State of play in amyotrophic lateral sclerosis genetics.

Artículos que citan State of play in amyotrophic lateral sclerosis genetics.

Título / Autor	Año
Guidelines for the use and interpretation of assays for monitoring autophagy DJ Klionsky, K Abdelmohsen, A Abe, MJ Abedin, H Abeliovich, ... Autophagy 12 (1), 1-222	2016
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ... Science 347 (6229), 1436-1441	2015
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia A Freischmidt, T Wieland, B Richter, W Ruf, V Schaeffer, K Müller, ... Nature neuroscience 18 (5), 631	2015
RNA mis-splicing in disease MM Scotti, MS Swanson Nature Reviews Genetics 17 (1), 19	2016
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ... Nature neuroscience 17 (5), 664	2014
Microglia function in the central nervous system during health and neurodegeneration M Colonna, O Butovsky Annual review of immunology 35, 441-468	2017
The phenotypic variability of amyotrophic lateral sclerosis B Swinnen, W Robberecht Nature Reviews Neurology 10 (11), 661	2014
Risk factors for amyotrophic lateral sclerosis C Ingre, PM Roos, F Piehl, F Kamel, F Fang Clinical epidemiology 7, 181	2015
The structure of the dynactin complex and its interaction with dynein L Urnavicius, K Zhang, AG Diamant, C Motz, MA Schlager, M Yu, NA Patel, ... Science 347 (6229), 1441-1446	2015
Antisense oligonucleotides in therapy for neurodegenerative disorders MM Evers, LJA Toonen, WMC van Roon-Mom Advanced drug delivery reviews 87, 90-103	2015
Amyotrophic lateral sclerosis O Hardiman, A Al-Chalabi, A Chio, EM Corr, G Logroscino, W Robberecht, ... Nature Reviews Disease Primers 3, 17071	2017
TDP-43 repression of nonconserved cryptic exons is compromised in ALS-FTD JP Ling, O Pletnikova, JC Troncoso, PC Wong Science 349 (6248), 650-655	2015
Amyotrophic lateral sclerosis MA van Es, O Hardiman, A Chio, A Al-Chalabi, RJ Pasterkamp, ... The Lancet 390 (10107), 2084-2098	2017
Protein phase separation: a new phase in cell biology S Boeynaems, S Alberti, NL Fawzi, T Mittag, M Polymenidou, F Rousseau, ... Trends in cell biology 28 (6), 420-435	2018
Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viability AC Devlin, K Burr, S Borooah, JD Foster, EM Cleary, I Geti, L Vallier, ... Nature communications 6, 5999	2015
ALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the disease EB Moloney, F de Winter, J Verhaagen Frontiers in neuroscience 8, 252	2014
Human C9ORF72 hexanucleotide expansion reproduces RNA foci and dipeptide repeat proteins but not neurodegeneration in BAC transgenic mice OM Peters, GT Cabrera, H Tran, TF Gendron, JE McKeon, J Metterville, ... Neuron 88 (5), 902-909	2015
Protective and toxic neuroinflammation in amyotrophic lateral sclerosis KG Hooten, DR Beers, W Zhao, SH Appel Neurotherapeutics 12 (2), 364-375	2015
TDP-43 proteinopathy and ALS: insights into disease mechanisms and therapeutic targets EL Scotter, HJ Chen, CE Shaw Neurotherapeutics 12 (2), 352-363	2015
Phase separation of C9orf72 dipeptide repeats perturbs stress granule dynamics S Boeynaems, E Bogaert, D Kovacs, A Konijnenberg, E Timmerman, ... Molecular cell 65 (6), 1044-1055. e5	2017

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