-
1
-
-
77953870821
-
TDP-43 pathology in sporadic ALS occurs in motor neurons lacking the RNA editing enzyme ADAR2
-
H. Aizawa TDP-43 pathology in sporadic ALS occurs in motor neurons lacking the RNA editing enzyme ADAR2 Acta Neuropathol. 120 2010 75 84
-
(2010)
Acta Neuropathol.
, vol.120
, pp. 75-84
-
-
Aizawa, H.1
-
2
-
-
33750716074
-
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
T. Arai TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis Biochem. Biophys. Res. Commun. 351 2006 602 611
-
(2006)
Biochem. Biophys. Res. Commun.
, vol.351
, pp. 602-611
-
-
Arai, T.1
-
3
-
-
0029610443
-
Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice
-
R. Brusa Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice Science 270 1995 1677 1680
-
(1995)
Science
, vol.270
, pp. 1677-1680
-
-
Brusa, R.1
-
4
-
-
77957317483
-
The multiple roles of TDP-43 in pre-mRNA processing and gene expression regulation
-
E. Buratti, and F.E. Baralle The multiple roles of TDP-43 in pre-mRNA processing and gene expression regulation RNA Biol. 7 2010 420 429
-
(2010)
RNA Biol.
, vol.7
, pp. 420-429
-
-
Buratti, E.1
Baralle, F.E.2
-
5
-
-
0030015076
-
Motor neurons are selectively vulnerable to AMPA/kainate receptor-mediated injury in vitro
-
S.G. Carriedo, H.Z. Yin, and J.H. Weiss Motor neurons are selectively vulnerable to AMPA/kainate receptor-mediated injury in vitro J. Neurosci. 16 1996 4069 4079
-
(1996)
J. Neurosci.
, vol.16
, pp. 4069-4079
-
-
Carriedo, S.G.1
Yin, H.Z.2
Weiss, J.H.3
-
6
-
-
84872564405
-
Transcriptome-wide identification of A>I RNA editing sites by inosine specific cleavage
-
P.B. Cattenoz Transcriptome-wide identification of A>I RNA editing sites by inosine specific cleavage RNA 19 2013 257 270
-
(2013)
RNA
, vol.19
, pp. 257-270
-
-
Cattenoz, P.B.1
-
8
-
-
0034078399
-
A third member of the RNA-specific adenosine deaminase gene family, ADAR3, contains both single- and double-stranded RNA binding domains
-
C.X. Chen A third member of the RNA-specific adenosine deaminase gene family, ADAR3, contains both single- and double-stranded RNA binding domains RNA 6 2000 755 767
-
(2000)
RNA
, vol.6
, pp. 755-767
-
-
Chen, C.X.1
-
9
-
-
84860863883
-
TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells
-
C. Colombrita TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells J. Biol. Chem. 287 2012 15635 15647
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 15635-15647
-
-
Colombrita, C.1
-
10
-
-
62149146109
-
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis
-
H. Daoud Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis J. Med. Genet. 46 2009 112 114
-
(2009)
J. Med. Genet.
, vol.46
, pp. 112-114
-
-
Daoud, H.1
-
11
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
M. DeJesus-Hernandez Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS Neuron 72 2011 245 256
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
Dejesus-Hernandez, M.1
-
12
-
-
84885808774
-
RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention
-
C.J. Donnelly RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention Neuron 80 2013 415 428
-
(2013)
Neuron
, vol.80
, pp. 415-428
-
-
Donnelly, C.J.1
-
13
-
-
67650432367
-
Proteolytic processing of TAR DNA binding protein-43 by caspases produces C-terminal fragments with disease defining properties independent of progranulin
-
D. Dormann Proteolytic processing of TAR DNA binding protein-43 by caspases produces C-terminal fragments with disease defining properties independent of progranulin J. Neurochem. 110 2009 1082 1094
-
(2009)
J. Neurochem.
, vol.110
, pp. 1082-1094
-
-
Dormann, D.1
-
14
-
-
0033364166
-
Neurological dysfunctions in mice expressing different levels of the Q/R site-unedited AMPAR subunit GluR-B
-
D. Feldmeyer Neurological dysfunctions in mice expressing different levels of the Q/R site-unedited AMPAR subunit GluR-B Nat. Neurosci. 2 1999 57 64
-
(1999)
Nat. Neurosci.
