Amyotrophic lateral sclerosis caused by TARDBP mutations: from genetics to TDP-43 proteinopathy.
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| Title: | Amyotrophic lateral sclerosis caused by TARDBP mutations: from genetics to TDP-43 proteinopathy. |
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| Authors: | Balendra R; Human Stem Cells and Neurodegeneration Laboratory, The Francis Crick Institute, London, UK; UK Dementia Research Institute at UCL, London, UK. Electronic address: r.balendra@ucl.ac.uk., Sreedharan J; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK., Hallegger M; UK Dementia Research Institute at King's, London, UK; The Francis Crick Institute, London, UK; Oxford-GSK Institute of Molecular and Computational Medicine, Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK., Luisier R; Genomics and Health Informatics Group, Idiap Research Institute, Martigny, Switzerland., Lashuel HA; Laboratory of Molecular and Chemical Biology of Neurodegeneration, Institute of Bioengineering, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland; Qatar Foundation, Doha, Qatar., Gregory JM; Institute of Medical Sciences, University of Aberdeen, UK., Patani R; Human Stem Cells and Neurodegeneration Laboratory, The Francis Crick Institute, London, UK; Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology, London, UK. Electronic address: rickie.patani@ucl.ac.uk. |
| Source: | The Lancet. Neurology [Lancet Neurol] 2025 May; Vol. 24 (5), pp. 456-470. |
| Publication Type: | Journal Article; Review |
| Journal Info: | Publisher: Lancet Pub. Group Country of Publication: England NLM ID: 101139309 Publication Model: Print Cited Medium: Internet ISSN: 1474-4465 (Electronic) Linking ISSN: 14744422 NLM ISO Abbreviation: Lancet Neurol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40252666 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Amyotrophic lateral sclerosis caused by TARDBP mutations: from genetics to TDP-43 proteinopathy. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Balendra+R%22">Balendra R</searchLink>; Human Stem Cells and Neurodegeneration Laboratory, The Francis Crick Institute, London, UK; UK Dementia Research Institute at UCL, London, UK. Electronic address: r.balendra@ucl.ac.uk.<br /><searchLink fieldCode="AU" term="%22Sreedharan+J%22">Sreedharan J</searchLink>; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Hallegger+M%22">Hallegger M</searchLink>; UK Dementia Research Institute at King's, London, UK; The Francis Crick Institute, London, UK; Oxford-GSK Institute of Molecular and Computational Medicine, Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Luisier+R%22">Luisier R</searchLink>; Genomics and Health Informatics Group, Idiap Research Institute, Martigny, Switzerland.<br /><searchLink fieldCode="AU" term="%22Lashuel+HA%22">Lashuel HA</searchLink>; Laboratory of Molecular and Chemical Biology of Neurodegeneration, Institute of Bioengineering, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland; Qatar Foundation, Doha, Qatar.<br /><searchLink fieldCode="AU" term="%22Gregory+JM%22">Gregory JM</searchLink>; Institute of Medical Sciences, University of Aberdeen, UK.<br /><searchLink fieldCode="AU" term="%22Patani+R%22">Patani R</searchLink>; Human Stem Cells and Neurodegeneration Laboratory, The Francis Crick Institute, London, UK; Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology, London, UK. Electronic address: rickie.patani@ucl.ac.uk. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101139309%22">The Lancet. Neurology</searchLink> [Lancet Neurol] 2025 May; Vol. 24 (5), pp. 456-470. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Review – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lancet+Pub%2E+Group%22">Lancet Pub. Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101139309 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1474-4465 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214744422%22">14744422 </searchLink><i>NLM ISO Abbreviation: </i>Lancet Neurol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40252666 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/S1474-4422(25)00109-7 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 456 Titles: – TitleFull: Amyotrophic lateral sclerosis caused by TARDBP mutations: from genetics to TDP-43 proteinopathy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Balendra R – PersonEntity: Name: NameFull: Sreedharan J – PersonEntity: Name: NameFull: Hallegger M – PersonEntity: Name: NameFull: Luisier R – PersonEntity: Name: NameFull: Lashuel HA – PersonEntity: Name: NameFull: Gregory JM – PersonEntity: Name: NameFull: Patani R IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: 2025 May Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1474-4465 Numbering: – Type: volume Value: 24 – Type: issue Value: 5 Titles: – TitleFull: The Lancet. Neurology Type: main |
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