Activation of Rho GTPases in Smith-Lemli-Opitz syndrome: pathophysiological and clinical implications.
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| Title: | Activation of Rho GTPases in Smith-Lemli-Opitz syndrome: pathophysiological and clinical implications. |
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| Authors: | Jiang XS; Section on Molecular Dysmorphology, Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health, National Institutes of Health, Bethesda, MD 20892, USA., Wassif CA, Backlund PS, Song L, Holtzclaw LA, Li Z, Yergey AL, Porter FD |
| Source: | Human molecular genetics [Hum Mol Genet] 2010 Apr 01; Vol. 19 (7), pp. 1347-57. Date of Electronic Publication: 2010 Jan 12. |
| Publication Type: | Journal Article; Research Support, N.I.H., Intramural |
| 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: 20067919 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Activation of Rho GTPases in Smith-Lemli-Opitz syndrome: pathophysiological and clinical implications. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Jiang+XS%22">Jiang XS</searchLink>; Section on Molecular Dysmorphology, Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health, National Institutes of Health, Bethesda, MD 20892, USA.<br /><searchLink fieldCode="AU" term="%22Wassif+CA%22">Wassif CA</searchLink><br /><searchLink fieldCode="AU" term="%22Backlund+PS%22">Backlund PS</searchLink><br /><searchLink fieldCode="AU" term="%22Song+L%22">Song L</searchLink><br /><searchLink fieldCode="AU" term="%22Holtzclaw+LA%22">Holtzclaw LA</searchLink><br /><searchLink fieldCode="AU" term="%22Li+Z%22">Li Z</searchLink><br /><searchLink fieldCode="AU" term="%22Yergey+AL%22">Yergey AL</searchLink><br /><searchLink fieldCode="AU" term="%22Porter+FD%22">Porter FD</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2010 Apr 01; Vol. 19 (7), pp. 1347-57. <i>Date of Electronic Publication: </i>2010 Jan 12. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Intramural – 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=20067919 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/ddq011 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1347 Titles: – TitleFull: Activation of Rho GTPases in Smith-Lemli-Opitz syndrome: pathophysiological and clinical implications. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Jiang XS – PersonEntity: Name: NameFull: Wassif CA – PersonEntity: Name: NameFull: Backlund PS – PersonEntity: Name: NameFull: Song L – PersonEntity: Name: NameFull: Holtzclaw LA – PersonEntity: Name: NameFull: Li Z – PersonEntity: Name: NameFull: Yergey AL – PersonEntity: Name: NameFull: Porter FD IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 04 Text: 2010 Apr 01 Type: published Y: 2010 Identifiers: – Type: issn-electronic Value: 1460-2083 Numbering: – Type: volume Value: 19 – Type: issue Value: 7 Titles: – TitleFull: Human molecular genetics Type: main |
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