-
1
-
-
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, Panagopoulos I, Lassen C, Fioretos T, Mencinger M, Toresson H, et al. Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS. Genomics 1996; 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
-
2
-
-
48249083430
-
The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response
-
Andersson MK, Stahlberg A, Arvidsson Y, Olofsson A, Semb H, Stenman G, et al. The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response. BMC Cell Biol 2008; 9: 37.
-
(2008)
BMC Cell Biol
, vol.9
, pp. 37
-
-
Andersson, M.K.1
Stahlberg, A.2
Arvidsson, Y.3
Olofsson, A.4
Semb, H.5
Stenman, G.6
-
3
-
-
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, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, Mori H, et al. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 2006; 351: 602-11. (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
-
4
-
-
79451469349
-
The spectrum and severity of FUS-immunoreactive inclusions in the frontal and temporal lobes of ten cases of neuronal intermediate filament inclusion disease
-
Armstrong RA, Gearing M, Bigio EH, Cruz-Sanchez FF, Duyckaerts C, Mackenzie IR, et al. The spectrum and severity of FUS-immunoreactive inclusions in the frontal and temporal lobes of ten cases of neuronal intermediate filament inclusion disease. Acta Neuropathol 2011; 121: 219-28.
-
(2011)
Acta Neuropathol
, vol.121
, pp. 219-228
-
-
Armstrong, R.A.1
Gearing, M.2
Bigio, E.H.3
Cruz-Sanchez, F.F.4
Duyckaerts, C.5
MacKenzie, I.R.6
-
5
-
-
0033607753
-
Human 75-kDa DNA-pairing protein is identical to the pro-oncoprotein TLS/FUS and is able to promote D-loop formation
-
Baechtold H, Kuroda M, Sok J, Ron D, Lopez BS, Akhmedov AT. Human 75-kDa DNA-pairing protein is identical to the pro-oncoprotein TLS/FUS and is able to promote D-loop formation. J Biol Chem 1999; 274: 34337-42. (Pubitemid 129511776)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.48
, pp. 34337-34342
-
-
Baechtold, H.1
Kuroda, M.2
Sok, J.3
Ron, D.4
Lopez, B.S.5
Akhmedov, A.T.6
-
6
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
DOI 10.1038/nature05016, PII NATURE05016
-
Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, Lindholm C, et al. Mutations in progranulin cause tau-negative fron-totemporal dementia linked to chromosome 17. Nature, 2006; 442, 916-9. (Pubitemid 44285946)
-
(2006)
Nature
, vol.442
, Issue.7105
, pp. 916-919
-
-
Baker, M.1
Mackenzie, I.R.2
Pickering-Brown, S.M.3
Gass, J.4
Rademakers, R.5
Lindholm, C.6
Snowden, J.7
Adamson, J.8
Sadovnick, A.D.9
Rollinson, S.10
Cannon, A.11
Dwosh, E.12
Neary, D.13
Melquist, S.14
Richardson, A.15
Dickson, D.16
Berger, Z.17
Eriksen, J.18
Robinson, T.19
Zehr, C.20
Dickey, C.A.21
Crook, R.22
McGowan, E.23
Mann, D.24
Boeve, B.25
Feldman, H.26
Hutton, M.27
more..
