-
1
-
-
0000244405
-
Uber die Beziehungen der senilen Hirnatrophie zur Aphasie
-
Pick A. Uber die Beziehungen der senilen Hirnatrophie zur Aphasie. Prager Med Wochenschr 17: 165-167 (1892).
-
(1892)
Prager Med Wochenschr
, vol.17
, pp. 165-167
-
-
Pick, A.1
-
2
-
-
0025341975
-
Dementia lacking distinctive histologic features: A common non-Alzheimer degenerative dementia
-
Knopman DS, Mastri AR, Frey WH 2nd, Sung JH, Rustan T. Dementia lacking distinctive histologic features: a common non-Alzheimer degenerative dementia. Neurology 40: 251-256 (1990).
-
(1990)
Neurology
, vol.40
, pp. 251-256
-
-
Knopman, D.S.1
Mastri, A.R.2
Frey 2nd, W.H.3
Sung, J.H.4
Rustan, T.5
-
3
-
-
0028223015
-
The Lund and Manchester Groups
-
Clinical and neuropathological criteria for frontotemporal dementia
-
Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups. J Neurosurg Psychiatry 57(4): 416-418 (1994).
-
(1994)
J Neurosurg Psychiatry
, vol.57
, Issue.4
, pp. 416-418
-
-
-
4
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus of clinical diagnostic criteria
-
Neary D, Snowden JS, Gustafson L, Passant U, Stuss D, Black S, et al. Frontotemporal lobar degeneration: A consensus of clinical diagnostic criteria. Neurology 51(6): 1546-1554 (1998).
-
(1998)
Neurology
, vol.51
, Issue.6
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
Passant, U.4
Stuss, D.5
Black, S.6
-
5
-
-
8944226575
-
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): Report of the NINDS-SPSP international workshop
-
Litvan I, Agid Y, Calne D, Campbell G, Dubois B, Duvoisin RC, et al. Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop. Neurology 47(1): 1-9 (1996).
-
(1996)
Neurology
, vol.47
, Issue.1
, pp. 1-9
-
-
Litvan, I.1
Agid, Y.2
Calne, D.3
Campbell, G.4
Dubois, B.5
Duvoisin, R.C.6
-
6
-
-
0001111974
-
Cortical-basal ganglionic degeneration
-
Saunders (Ed.)
-
Lang A. Cortical-basal ganglionic degeneration. In Saunders (Ed.), Neurodegenerative Dis 877-894 (1994).
-
(1994)
Neurodegenerative Dis
, pp. 877-894
-
-
Lang, A.1
-
7
-
-
0034764622
-
Clinical and pathological diagnosis of frontotemporal dementia. Report of the work group on frontotemporal dementia and Pick's disease
-
McKhann GM, Albert MS, Grossman M, Miller B, Dickson D, Trojanowski JQ. Clinical and Pathological Diagnosis of Frontotemporal Dementia. Report of the work group on frontotemporal dementia and Pick's disease. Arch Neurol 58: 1803-1809 (2001).
-
(2001)
Arch Neurol
, vol.58
, pp. 1803-1809
-
-
McKhann, G.M.1
Albert, M.S.2
Grossman, M.3
Miller, B.4
Dickson, D.5
Trojanowski, J.Q.6
-
8
-
-
24344457727
-
The evolution and pathology of frontotemporal dementia
-
Kertesz A, McMonagle P, Blair M, Davidson W, Munoz DG. The evolution and pathology of frontotemporal dementia. Brain 128: 1996-2005 (2005).
-
(2005)
Brain
, vol.128
, pp. 1996-2005
-
-
Kertesz, A.1
McMonagle, P.2
Blair, M.3
Davidson, W.4
Munoz, D.G.5
-
9
-
-
33751001753
-
Progression in frontotemporal dementia: Identifying a benign behavioral variant by magnetic resonance imaging
-
Davies RR, Kipps CM, Mitchell J, Kril JJ, Halliday GM, Hodges JR. Progression in frontotemporal dementia: identifying a benign behavioral variant by magnetic resonance imaging. Arch Neurol 63(11): 1627-1631 (2006).
-
(2006)
Arch Neurol
, vol.63
, Issue.11
, pp. 1627-1631
-
-
Davies, R.R.1
Kipps, C.M.2
Mitchell, J.3
Kril, J.J.4
Halliday, G.M.5
Hodges, J.R.6
-
10
-
-
62149149465
-
Survival in frontotemporal lobar degeneration and related disorders: Latent class predictors and brain functional correlates
-
Borroni B, Grassi M, Agosti C, Premi E, Alberici A, Paghera B, et al. Survival in frontotemporal lobar degeneration and related disorders: latent class predictors and brain functional correlates. Rejuvenation Res 12(1): 33-44 (2009).
-
(2009)
Rejuvenation Res
, vol.12
, Issue.1
, pp. 33-44
-
-
Borroni, B.1
Grassi, M.2
Agosti, C.3
Premi, E.4
Alberici, A.5
Paghera, B.6
-
11
-
-
0042626056
-
Survival in frontotemporal dementia
-
Hodges JR, Davies R, Xuereb J, Kril J, Halliday G. Survival in frontotemporal dementia. Neurology 61(3): 349-354 (2003).
-
(2003)
Neurology
, vol.61
, Issue.3
, pp. 349-354
-
-
Hodges, J.R.1
Davies, R.2
Xuereb, J.3
Kril, J.4
Halliday, G.5
-
12
-
-
74249101783
-
Semantic dementia: Demography, familial factors and survival in a consecutive series of 100 cases
-
Hodges JR, Mitchell J, Dawson K, Spillantini MG, Xuereb JH, McMonagle P, et al. Semantic dementia: demography, familial factors and survival in a consecutive series of 100 cases. Brain 133: 300-306 (2010).
