Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.
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| Title: | Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration. |
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| Authors: | Joyce PI; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Fratta P; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Landman AS; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Mcgoldrick P; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Wackerhage H; Health Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK., Groves M; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Busam BS; Health Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK., Galino J; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK., Corrochano S; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Beskina OA; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Esapa C; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Ryder E; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK., Carter S; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Stewart M; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Codner G; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Hilton H; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Teboul L; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Tucker J; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Lionikas A; Health Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK., Estabel J; Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK and., Ramirez-Solis R; Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK and., White JK; Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK and., Brandner S; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Plagnol V; UCL Genetics Institute, London WC1E 6BT, UK., Bennet DL; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK., Abramov AY; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Greensmith L; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK, a.acevedo@har.mrc.ac.uk e.fisher@prion.ucl.ac.uk l.greensmith@ucl.ac.uk., Fisher EM; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK, a.acevedo@har.mrc.ac.uk e.fisher@prion.ucl.ac.uk l.greensmith@ucl.ac.uk., Acevedo-Arozena A; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK, a.acevedo@har.mrc.ac.uk e.fisher@prion.ucl.ac.uk l.greensmith@ucl.ac.uk. |
| Source: | Human molecular genetics [Hum Mol Genet] 2016 Jan 15; Vol. 25 (2), pp. 291-307. Date of Electronic Publication: 2015 Nov 24. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 26604141 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Joyce+PI%22">Joyce PI</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Fratta+P%22">Fratta P</searchLink>; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Landman+AS%22">Landman AS</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Mcgoldrick+P%22">Mcgoldrick P</searchLink>; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Wackerhage+H%22">Wackerhage H</searchLink>; Health Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK.<br /><searchLink fieldCode="AU" term="%22Groves+M%22">Groves M</searchLink>; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Busam+BS%22">Busam BS</searchLink>; Health Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK.<br /><searchLink fieldCode="AU" term="%22Galino+J%22">Galino J</searchLink>; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK.<br /><searchLink fieldCode="AU" term="%22Corrochano+S%22">Corrochano S</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Beskina+OA%22">Beskina OA</searchLink>; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Esapa+C%22">Esapa C</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Ryder+E%22">Ryder E</searchLink>; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK.<br /><searchLink fieldCode="AU" term="%22Carter+S%22">Carter S</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Stewart+M%22">Stewart M</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Codner+G%22">Codner G</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Hilton+H%22">Hilton H</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Teboul+L%22">Teboul L</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Tucker+J%22">Tucker J</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Lionikas+A%22">Lionikas A</searchLink>; Health Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK.<br /><searchLink fieldCode="AU" term="%22Estabel+J%22">Estabel J</searchLink>; Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK and.<br /><searchLink fieldCode="AU" term="%22Ramirez-Solis+R%22">Ramirez-Solis R</searchLink>; Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK and.<br /><searchLink fieldCode="AU" term="%22White+JK%22">White JK</searchLink>; Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK and.<br /><searchLink fieldCode="AU" term="%22Brandner+S%22">Brandner S</searchLink>; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Plagnol+V%22">Plagnol V</searchLink>; UCL Genetics Institute, London WC1E 6BT, UK.<br /><searchLink fieldCode="AU" term="%22Bennet+DL%22">Bennet DL</searchLink>; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK.<br /><searchLink fieldCode="AU" term="%22Abramov+AY%22">Abramov AY</searchLink>; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Greensmith+L%22">Greensmith L</searchLink>; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK, a.acevedo@har.mrc.ac.uk e.fisher@prion.ucl.ac.uk l.greensmith@ucl.ac.uk.<br /><searchLink fieldCode="AU" term="%22Fisher+EM%22">Fisher EM</searchLink>; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK, a.acevedo@har.mrc.ac.uk e.fisher@prion.ucl.ac.uk l.greensmith@ucl.ac.uk.<br /><searchLink fieldCode="AU" term="%22Acevedo-Arozena+A%22">Acevedo-Arozena A</searchLink>; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK, a.acevedo@har.mrc.ac.uk e.fisher@prion.ucl.ac.uk l.greensmith@ucl.ac.uk. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2016 Jan 15; Vol. 25 (2), pp. 291-307. <i>Date of Electronic Publication: </i>2015 Nov 24. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=26604141 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/ddv471 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 291 Titles: – TitleFull: Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Joyce PI – PersonEntity: Name: NameFull: Fratta P – PersonEntity: Name: NameFull: Landman AS – PersonEntity: Name: NameFull: Mcgoldrick P – PersonEntity: Name: NameFull: Wackerhage H – PersonEntity: Name: NameFull: Groves M – PersonEntity: Name: NameFull: Busam BS – PersonEntity: Name: NameFull: Galino J – PersonEntity: Name: NameFull: Corrochano S – PersonEntity: Name: NameFull: Beskina OA – PersonEntity: Name: NameFull: Esapa C – PersonEntity: Name: NameFull: Ryder E – PersonEntity: Name: NameFull: Carter S – PersonEntity: Name: NameFull: Stewart M – PersonEntity: Name: NameFull: Codner G – PersonEntity: Name: NameFull: Hilton H – PersonEntity: Name: NameFull: Teboul L – PersonEntity: Name: NameFull: Tucker J – PersonEntity: Name: NameFull: Lionikas A – PersonEntity: Name: NameFull: Estabel J – PersonEntity: Name: NameFull: Ramirez-Solis R – PersonEntity: Name: NameFull: White JK – PersonEntity: Name: NameFull: Brandner S – PersonEntity: Name: NameFull: Plagnol V – PersonEntity: Name: NameFull: Bennet DL – PersonEntity: Name: NameFull: Abramov AY – PersonEntity: Name: NameFull: Greensmith L – PersonEntity: Name: NameFull: Fisher EM – PersonEntity: Name: NameFull: Acevedo-Arozena A IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 01 Text: 2016 Jan 15 Type: published Y: 2016 Identifiers: – Type: issn-electronic Value: 1460-2083 Numbering: – Type: volume Value: 25 – Type: issue Value: 2 Titles: – TitleFull: Human molecular genetics Type: main |
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