-
1
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
Dejesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, Rutherford NJ, et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 2011; 72: 245-256.
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
Dejesus-Hernandez, M.1
MacKenzie, I.R.2
Boeve, B.F.3
Boxer, A.L.4
Baker, M.5
Rutherford, N.J.6
-
2
-
-
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, Van Langenhove T, van der Zee J, Sleegers K, Philtjens S, Kleinberger G, et al. 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 2012; 11: 54-65.
-
(2012)
Lancet Neurol
, vol.11
, pp. 54-65
-
-
Gijselinck, I.1
Van Langenhove, T.2
Van Der Zee, J.3
Sleegers, K.4
Philtjens, S.5
Kleinberger, G.6
-
3
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
Renton AE, Majounie E, Waite A, Simon-Sanchez J, Rollinson S, Gibbs JR, et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 2011; 72: 257-268.
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
Majounie, E.2
Waite, A.3
Simon-Sanchez, J.4
Rollinson, S.5
Gibbs, J.R.6
-
4
-
-
84901038797
-
C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking
-
Farg MA, Sundaramoorthy V, Sultana JM, Yang S, Atkinson RA, Levina V, et al. C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking. Hum Mol Genet 2014; 23: 3579-3595.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 3579-3595
-
-
Farg, M.A.1
Sundaramoorthy, V.2
Sultana, J.M.3
Yang, S.4
Atkinson, R.A.5
Levina, V.6
-
5
-
-
84919912448
-
Aggregation-prone c9FTD/ALS poly(GA) RAN-Translated proteins cause neurotoxicity by inducing ER stress
-
Zhang YJ, Jansen-West K, Xu YF, Gendron TF, Bieniek KF, Lin WL, et al. Aggregation-prone c9FTD/ALS poly(GA) RAN-Translated proteins cause neurotoxicity by inducing ER stress. Acta Neuropathol 2014; 128: 505-524.
-
(2014)
Acta Neuropathol
, vol.128
, pp. 505-524
-
-
Zhang, Y.J.1
Jansen-West, K.2
Xu, Y.F.3
Gendron, T.F.4
Bieniek, K.F.5
Lin, W.L.6
-
6
-
-
85056706559
-
Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion
-
Waite AJ, Baumer D, East S, Neal J, Morris HR, Ansorge O, et al. Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion. Neurobiol Aging 2014; 35: 1779.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 1779
-
-
Waite, A.J.1
Baumer, D.2
East, S.3
Neal, J.4
Morris, H.R.5
Ansorge, O.6
-
7
-
-
84881531855
-
Loss of function of C9orf72 causes motor deficits in a zebrafish model of Amyotrophic Lateral Sclerosis
-
Ciura S, Lattante S, Le BI, Latouche M, Tostivint H, Brice A, et al. Loss of function of C9orf72 causes motor deficits in a zebrafish model of Amyotrophic Lateral Sclerosis. Ann Neurol 2013; 74: 180-187.
-
(2013)
Ann Neurol
, vol.74
, pp. 180-187
-
-
Ciura, S.1
Lattante, S.2
Le, B.I.3
Latouche, M.4
Tostivint, H.5
Brice, A.6
-
8
-
-
84883460229
-
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia
-
Fratta P, Poulter M, Lashley T, Rohrer JD, Polke JM, Beck J, et al. Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia. Acta Neuropathol 2013; 126: 401-409.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 401-409
-
-
Fratta, P.1
Poulter, M.2
Lashley, T.3
Rohrer, J.D.4
Polke, J.M.5
Beck, J.6
-
9
-
-
84892596606
-
Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood
-
Belzil VV, Bauer PO, Prudencio M, Gendron TF, Stetler CT, Yan IK, et al. Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood. Acta Neuropathol 2013; 126: 895-905.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 895-905
-
-
Belzil, V.V.1
Bauer, P.O.2
Prudencio, M.3
Gendron, T.F.4
Stetler, C.T.5
Yan, I.K.6
-
10
-
-
84939941360
-
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients
-
Xi Z, Zhang M, Bruni AC, Maletta RG, Colao R, Fratta P, et al. The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients. Acta Neuropathol 2015; 129: 715-727.
-
(2015)
Acta Neuropathol
, vol.129
, pp. 715-727
-
-
Xi, Z.1
Zhang, M.2
Bruni, A.C.3
Maletta, R.G.4
Colao, R.5
Fratta, P.6
-
11
-
-
84907681995
-
Characterization of DNA hypermethylation in the cerebellum of c9FTD/ALS patients
-
Belzil VV, Bauer PO, Gendron TF, Murray ME, Dickson D, Petrucelli L. Characterization of DNA hypermethylation in the cerebellum of c9FTD/ALS patients. Brain Res 2014; 1584: 15-21.
