A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human.
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| Title: | A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human. |
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| Authors: | Madelaine R; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA., Notwell JH; Department of Computer Science, Stanford, CA 94305, USA., Skariah G; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA., Halluin C; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA., Chen CC; Department of Computer Science, Stanford, CA 94305, USA., Bejerano G; Department of Computer Science, Stanford, CA 94305, USA.; Department of Developmental Biology, Stanford, CA 94305, USA.; Division of Medical Genetics, Department of Pediatrics, Stanford, CA 94305, USA., Mourrain P; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA.; INSERM 1024, Ecole Normale Supérieure Paris, 75005, France. |
| Source: | Nucleic acids research [Nucleic Acids Res] 2018 Apr 20; Vol. 46 (7), pp. 3517-3531. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. |
| Journal Info: | Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium: Internet ISSN: 1362-4962 (Electronic) Linking ISSN: 03051048 NLM ISO Abbreviation: Nucleic Acids Res Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 29518216 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Madelaine+R%22">Madelaine R</searchLink>; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA.<br /><searchLink fieldCode="AU" term="%22Notwell+JH%22">Notwell JH</searchLink>; Department of Computer Science, Stanford, CA 94305, USA.<br /><searchLink fieldCode="AU" term="%22Skariah+G%22">Skariah G</searchLink>; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA.<br /><searchLink fieldCode="AU" term="%22Halluin+C%22">Halluin C</searchLink>; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA.<br /><searchLink fieldCode="AU" term="%22Chen+CC%22">Chen CC</searchLink>; Department of Computer Science, Stanford, CA 94305, USA.<br /><searchLink fieldCode="AU" term="%22Bejerano+G%22">Bejerano G</searchLink>; Department of Computer Science, Stanford, CA 94305, USA.; Department of Developmental Biology, Stanford, CA 94305, USA.; Division of Medical Genetics, Department of Pediatrics, Stanford, CA 94305, USA.<br /><searchLink fieldCode="AU" term="%22Mourrain+P%22">Mourrain P</searchLink>; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA.; INSERM 1024, Ecole Normale Supérieure Paris, 75005, France. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220411011%22">Nucleic acids research</searchLink> [Nucleic Acids Res] 2018 Apr 20; Vol. 46 (7), pp. 3517-3531. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Oxford+University+Press%22">Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>0411011 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1362-4962 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2203051048%22">03051048 </searchLink><i>NLM ISO Abbreviation: </i>Nucleic Acids Res <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=29518216 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/nar/gky166 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 3517 Titles: – TitleFull: A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Madelaine R – PersonEntity: Name: NameFull: Notwell JH – PersonEntity: Name: NameFull: Skariah G – PersonEntity: Name: NameFull: Halluin C – PersonEntity: Name: NameFull: Chen CC – PersonEntity: Name: NameFull: Bejerano G – PersonEntity: Name: NameFull: Mourrain P IsPartOfRelationships: – BibEntity: Dates: – D: 20 M: 04 Text: 2018 Apr 20 Type: published Y: 2018 Identifiers: – Type: issn-electronic Value: 1362-4962 Numbering: – Type: volume Value: 46 – Type: issue Value: 7 Titles: – TitleFull: Nucleic acids research Type: main |
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