Senataxin mutations elicit motor neuron degeneration phenotypes and yield TDP-43 mislocalization in ALS4 mice and human patients.
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| Title: | Senataxin mutations elicit motor neuron degeneration phenotypes and yield TDP-43 mislocalization in ALS4 mice and human patients. |
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| Authors: | Bennett CL; Department of Neurology, Duke University School of Medicine, Durham, USA., Dastidar SG; Department of Neurology, Duke University School of Medicine, Durham, USA., Ling SC; Department of Physiology, National University of Singapore, Singapore, Singapore., Malik B; Sobell Department of Motor Neuroscience and Movement Disorders, University College London Institute of Neurology, London, UK., Ashe T; Department of Pediatrics, University of California, San Diego, LA JOLLA, USA., Wadhwa M; Department of Neurology, Duke University School of Medicine, Durham, USA., Miller DB; Department of Pediatrics, University of California, San Diego, LA JOLLA, USA., Lee C; Department of Pediatrics, University of California, San Diego, LA JOLLA, USA., Mitchell MB; Department of Pediatrics, University of California, San Diego, LA JOLLA, USA., van Es MA; Department of Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands., Grunseich C; Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, USA., Chen Y; Department of Pediatrics, University of Washington Medical Center, Seattle, USA., Sopher BL; Department of Neurology, University of Washington Medical Center, Seattle, USA., Greensmith L; Sobell Department of Motor Neuroscience and Movement Disorders, University College London Institute of Neurology, London, UK.; The MRC Centre for Neuromuscular Diseases, University College London Institute of Neurology, London, UK., Cleveland DW; Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, USA.; Department of Neurosciences, University of California, San Diego, La Jolla, USA.; The Ludwig Institute for Cancer Research, University of California, San Diego, La Jolla, USA., La Spada AR; Department of Neurology, Duke University School of Medicine, Durham, USA. al.laspada@duke.edu.; Department of Pediatrics, University of California, San Diego, LA JOLLA, USA. al.laspada@duke.edu.; Department of Neurobiology, Duke University School of Medicine, Durham, USA. al.laspada@duke.edu.; Department of Cell Biology, Duke University School of Medicine, Durham, USA. al.laspada@duke.edu.; Duke Center for Neurodegeneration and Neurotherapeutics, Duke University School of Medicine, Bryan Building, Room 401-E, DUMC 2900, Durham, NC, 27710, USA. al.laspada@duke.edu. |
| Source: | Acta neuropathologica [Acta Neuropathol] 2018 Sep; Vol. 136 (3), pp. 425-443. Date of Electronic Publication: 2018 May 03. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Springer Verlag Country of Publication: Germany NLM ID: 0412041 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-0533 (Electronic) Linking ISSN: 00016322 NLM ISO Abbreviation: Acta Neuropathol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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