-
(2010)
Brain
, vol.133
, pp. 300-306
-
-
Hodges, J.R.1
Mitchell, J.2
Dawson, K.3
Spillantini, M.G.4
Xuereb, J.H.5
McMonagle, P.6
-
13
-
-
47049107932
-
Measuring progression in frontotemporal dementia: Implications for therapeutic interventions
-
Kipps CM, Nestor PJ, Dawson CE, Mitchell J, Hodges JR. Measuring progression in frontotemporal dementia: implications for therapeutic interventions. Neurology 70(22): 2046-2052 (2008).
-
(2008)
Neurology
, vol.70
, Issue.22
, pp. 2046-2052
-
-
Kipps, C.M.1
Nestor, P.J.2
Dawson, C.E.3
Mitchell, J.4
Hodges, J.R.5
-
14
-
-
55749085637
-
Development of methodology for conducting clinical trials in frontotemporal lobar degeneration
-
Knopman DS, Kramer JH, Boeve BF, Caselli RJ, Graff-Radford NR, Mendez MF, et al. Development of methodology for conducting clinical trials in frontotemporal lobar degeneration. Brain 13: 2957-2968 (2008).
-
(2008)
Brain
, vol.13
, pp. 2957-2968
-
-
Knopman, D.S.1
Kramer, J.H.2
Boeve, B.F.3
Caselli, R.J.4
Graff-Radford, N.R.5
Mendez, M.F.6
-
15
-
-
20844443269
-
Frontotemporal lobar degeneration: Demographic characteristics of 353 patients
-
Johnson JK, Diehl J, Mendez MF, Neuhaus J, Shapira JS, Forman M, et al. Frontotemporal lobar degeneration: demographic characteristics of 353 patients. Arch Neurol 62(6): 925-930 (2005).
-
(2005)
Arch Neurol
, vol.62
, Issue.6
, pp. 925-930
-
-
Johnson, J.K.1
Diehl, J.2
Mendez, M.F.3
Neuhaus, J.4
Shapira, J.S.5
Forman, M.6
-
16
-
-
56149118607
-
Incidence of early-onset dementias in Cambridgeshire, United Kingdom
-
Mercy L, Hodges JR, Dawson K, Barker RA, Brayne C. Incidence of early-onset dementias in Cambridgeshire, United Kingdom. Neurology 71(19): 1496-9 (2008).
-
(2008)
Neurology
, vol.71
, Issue.19
, pp. 1496-1499
-
-
Mercy, L.1
Hodges, J.R.2
Dawson, K.3
Barker, R.A.4
Brayne, C.5
-
17
-
-
0037062609
-
The prevalence of frontotemporal dementia
-
Ratnavalli E, Brayne C, Dawson K, Hodges JR. The prevalence of frontotemporal dementia. Neurology 58(11): 1615-1621 (2002).
-
(2002)
Neurology
, vol.58
, Issue.11
, pp. 1615-1621
-
-
Ratnavalli, E.1
Brayne, C.2
Dawson, K.3
Hodges, J.R.4
-
18
-
-
0041320789
-
Frontotemporal dementia in The Netherlands: Patient characteristics and prevalence estimates from a populationbased study
-
Rosso SM, Donker Kaat L, Baks T, Joosse M, de Koning I, Pijnenburg Y, et al. Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a populationbased study. Brain 126(Pt 9): 2016-2022 (2003).
-
(2003)
Brain
, vol.126
, Issue.PART 9
, pp. 2016-2022
-
-
Rosso, S.M.1
Donker, K.L.2
Baks, T.3
Joosse, M.4
de Koning, I.5
Pijnenburg, Y.6
-
19
-
-
0037804089
-
The prevalence of frontal variant frontotemporal dementia and the frontal lobe syn-drome in a population based sample of 85 year olds
-
Gislason TB, Sjögren M, Larsson L, Skoog I. The prevalence of frontal variant frontotemporal dementia and the frontal lobe syn-drome in a population based sample of 85 year olds. J Neurol Neurosurg Psychiatry 74(7): 867-871 (2003).
-
(2003)
J Neurol Neurosurg Psychiatry
, vol.74
, Issue.7
, pp. 867-871
-
-
Gislason, T.B.1
Sjögren, M.2
Larsson, L.3
Skoog, I.4
-
20
-
-
75149132914
-
Is frontotemporal lobar degeneration a rare disorder? Evidence from a preliminary study in brescia county, Italy
-
Borroni B, Alberici A, Grassi M, Turla M, Zanetti O, Bianchetti A, et al. Is Frontotemporal Lobar Degeneration a Rare Disorder? Evidence from a preliminary study in brescia county, Italy. J Alzheimers Dis 19(1): 111-116 (2010).
-
(2010)
J Alzheimers Dis
, vol.19
, Issue.1
, pp. 111-116
-
-
Borroni, B.1
Alberici, A.2
Grassi, M.3
Turla, M.4
Zanetti, O.5
Bianchetti, A.6
-
21
-
-
51849177331
-
Klinish-genealogischer Nachweis von Erblichkeit bei Pickscher Krankheit
-
Gruntal E. Klinish-genealogischer Nachweis von Erblichkeit bei Pickscher Krankheit. Zeitschrift Fur gesante Neurologie Psychiatrie 136: 464 (1931).
-
(1931)
Zeitschrift Fur Gesante Neurologie Psychiatrie
, vol.136
, pp. 464
-
-
Gruntal, E.1
-
23
-
-
0031800415
-
Familial aggregation in frontotemporal dementia
-
Stevens M, van Duijn CM, Kamphorst W, de Knijff P, Heutink P, van Gool WA, et al. Familial aggregation in frontotemporal dementia. Neurology 50(6): 1541-1545 (1998).
-
(1998)
Neurology
, vol.50
, Issue.6
, pp. 1541-1545
-
-
Stevens, M.1
van Duijn, C.M.2
Kamphorst, W.3
de Knijff, P.4
Heutink, P.5
van Gool, W.A.6
-
24
-
-
23044471011
-
Mutations in the endosomal ESCRTIIIcomplex subunit CHMP2B in frontotemporal dementia
-
Skibinski G, Parkinson NJ, Brown JM, Chakrabarti L, Lloyd SL, Hummerich H, et al. Mutations in the endosomal ESCRTIIIcomplex subunit CHMP2B in frontotemporal dementia. Nat Genet 37(8): 806-808 (2005).