, vol.2
, pp. 57-64
-
-
Feldmeyer, D.1
-
15
-
-
80755163102
-
Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis
-
L. Ferraiuolo Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis Nat. Rev. Neurol. 7 2011 616 630
-
(2011)
Nat. Rev. Neurol.
, vol.7
, pp. 616-630
-
-
Ferraiuolo, L.1
-
16
-
-
79956307266
-
Increased RNA editing in EAAT2 pre-mRNA from amyotrophic lateral sclerosis patients: Involvement of a cryptic polyadenylation site
-
R. Flomen, and A. Makoff Increased RNA editing in EAAT2 pre-mRNA from amyotrophic lateral sclerosis patients: involvement of a cryptic polyadenylation site Neurosci. Lett. 497 2011 139 143
-
(2011)
Neurosci. Lett.
, vol.497
, pp. 139-143
-
-
Flomen, R.1
Makoff, A.2
-
17
-
-
84874618556
-
A high-throughput screen to identify enhancers of ADAR-mediated RNA-editing
-
W. Garncarz A high-throughput screen to identify enhancers of ADAR-mediated RNA-editing RNA Biol. 10 2013 192 204
-
(2013)
RNA Biol.
, vol.10
, pp. 192-204
-
-
Garncarz, W.1
-
18
-
-
80855138138
-
Rodent models of TDP-43 proteinopathy: Investigating the mechanisms of TDP-43-mediated neurodegeneration
-
T.F. Gendron, and L. Petrucelli Rodent models of TDP-43 proteinopathy: investigating the mechanisms of TDP-43-mediated neurodegeneration J. Mol. Neurosci. 45 2011 486 499
-
(2011)
J. Mol. Neurosci.
, vol.45
, pp. 486-499
-
-
Gendron, T.F.1
Petrucelli, L.2
-
19
-
-
84892590289
-
Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS
-
T.F. Gendron Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS Acta Neuropathol. 126 2013 829 844
-
(2013)
Acta Neuropathol.
, vol.126
, pp. 829-844
-
-
Gendron, T.F.1
-
20
-
-
77957966260
-
Pathological 43-kDa transactivation response DNA-binding protein in older adults with and without severe mental illness
-
F. Geser Pathological 43-kDa transactivation response DNA-binding protein in older adults with and without severe mental illness Arch. Neurol. 67 2010 1238 1250
-
(2010)
Arch. Neurol.
, vol.67
, pp. 1238-1250
-
-
Geser, F.1
-
21
-
-
41949119043
-
TDP-43 A315T mutation in familial motor neuron disease
-
M.A. Gitcho TDP-43 A315T mutation in familial motor neuron disease Ann. Neurol. 63 2008 535 538
-
(2008)
Ann. Neurol.
, vol.63
, pp. 535-538
-
-
Gitcho, M.A.1
-
22
-
-
47949086625
-
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
M. Hasegawa Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis Ann. Neurol. 64 2008 60 70
-
(2008)
Ann. Neurol.
, vol.64
, pp. 60-70
-
-
Hasegawa, M.1
-
23
-
-
84865360706
-
Asparaginyl endopeptidase cleaves TDP-43 in brain
-
J.H. Herskowitz Asparaginyl endopeptidase cleaves TDP-43 in brain Proteomics 12 2012 2455 2463
-
(2012)
Proteomics
, vol.12
, pp. 2455-2463
-
-
Herskowitz, J.H.1
-
24
-
-
77956565399
-
Induced loss of ADAR2 engenders slow death of motor neurons from Q/R site-unedited GluR2
-
T. Hideyama Induced loss of ADAR2 engenders slow death of motor neurons from Q/R site-unedited GluR2 J. Neurosci. 30 2010 11917 11925
-
(2010)
J. Neurosci.
, vol.30
, pp. 11917-11925
-
-
Hideyama, T.1
-
25
-
-
84856565045
-
When does ALS start? ADAR2-GluA2 hypothesis for the etiology of sporadic ALS
-
T. Hideyama, and S. Kwak When does ALS start? ADAR2-GluA2 hypothesis for the etiology of sporadic ALS Front. Mol. Neurosci. 4 2011 33
-
(2011)
Front. Mol. Neurosci.
