PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells.
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| Title: | PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells. |
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| Authors: | Hofvander J; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden., Jo VY; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA., Fletcher CDM; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA., Puls F; Department of Clinical Pathology and Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden., Flucke U; Department of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands., Nilsson J; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden., Magnusson L; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden., Mertens F; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. Fredrik.mertens@med.lu.se.; Department of Clinical Genetics and Pathology, Skåne University Hospital, SE-221 85, Lund, Sweden. Fredrik.mertens@med.lu.se. |
| Source: | Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc [Mod Pathol] 2020 Jul; Vol. 33 (7), pp. 1331-1340. Date of Electronic Publication: 2020 Jan 13. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Elsevier Inc Country of Publication: United States NLM ID: 8806605 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0285 (Electronic) Linking ISSN: 08933952 NLM ISO Abbreviation: Mod Pathol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 31932680 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Hofvander+J%22">Hofvander J</searchLink>; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.<br /><searchLink fieldCode="AU" term="%22Jo+VY%22">Jo VY</searchLink>; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.<br /><searchLink fieldCode="AU" term="%22Fletcher+CDM%22">Fletcher CDM</searchLink>; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.<br /><searchLink fieldCode="AU" term="%22Puls+F%22">Puls F</searchLink>; Department of Clinical Pathology and Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden.<br /><searchLink fieldCode="AU" term="%22Flucke+U%22">Flucke U</searchLink>; Department of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Nilsson+J%22">Nilsson J</searchLink>; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.<br /><searchLink fieldCode="AU" term="%22Magnusson+L%22">Magnusson L</searchLink>; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.<br /><searchLink fieldCode="AU" term="%22Mertens+F%22">Mertens F</searchLink>; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. Fredrik.mertens@med.lu.se.; Department of Clinical Genetics and Pathology, Skåne University Hospital, SE-221 85, Lund, Sweden. Fredrik.mertens@med.lu.se. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%228806605%22">Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc</searchLink> [Mod Pathol] 2020 Jul; Vol. 33 (7), pp. 1331-1340. <i>Date of Electronic Publication: </i>2020 Jan 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="%22Elsevier+Inc%22">Elsevier Inc </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>8806605 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1530-0285 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2208933952%22">08933952 </searchLink><i>NLM ISO Abbreviation: </i>Mod Pathol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=31932680 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41379-020-0457-8 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1331 Titles: – TitleFull: PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Hofvander J – PersonEntity: Name: NameFull: Jo VY – PersonEntity: Name: NameFull: Fletcher CDM – PersonEntity: Name: NameFull: Puls F – PersonEntity: Name: NameFull: Flucke U – PersonEntity: Name: NameFull: Nilsson J – PersonEntity: Name: NameFull: Magnusson L – PersonEntity: Name: NameFull: Mertens F IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: 2020 Jul Type: published Y: 2020 Identifiers: – Type: issn-electronic Value: 1530-0285 Numbering: – Type: volume Value: 33 – Type: issue Value: 7 Titles: – TitleFull: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc Type: main |
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