-
(2005)
Nat Genet
, vol.37
, Issue.8
, pp. 806-808
-
-
Skibinski, G.1
Parkinson, N.J.2
Brown, J.M.3
Chakrabarti, L.4
Lloyd, S.L.5
Hummerich, H.6
-
25
-
-
1842483843
-
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosincontaining protein
-
Watts GD, Wymer J, Kovach MJ, Mehta SG, Mumm S, Darvish D, et al. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosincontaining protein. Nat Genet 36(4): 377-381 (2004).
-
(2004)
Nat Genet
, vol.36
, Issue.4
, pp. 377-381
-
-
Watts, G.D.1
Wymer, J.2
Kovach, M.J.3
Mehta, S.G.4
Mumm, S.5
Darvish, D.6
-
26
-
-
0034605478
-
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
-
Hosler BA, Siddique T, Sapp PC, Sailor W, Huang MC, Hossain A, et al. Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. JAMA 284(13): 1664-1669 (2000).
-
(2000)
JAMA
, vol.284
, Issue.13
, pp. 1664-1669
-
-
Hosler, B.A.1
Siddique, T.2
Sapp, P.C.3
Sailor, W.4
Huang, M.C.5
Hossain, A.6
-
27
-
-
33645062075
-
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
-
Morita M, Al-Chalabi A, Andersen PM, Hosler B, Sapp P, Englund E, et al. A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia. Neurology 66(6): 839-844 (2006).
-
(2006)
Neurology
, vol.66
, Issue.6
, pp. 839-844
-
-
Morita, M.1
Al-Chalabi, A.2
Andersen, P.M.3
Hosler, B.4
Sapp, P.5
Englund, E.6
-
28
-
-
33645069660
-
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3
-
Vance C, Al-Chalabi A, Ruddy D, Smith BN, Hu X, Sreedharan J, et al. Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3. Brain 129(Pt 4): 868-876. (2006).
-
(2006)
Brain
, vol.129
, Issue.PART 4
, pp. 868-876
-
-
Vance, C.1
Al-Chalabi, A.2
Ruddy, D.3
Smith, B.N.4
Hu, X.5
Sreedharan, J.6
-
29
-
-
0030977392
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference. Conference Participants
-
Foster NL, Wilhelmsen K, Sima AA, Jones MZ, D'Amato CJ, Gilman S. Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants. Ann Neurol 41(6): 706-715 (1997).
-
(1997)
Ann Neurol
, vol.41
, Issue.6
, pp. 706-715
-
-
Foster, N.L.1
Wilhelmsen, K.2
Sima, A.A.3
Jones, M.Z.4
D'Amato, C.J.5
Gilman, S.6
-
30
-
-
0032543684
-
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, et al. Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 18:393(6686): 702-705 (1998).
-
(1998)
Nature 18
, vol.393
, Issue.6686
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, H.6
-
31
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, Lindholm C, et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442: 916-919 (2006).
-
(2006)
Nature
, vol.442
, pp. 916-919
-
-
Baker, M.1
Mackenzie, I.R.2
Pickering-Brown, S.M.3
Gass, J.4
Rademakers, R.5
Lindholm, C.6
-
32
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, et al. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442: 920-924 (2006).
-
(2006)
Nature
, vol.442
, pp. 920-924
-
-
Cruts, M.1
Gijselinck, I.2
van der Zee, J.3
Engelborghs, S.4
Wils, H.5
Pirici, D.6
-
33
-
-
77649187519
-
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: An update
-
Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, et al. Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update. Acta Neuropathol 119: 1-4 (2010).
-
(2010)
Acta Neuropathol
, vol.119
, pp. 1-4
-
-
Mackenzie, I.R.1
Neumann, M.2
Bigio, E.H.3
Cairns, N.J.4
Alafuzoff, I.5
Kril, J.6
-
34
-
-
70350673956
-
A new subtype of frontotemporal lobar degeneration with FUS pathology
-
Neumann M, Rademakers R, Roeber S, Baker M, Kretzschmar HA, Mackenzie IR. A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain 132(Pt 11): 2922-2931 (2009).
-
(2009)
Brain
, vol.132
, Issue.PART 11
, pp. 2922-2931
-
-
Neumann, M.1
Rademakers, R.2
Roeber, S.3
Baker, M.4
Kretzschmar, H.A.5
Mackenzie, I.R.6
-
35
-
-
77953872890
-
FUS pathology in basophilic inclusion body disease
-
Urwin H, Josephs KA, Rohrer JD, Mackenzie IR, Neumann M, Authier A, et al. FUS pathology in basophilic inclusion body disease. Acta Neuropathol 120(1): 33-41 (2010).
-
(2010)
Acta Neuropathol
, vol.120
, Issue.1
, pp. 33-41
-
-
Urwin, H.1
Josephs, K.A.2
Rohrer, J.D.3
Mackenzie, I.R.4
Neumann, M.5
Authier, A.6
-
36
-
-
76349115779
-
Genetic contribution of FUS to frontotemporal lobar degeneration
-
Van Langenhove T, van der Zee J, Sleegers K, Engelborghs S, Vandenberghe R, Gijselinck I, et al. Genetic contribution of FUS to frontotemporal lobar degeneration. Neurology 74(5): 366-371 (2010).
-
(2010)
Neurology
, vol.74
, Issue.5
, pp. 366-371
-
-
van Langenhove, T.1
van der Zee, J.2
Sleegers, K.3
Engelborghs, S.4
Vandenberghe, R.5
Gijselinck, I.6
-
37
-
-
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 118(5):617-27 (2009).
-
(2009)
Acta Neuropathol
, vol.118
, Issue.5
, pp. 617-627
-
-
Munoz, D.G.1
Neumann, M.2
Kusaka, H.3
Yokota, O.4
Ishihara, K.5
Terada, S.6
-
38
-
-
0002792366
-
Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease: Identification as the microtubule-associated protein tau
-
Goedert M, Wischik CM, Crowther RA, Walker JE, Klug A. Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease: identification as the microtubule-associated protein tau. Proc Natl Acad Sci U S A 85(11): 4051-4055 (1988).