-
7
-
-
17444381645
-
Delocalization of the multifunctional RNA splicing factor TLS/FUS in hippocampal neurones: Exclusion from the nucleus and accumulation in dendritic granules and spine heads
-
DOI 10.1016/j.neulet.2004.12.071
-
Belly A, Moreau-Gachelin F, Sadoul R, Goldberg Y. Delocalization of the multifunctional RNA splicing factor TLS/FUS in hippocampal neurones: exclusion from the nucleus and accumulation in dendritic granules and spine heads. Neurosci Lett 2005; 379: 152-7. (Pubitemid 40544525)
-
(2005)
Neuroscience Letters
, vol.379
, Issue.3
, pp. 152-157
-
-
Belly, A.1
Moreau-Gachelin, F.2
Sadoul, R.3
Goldberg, Y.4
-
8
-
-
0033527059
-
Human POMp75 is identified as the pro-oncoprotein TLS/FUS: Both POMp75 and POMp100 DNA homologous pairing activities are associated to cell proliferation
-
DOI 10.1038/sj.onc.1203048
-
Bertrand P, Akhmedov AT, Delacote F, Durrbach A, Lopez BS. Human POMp75 is identified as the pro-oncoprotein TLS/FUS: both POMp75 and POMp100 DNA homologous pairing activities are associated to cell proliferation. Oncogene 1999; 18: 4515-21. (Pubitemid 29396659)
-
(1999)
Oncogene
, vol.18
, Issue.31
, pp. 4515-4521
-
-
Bertrand, P.1
Akhmedov, A.T.2
Delacote, F.3
Durrbach, A.4
Lopez, B.S.5
-
9
-
-
38449102667
-
Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease
-
DOI 10.2741/2727
-
Buratti E, Baralle FE. Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease. Front Biosci 2008; 13: 867-78. (Pubitemid 351594732)
-
(2008)
Frontiers in Bioscience
, vol.13
, Issue.3
, pp. 867-878
-
-
Buratti, E.1
Baralle, F.E.2
-
10
-
-
34447096691
-
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: Consensus of the Consortium for Frontotemporal Lobar Degeneration
-
DOI 10.1007/s00401-007-0237-2
-
Cairns NJ, Bigio EH, Mackenzie IR, Neumann M, Lee VM, Hatanpaa KJ, et al. Neuropathologic diagnostic and nosologic criteria for frontotem-poral lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration. Acta Neuropathol 2007; 114: 5-22. (Pubitemid 47029055)
-
(2007)
Acta Neuropathologica
, vol.114
, Issue.1
, pp. 5-22
-
-
Cairns, N.J.1
Bigio, E.H.2
Mackenzie, I.R.A.3
Neumann, M.4
Lee, V.M.-Y.5
Hatanpaa, K.J.6
White III, C.L.7
Schneider, J.A.8
Grinberg, L.T.9
Halliday, G.10
Duyckaerts, C.11
Lowe, J.S.12
Holm, I.E.13
Tolnay, M.14
Okamoto, K.15
Yokoo, H.16
Murayama, S.17
Woulfe, J.18
Munoz, D.G.19
Dickson, D.W.20
Ince, P.G.21
Trojanowski, J.Q.22
Mann, D.M.A.23
more..
-
11
-
-
2442684337
-
α-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease
-
Cairns NJ, Zhukareva V, Uryu K, Zhang B, Bigio E, Mackenzie IR, et al. Alpha-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease. Am J Pathol 2004; 164: 2153-61. (Pubitemid 38669362)
-
(2004)
American Journal of Pathology
, vol.164
, Issue.6
, pp. 2153-2161
-
-
Cairns, N.J.1
Zhukareva, V.2
Uryu, K.3
Zhang, B.4
Bigio, E.5
Mackenzie, I.R.A.6
Gearing, M.7
Duyckaerts, C.8
Yokoo, H.9
Nakazato, Y.10
Jaros, E.11
Perry, R.H.12
Lee, V.M.-Y.13
Trojanowski, J.Q.14
-
12
-
-
0027227651
-
Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma
-
DOI 10.1038/363640a0
-
Crozat A, Aman P, Mandahl N, Ron D. Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma. Nature 1993; 363: 640-4. (Pubitemid 23227627)
-
(1993)
Nature
, vol.363
, Issue.6430
, pp. 640-644
-
-
Crozat, A.1
Aman, P.2
Mandahl, N.3
Ron, D.4
-
13
-
-
33846055457
-
Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
DOI 10.2174/156720506779025251
-
Cruts M, Kumar-Singh S, Van BC. Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Curr Alzheimer Res 2006; 3: 485-91. (Pubitemid 46066424)
-
(2006)
Current Alzheimer Research
, vol.3
, Issue.5
, pp. 485-491
-
-
Cruts, M.1
Kumar-Singh, S.2
Van Broeckhoven, C.3
-
14
-
-
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, Kelley T, Mackenzie IR, Pickering-Brown S, Du PD, Neary D, et al. Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43. Acta Neuropathol 2007; 113: 521-33. (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 Plessis, D.5
Neary, D.6
Snowden, J.S.7
Mann, D.M.A.8
-
15
-
-
75949105684
-
TDP-43 redistribution is an early event in sporadic amyotrophic lateral sclerosis
-
Giordana MT, Piccinini M, Grifoni S, De MG, Vercellino M, Magistrello M, et al. TDP-43 redistribution is an early event in sporadic amyotrophic lateral sclerosis. Brain Pathol 2010; 20: 351-60.
