Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth.
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| Title: | Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth. |
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| Authors: | Jeanne M; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France., Vuillaume ML; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France., Ung DC; UMR 1253, iBrain, University of Tours, Inserm, Tours, France., Vancollie VE; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, Hinxton, UK., Wagner C; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France., Collins SC; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France., Vonwill S; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France., Haye D; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France., Chelloug N; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France., Pfundt R; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands., Kummeling J; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands., Moizard MP; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France., Marouillat S; UMR 1253, iBrain, University of Tours, Inserm, Tours, France., Kleefstra T; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands., Yalcin B; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France., Laumonnier F; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France. frederic.laumonnier@inserm.fr.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France. frederic.laumonnier@inserm.fr., Toutain A; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France. |
| Source: | Human genetics [Hum Genet] 2021 Jun; Vol. 140 (6), pp. 885-896. Date of Electronic Publication: 2021 Jan 08. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 33417013 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Jeanne+M%22">Jeanne M</searchLink>; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.<br /><searchLink fieldCode="AU" term="%22Vuillaume+ML%22">Vuillaume ML</searchLink>; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.<br /><searchLink fieldCode="AU" term="%22Ung+DC%22">Ung DC</searchLink>; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.<br /><searchLink fieldCode="AU" term="%22Vancollie+VE%22">Vancollie VE</searchLink>; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, Hinxton, UK.<br /><searchLink fieldCode="AU" term="%22Wagner+C%22">Wagner C</searchLink>; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France.<br /><searchLink fieldCode="AU" term="%22Collins+SC%22">Collins SC</searchLink>; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France.<br /><searchLink fieldCode="AU" term="%22Vonwill+S%22">Vonwill S</searchLink>; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.<br /><searchLink fieldCode="AU" term="%22Haye+D%22">Haye D</searchLink>; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.<br /><searchLink fieldCode="AU" term="%22Chelloug+N%22">Chelloug N</searchLink>; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.<br /><searchLink fieldCode="AU" term="%22Pfundt+R%22">Pfundt R</searchLink>; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Kummeling+J%22">Kummeling J</searchLink>; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Moizard+MP%22">Moizard MP</searchLink>; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.<br /><searchLink fieldCode="AU" term="%22Marouillat+S%22">Marouillat S</searchLink>; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.<br /><searchLink fieldCode="AU" term="%22Kleefstra+T%22">Kleefstra T</searchLink>; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Yalcin+B%22">Yalcin B</searchLink>; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France.<br /><searchLink fieldCode="AU" term="%22Laumonnier+F%22">Laumonnier F</searchLink>; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France. frederic.laumonnier@inserm.fr.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France. frederic.laumonnier@inserm.fr.<br /><searchLink fieldCode="AU" term="%22Toutain+A%22">Toutain A</searchLink>; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%227613873%22">Human genetics</searchLink> [Hum Genet] 2021 Jun; Vol. 140 (6), pp. 885-896. <i>Date of Electronic Publication: </i>2021 Jan 08. – 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="%22Springer+Verlag%22">Springer Verlag </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>7613873 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1432-1203 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2203406717%22">03406717 </searchLink><i>NLM ISO Abbreviation: </i>Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=33417013 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s00439-020-02252-1 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 885 Titles: – TitleFull: Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Jeanne M – PersonEntity: Name: NameFull: Vuillaume ML – PersonEntity: Name: NameFull: Ung DC – PersonEntity: Name: NameFull: Vancollie VE – PersonEntity: Name: NameFull: Wagner C – PersonEntity: Name: NameFull: Collins SC – PersonEntity: Name: NameFull: Vonwill S – PersonEntity: Name: NameFull: Haye D – PersonEntity: Name: NameFull: Chelloug N – PersonEntity: Name: NameFull: Pfundt R – PersonEntity: Name: NameFull: Kummeling J – PersonEntity: Name: NameFull: Moizard MP – PersonEntity: Name: NameFull: Marouillat S – PersonEntity: Name: NameFull: Kleefstra T – PersonEntity: Name: NameFull: Yalcin B – PersonEntity: Name: NameFull: Laumonnier F – PersonEntity: Name: NameFull: Toutain A IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: 2021 Jun Type: published Y: 2021 Identifiers: – Type: issn-electronic Value: 1432-1203 Numbering: – Type: volume Value: 140 – Type: issue Value: 6 Titles: – TitleFull: Human genetics Type: main |
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