-
(1988)
Proc Natl Acad Sci U S A
, vol.85
, Issue.11
, pp. 4051-4055
-
-
Goedert, M.1
Wischik, C.M.2
Crowther, R.A.3
Walker, J.E.4
Klug, A.5
-
39
-
-
0024387161
-
Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: Differential expression of tau protein mRNAs in human brain
-
Goedert M, Spillantini MG, Potier MC, Ulrich J, Crowther RA. Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain. EMBO J 8(2): 393-399 (1989).
-
(1989)
EMBO J
, vol.8
, Issue.2
, pp. 393-399
-
-
Goedert, M.1
Spillantini, M.G.2
Potier, M.C.3
Ulrich, J.4
Crowther, R.A.5
-
40
-
-
0024745894
-
Multiple isoforms of human microtubule-associated protein tau: Sequences and localization in neurofibrillary tangles of Alzheimer's disease
-
Goedert M, Spillantini MG, Jakes R, Rutherford D, Crowther RA. Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease. Neuron 3(4): 519-526 (1989).
-
(1989)
Neuron
, vol.3
, Issue.4
, pp. 519-526
-
-
Goedert, M.1
Spillantini, M.G.2
Jakes, R.3
Rutherford, D.4
Crowther, R.A.5
-
41
-
-
0027945346
-
Biopsy-derived adult human brain tau is phosphorylated at many of the same sites as Alzheimer's disease paired helical filament tau
-
Matsuo ES, Shin RW, Billingsley ML, Van deVoorde A, O'Connor M, Trojanowski JQ, et al. Biopsy-derived adult human brain tau is phosphorylated at many of the same sites as Alzheimer's disease paired helical filament tau. Neuron 13(4): 989-1002 (1994).
-
(1994)
Neuron
, vol.13
, Issue.4
, pp. 989-1002
-
-
Matsuo, E.S.1
Shin, R.W.2
Billingsley, M.L.3
van Devoorde, A.4
O'Connor, M.5
Trojanowski, J.Q.6
-
42
-
-
33645300736
-
The prolyl isomerase Pin1 regulates amyloid precursor protein processing and amyloid-beta production
-
Pastorino L, Sun A, Lu PJ, Zhou XZ, Balastik M, Finn G, et al. The prolyl isomerase Pin1 regulates amyloid precursor protein processing and amyloid-beta production. Nature 440(7083): 528-534 (2006).
-
(2006)
Nature
, vol.440
, Issue.7083
, pp. 528-534
-
-
Pastorino, L.1
Sun, A.2
Lu, P.J.3
Zhou, X.Z.4
Balastik, M.5
Finn, G.6
-
43
-
-
0033600242
-
The prolyl isomerase Pin1 restores the function of Alzheimer-associated phosphorylated tau protein
-
Lu PJ, Wulf G, Zhou XZ, Davies P, Lu KP. The prolyl isomerase Pin1 restores the function of Alzheimer-associated phosphorylated tau protein. Nature 399(6738): 784-788 (1999).
-
(1999)
Nature
, vol.399
, Issue.6738
, pp. 784-788
-
-
Lu, P.J.1
Wulf, G.2
Zhou, X.Z.3
Davies, P.4
Lu, K.P.5
-
44
-
-
39749165656
-
Differential regulation of dynein and kinesin motor proteins by tau
-
Dixit R, Ross JL, Goldman YE, Holzbaur EL. Differential regulation of dynein and kinesin motor proteins by tau. Science 319(5866): 1086-1089 (2008).
-
(2008)
Science
, vol.319
, Issue.5866
, pp. 1086-1089
-
-
Dixit, R.1
Ross, J.L.2
Goldman, Y.E.3
Holzbaur, E.L.4
-
45
-
-
0037128935
-
Tau blocks traffic of organelles, neurofilaments, and APP vesicles in neurons and enhances oxidative stress
-
Stamer K, Vogel R, Thies E, Mandelkow E, Mandelkow EM. Tau blocks traffic of organelles, neurofilaments, and APP vesicles in neurons and enhances oxidative stress. J Cell Biol 156(6): 1051-1063 (2002).
-
(2002)
J Cell Biol
, vol.156
, Issue.6
, pp. 1051-1063
-
-
Stamer, K.1
Vogel, R.2
Thies, E.3
Mandelkow, E.4
Mandelkow, E.M.5
-
46
-
-
35649028013
-
Interaction of tau protein with the dynactin complex
-
Magnani E, Fan J, Gasparini L, Golding M, Williams M, Schiavo G, et al. Interaction of tau protein with the dynactin complex. EMBO J 26(21): 4546-4554 (2007).
-
(2007)
EMBO J
, vol.26
, Issue.21
, pp. 4546-4554
-
-
Magnani, E.1
Fan, J.2
Gasparini, L.3
Golding, M.4
Williams, M.5
Schiavo, G.6
-
47
-
-
0037466656
-
Initiation and synergistic fibrillization of tau and alpha-synuclein
-
Giasson BI, Forman MS, Higuchi M, Golbe LI, Graves CL, Kotzbauer PT, et al. Initiation and synergistic fibrillization of tau and alpha-synuclein. Science 300(5619): 636-640 (2003).
-
(2003)
Science
, vol.300
, Issue.5619
, pp. 636-640
-
-
Giasson, B.I.1
Forman, M.S.2
Higuchi, M.3
Golbe, L.I.4
Graves, C.L.5
Kotzbauer, P.T.6
-
48
-
-
9144257938
-
DJ-1 colocalizes with tau inclusions: A link between parkinsonism and dementia
-
Rizzu P, Hinkle DA, Zhukareva V, Bonifati V, Severijnen LA, Martinez D, et al. DJ-1 colocalizes with tau inclusions: a link between parkinsonism and dementia. Ann Neurol 55(1): 113-118 (2004).
