Article thumbnail

Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

By Pietro Fratta, Prasanth Sivakumar, Jack Humphrey, Lo Kitty, Thomas Ricketts, Hugo Oliveira, Jose M Brito-Armas, Bernadett Kalmar, Agnieszka Ule, Yu Yichao, Nicol Birsa, Cristian Bodo, Toby Collins, Alexander E Conicella, Alan Mejia Maza, Alessandro Marrero-Gagliardi, Michelle Stewart, Joffrey Mianne, Silvia Corrochano, Warren Emmett, Gemma Codner, Michael Groves, Ryutaro Fukumura, Yoichi Gondo, Mark Lythgoe, Erwin Pauws, Emma Peskett, Philip Stanier, Lydia Teboul, Martina Hallegger, Andrea Calvo, Adriano Chiò, Adrian M Isaacs, Nicolas L Fawzi, Eric Wang, David E Housman, Francisco Baralle, Linda Greensmith, Emanuele Buratti, Vincent Plagnol, Elizabeth MC Fisher and Abraham Acevedo-Arozena
Topics: ALS; cryptic exon; skiptic exon; splicing; TDP-43; Neuroscience (all); Molecular Biology; Biochemistry, Genetics and Molecular Biology (all); Immunology and Microbiology (all)
Publisher: 'EMBO'
Year: 2018
DOI identifier: 10.15252/embj.201798684
OAI identifier: oai:iris.unito.it:2318/1673166

Suggested articles


To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.