-
(2014)
Brain Res
, vol.1584
, pp. 15-21
-
-
Belzil, V.V.1
Bauer, P.O.2
Gendron, T.F.3
Murray, M.E.4
Dickson, D.5
Petrucelli, L.6
-
12
-
-
84939886575
-
C9orf72 hypermethylation protects against repeat expansion-Associated pathology in ALS/FTD
-
Liu EY, Russ J, Wu K, Neal D, Suh E, McNally AG, et al. C9orf72 hypermethylation protects against repeat expansion-Associated pathology in ALS/FTD. Acta Neuropathol 2014; 128: 525-541.
-
(2014)
Acta Neuropathol
, vol.128
, pp. 525-541
-
-
Liu, E.Y.1
Russ, J.2
Wu, K.3
Neal, D.4
Suh, E.5
McNally, A.G.6
-
13
-
-
84911382953
-
Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients
-
Xi Z, Rainero I, Rubino E, Pinessi L, Bruni AC, Maletta RG, et al. Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients. Hum Mol Genet 2014; 23: 5630-5637.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 5630-5637
-
-
Xi, Z.1
Rainero, I.2
Rubino, E.3
Pinessi, L.4
Bruni, A.C.5
Maletta, R.G.6
-
14
-
-
84878863605
-
Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion
-
Xi Z, Zinman L, Moreno D, Schymick J, Liang Y, Sato C, et al. Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion. Am J Hum Genet 2013; 92: 981-989.
-
(2013)
Am J Hum Genet
, vol.92
, pp. 981-989
-
-
Xi, Z.1
Zinman, L.2
Moreno, D.3
Schymick, J.4
Liang, Y.5
Sato, C.6
-
15
-
-
84928157416
-
Hypermethylation of repeat expanded C9orf72 is a clinical and molecular disease modifier
-
Russ J, Liu EY, Wu K, Neal D, Suh E, Irwin DJ, et al. Hypermethylation of repeat expanded C9orf72 is a clinical and molecular disease modifier. Acta Neuropathol 2014; 129: 39-52.
-
(2014)
Acta Neuropathol
, vol.129
, pp. 39-52
-
-
Russ, J.1
Liu, E.Y.2
Wu, K.3
Neal, D.4
Suh, E.5
Irwin, D.J.6
-
16
-
-
0026339303
-
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
-
Oberle I, Rousseau F, Heitz D, Kretz C, Devys D, Hanauer A, et al. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome. Science 1991; 252: 1097-1102.
-
(1991)
Science
, vol.252
, pp. 1097-1102
-
-
Oberle, I.1
Rousseau, F.2
Heitz, D.3
Kretz, C.4
Devys, D.5
Hanauer, A.6
-
17
-
-
0027203684
-
Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
-
Knight SJ, Flannery AV, Hirst MC, Campbell L, Christodoulou Z, Phelps SR, et al. Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Cell 1993; 74: 127-134.
-
(1993)
Cell
, vol.74
, pp. 127-134
-
-
Knight, S.J.1
Flannery, A.V.2
Hirst, M.C.3
Campbell, L.4
Christodoulou, Z.5
Phelps, S.R.6
-
18
-
-
57349086192
-
DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients
-
Castaldo I, Pinelli M, Monticelli A, Acquaviva F, Giacchetti M, Filla A, et al. DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients. J Med Genet 2008; 45: 808-812.
-
(2008)
J Med Genet
, vol.45
, pp. 808-812
-
-
Castaldo, I.1
Pinelli, M.2
Monticelli, A.3
Acquaviva, F.4
Giacchetti, M.5
Filla, A.6
-
19
-
-
84877342215
-
Expanded ggggcc repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration
-
Xu Z, Poidevin M, Li X, Li Y, Shu L, Nelson DL, et al. Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration. Proc Natl Acad Sci USA 2013; 110: 7778-7783.
-
(2013)
Proc Natl Acad Sci USA
, vol.110
, pp. 7778-7783
-
-
Xu, Z.1
Poidevin, M.2
Li, X.3
Li, Y.4
Shu, L.5
Nelson, D.L.6
-
20
-
-
84892590289
-
Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-Associated non-ATG translation in c9FTD/.ALS
-
Gendron TF, Bieniek KF, Zhang YJ, Jansen-West K, Ash PE, Caulfield T, et al. Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-Associated non-ATG translation in c9FTD/.ALS. Acta Neuropathol 2013; 126: 829-844.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 829-844
-
-
Gendron, T.F.1
Bieniek, K.F.2
Zhang, Y.J.3
Jansen-West, K.4
Ash, P.E.5
Caulfield, T.6
-
21
-
-
84890233174
-
Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic
-
Lee YB, Chen HJ, Peres JN, Gomez-Deza J, Attig J, Stalekar M, et al. Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic. Cell Rep 2013; 5: 1178-1186.
