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Human Molecular Genetics|October 4, 2017
C9orf72 poly GA RAN-translated protein plays a key role in amyotrophic lateral sclerosis via aggregation and toxicityYoun-Bok Lee, Pranetha Baskaran, Jorge Gomez-Deza, et al.Neurobiology of Aging|August 9, 2014
Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's diseaseCeleste Sassi, Rita Guerreiro, Raphael Gibbs, et al.Cell Stem Cell|May 7, 2016
Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic CupsDavid A Parfitt, Amelia Lane, Conor M Ramsden, et al.Cell Reports|December 3, 2013
Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxicYoun-Bok Lee, Han-Jou Chen, João N Peres, et al.Brain : a Journal of Neurology|September 22, 2018
A feedback loop between dipeptide-repeat protein, TDP-43 and karyopherin-α mediates C9orf72-related neurodegenerationDaniel A Solomon, Alan Stepto, Wing Hei Au, et al.Science (New York, N.Y.)|March 3, 2009
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6Caroline Vance, Boris Rogelj, Tibor Hortobágyi, et al.Pageof 4