, vol.4
, pp. 33
-
-
Hideyama, T.1
Kwak, S.2
-
26
-
-
84865190331
-
Co-Occurrence of TDP-43 mislocalization with reduced activity of an RNA editing enzyme, ADAR2, in aged mouse motor neurons
-
T. Hideyama Co-Occurrence of TDP-43 mislocalization with reduced activity of an RNA editing enzyme, ADAR2, in aged mouse motor neurons PLoS One 7 2012 e43469
-
(2012)
PLoS One
, vol.7
, pp. 43469
-
-
Hideyama, T.1
-
27
-
-
84856580212
-
Profound downregulation of the RNA editing enzyme ADAR2 in ALS spinal motor neurons
-
T. Hideyama Profound downregulation of the RNA editing enzyme ADAR2 in ALS spinal motor neurons Neurobiol. Dis. 45 2012 1121 1128
-
(2012)
Neurobiol. Dis.
, vol.45
, pp. 1121-1128
-
-
Hideyama, T.1
-
28
-
-
0034612640
-
Point mutation in an AMPA receptor gene rescues lethality in mice deficient in the RNA-editing enzyme ADAR2
-
M. Higuchi Point mutation in an AMPA receptor gene rescues lethality in mice deficient in the RNA-editing enzyme ADAR2 Nature 406 2000 78 81
-
(2000)
Nature
, vol.406
, pp. 78-81
-
-
Higuchi, M.1
-
29
-
-
79551648715
-
RNA editing by mammalian ADARs
-
M. Hogg RNA editing by mammalian ADARs Adv. Genet. 73 2011 87 120
-
(2011)
Adv. Genet.
, vol.73
, pp. 87-120
-
-
Hogg, M.1
-
30
-
-
67649797399
-
Expression of TDP-43 C-terminal fragments in Vitro recapitulates pathological features of TDP-43 proteinopathies
-
L.M. Igaz Expression of TDP-43 C-terminal fragments in Vitro recapitulates pathological features of TDP-43 proteinopathies J. Biol. Chem. 284 2009 8516 8524
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 8516-8524
-
-
Igaz, L.M.1
-
31
-
-
69249092183
-
TDP-43 depletion induces neuronal cell damage through dysregulation of Rho family GTPases
-
Y. Iguchi TDP-43 depletion induces neuronal cell damage through dysregulation of Rho family GTPases J. Biol. Chem. 284 2009 22059 22066
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 22059-22066
-
-
Iguchi, Y.1
-
32
-
-
19944432585
-
Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis
-
Y.M. Jiang Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis Ann. Neurol. 57 2005 236 251
-
(2005)
Ann. Neurol.
, vol.57
, pp. 236-251
-
-
Jiang, Y.M.1
-
33
-
-
67749133873
-
TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity
-
B.S. Johnson TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity J. Biol. Chem. 284 2009 20329 20339
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 20329-20339
-
-
Johnson, B.S.1
-
34
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
E. Kabashi TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis Nat. Genet. 40 2008 572 574
-
(2008)
Nat. Genet.
, vol.40
, pp. 572-574
-
-
Kabashi, E.1
-
35
-
-
79952375490
-
Biochemical and histopathological alterations in TAR DNA-binding protein-43 after acute ischemic stroke in rats
-
M. Kanazawa Biochemical and histopathological alterations in TAR DNA-binding protein-43 after acute ischemic stroke in rats J. Neurochem. 116 2011 957 965
-
(2011)
