Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.
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| Title: | Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair. |
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| Authors: | Mianné J; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Chessum L; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Kumar S; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Aguilar C; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Codner G; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Hutchison M; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Parker A; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Mallon AM; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Wells S; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Simon MM; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Teboul L; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK., Brown SD; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK. s.brown@har.mrc.ac.uk., Bowl MR; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK. m.bowl@har.mrc.ac.uk. |
| Source: | Genome medicine [Genome Med] 2016 Feb 15; Vol. 8 (1), pp. 16. Date of Electronic Publication: 2016 Feb 15. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X (Electronic) Linking ISSN: 1756994X NLM ISO Abbreviation: Genome Med Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 26876963 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Mianné+J%22">Mianné J</searchLink>; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Chessum+L%22">Chessum L</searchLink>; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Kumar+S%22">Kumar S</searchLink>; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Aguilar+C%22">Aguilar C</searchLink>; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Codner+G%22">Codner G</searchLink>; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Hutchison+M%22">Hutchison M</searchLink>; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Parker+A%22">Parker A</searchLink>; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Mallon+AM%22">Mallon AM</searchLink>; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Wells+S%22">Wells S</searchLink>; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Simon+MM%22">Simon MM</searchLink>; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Teboul+L%22">Teboul L</searchLink>; Mary Lyon Centre, MRC Harwell, Harwell, Oxford, OX11 0RD, UK.<br /><searchLink fieldCode="AU" term="%22Brown+SD%22">Brown SD</searchLink>; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK. s.brown@har.mrc.ac.uk.<br /><searchLink fieldCode="AU" term="%22Bowl+MR%22">Bowl MR</searchLink>; Mammalian Genetics Unit, MRC Harwell, Harwell, Oxford, OX11 0RD, UK. m.bowl@har.mrc.ac.uk. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101475844%22">Genome medicine</searchLink> [Genome Med] 2016 Feb 15; Vol. 8 (1), pp. 16. <i>Date of Electronic Publication: </i>2016 Feb 15. – 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="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101475844 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1756-994X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%221756994X%22">1756994X </searchLink><i>NLM ISO Abbreviation: </i>Genome Med <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=26876963 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13073-016-0273-4 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 16 Titles: – TitleFull: Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Mianné J – PersonEntity: Name: NameFull: Chessum L – PersonEntity: Name: NameFull: Kumar S – PersonEntity: Name: NameFull: Aguilar C – PersonEntity: Name: NameFull: Codner G – PersonEntity: Name: NameFull: Hutchison M – PersonEntity: Name: NameFull: Parker A – PersonEntity: Name: NameFull: Mallon AM – PersonEntity: Name: NameFull: Wells S – PersonEntity: Name: NameFull: Simon MM – PersonEntity: Name: NameFull: Teboul L – PersonEntity: Name: NameFull: Brown SD – PersonEntity: Name: NameFull: Bowl MR IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 02 Text: 2016 Feb 15 Type: published Y: 2016 Identifiers: – Type: issn-electronic Value: 1756-994X Numbering: – Type: volume Value: 8 – Type: issue Value: 1 Titles: – TitleFull: Genome medicine Type: main |
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