-
(2013)
Cell Rep
, vol.5
, pp. 1178-1186
-
-
Lee, Y.B.1
Chen, H.J.2
Peres, J.N.3
Gomez-Deza, J.4
Attig, J.5
Stalekar, M.6
-
22
-
-
84874962380
-
The c9orf72 ggggcc repeat is translated into aggregating dipeptide-repeat proteins in ftld/.als
-
Mori K, Weng SM, Arzberger T, May S, Rentzsch K, Kremmer E, et al. The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/.ALS. Science 2013; 339: 1335-1338.
-
(2013)
Science
, vol.339
, pp. 1335-1338
-
-
Mori, K.1
Weng, S.M.2
Arzberger, T.3
May, S.4
Rentzsch, K.5
Kremmer, E.6
-
23
-
-
84874272095
-
Unconventional translation of c9orf72 ggggcc expansion generates insoluble polypeptides specific to c9ftd/als
-
Ash PE, Bieniek KF, Gendron TF, Caulfield T, Lin WL, Dejesus-Hernandez M, et al. Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS. Neuron 2013; 77: 639-646.
-
(2013)
Neuron
, vol.77
, pp. 639-646
-
-
Ash, P.E.1
Bieniek, K.F.2
Gendron, T.F.3
Caulfield, T.4
Lin, W.L.5
Dejesus-Hernandez, M.6
-
24
-
-
84892585689
-
Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins
-
Mori K, Arzberger T, Grasser FA, Gijselinck I, May S, Rentzsch K, et al. Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins. Acta Neuropathol 2013; 126: 881-893.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 881-893
-
-
Mori, K.1
Arzberger, T.2
Grasser, F.A.3
Gijselinck, I.4
May, S.5
Rentzsch, K.6
-
25
-
-
84873093810
-
A pan-European study of the C9orf72 repeat associated with FTLD: Geographic prevalence, genomic instability, and intermediate repeats
-
van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Engelborghs S, et al. A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats. Hum Mutat 2013; 34: 363-373.
-
(2013)
Hum Mutat
, vol.34
, pp. 363-373
-
-
Van Der Zee, J.1
Gijselinck, I.2
Dillen, L.3
Van Langenhove, T.4
Theuns, J.5
Engelborghs, S.6
-
26
-
-
84876411369
-
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population
-
Beck J, Poulter M, Hensman D, Rohrer JD, Mahoney CJ, Adamson G, et al. Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population. Am J Hum Genet 2013; 92: 345-353.
-
(2013)
Am J Hum Genet
, vol.92
, pp. 345-353
-
-
Beck, J.1
Poulter, M.2
Hensman, D.3
Rohrer, J.D.4
Mahoney, C.J.5
Adamson, G.6
-
27
-
-
84874230421
-
C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients
-
Dobson-Stone C, Hallupp M, Loy CT, Thompson EM, Haan E, Sue CM, et al. C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients. PLoS One 2013; 8: e56899.
-
(2013)
PLoS One
, vol.8
, pp. e56899
-
-
Dobson-Stone, C.1
Hallupp, M.2
Loy, C.T.3
Thompson, E.M.4
Haan, E.5
Sue, C.M.6
-
28
-
-
84866058216
-
C9orf72 repeat expansion in amyotrophic lateral sclerosis in the kii peninsula of Japan
-
Ishiura H, Takahashi Y, Mitsui J, Yoshida S, Kihira T, Kokubo Y, et al. C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of Japan. Arch Neurol 2012; 69: 1154-1158.
-
(2012)
Arch Neurol
, vol.69
, pp. 1154-1158
-
-
Ishiura, H.1
Takahashi, Y.2
Mitsui, J.3
Yoshida, S.4
Kihira, T.5
Kokubo, Y.6
-
29
-
-
84875840045
-
Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation
-
Buchman VL, Cooper-Knock J, Connor-Robson N, Higginbottom A, Kirby J, Razinskaya OD, et al. Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation. Mol Neurodegener 2013; 8: 12.
-
(2013)
Mol Neurodegener
, vol.8
, pp. 12
-
-
Buchman, V.L.1
Cooper-Knock, J.2
Connor-Robson, N.3
Higginbottom, A.4
Kirby, J.5
Razinskaya, O.D.6
-
30
-
-
84884163243
-
Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): A cross-sectional cohort study
-
van Blitterswijk M, Dejesus-Hernandez M, Niemantsverdriet E, Murray ME, Heckman MG, Diehl NN, et al. Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study. Lancet Neurol 2013; 12: 978-988.