-
(2004)
Ann Neurol
, vol.55
, Issue.1
, pp. 113-118
-
-
Rizzu, P.1
Hinkle, D.A.2
Zhukareva, V.3
Bonifati, V.4
Severijnen, L.A.5
Martinez, D.6
-
49
-
-
11144356089
-
CHIP and Hsp70 regulate tau ubiquitination, degradation and aggregation
-
Petrucelli L, Dickson D, Kehoe K, Taylor J, Snyder H, Grover A, et al. CHIP and Hsp70 regulate tau ubiquitination, degradation and aggregation. Hum Mol Genet 13(7): 703-714 (2004).
-
(2004)
Hum Mol Genet
, vol.13
, Issue.7
, pp. 703-714
-
-
Petrucelli, L.1
Dickson, D.2
Kehoe, K.3
Taylor, J.4
Snyder, H.5
Grover, A.6
-
50
-
-
58549092073
-
Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland
-
Kaivorinne AL, Krüger J, Kuivaniemi K, Tuominen H, Moilanen V, Majamaa K, et al. Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland. BMC Neurol 17: 8-48 (2008).
-
(2008)
BMC Neurol
, vol.17
, pp. 8-48
-
-
Kaivorinne, A.L.1
Krüger, J.2
Kuivaniemi, K.3
Tuominen, H.4
Moilanen, V.5
Majamaa, K.6
-
51
-
-
7344220963
-
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism
-
Dumanchin C, Camuzat A, Campion D, Verpillat P, Hannequin D, Dubois B, et al. Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism. Hum Mol Genet 7(11): 1825-1829 (1998).
-
(1998)
Hum Mol Genet
, vol.7
, Issue.11
, pp. 1825-1829
-
-
Dumanchin, C.1
Camuzat, A.2
Campion, D.3
Verpillat, P.4
Hannequin, D.5
Dubois, B.6
-
52
-
-
0032837303
-
Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia
-
Houlden H, Baker M, Adamson J, Grover A, Waring S, Dickson D, et al. Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia. Ann Neurol 46(2): 243-248 (1999).
-
(1999)
Ann Neurol
, vol.46
, Issue.2
, pp. 243-248
-
-
Houlden, H.1
Baker, M.2
Adamson, J.3
Grover, A.4
Waring, S.5
Dickson, D.6
-
53
-
-
0034756333
-
The genetic and pathological classification of familial frontotemporal dementia
-
Morris HR, Khan MN, Janssen JC, Brown JM, Perez-Tur J, Baker M, et al. The genetic and pathological classification of familial frontotemporal dementia. Arch Neurol 58(11): 1813-1816 (2001).
-
(2001)
Arch Neurol
, vol.58
, Issue.11
, pp. 1813-1816
-
-
Morris, H.R.1
Khan, M.N.2
Janssen, J.C.3
Brown, J.M.4
Perez-Tur, J.5
Baker, M.6
-
54
-
-
0035108754
-
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia
-
Poorkaj P, Grossman M, Steinbart E, Payami H, Sadovnick A, Nochlin D, et al. Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia. Arch Neurol 58(3): 383-387 (2001).
-
(2001)
Arch Neurol
, vol.58
, Issue.3
, pp. 383-387
-
-
Poorkaj, P.1
Grossman, M.2
Steinbart, E.3
Payami, H.4
Sadovnick, A.5
Nochlin, D.6
-
55
-
-
0033070197
-
High prevalence of mutations in the microtubuleassociated protein tau in a population study of frontotemporal dementia in the Netherlands
-
Rizzu P, Van Swieten JC, Joosse M, Hasegawa M, Stevens M, Tibben A, et al. High prevalence of mutations in the microtubuleassociated protein tau in a population study of frontotemporal dementia in the Netherlands. Am J Hum Genet 64 (2): 414-421 (1999).
-
(1999)
Am J Hum Genet
, vol.64
, Issue.2
, pp. 414-421
-
-
Rizzu, P.1
van Swieten, J.C.2
Joosse, M.3
Hasegawa, M.4
Stevens, M.5
Tibben, A.6
-
56
-
-
0037455980
-
Prevalence of TAU mutations in an Italian clinical series of familial frontotemporal patients
-
Binetti G, Nicosia F, Benussi L, Ghidoni R, Feudatari E, Barbiero L, et al. Prevalence of TAU mutations in an Italian clinical series of familial frontotemporal patients. Neurosci Lett 338(1): 85-87 (2003).
-
(2003)
Neurosci Lett
, vol.338
, Issue.1
, pp. 85-87
-
-
Binetti, G.1
Nicosia, F.2
Benussi, L.3
Ghidoni, R.4
Feudatari, E.5
Barbiero, L.6
-
57
-
-
42249085980
-
Refining frontotemporal dementia with parkinsonism linked to chromosome 17: Introducing FTDP-17 (MAPT) and FTDP-17 (PGRN)
-
Boeve BF, Hutton M. Refining frontotemporal dementia with parkinsonism linked to chromosome 17: introducing FTDP-17 (MAPT) and FTDP-17 (PGRN). Arch Neurol 65(4): 460-464 (2008).
-
(2008)
Arch Neurol
, vol.65
, Issue.4
, pp. 460-464
-
-
Boeve, B.F.1
Hutton, M.2
-
58
-
-
0035199224
-
Dementia and neurodevelopmental predisposition: Cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia
-
Geschwind DH, Robidoux J, Alarcón M, Miller BL, Wilhelmsen KC, Cummings JL, et al. Dementia and neurodevelopmental predisposition: cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia. Ann Neurol 50(6): 741-746 (2001).
-
(2001)
Ann Neurol
, vol.50
, Issue.6
, pp. 741-746
-
-
Geschwind, D.H.1
Robidoux, J.2
Alarcón, M.3
Miller, B.L.4
Wilhelmsen, K.C.5
Cummings, J.L.6
-
59
-
-
77956227571
-
Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations
-
Rohrer JD, Ridgway GR, Modat M, Ourselin S, Mead S, Fox NC, et al. Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations. Neuroimage 53(3): 1070-6 (2010).
