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 |
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