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Scientific Reports|August 31, 2012
Widespread binding of FUS along nascent RNA regulates alternative splicing in the brainBoris Rogelj, Laura E Easton, Gireesh K Bogu, et al.
Human Molecular Genetics|June 4, 2013
Drosophila TDP-43 dysfunction in glia and muscle cells cause cytological and behavioural phenotypes that characterize ALS and FTLDDanielle C Diaper, Yoshitsugu Adachi, Luke Lazarou, et al.
Neurobiology of Aging|October 24, 2018
Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementiaSoragia Athina Gkazi, Claire Troakes, Simon Topp, et al.
Plos One|March 11, 2014
An evaluation of a SVA retrotransposon in the FUS promoter as a transcriptional regulator and its association to ALSAbigail L Savage, Thomas P Wilm, Kejhal Khursheed, et al.
Nature Neuroscience|March 2, 2011
Characterizing the RNA targets and position-dependent splicing regulation by TDP-43James R Tollervey, Tomaž Curk, Boris Rogelj, et al.
Acta Neuropathologica Communications|July 19, 2019
C9orf72 intermediate expansions of 24-30 repeats are associated with ALSAlfredo Iacoangeli, Ahmad Al Khleifat, Ashley R Jones, et al.
Annals of Neurology|July 3, 2003
Ciliary neurotrophic factor genotype does not influence clinical phenotype in amyotrophic lateral sclerosisAmmar Al-Chalabi, Margaret D Scheffler, Bradley N Smith, et al.
Journal of Cell Science|February 13, 2019
Nuclear RNA foci from <i>C9ORF72</i> expansion mutation form paraspeckle-like bodiesAna Bajc Česnik, Simona Darovic, Sonja Prpar Mihevc, et al.
American Journal of Human Genetics|July 4, 2003
Two families with familial amyotrophic lateral sclerosis are linked to a novel locus on chromosome 16qDeborah M Ruddy, Matthew J Parton, Ammar Al-Chalabi, et al.
Stem Cells (Dayton, Ohio)|January 15, 2016
Maturation and electrophysiological properties of human pluripotent stem cell-derived oligodendrocytesMatthew R Livesey, Dario Magnani, Elaine M Cleary, et al.
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