-
(2010)
Neuroimage
, vol.53
, Issue.3
, pp. 1070-1076
-
-
Rohrer, J.D.1
Ridgway, G.R.2
Modat, M.3
Ourselin, S.4
Mead, S.5
Fox, N.C.6
-
60
-
-
43249106998
-
CSF biomarkers in frontotemporal lobar degeneration with known pathology
-
Bian H, Van Swieten JC, Leight S, Massimo L, Wood E, Forman M, et al. CSF biomarkers in frontotemporal lobar degeneration with known pathology. Neurology 70(19 Pt 2): 1827-1835 (2008).
-
(2008)
Neurology
, vol.70
, Issue.19 PART 2
, pp. 1827-1835
-
-
Bian, H.1
van Swieten, J.C.2
Leight, S.3
Massimo, L.4
Wood, E.5
Forman, M.6
-
61
-
-
0034624014
-
Structural and functional differences between 3-repeat and 4-repeat tau isoforms. Implications for normal tau function and the onset of neurodegenetative disease
-
Goode BL, Chau M, Denis PE, Feinstein SC. Structural and functional differences between 3-repeat and 4-repeat tau isoforms. Implications for normal tau function and the onset of neurodegenetative disease. J Biol Chem 275(49): 38182-38189 (2000).
-
(2000)
J Biol Chem
, vol.275
, Issue.49
, pp. 38182-38189
-
-
Goode, B.L.1
Chau, M.2
Denis, P.E.3
Feinstein, S.C.4
-
62
-
-
21044449225
-
Inhibition of glycogen synthase kinase-3 by lithium correlates with reduced tauopathy and degeneration in vivo
-
Noble W, Planel E, Zehr C, Olm V, Meyerson J, Suleman F, et al. Inhibition of glycogen synthase kinase-3 by lithium correlates with reduced tauopathy and degeneration in vivo. Proc Natl Acad Sci USA 102(19): 6990-6995 (2005).
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, Issue.19
, pp. 6990-6995
-
-
Noble, W.1
Planel, E.2
Zehr, C.3
Olm, V.4
Meyerson, J.5
Suleman, F.6
-
63
-
-
19944429064
-
Microtubule-binding drugs offset tau sequestration by stabilizing microtubules and reversing fast axonal transport deficits in a tauopathy model
-
Zhang B, Maiti A, Shively S, Lakhani F, McDonald-Jones G, Bruce J, et al. Microtubule-binding drugs offset tau sequestration by stabilizing microtubules and reversing fast axonal transport deficits in a tauopathy model. Proc Natl Acad Sci USA 102(1): 227-231 (2005).
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, Issue.1
, pp. 227-231
-
-
Zhang, B.1
Maiti, A.2
Shively, S.3
Lakhani, F.4
McDonald-Jones, G.5
Bruce, J.6
-
64
-
-
45049084534
-
Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease
-
Rovelet-Lecrux A, Deramecourt V, Legallic S, Maurage CA, Le Ber I, Brice A, et al. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease. Neurobiol Dis 31(1): 41-45 (2008).
-
(2008)
Neurobiol Dis
, vol.31
, Issue.1
, pp. 41-45
-
-
Rovelet-Lecrux, A.1
Deramecourt, V.2
Legallic, S.3
Maurage, C.A.4
Le Ber, I.5
Brice, A.6
-
65
-
-
63749104739
-
Partial deletion of the MAPT gene: A novel mechanism of FTDP-17
-
Rovelet-Lecrux A, Lecourtois M, Thomas-Anterion C, Le Ber I, Brice A, Frebourg T, et al. Partial deletion of the MAPT gene: a novel mechanism of FTDP-17. Hum Mutat 30(4): 591-602 (2009).
-
(2009)
Hum Mutat
, vol.30
, Issue.4
, pp. 591-602
-
-
Rovelet-Lecrux, A.1
Lecourtois, M.2
Thomas-Anterion, C.3
Le Ber, I.4
Brice, A.5
Frebourg, T.6
-
66
-
-
0026580016
-
Isolation and sequence of the granulin precursor cDNA from human bone marrow reveals tandem cysteine-rich granulin domains
-
Bhandari V, Palfree RG, Bateman A. Isolation and sequence of the granulin precursor cDNA from human bone marrow reveals tandem cysteine-rich granulin domains. Proc Natl Acad Sci USA 89(5): 1715-1719 (1992).
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, Issue.5
, pp. 1715-1719
-
-
Bhandari, V.1
Palfree, R.G.2
Bateman, A.3
-
67
-
-
0027506142
-
Acrogranin, an acrosomal cysteine-rich glycoprotein, is the precursor of the growth-modulating peptides, granulins, and epithelins, and is expressed in somatic as well as male germ cells
-
Baba T, Hoff HB 3rd, Nemoto H, Lee H, Orth J, Arai Y, et al. Acrogranin, an acrosomal cysteine-rich glycoprotein, is the precursor of the growth-modulating peptides, granulins, and epithelins, and is expressed in somatic as well as male germ cells. Mol Reprod Dev 34(3): 233-243 (1993).
-
(1993)
Mol Reprod Dev
, vol.34
, Issue.3
, pp. 233-243
-
-
Baba, T.1
Hoff 3rd, H.B.2
Nemoto, H.3
Lee, H.4
Orth, J.5
Arai, Y.6
-
68
-
-
0029780955
-
The hairpin stack fold, a novel protein architecture for a new family of protein growth factors
-
Hrabal R, Chen Z, James S, Bennett HP, Ni F. The hairpin stack fold, a novel protein architecture for a new family of protein growth factors. Nat Struct Biol 3(9): 747-752 (1996).
-
(1996)
Nat Struct Biol
, vol.3
, Issue.9
, pp. 747-752
-
-
Hrabal, R.1
Chen, Z.2
James, S.3
Bennett, H.P.4
Ni, F.5
-
69
-
-
0037074016
-
Conversion of proepithelin to epithelins: Roles of SLPI and elastase in host defense and wound repair
-
Zhu J, Nathan C, Jin W, Sim D, Ashcroft GS, Wahl SM, et al. Conversion of proepithelin to epithelins: roles of SLPI and elastase in host defense and wound repair. Cell 111(6): 867-878 (2002).