-
(2010)
Brain Pathol
, vol.20
, pp. 351-360
-
-
Giordana, M.T.1
Piccinini, M.2
Grifoni, S.3
De Mg Vercellino, M.4
Magistrello, M.5
-
16
-
-
0035137042
-
Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia
-
Holton JL, Ghiso J, Lashley T, Rostagno A, Guerin CJ, Gibb G, et al. Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia. Am J Pathol 2001; 158: 515-26. (Pubitemid 32158612)
-
(2001)
American Journal of Pathology
, vol.158
, Issue.2
, pp. 515-526
-
-
Holton, J.L.1
Ghiso, J.2
Lashley, T.3
Rostagno, A.4
Guerin, C.J.5
Gibb, G.6
Houlden, H.7
Ayling, H.8
Martinian, L.9
Anderton, B.H.10
Wood, N.W.11
Vidal, R.12
Plant, G.13
Frangione, B.14
Revesz, T.15
-
17
-
-
77954643023
-
Sustained expression of TDP-43 and FUS in motor neurons in rodent's lifetime
-
Huang C, Xia PY, Zhou H. Sustained expression of TDP-43 and FUS in motor neurons in rodent's lifetime. Int J Biol Sci 2010; 6: 396-406.
-
(2010)
Int J Biol Sci
, vol.6
, pp. 396-406
-
-
Huang, C.1
Xia, P.Y.2
Zhou, H.3
-
18
-
-
0242336433
-
Neurofilament inclusion body disease: A new proteinopathy?
-
DOI 10.1093/brain/awg231
-
Josephs KA, Holton JL, Rossor MN, Braendgaard H, Ozawa T, Fox NC, et al. Neurofilament inclusion body disease: a new proteinopathy? Brain 2003; 126: 2291-303. (Pubitemid 37432372)
-
(2003)
Brain
, vol.126
, Issue.10
, pp. 2291-2303
-
-
Josephs, K.A.1
Holton, J.L.2
Rossor, M.N.3
Braendgaard, H.4
Ozawa, T.5
Fox, N.C.6
Petersen, R.C.7
Pearl, G.S.8
Ganguly, M.9
Rosa, P.10
Laursen, H.11
Parisi, J.E.12
Waldemar, G.13
Quinn, N.P.14
Dickson, D.W.15
Revesz, T.16
-
19
-
-
4344642855
-
Frontotemporal lobar degeneration and ubiquitin immunohistochemistry
-
DOI 10.1111/j.1365-2990.2003.00545.x
-
Josephs KA, Holton JL, Rossor MN, Godbolt AK, Ozawa T, Strand K, et al. Frontotemporal lobar degeneration and ubiquitin immunohisto-chemistry. Neuropathol Appl Neurobiol 2004; 30: 369-73. (Pubitemid 39120298)
-
(2004)
Neuropathology and Applied Neurobiology
, vol.30
, Issue.4
, pp. 369-373
-
-
Josephs, K.A.1
Holton, J.L.2
Rossor, M.N.3
Godbolt, A.K.4
Ozawa, T.5
Strand, K.6
Khan, N.7
Al-Sarraj, S.8
Revesz, T.9
-
20
-
-
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, Russ C, et al. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 2009; 323: 1205-8.
-
(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
Russ, C.6
-
21
-
-
0025739379
-
Simplified mammalian DNA isolation procedure
-
Laird PW, Zijderveld A, Linders K, Rudnicki MA, Jaenisch R, Berns A, et al. Simplified mammalian DNA isolation procedure. Nucleic Acids Res 1991; 19: 4293.
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 4293
-
-
Laird, P.W.1
Zijderveld, A.2
Linders, K.3
Rudnicki, M.A.4
Jaenisch, R.5
Berns, A.6
-
22
-
-
78649846412
-
Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathology
-
Loy CT, McCusker E, Kril JJ, Kwok JB, Brooks WS, McCann H, et al. Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathology. Brain 2010; 133: e158.
-
(2010)
Brain
, vol.133
-
-
Loy, C.T.1
McCusker, E.2
Kril, J.J.3
Kwok, J.B.4
Brooks, W.S.5
McCann, H.6
-
23
-
-
33749668518
-
Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: Classification and relation to clinical phenotype
-
DOI 10.1007/s00401-006-0138-9
-
Mackenzie IR, Baborie A, Pickering-Brown S, Du PD, Jaros E, Perry RH, et al. Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype. Acta Neuropathol 2006; 112: 539-49. (Pubitemid 44550678)
-
(2006)
Acta Neuropathologica
, vol.112
, Issue.5
, pp. 539-549
-
-
Mackenzie, I.R.A.1
Baborie, A.2
Pickering-Brown, S.3
Plessis, D.D.4
Jaros, E.5
Perry, R.H.6
Neary, D.7
Snowden, J.S.8
Mann, D.M.A.9
-
24
-
-
79451472241
-
Distinct pathological subtypes of FTLD-FUS
-
Mackenzie IR, Munoz DG, Kusaka H, Yokota O, Ishihara K, Roeber S, et al. Distinct pathological subtypes of FTLD-FUS. Acta Neuropathol 2011; 121: 207-18.