-
(2013)
Lancet Neurol
, vol.12
, pp. 978-988
-
-
Van Blitterswijk, M.1
Dejesus-Hernandez, M.2
Niemantsverdriet, E.3
Murray, M.E.4
Heckman, M.G.5
Diehl, N.N.6
-
31
-
-
84892451456
-
Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia
-
Dols-Icardo O, Garcia-Redondo A, Rojas-Garcia R, Sanchez-Valle R, Noguera A, Gomez-Tortosa E, et al. Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia. Hum Mol Genet 2013; 23: 749-754.
-
(2013)
Hum Mol Genet
, vol.23
, pp. 749-754
-
-
Dols-Icardo, O.1
Garcia-Redondo, A.2
Rojas-Garcia, R.3
Sanchez-Valle, R.4
Noguera, A.5
Gomez-Tortosa, E.6
-
32
-
-
84893718348
-
Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases
-
Hubers A, Marroquin N, Schmoll B, Vielhaber S, Just M, Mayer B, et al. Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases. Neurobiol Aging 2014; 35: 1214-1216.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 1214-1216
-
-
Hubers, A.1
Marroquin, N.2
Schmoll, B.3
Vielhaber, S.4
Just, M.5
Mayer, B.6
-
33
-
-
84866093352
-
C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts
-
Dobson-Stone C, Hallupp M, Bartley L, Shepherd CE, Halliday GM, Schofield PR, et al. C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts. Neurology 2012; 79: 995-1001.
-
(2012)
Neurology
, vol.79
, pp. 995-1001
-
-
Dobson-Stone, C.1
Hallupp, M.2
Bartley, L.3
Shepherd, C.E.4
Halliday, G.M.5
Schofield, P.R.6
-
34
-
-
84871610298
-
Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwide
-
Garcia-Redondo A, Dols-Icardo O, Rojas-Garcia R, Esteban-Perez J, Cordero-Vazquez P, Munoz-Blanco JL, et al. Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwide. Hum Mutat 2013; 34: 79-82.
-
(2013)
Hum Mutat
, vol.34
, pp. 79-82
-
-
Garcia-Redondo, A.1
Dols-Icardo, O.2
Rojas-Garcia, R.3
Esteban-Perez, J.4
Cordero-Vazquez, P.5
Munoz-Blanco, J.L.6
-
35
-
-
84864392867
-
C9ORF72 repeat expansion in a large Italian ALS cohort: Evidence of a founder effect
-
Ratti A, Corrado L, Castellotti B, Del BR, Fogh I, Cereda C, et al. C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. Neurobiol Aging 2012; 33: 2528-14.
-
(2012)
Neurobiol Aging
, vol.33
, pp. 2528-2614
-
-
Ratti, A.1
Corrado, L.2
Castellotti, B.3
Del, B.R.4
Fogh, I.5
Cereda, C.6
-
36
-
-
84857516402
-
The clinical and pathological phenotype of C9orf72 hexanucleotide repeat expansions
-
Simon-Sanchez J, Dopper EG, Cohn-Hokke PE, Hukema RK, Nicolaou N, Seelaar H, et al. The clinical and pathological phenotype of C9orf72 hexanucleotide repeat expansions. Brain 2012; 135: 723-735.
-
(2012)
Brain
, vol.135
, pp. 723-735
-
-
Simon-Sanchez, J.1
Dopper, E.G.2
Cohn-Hokke, P.E.3
Hukema, R.K.4
Nicolaou, N.5
Seelaar, H.6
-
37
-
-
84871243649
-
Investigation of c9orf72 in 4 neurodegenerative disorders
-
Xi Z, Zinman L, Grinberg Y, Moreno D, Sato C, Bilbao JM, et al. Investigation of c9orf72 in 4 neurodegenerative disorders. Arch Neurol 2012; 69: 1583-1590.
-
(2012)
Arch Neurol
, vol.69
, pp. 1583-1590
-
-
Xi, Z.1
Zinman, L.2
Grinberg, Y.3
Moreno, D.4
Sato, C.5
Bilbao, J.M.6
-
38
-
-
84930747272
-
Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD
-
Nordin A, Akimoto C, Wuolikainen A, Alstermark H, Jonsson P, Birve A, et al. Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD. Hum Mol Genet 2015; 24: 3133-3142.
-
(2015)
Hum Mol Genet
, vol.24
, pp. 3133-3142
-
-
Nordin, A.1
Akimoto, C.2
Wuolikainen, A.3
Alstermark, H.4
Jonsson, P.5
Birve, A.6
-
39
-
-
0027485748
-
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy
-
Harley HG, Rundle SA, MacMillan JC, Myring J, Brook JD, Crow S, et al. Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. Am J Hum Genet 1993; 52: 1164-1174.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 1164-1174
-
-
Harley, H.G.1
Rundle, S.A.2
MacMillan, J.C.3
Myring, J.4
Brook, J.D.5
Crow, S.6
-
40
-
-
0029757676
-
The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia
-
Filla A, De MG, Cavalcanti F, Pianese L, Monticelli A, Campanella G, et al. The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia. Am J Hum Genet 1996; 59: 554-560.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 554-560
-
-
Filla, A.1
De Mg Cavalcanti, F.2
Pianese, L.3
Monticelli, A.4
Campanella, G.5
-
41
-
-
84874835620
-
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohorts
-
Van Langenhove T, van der Zee J, Gijselinck I, Engelborghs S, Vandenberghe R, Vandenbulcke M, et al. Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort. JAMA Neurol 2013; 70: 365-373.