-
(2002)
Cell
, vol.111
, Issue.6
, pp. 867-878
-
-
Zhu, J.1
Nathan, C.2
Jin, W.3
Sim, D.4
Ashcroft, G.S.5
Wahl, S.M.6
-
70
-
-
0037329891
-
Progranulin is a mediator of the wound response
-
He Z, Ong CH, Halper J, Bateman A. Progranulin is a mediator of the wound response. Nat Med 9(2): 225-229 (2003).
-
(2003)
Nat Med
, vol.9
, Issue.2
, pp. 225-229
-
-
He, Z.1
Ong, C.H.2
Halper, J.3
Bateman, A.4
-
71
-
-
0033168521
-
Progranulin gene expression regulates epithelial cell growth and promotes tumor growth in vivo
-
He Z, Bateman A. Progranulin gene expression regulates epithelial cell growth and promotes tumor growth in vivo. Cancer Res 59(13): 3222-3229 (1999).
-
(1999)
Cancer Res
, vol.59
, Issue.13
, pp. 3222-3229
-
-
He, Z.1
Bateman, A.2
-
72
-
-
0034163549
-
Identification of a human glioma-associated growth factor gene, granulin, using differential immuno-absorption
-
Liau LM, Lallone RL, Seitz RS, Buznikov A, Gregg JP, Kornblum HI, et al. Identification of a human glioma-associated growth factor gene, granulin, using differential immuno-absorption. Cancer Res 60(5): 1353-1360 (2000).
-
(2000)
Cancer Res
, vol.60
, Issue.5
, pp. 1353-1360
-
-
Liau, L.M.1
Lallone, R.L.2
Seitz, R.S.3
Buznikov, A.4
Gregg, J.P.5
Kornblum, H.I.6
-
73
-
-
42049087853
-
Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival
-
Van Damme P, Van Hoecke A, Lambrechts D, Vanacker P, Bogaert E, van Swieten J, et al. Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival. J Cell Biol 181(1): 37-41 (2008).
-
(2008)
J Cell Biol
, vol.181
, Issue.1
, pp. 37-41
-
-
van Damme, P.1
van Hoecke, A.2
Lambrechts, D.3
Vanacker, P.4
Bogaert, E.5
van Swieten, J.6
-
74
-
-
34247868937
-
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia
-
van der Zee J, Le Ber I, Maurer-Stroh S, Engelborghs S, Gijselinck I, Camuzat A, et al. Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia. Hum Mutat 28(4): 416 (2007).
-
(2007)
Hum Mutat
, vol.28
, Issue.4
, pp. 416
-
-
van der Zee, J.1
Le Ber, I.2
Maurer-Stroh, S.3
Engelborghs, S.4
Gijselinck, I.5
Camuzat, A.6
-
75
-
-
33749568019
-
Mutations in progranulin are a major cause of ubiquitinpositive frontotemporal lobar degeneration
-
Gass J, Cannon A, Mackenzie IR, Boeve B, Baker M, Adamson J, et al. Mutations in progranulin are a major cause of ubiquitinpositive frontotemporal lobar degeneration. Hum Mol Genet 15(20): 2988-3001 (2006).
-
(2006)
Hum Mol Genet
, 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
-
76
-
-
34447098853
-
Progranulin null mutations in both sporadic and familial frontotemporal dementia
-
Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, et al. Progranulin null mutations in both sporadic and familial frontotemporal dementia. Hum Mutat 28(9): 846-855 (2007).
-
(2007)
Hum Mutat
, vol.28
, Issue.9
, pp. 846-855
-
-
Le Ber, I.1
van der Zee, J.2
Hannequin, D.3
Gijselinck, I.4
Campion, D.5
Puel, M.6
-
77
-
-
46149083470
-
Progranulin genetic variations in frontotemporal lobar degeneration: Evidence for low mutation frequency in an Italian clinical series
-
Borroni B, Archetti S, Alberici A, Agosti C, Gennarelli M, Bigni B, et al. Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series. Neurogenetics 9(3): 197-205 (2008).
-
(2008)
Neurogenetics
, vol.9
, Issue.3
, pp. 197-205
-
-
Borroni, B.1
Archetti, S.2
Alberici, A.3
Agosti, C.4
Gennarelli, M.5
Bigni, B.6
-
78
-
-
34447340657
-
Heterogeneity within a large kindred with frontotemporal dementia: A novel progranulin mutation
-
Bruni AC, Momeni P, Bernardi L, Tomaino C, Frangipane F, Elder J, et al. Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation. Neurology 69(2): 140-147 (2007).
-
(2007)
Neurology
, vol.69
, Issue.2
, pp. 140-147
-
-
Bruni, A.C.1
Momeni, P.2
Bernardi, L.3
Tomaino, C.4
Frangipane, F.5
Elder, J.6
-
79
-
-
57449097370
-
Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration
-
Krüger J, Kaivorinne AL, Udd B, Majamaa K, Remes AM. Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration. Eur J Neurol 16(1): 27-30 (2009).
-
(2009)
Eur J Neurol
, vol.16
, Issue.1
, pp. 27-30
-
-
Krüger, J.1
Kaivorinne, A.L.2
Udd, B.3
Majamaa, K.4
Remes, A.M.5
-
80
-
-
51449107701
-
Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases
-
Guerreiro RJ, Santana I, Bras JM, Revesz T, Rebelo O, Ribeiro MH, et al. Novel progranulin mutation: screening for PGRN mutations in a Portuguese series of FTD/CBS cases. Mov Disord 23(9): 1269-1273 (2008).
-
(2008)
Mov Disord
, vol.23
, Issue.9
, pp. 1269-1273
-
-
Guerreiro, R.J.1
Santana, I.2
Bras, J.M.3
Revesz, T.4
Rebelo, O.5
Ribeiro, M.H.6
-
81
-
-
33947244850
-
Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations
-
Whitwell JL, Jack CR Jr, Baker M, Rademakers R, Adamson J, Boeve BF, et al. Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations. Arch Neurol 64(3): 371-376 (2007).