J. Neurochem.
, vol.116
, pp. 957-965
-
-
Kanazawa, M.1
-
36
-
-
0032506119
-
The AMPA receptor subunit GluR-B in its Q/R site-unedited form is not essential for brain development and function
-
K. Kask The AMPA receptor subunit GluR-B in its Q/R site-unedited form is not essential for brain development and function Proc. Natl. Acad. Sci. USA 95 1998 13777 13782
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 13777-13782
-
-
Kask, K.1
-
37
-
-
0038673599
-
Human spinal motoneurons express low relative abundance of GluR2 mRNA: An implication for excitotoxicity in ALS
-
Y. Kawahara Human spinal motoneurons express low relative abundance of GluR2 mRNA: an implication for excitotoxicity in ALS J. Neurochem. 85 2003 680 689
-
(2003)
J. Neurochem.
, vol.85
, pp. 680-689
-
-
Kawahara, Y.1
-
38
-
-
1542378930
-
Glutamate receptors: RNA editing and death of motor neurons
-
Y. Kawahara Glutamate receptors: RNA editing and death of motor neurons Nature 427 2004 801
-
(2004)
Nature
, vol.427
, pp. 801
-
-
Kawahara, Y.1
-
39
-
-
28944446370
-
Underediting of GluR2 mRNA, a neuronal death inducing molecular change in sporadic ALS, does not occur in motor neurons in ALS1 or SBMA
-
Y. Kawahara Underediting of GluR2 mRNA, a neuronal death inducing molecular change in sporadic ALS, does not occur in motor neurons in ALS1 or SBMA Neurosci. Res. 54 2006 11 14
-
(2006)
Neurosci. Res.
, vol.54
, pp. 11-14
-
-
Kawahara, Y.1
-
40
-
-
84875605133
-
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
-
H.J. Kim Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS Nature 495 2013 467 473
-
(2013)
Nature
, vol.495
, pp. 467-473
-
-
Kim, H.J.1
-
41
-
-
15044346521
-
Deficient RNA editing of GluR2 and neuronal death in amyotropic lateral sclerosis
-
S. Kwak, and Y. Kawahara Deficient RNA editing of GluR2 and neuronal death in amyotropic lateral sclerosis J. Mol. Med. 83 2005 110 120
-
(2005)
J. Mol. Med.
, vol.83
, pp. 110-120
-
-
Kwak, S.1
Kawahara, Y.2
-
42
-
-
61349156118
-
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
-
T.J. Kwiatkowski Jr. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis Science 323 2009 1205 1208
-
(2009)
Science
, vol.323
, pp. 1205-1208
-
-
Kwiatkowski, T.J.1
-
43
-
-
77953890823
-
TDP-43 and FUS/TLS: Emerging roles in RNA processing and neurodegeneration
-
C. Lagier-Tourenne, M. Polymenidou, and D.W. Cleveland TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration Hum. Mol. Genet. 19 2010 R46 R64
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 46-R64
-
-
Lagier-Tourenne, C.1
Polymenidou, M.2
Cleveland, D.W.3
-
44
-
-
84888098632
-
Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration
-
C. Lagier-Tourenne Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration Proc. Natl. Acad. Sci. USA 110 2013 E4530 E4539
-
(2013)
Proc. Natl. Acad. Sci. USA
, vol.110
, pp. 4530-E4539
-
-
Lagier-Tourenne, C.1
-
45
-
-
66349122954
-
Genome-wide identification of human RNA editing sites by parallel DNA capturing and sequencing
-
J.B. Li Genome-wide identification of human RNA editing sites by parallel DNA capturing and sequencing Science 324 2009 1210 1213
-
(2009)
Science
, vol.324
, pp. 1210-1213
-
-
Li, J.B.1
-
46
-
-
84907680636
-
The ADAR RNA editing enzyme controls neuronal excitability in Drosophila melanogaster
-
X. Li The ADAR RNA editing enzyme controls neuronal excitability in Drosophila melanogaster Nucleic Acids Res 2013
-
(2013)
Nucleic Acids Res
-
-
Li, X.1
-
47
-
-
81355123205
-
Conventional calpains and programmed cell death
-
P. Lopatniuk, and J.M. Witkowski Conventional calpains and programmed cell death Acta Biochim. Pol. 58 2011 287 296
-
(2011)
Acta Biochim. Pol.