-
(2013)
JAMA Neurol
, vol.70
, pp. 365-373
-
-
Van Langenhove, T.1
Van Der Zee, J.2
Gijselinck, I.3
Engelborghs, S.4
Vandenberghe, R.5
Vandenbulcke, M.6
-
42
-
-
84857522741
-
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
-
Chio A, Borghero G, Restagno G, Mora G, Drepper C, Traynor BJ, et al. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. Brain 2012; 135: 784-793.
-
(2012)
Brain
, vol.135
, pp. 784-793
-
-
Chio, A.1
Borghero, G.2
Restagno, G.3
Mora, G.4
Drepper, C.5
Traynor, B.J.6
-
43
-
-
84857587514
-
Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p
-
Hsiung GY, Dejesus-Hernandez M, Feldman HH, Sengdy P, Bouchard-Kerr P, Dwosh E, et al. Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p. Brain 2012; 135: 709-722.
-
(2012)
Brain
, vol.135
, pp. 709-722
-
-
Hsiung, G.Y.1
Dejesus-Hernandez, M.2
Feldman, H.H.3
Sengdy, P.4
Bouchard-Kerr, P.5
Dwosh, E.6
-
44
-
-
84857921617
-
Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p
-
Stewart H, Rutherford NJ, Briemberg H, Krieger C, Cashman N, Fabros M, et al. Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p. Acta Neuropathol 2012; 123: 409-417.
-
(2012)
Acta Neuropathol
, vol.123
, pp. 409-417
-
-
Stewart, H.1
Rutherford, N.J.2
Briemberg, H.3
Krieger, C.4
Cashman, N.5
Fabros, M.6
-
45
-
-
84863393788
-
Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
-
Boeve BF, Boylan KB, Graff-Radford NR, Dejesus-Hernandez M, Knopman DS, Pedraza O, et al. Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72. Brain 2012; 135: 765-783.
-
(2012)
Brain
, vol.135
, pp. 765-783
-
-
Boeve, B.F.1
Boylan, K.B.2
Graff-Radford, N.R.3
Dejesus-Hernandez, M.4
Knopman, D.S.5
Pedraza, O.6
-
46
-
-
84865613274
-
Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: Psychiatric clinical presentations
-
Arighi A, Fumagalli GG, Jacini F, Fenoglio C, Ghezzi L, Pietroboni AM, et al. Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentations. J Alzheimers Dis 2012; 31: 447-452.
-
(2012)
J Alzheimers Dis
, vol.31
, pp. 447-452
-
-
Arighi, A.1
Fumagalli, G.G.2
Jacini, F.3
Fenoglio, C.4
Ghezzi, L.5
Pietroboni, A.M.6
-
47
-
-
79952823979
-
Classification of primary progressive aphasia and its variants
-
Gorno-Tempini ML, Hillis AE, Weintraub S, Kertesz A, Mendez M, Cappa SF, et al. Classification of primary progressive aphasia and its variants. Neurology 2011; 76: 1006-1014.
-
(2011)
Neurology
, vol.76
, pp. 1006-1014
-
-
Gorno-Tempini, M.L.1
Hillis, A.E.2
Weintraub, S.3
Kertesz, A.4
Mendez, M.5
Cappa, S.F.6
-
48
-
-
80052938441
-
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
-
Rascovsky K, Hodges JR, Knopman D, Mendez MF, Kramer JH, Neuhaus J, et al. Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 2011; 134: 2456-2477.
-
(2011)
Brain
, vol.134
, pp. 2456-2477
-
-
Rascovsky, K.1
Hodges, J.R.2
Knopman, D.3
Mendez, M.F.4
Kramer, J.H.5
Neuhaus, J.6
-
50
-
-
39049153337
-
Electrodiagnostic criteria for diagnosis of ALS
-
deCarvalho M, Dengler R, Eisen A, England JD, Kaji R, Kimura J, et al. Electrodiagnostic criteria for diagnosis of ALS. Clin Neurophysiol 2008; 119: 497-503.
