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

Journal: The EMBO Journal

Published: 2018-05-15

DOI: 10.15252/embj.201798684

Affiliations: 19

Authors: 42

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Institutions FC
MRC Centre for Neuromuscular Diseases (London), United Kingdom (UK) 0.28
MRC Mary Lyon Centre, United Kingdom (UK) 0.10
UCL Genetics Institute (UGI), United Kingdom (UK) 0.08
MRC Mammalian Genetics Unit (MGU), United Kingdom (UK) 0.08
UCL Great Ormond Street Institute of Child Health (ICH), United Kingdom (UK) 0.07
MIT Department of Biology, United States of America (USA) 0.05
Rita Levi Montalcini Department of Neuroscience, UNITO, Italy 0.05
RIKEN Mutagenesis and Genomics Team, Japan 0.05
UCL Centre for Advanced Biomedical Imaging (CABI), United Kingdom (UK) 0.05
ICGEB Trieste, Italy 0.05
Department of Molecular Biology, Cell Biology, and Biochemistry, Brown University, United States of America (USA) 0.02
Department of Molecular Pharmacology, Physiology and Biotechnology (MPPB), Brown University, United States of America (USA) 0.02
University Hospital of the Canary Islands, ULL, Spain 0.02
Centro de Investigaciones Biomédicas de Canarias (CIBICAN), ULL, Spain 0.02
Instituto Universitario de Tecnologías Biomédicas (ITB), ULL, Spain 0.02
UCL Queen Square Institute of Neurology (IoN), United Kingdom (UK) 0.02
The Francis Crick Institute, United Kingdom (UK) 0.01
UCL Dementia Research Centre (DRC), United Kingdom (UK) 0.01

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