Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect.
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| Title: | Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect. |
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| Authors: | Olley G; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK., Pradeepa MM; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK.; Blizard institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK., Grimes GR; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK., Piquet S; Epigenetics and Cell Fate Centre, UMR7216 CNRS, Université de Paris, Paris, France., Polo SE; Epigenetics and Cell Fate Centre, UMR7216 CNRS, Université de Paris, Paris, France., FitzPatrick DR; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK., Bickmore WA; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK. Wendy.Bickmore@igmm.ed.ac.uk., Boumendil C; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK. Charlene.BOUMENDIL@ijm.fr.; Université de Paris, CNRS, Institut Jacques Monod, Paris, France. Charlene.BOUMENDIL@ijm.fr. |
| Source: | Nature communications [Nat Commun] 2021 May 25; Vol. 12 (1), pp. 3127. Date of Electronic Publication: 2021 May 25. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 34035299 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Olley+G%22">Olley G</searchLink>; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK.<br /><searchLink fieldCode="AU" term="%22Pradeepa+MM%22">Pradeepa MM</searchLink>; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK.; Blizard institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.<br /><searchLink fieldCode="AU" term="%22Grimes+GR%22">Grimes GR</searchLink>; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK.<br /><searchLink fieldCode="AU" term="%22Piquet+S%22">Piquet S</searchLink>; Epigenetics and Cell Fate Centre, UMR7216 CNRS, Université de Paris, Paris, France.<br /><searchLink fieldCode="AU" term="%22Polo+SE%22">Polo SE</searchLink>; Epigenetics and Cell Fate Centre, UMR7216 CNRS, Université de Paris, Paris, France.<br /><searchLink fieldCode="AU" term="%22FitzPatrick+DR%22">FitzPatrick DR</searchLink>; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK.<br /><searchLink fieldCode="AU" term="%22Bickmore+WA%22">Bickmore WA</searchLink>; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK. Wendy.Bickmore@igmm.ed.ac.uk.<br /><searchLink fieldCode="AU" term="%22Boumendil+C%22">Boumendil C</searchLink>; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK. Charlene.BOUMENDIL@ijm.fr.; Université de Paris, CNRS, Institut Jacques Monod, Paris, France. Charlene.BOUMENDIL@ijm.fr. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101528555%22">Nature communications</searchLink> [Nat Commun] 2021 May 25; Vol. 12 (1), pp. 3127. <i>Date of Electronic Publication: </i>2021 May 25. – 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="%22Nature+Pub%2E+Group%22">Nature Pub. Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101528555 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2041-1723 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220411723%22">20411723 </searchLink><i>NLM ISO Abbreviation: </i>Nat Commun <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=34035299 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41467-021-23500-6 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 3127 Titles: – TitleFull: Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Olley G – PersonEntity: Name: NameFull: Pradeepa MM – PersonEntity: Name: NameFull: Grimes GR – PersonEntity: Name: NameFull: Piquet S – PersonEntity: Name: NameFull: Polo SE – PersonEntity: Name: NameFull: FitzPatrick DR – PersonEntity: Name: NameFull: Bickmore WA – PersonEntity: Name: NameFull: Boumendil C IsPartOfRelationships: – BibEntity: Dates: – D: 25 M: 05 Text: 2021 May 25 Type: published Y: 2021 Identifiers: – Type: issn-electronic Value: 2041-1723 Numbering: – Type: volume Value: 12 – Type: issue Value: 1 Titles: – TitleFull: Nature communications Type: main |
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