-
(2008)
Clin Neurophysiol
, vol.119
, pp. 497-503
-
-
De Carvalho, M.1
Dengler, R.2
Eisen, A.3
England, J.D.4
Kaji, R.5
Kimura, J.6
-
51
-
-
79959599081
-
A harmonized classification system for FTLD-TDP pathology
-
Mackenzie IR, Neumann M, Baborie A, Sampathu DM, Du PD, Jaros E, et al. A harmonized classification system for FTLD-TDP pathology. Acta Neuropathol 2011; 122: 111-113.
-
(2011)
Acta Neuropathol
, vol.122
, pp. 111-113
-
-
MacKenzie, I.R.1
Neumann, M.2
Baborie, A.3
Sampathu, D.M.4
Du, P.D.5
Jaros, E.6
-
52
-
-
84920417120
-
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion
-
Fratta P, Polke JM, Newcombe J, Mizielinska S, Lashley T, Poulter M, et al. Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion. Neurobiol Aging 2015; 36: 546-547.
-
(2015)
Neurobiol Aging
, vol.36
, pp. 546-547
-
-
Fratta, P.1
Polke, J.M.2
Newcombe, J.3
Mizielinska, S.4
Lashley, T.5
Poulter, M.6
-
53
-
-
84930637080
-
Neurodegeneration C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits
-
Chew J, Gendron TF, Prudencio M, Sasaguri H, Zhang YJ, Castanedes-Casey M, et al. Neurodegeneration. C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits. Science 2015; 348: 1151-1154.
-
(2015)
Science
, vol.348
, pp. 1151-1154
-
-
Chew, J.1
Gendron, T.F.2
Prudencio, M.3
Sasaguri, H.4
Zhang, Y.J.5
Castanedes-Casey, M.6
-
54
-
-
84920504317
-
Identical twins with the C9orf72 repeat expansion are discordant for ALS
-
Xi Z, Yunusova Y, van BM, Dib S, Ghani M, Moreno D, et al. Identical twins with the C9orf72 repeat expansion are discordant for ALS. Neurology 2014; 83: 1476-1478.
-
(2014)
Neurology
, vol.83
, pp. 1476-1478
-
-
Xi, Z.1
Yunusova, Y.2
Van Bm Dib, S.3
Ghani, M.4
Moreno, D.5
-
56
-
-
84863596527
-
Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion
-
Fong JC, Karydas AM, Goldman JS. Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion. Alzheimers Res Ther 2012; 4: 27.
-
(2012)
Alzheimers Res Ther
, vol.4
, pp. 27
-
-
Fong, J.C.1
Karydas, A.M.2
Goldman, J.S.3
-
57
-
-
84892611020
-
Dipeptide repeat protein pathology in C9ORF72 mutation cases: Clinico-pathological correlations
-
Mackenzie IR, Arzberger T, Kremmer E, Troost D, Lorenzl S, Mori K, et al. Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations. Acta Neuropathol 2013; 126: 859-879.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 859-879
-
-
MacKenzie, I.R.1
Arzberger, T.2
Kremmer, E.3
Troost, D.4
Lorenzl, S.5
Mori, K.6
-
58
-
-
84896718565
-
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia
-
van Blitterswijk M, Mullen B, Nicholson AM, Bieniek KF, Heckman MG, Baker MC, et al. TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia. Acta Neuropathol 2014; 127: 397-406.
-
(2014)
Acta Neuropathol
, vol.127
, pp. 397-406
-
-
Van Blitterswijk, M.1
Mullen, B.2
Nicholson, A.M.3
Bieniek, K.F.4
Heckman, M.G.5
Baker, M.C.6
-
59
-
-
84903819005
-
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers
-
van Blitterswijk M, Mullen B, Heckman MG, Baker MC, Dejesus-Hernandez M, Brown PH, et al. Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers. Neurobiol Aging 2014; 35: 2421-2427.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 2421-2427
-
-
Van Blitterswijk, M.1
Mullen, B.2
Heckman, M.G.3
Baker, M.C.4
Dejesus-Hernandez, M.5
Brown, P.H.6
-
60
-
-
84908320047
-
Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders
-
Lattante S, Millecamps S, Stevanin G, Rivaud-Pechoux S, Moigneu C, Camuzat A, et al. Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders. Neurology 2014; 83: 990-995.
-
(2014)
Neurology
, vol.83
, pp. 990-995
-
-
Lattante, S.1
Millecamps, S.2
Stevanin, G.3
Rivaud-Pechoux, S.4
Moigneu, C.5
Camuzat, A.6
-
61
-
-
84928769147
-
Defining the genetic connection linking amyotrophic lateral sclerosis (ALS with frontotemporal dementia (FTD
-
Lattante S, Ciura S, Rouleau GA, Kabashi E. Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD). Trends Genet 2015; 31: 263-273.
