Loss-of-function point mutations associated with renal tubular dysgenesis provide insights about renin function and cellular trafficking.
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| Title: | Loss-of-function point mutations associated with renal tubular dysgenesis provide insights about renin function and cellular trafficking. |
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| Authors: | Michaud A; INSERM, U833, Paris, France. annie.michaud@college-de-france.fr, Bur D, Gribouval O, Muller L, Iturrioz X, Clemessy M, Gasc JM, Gubler MC, Corvol P |
| Source: | Human molecular genetics [Hum Mol Genet] 2011 Jan 15; Vol. 20 (2), pp. 301-11. Date of Electronic Publication: 2010 Oct 29. |
| Publication Type: | Journal Article |
| 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: 21036942 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Loss-of-function point mutations associated with renal tubular dysgenesis provide insights about renin function and cellular trafficking. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Michaud+A%22">Michaud A</searchLink>; INSERM, U833, Paris, France. annie.michaud@college-de-france.fr<br /><searchLink fieldCode="AU" term="%22Bur+D%22">Bur D</searchLink><br /><searchLink fieldCode="AU" term="%22Gribouval+O%22">Gribouval O</searchLink><br /><searchLink fieldCode="AU" term="%22Muller+L%22">Muller L</searchLink><br /><searchLink fieldCode="AU" term="%22Iturrioz+X%22">Iturrioz X</searchLink><br /><searchLink fieldCode="AU" term="%22Clemessy+M%22">Clemessy M</searchLink><br /><searchLink fieldCode="AU" term="%22Gasc+JM%22">Gasc JM</searchLink><br /><searchLink fieldCode="AU" term="%22Gubler+MC%22">Gubler MC</searchLink><br /><searchLink fieldCode="AU" term="%22Corvol+P%22">Corvol P</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2011 Jan 15; Vol. 20 (2), pp. 301-11. <i>Date of Electronic Publication: </i>2010 Oct 29. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – 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=21036942 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/ddq465 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 301 Titles: – TitleFull: Loss-of-function point mutations associated with renal tubular dysgenesis provide insights about renin function and cellular trafficking. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Michaud A – PersonEntity: Name: NameFull: Bur D – PersonEntity: Name: NameFull: Gribouval O – PersonEntity: Name: NameFull: Muller L – PersonEntity: Name: NameFull: Iturrioz X – PersonEntity: Name: NameFull: Clemessy M – PersonEntity: Name: NameFull: Gasc JM – PersonEntity: Name: NameFull: Gubler MC – PersonEntity: Name: NameFull: Corvol P IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 01 Text: 2011 Jan 15 Type: published Y: 2011 Identifiers: – Type: issn-electronic Value: 1460-2083 Numbering: – Type: volume Value: 20 – Type: issue Value: 2 Titles: – TitleFull: Human molecular genetics Type: main |
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