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In-depth Genetic Analysis of Sclerosing Epithelioid Fibrosarcoma Reveals Recurrent Genomic Alterations and Potential Treatment Targets.

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Title: In-depth Genetic Analysis of Sclerosing Epithelioid Fibrosarcoma Reveals Recurrent Genomic Alterations and Potential Treatment Targets.
Authors: Arbajian E; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. elsa.arbajian@med.lu.se., Puls F; Department of Pathology and Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden., Antonescu CR; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York., Amary F; Department of Histopathology, Royal National Orthopaedic Hospital, Stanmore, United Kingdom., Sciot R; Department of Pathology, KU Leuven and University Hospitals, Leuven, Belgium., Debiec-Rychter M; Center for Human Genetics, KU Leuven and University Hospitals, Leuven, Belgium., Sumathi VP; Department of Musculoskeletal Pathology, Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham, United Kingdom., Järås M; 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., Nilsson J; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden., Hofvander J; 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.; Department of Clinical Genetics, Office for Medical Services, Division of Laboratory Medicine, Lund, Sweden.
Source: Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2017 Dec 01; Vol. 23 (23), pp. 7426-7434. Date of Electronic Publication: 2017 Sep 22.
Publication Type: Journal Article
Journal Info: Publisher: American Association for Cancer Research Country of Publication: United States NLM ID: 9502500 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-3265 (Electronic) Linking ISSN: 10780432 NLM ISO Abbreviation: Clin Cancer Res Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: In-depth Genetic Analysis of Sclerosing Epithelioid Fibrosarcoma Reveals Recurrent Genomic Alterations and Potential Treatment Targets.
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  Data: <searchLink fieldCode="AU" term="%22Arbajian+E%22">Arbajian E</searchLink>; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. elsa.arbajian@med.lu.se.<br /><searchLink fieldCode="AU" term="%22Puls+F%22">Puls F</searchLink>; Department of Pathology and Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden.<br /><searchLink fieldCode="AU" term="%22Antonescu+CR%22">Antonescu CR</searchLink>; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.<br /><searchLink fieldCode="AU" term="%22Amary+F%22">Amary F</searchLink>; Department of Histopathology, Royal National Orthopaedic Hospital, Stanmore, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Sciot+R%22">Sciot R</searchLink>; Department of Pathology, KU Leuven and University Hospitals, Leuven, Belgium.<br /><searchLink fieldCode="AU" term="%22Debiec-Rychter+M%22">Debiec-Rychter M</searchLink>; Center for Human Genetics, KU Leuven and University Hospitals, Leuven, Belgium.<br /><searchLink fieldCode="AU" term="%22Sumathi+VP%22">Sumathi VP</searchLink>; Department of Musculoskeletal Pathology, Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Järås+M%22">Järås M</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="%22Nilsson+J%22">Nilsson J</searchLink>; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.<br /><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="%22Mertens+F%22">Mertens F</searchLink>; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.; Department of Clinical Genetics, Office for Medical Services, Division of Laboratory Medicine, Lund, Sweden.
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  Data: <searchLink fieldCode="JN" term="%229502500%22">Clinical cancer research : an official journal of the American Association for Cancer Research</searchLink> [Clin Cancer Res] 2017 Dec 01; Vol. 23 (23), pp. 7426-7434. <i>Date of Electronic Publication: </i>2017 Sep 22.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22American+Association+for+Cancer+Research%22">American Association for Cancer Research </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9502500 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1557-3265 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210780432%22">10780432 </searchLink><i>NLM ISO Abbreviation: </i>Clin Cancer Res <i>Subsets: </i>MEDLINE
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