 805-810
-
-
Arrasate, M.1
Mitra, S.2
Schweitzer, E.S.3
Segal, M.R.4
Finkbeiner, S.5
-
43
-
-
70350045802
-
Mutations in FUS cause FALS and SALS in French and French Canadian populations
-
Belzil VV, Valdmanis PN, Dion PA, Daoud H, Kabashi E, et al. (2009) Mutations in FUS cause FALS and SALS in French and French Canadian populations. Neurology 73: 1176-1179.
-
(2009)
Neurology
, vol.73
, pp. 1176-1179
-
-
Belzil, V.V.1
Valdmanis, P.N.2
Dion, P.A.3
Daoud, H.4
Kabashi, E.5
-
44
-
-
70449521091
-
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
-
Neumann M, Roeber S, Kretzschmar HA, Rademakers R, et al. (2009) Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease. Acta Neuropathol 118: 605-616.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 605-616
-
-
Neumann, M.1
Roeber, S.2
Kretzschmar, H.A.3
Rademakers, R.4
-
45
-
-
77949760219
-
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
-
Corrado L, (2010) Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. J Med Genet 47: 190-194.
-
(2010)
J Med Genet
, vol.47
, pp. 190-194
-
-
Corrado, L.1
-
46
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
Vance C, (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
-
47
-
-
70350673956
-
A new subtype of frontotemporal lobar degeneration with FUS pathology
-
Neumann M, Rademakers R, Roeber S, Baker M, Kretzschmar HA, et al. (2009) A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain 132: 2922-2931.
-
(2009)
Brain
, vol.132
, pp. 2922-2931
-
-
Neumann, M.1
Rademakers, R.2
Roeber, S.3
Baker, M.4
Kretzschmar, H.A.5
-
48
-
-
14644437074
-
Transcriptional down-regulation through nuclear exclusion of EWS methylated by PRMT1
-
Araya N, Hiraga H, Kako K, Arao Y, Kato S, et al. (2005) Transcriptional down-regulation through nuclear exclusion of EWS methylated by PRMT1. Biochem Biophys Res Commun 329: 653-660.
-
(2005)
Biochem Biophys Res Commun
, vol.329
, pp. 653-660
-
-
Araya, N.1
Hiraga, H.2
Kako, K.3
Arao, Y.4
Kato, S.5
-
49
-
-
63049100536
-
PRMT1 mediated methylation of TAF15 is required for its positive gene regulatory function
-
Jobert L, Argentini M, Tora L, (2009) PRMT1 mediated methylation of TAF15 is required for its positive gene regulatory function. Exp Cell Res 315: 1273-1286.
-
(2009)
Exp Cell Res
, vol.315
, pp. 1273-1286
-
-
Jobert, L.1
Argentini, M.2
Tora, L.3
-
50
-
-
0033968408
-
Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death
-
Hicks GG, Singh N, Nashabi A, Mai S, Bozek G, et al. (2000) Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death. Nat Genet 24: 175-179.
-
(2000)
Nat Genet
, vol.24
, pp. 175-179
-
-
Hicks, G.G.1
Singh, N.2
Nashabi, A.3
Mai, S.4
Bozek, G.5
-
51
-
-
0034142209
-
Male sterility and enhanced radiation sensitivity in TLS(-/-) mice
-
Kuroda M, Sok J, Webb L, Baechtold H, Urano F, et al. (2000) Male sterility and enhanced radiation sensitivity in TLS(-/-) mice. EMBO J 19: 453-462.
-
(2000)
EMBO J
, vol.19
, pp. 453-462
-
-
Kuroda, M.1
Sok, J.2
Webb, L.3
Baechtold, H.4
Urano, F.5
-
52
-
-
0029812470
-
hTAF(II)68, a novel RNA/ssDNA-binding protein with homology to the pro-oncoproteins TLS/FUS and EWS is associated with both TFIID and RNA polymerase II
-
Bertolotti A, Lutz Y, Heard DJ, Chambon P, Tora L, (1996) hTAF(II)68, a novel RNA/ssDNA-binding protein with homology to the pro-oncoproteins TLS/FUS and EWS is associated with both TFIID and RNA polymerase II. EMBO J 15: 5022-5031.
-
(1996)
EMBO J
, vol.15
, pp. 5022-5031
-
-
Bertolotti, A.1
Lutz, Y.2
Heard, D.J.3
Chambon, P.4
Tora, L.5
-
53
-
-
80053646130
-
Nuclear localization sequence of FUS and induction of stress granules by ALS mutants
-
Gal J, Zhang J, Kwinter DM, Zhai J, Jia H, et al. (2011) Nuclear localization sequence of FUS and induction of stress granules by ALS mutants. Neurobiol Aging 32: 2323 e2327-2340.
-
(2011)
Neurobiol Aging
, vol.32
-
-
Gal, J.1
Zhang, J.2
Kwinter, D.M.3
Zhai, J.4
Jia, H.5
|