Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity.
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| Title: | Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity. |
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| Authors: | Liang ZS; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom., Cimino I; MRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom., Yalcin B; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique, Institut National de la Santé et de la Recherche Médicale, Université de Strasbourg, France., Raghupathy N; The Jackson Laboratory, Bar Harbor, Maine, United States of America., Vancollie VE; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom., Ibarra-Soria X; Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom., Firth HV; Department of Clinical Genetics, Addenbrooke's Hospital, Cambridge, United Kingdom., Rimmington D; MRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom., Farooqi IS; University of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Addenbrooke's Hospital, Cambridge, United Kingdom., Lelliott CJ; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom., Munger SC; The Jackson Laboratory, Bar Harbor, Maine, United States of America., O'Rahilly S; MRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom., Ferguson-Smith AC; Department of Genetics, University of Cambridge, Cambridge, United Kingdom., Coll AP; MRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom., Logan DW; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom. |
| Source: | PLoS genetics [PLoS Genet] 2020 Sep 02; Vol. 16 (9), pp. e1008916. Date of Electronic Publication: 2020 Sep 02 (Print Publication: 2020). |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 32877400 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Liang+ZS%22">Liang ZS</searchLink>; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Cimino+I%22">Cimino I</searchLink>; MRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Yalcin+B%22">Yalcin B</searchLink>; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique, Institut National de la Santé et de la Recherche Médicale, Université de Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Raghupathy+N%22">Raghupathy N</searchLink>; The Jackson Laboratory, Bar Harbor, Maine, United States of America.<br /><searchLink fieldCode="AU" term="%22Vancollie+VE%22">Vancollie VE</searchLink>; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Ibarra-Soria+X%22">Ibarra-Soria X</searchLink>; Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Firth+HV%22">Firth HV</searchLink>; Department of Clinical Genetics, Addenbrooke's Hospital, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Rimmington+D%22">Rimmington D</searchLink>; MRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Farooqi+IS%22">Farooqi IS</searchLink>; University of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Addenbrooke's Hospital, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Lelliott+CJ%22">Lelliott CJ</searchLink>; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Munger+SC%22">Munger SC</searchLink>; The Jackson Laboratory, Bar Harbor, Maine, United States of America.<br /><searchLink fieldCode="AU" term="%22O'Rahilly+S%22">O'Rahilly S</searchLink>; MRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Ferguson-Smith+AC%22">Ferguson-Smith AC</searchLink>; Department of Genetics, University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Coll+AP%22">Coll AP</searchLink>; MRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Logan+DW%22">Logan DW</searchLink>; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101239074%22">PLoS genetics</searchLink> [PLoS Genet] 2020 Sep 02; Vol. 16 (9), pp. e1008916. <i>Date of Electronic Publication: </i>2020 Sep 02 (<i>Print Publication: </i>2020). – 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="%22Public+Library+of+Science%22">Public Library of Science </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101239074 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>1553-7404 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215537390%22">15537390 </searchLink><i>NLM ISO Abbreviation: </i>PLoS Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32877400 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1371/journal.pgen.1008916 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: e1008916 Titles: – TitleFull: Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Liang ZS – PersonEntity: Name: NameFull: Cimino I – PersonEntity: Name: NameFull: Yalcin B – PersonEntity: Name: NameFull: Raghupathy N – PersonEntity: Name: NameFull: Vancollie VE – PersonEntity: Name: NameFull: Ibarra-Soria X – PersonEntity: Name: NameFull: Firth HV – PersonEntity: Name: NameFull: Rimmington D – PersonEntity: Name: NameFull: Farooqi IS – PersonEntity: Name: NameFull: Lelliott CJ – PersonEntity: Name: NameFull: Munger SC – PersonEntity: Name: NameFull: O'Rahilly S – PersonEntity: Name: NameFull: Ferguson-Smith AC – PersonEntity: Name: NameFull: Coll AP – PersonEntity: Name: NameFull: Logan DW IsPartOfRelationships: – BibEntity: Dates: – D: 02 M: 09 Text: 2020 Sep 02 Type: published Y: 2020 Identifiers: – Type: issn-electronic Value: 1553-7404 Numbering: – Type: volume Value: 16 – Type: issue Value: 9 Titles: – TitleFull: PLoS genetics Type: main |
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