-
(2011)
Acta Neuropathol
, vol.121
, pp. 207-218
-
-
MacKenzie, I.R.1
Munoz, D.G.2
Kusaka, H.3
Yokota, O.4
Ishihara, K.5
Roeber, S.6
-
25
-
-
47949099336
-
Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia
-
Mori F, Tanji K, Zhang HX, Nishihira Y, Tan CF, Takahashi H, et al. Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia. Acta Neuropathol 2008; 116: 193-203.
-
(2008)
Acta Neuropathol
, vol.116
, pp. 193-203
-
-
Mori, F.1
Tanji, K.2
Zhang, H.X.3
Nishihira, Y.4
Tan, C.F.5
Takahashi, H.6
-
26
-
-
70449517359
-
FUS pathology in basophilic inclusion body disease
-
Munoz DG, Neumann M, Kusaka H, Yokota O, Ishihara K, Terada S, et al. FUS pathology in basophilic inclusion body disease. Acta Neuropathol 2009; 118: 617-27.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 617-627
-
-
Munoz, D.G.1
Neumann, M.2
Kusaka, H.3
Yokota, O.4
Ishihara, K.5
Terada, S.6
-
27
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
Neary D, Snowden JS, Gustafson L, Passant U, Stuss D, Black S, et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 1998; 51: 1546-54.
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
Passant, U.4
Stuss, D.5
Black, S.6
-
28
-
-
70350673956
-
A new subtype of frontotemporal lobar degeneration with FUS pathology
-
Neumann M, Rademakers R, Roeber S, Baker M, Kretzschmar HA, Mackenzie IR, et al. A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain 2009a; 132: 2922-31.
-
(2009)
Brain
, vol.132
, pp. 2922-2931
-
-
Neumann, M.1
Rademakers, R.2
Roeber, S.3
Baker, M.4
Kretzschmar, H.A.5
MacKenzie, I.R.6
-
29
-
-
70449521091
-
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
-
Neumann M, Roeber S, Kretzschmar HA, Rademakers R, Baker M, Mackenzie IR. Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease. Acta Neuropathol 2009b; 118: 605-16.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 605-616
-
-
Neumann, M.1
Roeber, S.2
Kretzschmar, H.A.3
Rademakers, R.4
Baker, M.5
MacKenzie, I.R.6
-
30
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
DOI 10.1126/science.1134108
-
Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 2006; 314: 130-33. (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
-
31
-
-
8144227320
-
Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: Broadening the clinical picture to include progressive supranuclear palsy
-
DOI 10.1093/brain/awh265
-
Paviour DC, Lees AJ, Josephs KA, Ozawa T, Ganguly M, Strand C, et al. Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: broadening the clinical picture to include progressive supranuclear palsy. Brain 2004; 127 (Pt 11): 2441-51. (Pubitemid 39472972)
-
(2004)
Brain
, vol.127
, Issue.11
, pp. 2441-2451
-
-
Paviour, D.C.1
Lees, A.J.2
Josephs, K.A.3
Ozawa, T.4
Ganguly, M.5
Strand, C.6
Godbolt, A.7
Howard, R.S.8
Revesz, T.9
Holton, J.L.10
-
32
-
-
0032479980
-
TLS/FUS, a pro-oncogene involved in multiple chromosomal translocations, is a novel regulator of BCR/ABL-mediated leukemogenesis
-
DOI 10.1093/emboj/17.15.4442
-
Perrotti D, Bonatti S, Trotta R, Martinez R, Skorski T, Salomoni P, et al. TLS/FUS, a pro-oncogene involved in multiple chromosomal transloca-tions, is a novel regulator of BCR/ABL-mediated leukemogenesis. EMBO J 1998; 17: 4442-55. (Pubitemid 28362633)
-
(1998)
EMBO Journal
, vol.17
, Issue.15
, pp. 4442-4455
-
-
Perrotti, D.1
Bonatti, S.2
Trotta, R.3
Martinez, R.4
Skorski, T.5
Salomoni, P.6
Grassilli, E.7
Iozzo, R.V.8
Cooper, D.R.9
Calabretta, B.10
-
33
-
-
0027948152
-
TLS/FUS fusion domain of TLS/FUS-erg chimeric protein resulting from the t(16;21) chromosomal translocation in human myeloid leukemia functions as a transcriptional activation domain
-
Prasad DD, Ouchida M, Lee L, Rao VN, Reddy ES. TLS/FUS fusion domain of TLS/FUS-erg chimeric protein resulting from the t(16;21) chromosomal translocation in human myeloid leukemia functions as a transcriptional activation domain. Oncogene 1994; 9: 3717-29. (Pubitemid 24359413)
-
(1994)
Oncogene
, vol.9
, Issue.12
, pp. 3717-3729
-
-
Prasad, D.D.K.1
Ouchida, M.2
Lee, L.3
Rao, V.N.4
Reddy, E.S.P.5
-
34
-
-
47949123961
-
TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD
-
Roeber S, Mackenzie IR, Kretzschmar HA, Neumann M. TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD. Acta Neuropathol 2008; 116: 147-57.
