Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome.
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| Title: | Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome. |
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| Authors: | Wang S; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA., Yazawa E; Division of Newborn Medicine, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA., Keating EM; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA., Mazumdar N; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA., Hauschild A; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA., Ma Q; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA., Wu H; Department of Pharmacology, Sichuan University West China School of Basic Sciences and Forensic Medicine, Chengdu, Sichuan, China., Xu Y; Department of Anesthesiology, New York University School of Medicine, New York, NY, USA., Shi X; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA., Strathdee D; Transgenic Technology Laboratory, Cancer Research UK Beatson Institute, Glasgow, UK., Gerszten RE; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA., Schlame M; Department of Anesthesiology, New York University School of Medicine, New York, NY, USA., Pu WT; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA.; Transgenic Technology Laboratory, Cancer Research UK Beatson Institute, Glasgow, UK.; Harvard Stem Cell Institute, Harvard University, 02138 Beatson, Cambridge, MA G61 1BD, USA. |
| Source: | Human molecular genetics [Hum Mol Genet] 2023 Jun 05; Vol. 32 (12), pp. 2055-2067. |
| Publication Type: | Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, N.I.H., Extramural; 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 Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 36917259 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Wang+S%22">Wang S</searchLink>; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA.<br /><searchLink fieldCode="AU" term="%22Yazawa+E%22">Yazawa E</searchLink>; Division of Newborn Medicine, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA.<br /><searchLink fieldCode="AU" term="%22Keating+EM%22">Keating EM</searchLink>; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA.<br /><searchLink fieldCode="AU" term="%22Mazumdar+N%22">Mazumdar N</searchLink>; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA.<br /><searchLink fieldCode="AU" term="%22Hauschild+A%22">Hauschild A</searchLink>; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA.<br /><searchLink fieldCode="AU" term="%22Ma+Q%22">Ma Q</searchLink>; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA.<br /><searchLink fieldCode="AU" term="%22Wu+H%22">Wu H</searchLink>; Department of Pharmacology, Sichuan University West China School of Basic Sciences and Forensic Medicine, Chengdu, Sichuan, China.<br /><searchLink fieldCode="AU" term="%22Xu+Y%22">Xu Y</searchLink>; Department of Anesthesiology, New York University School of Medicine, New York, NY, USA.<br /><searchLink fieldCode="AU" term="%22Shi+X%22">Shi X</searchLink>; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA.<br /><searchLink fieldCode="AU" term="%22Strathdee+D%22">Strathdee D</searchLink>; Transgenic Technology Laboratory, Cancer Research UK Beatson Institute, Glasgow, UK.<br /><searchLink fieldCode="AU" term="%22Gerszten+RE%22">Gerszten RE</searchLink>; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA.<br /><searchLink fieldCode="AU" term="%22Schlame+M%22">Schlame M</searchLink>; Department of Anesthesiology, New York University School of Medicine, New York, NY, USA.<br /><searchLink fieldCode="AU" term="%22Pu+WT%22">Pu WT</searchLink>; Department of Cardiology, Boston Children's Hospital, Boston, MA 02215NYU 10016, USA.; Transgenic Technology Laboratory, Cancer Research UK Beatson Institute, Glasgow, UK.; Harvard Stem Cell Institute, Harvard University, 02138 Beatson, Cambridge, MA G61 1BD, USA. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2023 Jun 05; Vol. 32 (12), pp. 2055-2067. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, N.I.H., Extramural; 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 <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=36917259 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/ddad041 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 2055 Titles: – TitleFull: Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Wang S – PersonEntity: Name: NameFull: Yazawa E – PersonEntity: Name: NameFull: Keating EM – PersonEntity: Name: NameFull: Mazumdar N – PersonEntity: Name: NameFull: Hauschild A – PersonEntity: Name: NameFull: Ma Q – PersonEntity: Name: NameFull: Wu H – PersonEntity: Name: NameFull: Xu Y – PersonEntity: Name: NameFull: Shi X – PersonEntity: Name: NameFull: Strathdee D – PersonEntity: Name: NameFull: Gerszten RE – PersonEntity: Name: NameFull: Schlame M – PersonEntity: Name: NameFull: Pu WT IsPartOfRelationships: – BibEntity: Dates: – D: 05 M: 06 Text: 2023 Jun 05 Type: published Y: 2023 Identifiers: – Type: issn-electronic Value: 1460-2083 Numbering: – Type: volume Value: 32 – Type: issue Value: 12 Titles: – TitleFull: Human molecular genetics Type: main |
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