, vol.58
, pp. 287-296
-
-
Lopatniuk, P.1
Witkowski, J.M.2
-
48
-
-
80052273429
-
Genome-wide evaluation and discovery of vertebrate A-to-I RNA editing sites
-
S. Maas Genome-wide evaluation and discovery of vertebrate A-to-I RNA editing sites Biochem. Biophys. Res. Commun. 412 2011 407 412
-
(2011)
Biochem. Biophys. Res. Commun.
, vol.412
, pp. 407-412
-
-
Maas, S.1
-
49
-
-
34249946466
-
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
-
I.R. Mackenzie Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations Ann. Neurol. 61 2007 427 434
-
(2007)
Ann. Neurol.
, vol.61
, pp. 427-434
-
-
Mackenzie, I.R.1
-
50
-
-
77957285745
-
TDP-43 proteinopathy and motor neuron disease in chronic traumatic encephalopathy
-
A.C. McKee TDP-43 proteinopathy and motor neuron disease in chronic traumatic encephalopathy J. Neuropathol. Exp. Neurol. 69 2010 918 929
-
(2010)
J. Neuropathol. Exp. Neurol.
, vol.69
, pp. 918-929
-
-
McKee, A.C.1
-
51
-
-
0030051809
-
A mammalian RNA editing enzyme
-
T. Melcher A mammalian RNA editing enzyme Nature 379 1996 460 464
-
(1996)
Nature
, vol.379
, pp. 460-464
-
-
Melcher, T.1
-
52
-
-
58049221032
-
Divergent patterns of cytosolic TDP-43 and neuronal progranulin expression following axotomy: Implications for TDP-43 in the physiological response to neuronal injury
-
K. Moisse 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 2009 202 211
-
(2009)
Brain Res.
, vol.1249
, pp. 202-211
-
-
Moisse, K.1
-
53
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
M. Neumann Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis Science 314 2006 130 133
-
(2006)
Science
, vol.314
, pp. 130-133
-
-
Neumann, M.1
-
54
-
-
77949882769
-
Characterization of alternative isoforms and inclusion body of the TAR DNA binding protein-43
-
Y. Nishimoto Characterization of alternative isoforms and inclusion body of the TAR DNA binding protein-43 J. Biol. Chem 2009
-
(2009)
J. Biol. Chem
-
-
Nishimoto, Y.1
-
55
-
-
84879811291
-
The long non-coding RNA nuclear-enriched abundant transcript 12 induces paraspeckle formation in the motor neuron during the early phase of amyotrophic lateral sclerosis
-
Y. Nishimoto The long non-coding RNA nuclear-enriched abundant transcript 12 induces paraspeckle formation in the motor neuron during the early phase of amyotrophic lateral sclerosis Mol. Brain 6 2013 31
-
(2013)
Mol. Brain
, vol.6
, pp. 31
-
-
Nishimoto, Y.1
-
56
-
-
67650113333
-
Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43
-
T. Nonaka Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43 Hum. Mol. Genet. 18 2009 3353 3364
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3353-3364
-
-
Nonaka, T.1
-
57
-
-
84863229628
-
Comprehensive analysis of RNA-Seq data reveals extensive RNA editing in a human transcriptome
-
Z. Peng Comprehensive analysis of RNA-Seq data reveals extensive RNA editing in a human transcriptome Nat. Biotechnol. 30 2012 253 260
-
(2012)
Nat. Biotechnol.
, vol.30
, pp. 253-260
-
-
Peng, Z.1
-
58
-
-
79953185674
-
Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43
-
M. Polymenidou Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43 Nat. Neurosci. 14 2011 459 468
-
(2011)
Nat. Neurosci.
, vol.14
, pp. 459-468
-
-
Polymenidou, M.1
-
59
-
-
84873730841
-
Motor neuron disease in 2012: Novel causal genes and disease modifiers
-
R. Rademakers, and M. van Blitterswijk Motor neuron disease in 2012: novel causal genes and disease modifiers Nat. Rev. Neurol. 9 2013 63 64
-
(2013)
Nat. Rev. Neurol.
