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 |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 29725819 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Senataxin mutations elicit motor neuron degeneration phenotypes and yield TDP-43 mislocalization in ALS4 mice and human patients. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Bennett+CL%22">Bennett CL</searchLink>; Department of Neurology, Duke University School of Medicine, Durham, USA.<br /><searchLink fieldCode="AU" term="%22Dastidar+SG%22">Dastidar SG</searchLink>; Department of Neurology, Duke University School of Medicine, Durham, USA.<br /><searchLink fieldCode="AU" term="%22Ling+SC%22">Ling SC</searchLink>; Department of Physiology, National University of Singapore, Singapore, Singapore.<br /><searchLink fieldCode="AU" term="%22Malik+B%22">Malik B</searchLink>; Sobell Department of Motor Neuroscience and Movement Disorders, University College London Institute of Neurology, London, UK.<br /><searchLink fieldCode="AU" term="%22Ashe+T%22">Ashe T</searchLink>; Department of Pediatrics, University of California, San Diego, LA JOLLA, USA.<br /><searchLink fieldCode="AU" term="%22Wadhwa+M%22">Wadhwa M</searchLink>; Department of Neurology, Duke University School of Medicine, Durham, USA.<br /><searchLink fieldCode="AU" term="%22Miller+DB%22">Miller DB</searchLink>; Department of Pediatrics, University of California, San Diego, LA JOLLA, USA.<br /><searchLink fieldCode="AU" term="%22Lee+C%22">Lee C</searchLink>; Department of Pediatrics, University of California, San Diego, LA JOLLA, USA.<br /><searchLink fieldCode="AU" term="%22Mitchell+MB%22">Mitchell MB</searchLink>; Department of Pediatrics, University of California, San Diego, LA JOLLA, USA.<br /><searchLink fieldCode="AU" term="%22van+Es+MA%22">van Es MA</searchLink>; Department of Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Grunseich+C%22">Grunseich C</searchLink>; Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, USA.<br /><searchLink fieldCode="AU" term="%22Chen+Y%22">Chen Y</searchLink>; Department of Pediatrics, University of Washington Medical Center, Seattle, USA.<br /><searchLink fieldCode="AU" term="%22Sopher+BL%22">Sopher BL</searchLink>; Department of Neurology, University of Washington Medical Center, Seattle, USA.<br /><searchLink fieldCode="AU" term="%22Greensmith+L%22">Greensmith L</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Cleveland+DW%22">Cleveland DW</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22La+Spada+AR%22">La Spada AR</searchLink>; 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. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220412041%22">Acta neuropathologica</searchLink> [Acta Neuropathol] 2018 Sep; Vol. 136 (3), pp. 425-443. <i>Date of Electronic Publication: </i>2018 May 03. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Springer+Verlag%22">Springer Verlag </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>0412041 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1432-0533 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200016322%22">00016322 </searchLink><i>NLM ISO Abbreviation: </i>Acta Neuropathol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=29725819 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s00401-018-1852-9 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 425 Titles: – TitleFull: Senataxin mutations elicit motor neuron degeneration phenotypes and yield TDP-43 mislocalization in ALS4 mice and human patients. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Bennett CL – PersonEntity: Name: NameFull: Dastidar SG – PersonEntity: Name: NameFull: Ling SC – PersonEntity: Name: NameFull: Malik B – PersonEntity: Name: NameFull: Ashe T – PersonEntity: Name: NameFull: Wadhwa M – PersonEntity: Name: NameFull: Miller DB – PersonEntity: Name: NameFull: Lee C – PersonEntity: Name: NameFull: Mitchell MB – PersonEntity: Name: NameFull: van Es MA – PersonEntity: Name: NameFull: Grunseich C – PersonEntity: Name: NameFull: Chen Y – PersonEntity: Name: NameFull: Sopher BL – PersonEntity: Name: NameFull: Greensmith L – PersonEntity: Name: NameFull: Cleveland DW – PersonEntity: Name: NameFull: La Spada AR IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 09 Text: 2018 Sep Type: published Y: 2018 Identifiers: – Type: issn-electronic Value: 1432-0533 Numbering: – Type: volume Value: 136 – Type: issue Value: 3 Titles: – TitleFull: Acta neuropathologica Type: main |
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