-
1
-
-
80855130688
-
Making connections: Pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia
-
Fecto F, Siddique T (2011) Making connections: Pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia. J Mol Neurosci 45(3): 663-675.
-
(2011)
J Mol Neurosci
, vol.45
, Issue.3
, pp. 663-675
-
-
Fecto, F.1
Siddique, T.2
-
2
-
-
23844511513
-
Prevalence and patterns of cognitive impairment in sporadic ALS
-
Ringholz GM, et al. (2005) Prevalence and patterns of cognitive impairment in sporadic ALS. Neurology 65(4): 586-590.
-
(2005)
Neurology
, vol.65
, Issue.4
, pp. 586-590
-
-
Ringholz, G.M.1
-
3
-
-
0037044240
-
The overlap of amyotrophic lateral sclerosis and frontotemporal dementia
-
Lomen-Hoerth C, Anderson T, Miller B (2002) The overlap of amyotrophic lateral sclerosis and frontotemporal dementia. Neurology 59(7): 1077-1079.
-
(2002)
Neurology
, vol.59
, Issue.7
, pp. 1077-1079
-
-
Lomen-Hoerth, C.1
Anderson, T.2
Miller, B.3
-
4
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann M, et al. (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314(5796): 130-133.
-
(2006)
Science
, vol.314
, Issue.5796
, pp. 130-133
-
-
Neumann, M.1
-
5
-
-
34249946466
-
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
-
Mackenzie IR, et al. (2007) Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations. Ann Neurol 61(5): 427-434.
-
(2007)
Ann Neurol
, vol.61
, Issue.5
, pp. 427-434
-
-
MacKenzie, I.R.1
-
6
-
-
62149146109
-
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis
-
Daoud H, et al. (2009) Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis. J Med Genet 46(2): 112-114.
-
(2009)
J Med Genet
, vol.46
, Issue.2
, pp. 112-114
-
-
Daoud, H.1
-
7
-
-
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(5918): 1208-1211.
-
(2009)
Science
, vol.323
, Issue.5918
, pp. 1208-1211
-
-
Vance, C.1
-
8
-
-
61349156118
-
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
-
Kwiatkowski TJ, Jr., et al. (2009) Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323(5918): 1205-1208.
-
(2009)
Science
, vol.323
, Issue.5918
, pp. 1205-1208
-
-
Kwiatkowski Jr., T.J.1
-
9
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
Kabashi E, et al. (2008) TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat Genet 40(5): 572-574.
-
(2008)
Nat Genet
, vol.40
, Issue.5
, pp. 572-574
-
-
Kabashi, E.1
-
10
-
-
84864981763
-
Advances in understanding the molecular basis of frontotemporal dementia
-
Rademakers R, Neumann M, Mackenzie IR (2012) Advances in understanding the molecular basis of frontotemporal dementia. Nat Rev Neurol 8: 423-434.
-
(2012)
Nat Rev Neurol
, vol.8
, pp. 423-434
-
-
Rademakers, R.1
Neumann, M.2
MacKenzie, I.R.3
-
11
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
DeJesus-Hernandez M, et al. (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72(2): 245-256.
-
(2011)
Neuron
, vol.72
, Issue.2
, pp. 245-256
-
-
Dejesus-Hernandez, M.1
-
12
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
ITALSGEN Consortium
-
Renton AE, et al.; ITALSGEN Consortium (2011) A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72(2): 257-268.
-
(2011)
Neuron
, vol.72
, Issue.2
, pp. 257-268
-
-
Renton, A.E.1
-
13
-
-
83555166183
-
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: A gene identification study
-
Gijselinck I, et al. (2012) A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: A gene identification study. Lancet Neurol 11(1): 54-65.
-
(2012)
Lancet Neurol
, vol.11
, Issue.1
, pp. 54-65
-
-
Gijselinck, I.1
-
14
-
-
84858622829
-
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study
-
Chromosome 9-ALS/FTD Consortium; French Research Network on FTLD/FTLD/ALS; ITALSGEN Consortium
-
Majounie E, et al.; Chromosome 9-ALS/FTD Consortium; French Research Network on FTLD/FTLD/ALS; ITALSGEN Consortium (2012) Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study. Lancet Neurol 11(4): 323-330.
-
(2012)
Lancet Neurol
, vol.11
, Issue.4
, pp. 323-330
-
-
Majounie, E.1
-
15
-
-
33748373580
-
RNA-mediated neuromuscular disorders
-
Ranum LP, Cooper TA (2006) RNA-mediated neuromuscular disorders. Annu Rev Neurosci 29: 259-277.
-
(2006)
Annu Rev Neurosci
, vol.29
, pp. 259-277
-
-
Ranum, L.P.1
Cooper, T.A.2
-
16
-
-
78651105614
-
Non-ATG-initiated translation directed by microsatellite expansions
-
Zu T, et al. (2011) Non-ATG-initiated translation directed by microsatellite expansions. Proc Natl Acad Sci USA 108(1): 260-265.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, Issue.1
, pp. 260-265
-
-
Zu, T.1
-
17
-
-
84866760281
-
Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype
-
Rutherford NJ, et al. (2012) Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype. Neurobiol Aging 33(12):2950.e5-2950. e7.
