Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome.
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| Title: | Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome. |
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| Authors: | Poll SR; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Martin R; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Wohler E; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Partan ES; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Walek E; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Salman S; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Groepper D; Department of Pediatrics, Southern Illinois University School of Medicine, Springfield, Illinois, United States of America., Kratz L; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Cernach M; Universidade Metropolitana de Santos, Santos, São Paulo, Brazil., Jesus-Garcia R; Department of Orthopedics-Oncology, Universidade Federal de São Paulo, São Paulo, Brazil., Haldeman-Englert C; Mission Fullerton Genetics Center, Asheville, North Carolina, United States of America., Choi YJ; Department of Neurology, University of California, Irvine, California, United States of America., Morris CD; Department of Orthopedic Surgery, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.; Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America., Cohen B; Department of Dermatology, Johns Hopkins School of Medicine, Baltimore, Maryland, Untied States of America., Hoover-Fong J; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Valle D; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Semenza GL; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Sobreira NLM; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America. |
| Source: | PLoS genetics [PLoS Genet] 2022 Dec 08; Vol. 18 (12), pp. e1010504. Date of Electronic Publication: 2022 Dec 08 (Print Publication: 2022). |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural |
| 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: 36480544 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Poll+SR%22">Poll SR</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Martin+R%22">Martin R</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Wohler+E%22">Wohler E</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Partan+ES%22">Partan ES</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Walek+E%22">Walek E</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Salman+S%22">Salman S</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Groepper+D%22">Groepper D</searchLink>; Department of Pediatrics, Southern Illinois University School of Medicine, Springfield, Illinois, United States of America.<br /><searchLink fieldCode="AU" term="%22Kratz+L%22">Kratz L</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Cernach+M%22">Cernach M</searchLink>; Universidade Metropolitana de Santos, Santos, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Jesus-Garcia+R%22">Jesus-Garcia R</searchLink>; Department of Orthopedics-Oncology, Universidade Federal de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Haldeman-Englert+C%22">Haldeman-Englert C</searchLink>; Mission Fullerton Genetics Center, Asheville, North Carolina, United States of America.<br /><searchLink fieldCode="AU" term="%22Choi+YJ%22">Choi YJ</searchLink>; Department of Neurology, University of California, Irvine, California, United States of America.<br /><searchLink fieldCode="AU" term="%22Morris+CD%22">Morris CD</searchLink>; Department of Orthopedic Surgery, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.; Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Cohen+B%22">Cohen B</searchLink>; Department of Dermatology, Johns Hopkins School of Medicine, Baltimore, Maryland, Untied States of America.<br /><searchLink fieldCode="AU" term="%22Hoover-Fong+J%22">Hoover-Fong J</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Valle+D%22">Valle D</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Semenza+GL%22">Semenza GL</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Sobreira+NLM%22">Sobreira NLM</searchLink>; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101239074%22">PLoS genetics</searchLink> [PLoS Genet] 2022 Dec 08; Vol. 18 (12), pp. e1010504. <i>Date of Electronic Publication: </i>2022 Dec 08 (<i>Print Publication: </i>2022). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural – 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=36480544 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1371/journal.pgen.1010504 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: e1010504 Titles: – TitleFull: Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Poll SR – PersonEntity: Name: NameFull: Martin R – PersonEntity: Name: NameFull: Wohler E – PersonEntity: Name: NameFull: Partan ES – PersonEntity: Name: NameFull: Walek E – PersonEntity: Name: NameFull: Salman S – PersonEntity: Name: NameFull: Groepper D – PersonEntity: Name: NameFull: Kratz L – PersonEntity: Name: NameFull: Cernach M – PersonEntity: Name: NameFull: Jesus-Garcia R – PersonEntity: Name: NameFull: Haldeman-Englert C – PersonEntity: Name: NameFull: Choi YJ – PersonEntity: Name: NameFull: Morris CD – PersonEntity: Name: NameFull: Cohen B – PersonEntity: Name: NameFull: Hoover-Fong J – PersonEntity: Name: NameFull: Valle D – PersonEntity: Name: NameFull: Semenza GL – PersonEntity: Name: NameFull: Sobreira NLM IsPartOfRelationships: – BibEntity: Dates: – D: 08 M: 12 Text: 2022 Dec 08 Type: published Y: 2022 Identifiers: – Type: issn-electronic Value: 1553-7404 Numbering: – Type: volume Value: 18 – Type: issue Value: 12 Titles: – TitleFull: PLoS genetics Type: main |
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