, vol.9
, pp. 63-64
-
-
Rademakers, R.1
Van Blitterswijk, M.2
-
60
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
A.E. Renton A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD Neuron 72 2011 257 268
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
-
61
-
-
34249313704
-
Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS
-
J. Robertson Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS Neurosci. Lett. 420 2007 128 132
-
(2007)
Neurosci. Lett.
, vol.420
, pp. 128-132
-
-
Robertson, J.1
-
62
-
-
0027401203
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
D.R. Rosen Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis Nature 362 1993 59 62
-
(1993)
Nature
, vol.362
, pp. 59-62
-
-
Rosen, D.R.1
-
63
-
-
84886389563
-
Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion
-
(208ra149)
-
D. Sareen Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion Sci. Transl. Med. 5 2013 (208ra149)
-
(2013)
Sci. Transl. Med.
, vol.5
-
-
Sareen, D.1
-
64
-
-
0037014475
-
A-to-I editing: New and old sites, functions and speculations
-
P.H. Seeburg A-to-I editing: new and old sites, functions and speculations Neuron 35 2002 17 20
-
(2002)
Neuron
, vol.35
, pp. 17-20
-
-
Seeburg, P.H.1
-
65
-
-
78651408754
-
Identification of neuronal RNA targets of TDP-43-containing ribonucleoprotein complexes
-
C.F. Sephton Identification of neuronal RNA targets of TDP-43-containing ribonucleoprotein complexes J. Biol. Chem. 286 2011 1204 1215
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 1204-1215
-
-
Sephton, C.F.1
-
66
-
-
84876513474
-
Global regulation of alternative splicing by adenosine deaminase acting on RNA (ADAR)
-
O. Solomon Global regulation of alternative splicing by adenosine deaminase acting on RNA (ADAR) RNA 19 2013 591 604
-
(2013)
RNA
, vol.19
, pp. 591-604
-
-
Solomon, O.1
-
67
-
-
0025995296
-
RNA editing in brain controls a determinant of ion flow in glutamate-gated channels
-
B. Sommer RNA editing in brain controls a determinant of ion flow in glutamate-gated channels Cell 67 1991 11 19
-
(1991)
Cell
, vol.67
, pp. 11-19
-
-
Sommer, B.1
-
68
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
J. Sreedharan TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis Science 319 2008 1668 1672
-
(2008)
Science
, vol.319
, pp. 1668-1672
-
-
Sreedharan, J.1
-
69
-
-
20144364376
-
Expression profile of AMPA receptor subunit mRNA in single adult rat brain and spinal cord neurons in situ
-
H. Sun Expression profile of AMPA receptor subunit mRNA in single adult rat brain and spinal cord neurons in situ Neurosci. Res. 52 2005 228 234
-
(2005)
Neurosci. Res.
, vol.52
, pp. 228-234
-
-
Sun, H.1
-
70
-
-
18144407551
-
Calpain mediates excitotoxic DNA fragmentation via mitochondrial pathways in adult brains: Evidence from calpastatin mutant mice
-
J. Takano Calpain mediates excitotoxic DNA fragmentation via mitochondrial pathways in adult brains: evidence from calpastatin mutant mice J. Biol. Chem. 280 2005 16175 16184
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 16175-16184
-
-
Takano, J.1
-
71
-
-
0032752054
-
Reduction of GluR2 RNA editing, a molecular change that increases calcium influx through AMPA receptors, selective in the spinal ventral gray of patients with amyotrophic lateral sclerosis
-
H. Takuma Reduction of GluR2 RNA editing, a molecular change that increases calcium influx through AMPA receptors, selective in the spinal ventral gray of patients with amyotrophic lateral sclerosis Ann. Neurol. 46 1999 806 815
-
(1999)
Ann. Neurol.
, vol.46
, pp. 806-815
-
-
Takuma, H.1
-
72
-
-
34247606414
-
TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation
-
C.F. Tan TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation Acta Neuropathol. 113 2007 535 542
-
(2007)
Acta Neuropathol.