-
(2007)
Arch Neurol
, vol.64
, Issue.3
, pp. 371-376
-
-
Whitwell, J.L.1
Jack Jr., C.R.2
Baker, M.3
Rademakers, R.4
Adamson, J.5
Boeve, B.F.6
-
82
-
-
42249094592
-
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene
-
Rohrer JD, Warren JD, Omar R, Mead S, Beck J, Revesz T, et al. Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene. Arch Neurol 65(4): 506-513 (2008).
-
(2008)
Arch Neurol
, vol.65
, Issue.4
, pp. 506-513
-
-
Rohrer, J.D.1
Warren, J.D.2
Omar, R.3
Mead, S.4
Beck, J.5
Revesz, T.6
-
83
-
-
54449085260
-
Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
-
Ghidoni R, Benussi L, Glionna M, Franzoni M, Binetti G. Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration. Neurology 71(16): 1235-1239 (2008).
-
(2008)
Neurology
, vol.71
, Issue.16
, pp. 1235-1239
-
-
Ghidoni, R.1
Benussi, L.2
Glionna, M.3
Franzoni, M.4
Binetti, G.5
-
84
-
-
64849103956
-
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
-
Finch N, Baker M, Crook R, Swanson K, Kuntz K, Surtees R, et al. Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members. Brain 132(Pt 3): 583-591 (2009).
-
(2009)
Brain
, vol.132
, Issue.PART 3
, pp. 583-591
-
-
Finch, N.1
Baker, M.2
Crook, R.3
Swanson, K.4
Kuntz, K.5
Surtees, R.6
-
85
-
-
0035794665
-
Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping
-
Buratti E, Dörk T, Zuccato E, Pagani F, Romano M, Baralle FE. Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping. EMBO J 20(7): 1774-1784 (2001).
-
(2001)
EMBO J
, vol.20
, Issue.7
, pp. 1774-1784
-
-
Buratti, E.1
Dörk, T.2
Zuccato, E.3
Pagani, F.4
Romano, M.5
Baralle, F.E.6
-
86
-
-
38449102667
-
Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease
-
Buratti E, Baralle FE. Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease. Front Biosci 13: 867-878 (2008).
-
(2008)
Front Biosci
, vol.13
, pp. 867-878
-
-
Buratti, E.1
Baralle, F.E.2
-
87
-
-
70350721803
-
Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease
-
Borroni B, Bonvicini C, Alberici A, Buratti E, Agosti C, Archetti S, et al. Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease. Hum Mutat 30(11): 974-983 (2009).
-
(2009)
Hum Mutat
, vol.30
, Issue.11
, pp. 974-983
-
-
Borroni, B.1
Bonvicini, C.2
Alberici, A.3
Buratti, E.4
Agosti, C.5
Archetti, S.6
-
88
-
-
65649112431
-
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration
-
Benajiba L, Le Ber I, Camuzat A, Lacoste M, Thomas-Anterion C, Couratier P, et al. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Ann Neurol 65(4): 470-473 (2009).
-
(2009)
Ann Neurol
, vol.65
, Issue.4
, pp. 470-473
-
-
Benajiba, L.1
Le Ber, I.2
Camuzat, A.3
Lacoste, M.4
Thomas-Anterion, C.5
Couratier, P.6
-
89
-
-
70350572209
-
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
-
Kovacs GG, Murrell JR, Horvath S, Haraszti L, Majtenyi K, Molnar MJ, et al. TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Mov Disord 24(12): 1843-1847 (2009).
-
(2009)
Mov Disord
, vol.24
, Issue.12
, pp. 1843-1847
-
-
Kovacs, G.G.1
Murrell, J.R.2
Horvath, S.3
Haraszti, L.4
Majtenyi, K.5
Molnar, M.J.6
-
90
-
-
34848921202
-
Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43
-
Zhang YJ, Xu YF, Dickey CA, Buratti E, Baralle F, Bailey R, et al. Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43. J Neurosci 27(39): 10530-10534 (2007).
-
(2007)
J Neurosci
, vol.27
, Issue.39
, pp. 10530-10534
-
-
Zhang, Y.J.1
Xu, Y.F.2
Dickey, C.A.3
Buratti, E.4
Baralle, F.5
Bailey, R.6
-
91
-
-
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, Volkening K, Leystra-Lantz C, Welch I, Hill T, Strong MJ. 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).
-
(2009)
Brain Res
, vol.1249
, pp. 202-211
-
-
Moisse, K.1
Volkening, K.2
Leystra-Lantz, C.3
Welch, I.4
Hill, T.5
Strong, M.J.6
-
92
-
-
7244223202
-
Frontotemporal dementia: Impact of P301L tau mutation on a healthy carrier
-
Alberici A, Gobbo C, Panzacchi A, Nicosia F, Ghidoni R, Benussi L, et al. Frontotemporal dementia: impact of P301L tau mutation on a healthy carrier. J Neurosurg Psychiatry 75: 1607-1610 (2004).
-
(2004)
J Neurosurg Psychiatry
, vol.75
, pp. 1607-1610
-
-
Alberici, A.1
Gobbo, C.2
Panzacchi, A.3
Nicosia, F.4
Ghidoni, R.5
Benussi, L.6
-
93
-
-
46449123028
-
Brain magnetic resonance imaging structural changes in a pedigree of asymptomatic progranulin mutation carriers
-
Borroni B, Alberici A, Premi E, Archetti S, Garibotto V, Agosti C, et al. Brain magnetic resonance imaging structural changes in a pedigree of asymptomatic progranulin mutation carriers. Rejuvenation Res 11(3): 585-595 (2008).
-
(2008)
Rejuvenation Res
, vol.11
, Issue.3
, pp. 585-595
-
-
Borroni, B.1
Alberici, A.2
Premi, E.3
Archetti, S.4
Garibotto, V.5
Agosti, C.6
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