-
(2015)
Trends Genet
, vol.31
, pp. 263-273
-
-
Lattante, S.1
Ciura, S.2
Rouleau, G.A.3
Kabashi, E.4
-
62
-
-
84902509590
-
Frontotemporal dementia and its subtypes: A genome-wide association study
-
Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JB, et al. Frontotemporal dementia and its subtypes: a genome-wide association study. Lancet Neurol 2014; 13: 686-699.
-
(2014)
Lancet Neurol
, vol.13
, pp. 686-699
-
-
Ferrari, R.1
Hernandez, D.G.2
Nalls, M.A.3
Rohrer, J.D.4
Ramasamy, A.5
Kwok, J.B.6
-
63
-
-
84945749129
-
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
-
Cirulli ET, Lasseigne BN, Petrovski S, Sapp PC, Dion PA, Leblond CS, et al. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways. Science 2015; 347: 1436-1441.
-
(2015)
Science
, vol.347
, pp. 1436-1441
-
-
Cirulli, E.T.1
Lasseigne, B.N.2
Petrovski, S.3
Sapp, P.C.4
Dion, P.A.5
Leblond, C.S.6
-
64
-
-
79952036163
-
Distinct DNA methylation changes highly correlated with chronological age in the human brain
-
Hernandez DG, Nalls MA, Gibbs JR, Arepalli S, van der Brug M, Chong S, et al. Distinct DNA methylation changes highly correlated with chronological age in the human brain. Hum Mol Genet 2011; 20: 1164-1172.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 1164-1172
-
-
Hernandez, D.G.1
Nalls, M.A.2
Gibbs, J.R.3
Arepalli, S.4
Van Der Brug, M.5
Chong, S.6
-
65
-
-
84871801926
-
C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes
-
Fratta P, Mizielinska S, Nicoll AJ, Zloh M, Fisher EM, Parkinson G, et al. C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes. Sci Rep 2012; 2: 1016.
-
(2012)
Sci Rep
, vol.2
, pp. 1016
-
-
Fratta, P.1
Mizielinska, S.2
Nicoll, A.J.3
Zloh, M.4
Fisher, E.M.5
Parkinson, G.6
-
66
-
-
0026922707
-
DNA methylation represses FMR-1 transcription in fragile X syndrome
-
Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, et al. DNA methylation represses FMR-1 transcription in fragile X syndrome. Hum Mol Genet 1992; 1: 397-400.
-
(1992)
Hum Mol Genet
, vol.1
, pp. 397-400
-
-
Sutcliffe, J.S.1
Nelson, D.L.2
Zhang, F.3
Pieretti, M.4
Caskey, C.T.5
Saxe, D.6
-
67
-
-
84857045643
-
FXN methylation predicts expression and clinical outcome in Friedreich ataxia
-
Evans-Galea MV, Carrodus N, Rowley SM, Corben LA, Tai G, Saffery R, et al. FXN methylation predicts expression and clinical outcome in Friedreich ataxia. Ann Neurol 2012; 71: 487-497.
-
(2012)
Ann Neurol
, vol.71
, pp. 487-497
-
-
Evans-Galea, M.V.1
Carrodus, N.2
Rowley, S.M.3
Corben, L.A.4
Tai, G.5
Saffery, R.6
-
68
-
-
84892597871
-
Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C elegans
-
Therrien M, Rouleau GA, Dion PA, Parker JA. Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C elegans. PLoS One 2013; 8: e83450.
-
(2013)
PLoS One
, vol.8
, pp. e83450
-
-
Therrien, M.1
Rouleau, G.A.2
Dion, P.A.3
Parker, J.A.4
-
69
-
-
84883465132
-
Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons
-
Almeida S, Gascon E, Tran H, Chou HJ, Gendron TF, Degroot S, et al. Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons. Acta Neuropathol 2013; 126: 385-399.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 385-399
-
-
Almeida, S.1
Gascon, E.2
Tran, H.3
Chou, H.J.4
Gendron, T.F.5
Degroot, S.6
-
70
-
-
84886389563
-
Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion
-
208ra149
-
Sareen D, O'Rourke JG, Meera P, Muhammad AK, Grant S, Simpkinson M, et al. Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion. Sci Transl Med 2013; 5: 208ra149.
-
(2013)
Sci Transl Med
, vol.5
-
-
Sareen, D.1
O'Rourke, J.G.2
Meera, P.3
Muhammad, A.K.4
Grant, S.5
Simpkinson, M.6
-
71
-
-
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, Lammich S, Mackenzie IR, Forne I, Zilow S, Kretzschmar H, et al. 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 2013; 125: 413-423.
-
(2013)
Acta Neuropathol
, vol.125
, pp. 413-423
-
-
Mori, K.1
Lammich, S.2
MacKenzie, I.R.3
Forne, I.4
Zilow, S.5
Kretzschmar, H.6
-
72
-
-
84907188956
-
C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins
-
Mizielinska S, Gronke S, Niccoli T, Ridler CE, Clayton EL, Devoy A, et al. C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins. Science 2014; 345: 1192-1194.