-
(2012)
Neurobiol Aging
, vol.33
, Issue.12
-
-
Rutherford, N.J.1
-
18
-
-
0027160708
-
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
-
Brand AH, Perrimon N (1993) Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 118(2): 401-415.
-
(1993)
Development
, vol.118
, Issue.2
, pp. 401-415
-
-
Brand, A.H.1
Perrimon, N.2
-
19
-
-
34547681603
-
Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome
-
Jin P, et al. (2007) Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome. Neuron 55(4): 556-564.
-
(2007)
Neuron
, vol.55
, Issue.4
, pp. 556-564
-
-
Jin, P.1
-
20
-
-
34547697173
-
RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS
-
Sofola OA, et al. (2007) RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS. Neuron 55(4): 565-571.
-
(2007)
Neuron
, vol.55
, Issue.4
, pp. 565-571
-
-
Sofola, O.A.1
-
21
-
-
82355180826
-
P62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
-
Al-Sarraj S, et al. (2011) p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS. Acta Neuropathol 122(6): 691-702.
-
(2011)
Acta Neuropathol
, vol.122
, Issue.6
, pp. 691-702
-
-
Al-Sarraj, S.1
-
22
-
-
84863393065
-
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
-
Snowden JS, et al. (2012) Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations. Brain 135(Pt 3): 693-708.
-
(2012)
Brain
, vol.135
, Issue.PART 3
, pp. 693-708
-
-
Snowden, J.S.1
-
23
-
-
84857516402
-
The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions
-
Simón-Sánchez J, et al. (2012) The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions. Brain 135(Pt 3): 723-735.
-
(2012)
Brain
, vol.135
, Issue.PART 3
, pp. 723-735
-
-
Simón-Sánchez, J.1
-
24
-
-
84874963127
-
HnRNP A3 binds to GGGGCC repeats and is a constituent of p62- positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations
-
Mori K, et al. (2013) hnRNP A3 binds to GGGGCC repeats and is a constituent of p62- positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations. Acta Neuropathol 125(3): 413-23.
-
(2013)
Acta Neuropathol
, vol.125
, Issue.3
, pp. 413-423
-
-
Mori, K.1
-
25
-
-
59449092121
-
Multiple roles for Pur-α in cellular and viral regulation
-
White MK, Johnson EM, Khalili K (2009) Multiple roles for Pur-α in cellular and viral regulation. Cell Cycle 8(3): 414-420.
-
(2009)
Cell Cycle
, vol.8
, Issue.3
, pp. 414-420
-
-
White, M.K.1
Johnson, E.M.2
Khalili, K.3
-
26
-
-
4143088149
-
Kinesin transports RNA: Isolation and characterization of an RNA-transporting granule
-
Kanai Y, Dohmae N, Hirokawa N (2004) Kinesin transports RNA: Isolation and characterization of an RNA-transporting granule. Neuron 43(4): 513-525.
-
(2004)
Neuron
, vol.43
, Issue.4
, pp. 513-525
-
-
Kanai, Y.1
Dohmae, N.2
Hirokawa, N.3
-
27
-
-
14244261725
-
Axonal transport defects: A common theme in neurodegenerative diseases
-
Roy S, Zhang B, Lee VMY, Trojanowski JQ (2005) Axonal transport defects: A common theme in neurodegenerative diseases. Acta Neuropathol 109(1): 5-13.
-
(2005)
Acta Neuropathol
, vol.109
, Issue.1
, pp. 5-13
-
-
Roy, S.1
Zhang, B.2
Lee, V.M.Y.3
Trojanowski, J.Q.4
-
28
-
-
84874962380
-
The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS
-
Mori K, et al. (2013) The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS. Science 339(6125): 1335-8.
-
(2013)
Science
, vol.339
, Issue.6125
, pp. 1335-1338
-
-
Mori, K.1
-
29
-
-
84874272095
-
Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS
-
Ash PEA, et al. (2013) Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS. Neuron 77(4): 639-646.
-
(2013)
Neuron
, vol.77
, Issue.4
, pp. 639-646
-
-
Ash, P.E.A.1
-
30
-
-
0041880131
-
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila
-
Jin P, et al. (2003) RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila. Neuron 39(5): 739-747.
-
(2003)
Neuron
, vol.39
, Issue.5
, pp. 739-747
-
-
Jin, P.1
-
31
-
-
84860617820
-
Quantitative analysis of the detergent-insoluble brain proteome in frontotemporal lobar degeneration using SILAC internal standards
-
Seyfried NT, et al. (2012) Quantitative analysis of the detergent-insoluble brain proteome in frontotemporal lobar degeneration using SILAC internal standards. J Proteome Res 11(5): 2721-2738.
-
(2012)
J Proteome Res
, vol.11
, Issue.5
, pp. 2721-2738
-
-
Seyfried, N.T.1
|