, vol.113
, pp. 535-542
-
-
Tan, C.F.1
-
73
-
-
79953180492
-
Characterizing the RNA targets and position-dependent splicing regulation by TDP-43
-
J.R. Tollervey Characterizing the RNA targets and position-dependent splicing regulation by TDP-43 Nat. Neurosci. 14 2011 452 458
-
(2011)
Nat. Neurosci.
, vol.14
, pp. 452-458
-
-
Tollervey, J.R.1
-
74
-
-
41949100148
-
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: A genetic and histopathological analysis
-
V.M. Van Deerlin TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis Lancet Neurol. 7 2008 409 416
-
(2008)
Lancet Neurol.
, vol.7
, pp. 409-416
-
-
Van Deerlin, V.M.1
-
75
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
C. Vance Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6 Science 323 2009 1208 1211
-
(2009)
Science
, vol.323
, pp. 1208-1211
-
-
Vance, C.1
-
76
-
-
79958098783
-
TDP-43 in aging and Alzheimer's disease - A review
-
A.C. Wilson TDP-43 in aging and Alzheimer's disease - a review Int. J. Clin. Exp. Pathol. 4 2011 147 155
-
(2011)
Int. J. Clin. Exp. Pathol.
, vol.4
, pp. 147-155
-
-
Wilson, A.C.1
-
77
-
-
84871734357
-
A role for calpain-dependent cleavage of TDP-43 in amyotrophic lateral sclerosis pathology
-
T. Yamashita A role for calpain-dependent cleavage of TDP-43 in amyotrophic lateral sclerosis pathology Nat. Commun. 3 2012 1307
-
(2012)
Nat. Commun.
, vol.3
, pp. 1307
-
-
Yamashita, T.1
-
78
-
-
84860320548
-
The abnormal processing of TDP-43 is not an upstream event of reduced ADAR2 activity in ALS motor neurons
-
T. Yamashita The abnormal processing of TDP-43 is not an upstream event of reduced ADAR2 activity in ALS motor neurons Neurosci. Res. 73 2012 153 160
-
(2012)
Neurosci. Res.
, vol.73
, pp. 153-160
-
-
Yamashita, T.1
-
79
-
-
84887084505
-
Rescue of amyotrophic lateral sclerosis phenotype in a mouse model by intravenous AAV9-ADAR2 delivery to motor neurons
-
T. Yamashita Rescue of amyotrophic lateral sclerosis phenotype in a mouse model by intravenous AAV9-ADAR2 delivery to motor neurons EMBO Mol. Med. 5 2013 1710 1719
-
(2013)
EMBO Mol. Med.
, vol.5
, pp. 1710-1719
-
-
Yamashita, T.1
-
80
-
-
42949094584
-
TDP-43 mutation in familial amyotrophic lateral sclerosis
-
A. Yokoseki TDP-43 mutation in familial amyotrophic lateral sclerosis Ann. Neurol. 63 2008 538 542
-
(2008)
Ann. Neurol.
, vol.63
, pp. 538-542
-
-
Yokoseki, A.1
-
81
-
-
34848921202
-
Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43
-
Y.J. Zhang Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43 J. Neurosci. 27 2007 10530 10534
-
(2007)
J. Neurosci.
, vol.27
, pp. 10530-10534
-
-
Zhang, Y.J.1
-
82
-
-
66149114101
-
Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity
-
Y.J. Zhang Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity Proc. Natl. Acad. Sci. USA 106 2009 7607 7612
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 7607-7612
-
-
Zhang, Y.J.1
-
83
-
-
84875361309
-
Prediction of constitutive A-to-I editing sites from human transcriptomes in the absence of genomic sequences
-
S. Zhu Prediction of constitutive A-to-I editing sites from human transcriptomes in the absence of genomic sequences BMC Genom. 14 2013 206
-
(2013)
BMC Genom.
, vol.14
, pp. 206
-
-
Zhu, S.1
-
84
-
-
84890837640
-
RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia
-
T. Zu RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia Proc. Natl. Acad. Sci. USA 2013
-
(2013)
Proc. Natl. Acad. Sci. USA
-
-
Zu, T.1
|