The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein.
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| Title: | The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein. |
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| Authors: | Neumann LC; Institut für Humangenetik, Universitätsklinikum Essen, D-45122 Essen, Germany., Markaki Y, Mladenov E, Hoffmann D, Buiting K, Horsthemke B |
| Source: | Human molecular genetics [Hum Mol Genet] 2012 Sep 15; Vol. 21 (18), pp. 4038-48. Date of Electronic Publication: 2012 Jun 13. |
| Publication Type: | Journal Article; 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-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: 22694955 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Neumann+LC%22">Neumann LC</searchLink>; Institut für Humangenetik, Universitätsklinikum Essen, D-45122 Essen, Germany.<br /><searchLink fieldCode="AU" term="%22Markaki+Y%22">Markaki Y</searchLink><br /><searchLink fieldCode="AU" term="%22Mladenov+E%22">Mladenov E</searchLink><br /><searchLink fieldCode="AU" term="%22Hoffmann+D%22">Hoffmann D</searchLink><br /><searchLink fieldCode="AU" term="%22Buiting+K%22">Buiting K</searchLink><br /><searchLink fieldCode="AU" term="%22Horsthemke+B%22">Horsthemke B</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2012 Sep 15; Vol. 21 (18), pp. 4038-48. <i>Date of Electronic Publication: </i>2012 Jun 13. – 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="%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=22694955 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/dds228 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 4038 Titles: – TitleFull: The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Neumann LC – PersonEntity: Name: NameFull: Markaki Y – PersonEntity: Name: NameFull: Mladenov E – PersonEntity: Name: NameFull: Hoffmann D – PersonEntity: Name: NameFull: Buiting K – PersonEntity: Name: NameFull: Horsthemke B IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 09 Text: 2012 Sep 15 Type: published Y: 2012 Identifiers: – Type: issn-electronic Value: 1460-2083 Numbering: – Type: volume Value: 21 – Type: issue Value: 18 Titles: – TitleFull: Human molecular genetics Type: main |
| ResultId | 1 |