-
(2008)
Acta Neuropathol
, vol.116
, pp. 147-157
-
-
Roeber, S.1
MacKenzie, I.R.2
Kretzschmar, H.A.3
Neumann, M.4
-
35
-
-
70449365115
-
The heritability and genetics of frontotemporal lobar degeneration
-
Rohrer JD, Guerreiro R, Vandrovcova J, Uphill J, Reiman D, Beck J, et al. The heritability and genetics of frontotemporal lobar degeneration. Neurology 2009; 73: 1451-6.
-
(2009)
Neurology
, vol.73
, pp. 1451-1456
-
-
Rohrer, J.D.1
Guerreiro, R.2
Vandrovcova, J.3
Uphill, J.4
Reiman, D.5
Beck, J.6
-
36
-
-
80855136461
-
The clinical and neuroanatomical phenotype of FUS associated frontotem-poral lobar degeneration
-
July 16. [Epub ahead of print] doi:10.1136/jnnp.2010.214437
-
Rohrer JD, Lashley T, Holton J, Revesz T, Urwin H, Isaacs AM, et al. The clinical and neuroanatomical phenotype of FUS associated frontotem-poral lobar degeneration. J Neurol Neurosurg Psychiatry 2010. July 16. [Epub ahead of print] doi:10.1136/jnnp.2010.214437.
-
(2010)
J Neurol Neurosurg Psychiatry
-
-
Rohrer, J.D.1
Lashley, T.2
Holton, J.3
Revesz, T.4
Urwin, H.5
Isaacs, A.M.6
-
37
-
-
77953872890
-
FUS pathology defines the majority of tau-and TDP-43-negative frontotemporal lobar degeneration
-
Urwin H, Josephs KA, Rohrer JD, Mackenzie IR, Neumann M, Authier A, et al. FUS pathology defines the majority of tau-and TDP-43-negative frontotemporal lobar degeneration. Acta Neuropathol 2010; 120: 33-41.
-
(2010)
Acta Neuropathol
, vol.120
, pp. 33-41
-
-
Urwin, H.1
Josephs, K.A.2
Rohrer, J.D.3
MacKenzie, I.R.4
Neumann, M.5
Authier, A.6
-
38
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
Vance C, Rogelj B, Hortobagyi T, De Vos KJ, Nishimura AL, Sreedharan J, et al. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 2009; 323: 1208-11.
-
(2009)
Science
, vol.323
, pp. 1208-1211
-
-
Vance, C.1
Rogelj, B.2
Hortobagyi, T.3
De Vos, K.J.4
Nishimura, A.L.5
Sreedharan, J.6
-
39
-
-
77955093329
-
Fused in sarcoma/translocated in liposarcoma: A multifunctional DNA/RNA binding protein
-
Yang S, Warraich ST, Nicholson GA, Blair IP. Fused in sarcoma/translocated in liposarcoma: a multifunctional DNA/RNA binding protein. Int J Biochem Cell Biol 2010; 42: 1408-11.
-
(2010)
Int J Biochem Cell Biol
, vol.42
, pp. 1408-1411
-
-
Yang, S.1
Warraich, S.T.2
Nicholson, G.A.3
Blair, I.P.4
-
40
-
-
0030746523
-
TLS (FUS) binds RNA in vivo and engages in nucleo-cytoplasmic shuttling
-
Zinszner H, Sok J, Immanuel D, Yin Y, Ron D. TLS (FUS) binds RNA in vivo and engages in nucleo-cytoplasmic shuttling. J Cell Sci 1997; 110 (Pt 15): 1741-50. (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
|