-
(2014)
Science
, vol.345
, pp. 1192-1194
-
-
Mizielinska, S.1
Gronke, S.2
Niccoli, T.3
Ridler, C.E.4
Clayton, E.L.5
Devoy, A.6
-
73
-
-
84930000577
-
C9orf72 FTLD/ALS-Associated Gly- Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration
-
May S, Hornburg D, Schludi MH, Arzberger T, Rentzsch K, Schwenk BM, et al. C9orf72 FTLD/ALS-Associated Gly-Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration. Acta Neuropathol 2014; 128: 485-503.
-
(2014)
Acta Neuropathol
, vol.128
, pp. 485-503
-
-
May, S.1
Hornburg, D.2
Schludi, M.H.3
Arzberger, T.4
Rentzsch, K.5
Schwenk, B.M.6
-
74
-
-
84892585908
-
C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci
-
Mizielinska S, Lashley T, Norona FE, Clayton EL, Ridler CE, Fratta P, et al. C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci. Acta Neuropathol 2013; 126: 845-857.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 845-857
-
-
Mizielinska, S.1
Lashley, T.2
Norona, F.E.3
Clayton, E.L.4
Ridler, C.E.5
Fratta, P.6
-
75
-
-
84928139474
-
C9orf72 promoter hypermethylation is neuroprotective: Neuroimaging and neuropathologic evidence
-
McMillan CT, Russ J, Wood EM, Irwin DJ, Grossman M, McCluskey L, et al. C9orf72 promoter hypermethylation is neuroprotective: neuroimaging and neuropathologic evidence. Neurology 2015; 84: 1622-1630.
-
(2015)
Neurology
, vol.84
, pp. 1622-1630
-
-
McMillan, C.T.1
Russ, J.2
Wood, E.M.3
Irwin, D.J.4
Grossman, M.5
McCluskey, L.6
-
76
-
-
85005929986
-
Promoter DNA methylation regulates progranulin expression and is altered in FTLD
-
Banzhaf-Strathmann J, Claus R, Mücke O, Rentzsch K, van der Zee J, Engelborghs S, et al. Promoter DNA methylation regulates progranulin expression and is altered in FTLD. Acta Neuropathol 2013; 1: 16.
-
(2013)
Acta Neuropathol
, vol.1
, pp. 16
-
-
Banzhaf-Strathmann, J.1
Claus, R.2
Mücke, O.3
Rentzsch, K.4
Van Der Zee, J.5
Engelborghs, S.6
-
77
-
-
81255143014
-
Epigenetic regulation of motor neuron cell death through DNA methylation
-
Chestnut BA, Chang Q, Price A, Lesuisse C, Wong M, Martin LJ. Epigenetic regulation of motor neuron cell death through DNA methylation. J Neurosci 2011; 31: 16619-16636.
-
(2011)
J Neurosci
, vol.31
, pp. 16619-16636
-
-
Chestnut, B.A.1
Chang, Q.2
Price, A.3
Lesuisse, C.4
Wong, M.5
Martin, L.J.6
-
78
-
-
70450158919
-
A genome-wide analysis of brain DNA methylation identifies new candidate genes for sporadic amyotrophic lateral sclerosis
-
Morahan JM, Yu B, Trent RJ, Pamphlett R. A genome-wide analysis of brain DNA methylation identifies new candidate genes for sporadic amyotrophic lateral sclerosis. Amyotroph Lateral Scler 2009; 10: 418-429.
-
(2009)
Amyotroph Lateral Scler
, vol.10
, pp. 418-429
-
-
Morahan, J.M.1
Yu, B.2
Trent, R.J.3
Pamphlett, R.4
-
79
-
-
84885808774
-
RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention
-
Donnelly CJ, Zhang PW, Pham JT, Heusler AR, Mistry NA, Vidensky S, et al. RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention. Neuron 2013; 80: 415-428.
-
(2013)
Neuron
, vol.80
, pp. 415-428
-
-
Donnelly, C.J.1
Zhang, P.W.2
Pham, J.T.3
Heusler, A.R.4
Mistry, N.A.5
Vidensky, S.6
-
80
-
-
84888098632
-
Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration
-
Lagier-Tourenne C, Baughn M, Rigo F, Sun S, Liu P, Li HR, et al. Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration. Proc Natl Acad Sci USA 2013; 110: E4530-E4539.
-
(2013)
Proc Natl Acad Sci USA
, vol.110
, pp. E4530-E4539
-
-
Lagier-Tourenne, C.1
Baughn, M.2
Rigo, F.3
Sun, S.4
Liu, P.5
Li, H.R.6
|