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Journal Abstract Search

825 related items for PubMed ID: 32506986

  • 1. An EWSR1-CREB3L1 Fusion Gene in Extraskeletal Undifferentiated Round Cell Sarcoma Expands the Spectrum of Genetic Landscape in the "Ewing-Like" Undifferentiated Round Cell Sarcomas.
    Bissonnette C, Shilo K, Liebner D, Rogers A, Pollock RE, Iwenofu OH.
    Int J Surg Pathol; 2021 Feb; 29(1):109-116. PubMed ID: 32506986
    [Abstract] [Full Text] [Related]

  • 2. Expanding the molecular landscape of undifferentiated sarcomas of bone with a novel EWSR1-SSX3 gene fusion.
    Fumagalli C, Orellana R, Ferré M, Gonzalez A, Catasús L, Vázquez T, Sebio A, López-Pousa A, Llauger J, Peiró A, Antonescu CR.
    Genes Chromosomes Cancer; 2024 Jan; 63(1):e23215. PubMed ID: 38050902
    [Abstract] [Full Text] [Related]

  • 3. Superficial Neurocristic EWSR1::FLI1 Fusion Tumor: A Distinctive, Clinically Indolent, S100 Protein/SOX10-Positive Neoplasm.
    Folpe AL, Tetzlaff MT, Billings SD, Torres-Mora J, Borowsky AD, Santiago TC, Ameline B, Baumhoer D.
    Mod Pathol; 2024 Aug; 37(8):100537. PubMed ID: 38866368
    [Abstract] [Full Text] [Related]

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  • 5. Review with novel markers facilitates precise categorization of 41 cases of diagnostically challenging, "undifferentiated small round cell tumors". A clinicopathologic, immunophenotypic and molecular analysis.
    Machado I, Yoshida A, Morales MGN, Abrahão-Machado LF, Navarro S, Cruz J, Lavernia J, Parafioriti A, Picci P, Llombart-Bosch A.
    Ann Diagn Pathol; 2018 Jun; 34():1-12. PubMed ID: 29661713
    [Abstract] [Full Text] [Related]

  • 6. Primary Renal Hybrid Low-grade Fibromyxoid Sarcoma-Sclerosing Epithelioid Fibrosarcoma: An Unusual Pediatric Case With EWSR1-CREB3L1 Fusion.
    Mok Y, Pang YH, Sanjeev JS, Kuick CH, Chang KT.
    Pediatr Dev Pathol; 2018 Jun; 21(6):574-579. PubMed ID: 29426275
    [Abstract] [Full Text] [Related]

  • 7. Defining Ewing and Ewing-like small round cell tumors (SRCT): The need for molecular techniques in their categorization and differential diagnosis. A study of 200 cases.
    Machado I, Navarro L, Pellin A, Navarro S, Agaimy A, Tardío JC, Karseladze A, Petrov S, Scotlandi K, Picci P, Llombart-Bosch A.
    Ann Diagn Pathol; 2016 Jun; 22():25-32. PubMed ID: 27180056
    [Abstract] [Full Text] [Related]

  • 8. Clinicopathological and molecular spectrum of ewing sarcomas/PNETs, including validation of EWSR1 rearrangement by conventional and array FISH technique in certain cases.
    Rekhi B, Vogel U, Basak R, Desai SB, Jambhekar NA.
    Pathol Oncol Res; 2014 Jul; 20(3):503-16. PubMed ID: 24293381
    [Abstract] [Full Text] [Related]

  • 9. DNA methylation profiling distinguishes Ewing-like sarcoma with EWSR1-NFATc2 fusion from Ewing sarcoma.
    Koelsche C, Kriegsmann M, Kommoss FKF, Stichel D, Kriegsmann K, Vokuhl C, Grünewald TGP, Romero-Pérez L, Kirchner T, de Alava E, Diaz-Martin J, Hartmann W, Baumhoer D, Antonescu CR, Szuhai K, Flucke U, Dirksen U, Pfister SM, Jones DTW, Mechtersheimer G, von Deimling A.
    J Cancer Res Clin Oncol; 2019 May; 145(5):1273-1281. PubMed ID: 30895378
    [Abstract] [Full Text] [Related]

  • 10. A novel EWSR1-CREB3L1 fusion transcript in a case of small cell osteosarcoma.
    Debelenko LV, McGregor LM, Shivakumar BR, Dorfman HD, Raimondi SC.
    Genes Chromosomes Cancer; 2011 Dec; 50(12):1054-62. PubMed ID: 21987447
    [Abstract] [Full Text] [Related]

  • 11. Evaluation of NKX2-2 expression in round cell sarcomas and other tumors with EWSR1 rearrangement: imperfect specificity for Ewing sarcoma.
    Hung YP, Fletcher CD, Hornick JL.
    Mod Pathol; 2016 Apr; 29(4):370-80. PubMed ID: 26847175
    [Abstract] [Full Text] [Related]

  • 12. Ewing sarcoma and Ewing-like tumors.
    Sbaraglia M, Righi A, Gambarotti M, Dei Tos AP.
    Virchows Arch; 2020 Jan; 476(1):109-119. PubMed ID: 31802230
    [Abstract] [Full Text] [Related]

  • 13. Report and literature review of four cases of EWSR1::NFATC2 round cell sarcoma.
    Liu L, Li L, Ding Y, Kong F, Mo W, Ye H, Shen D.
    Diagn Pathol; 2024 Jan 22; 19(1):19. PubMed ID: 38254207
    [Abstract] [Full Text] [Related]

  • 14. Distinct transcriptional signature and immunoprofile of CIC-DUX4 fusion-positive round cell tumors compared to EWSR1-rearranged Ewing sarcomas: further evidence toward distinct pathologic entities.
    Specht K, Sung YS, Zhang L, Richter GH, Fletcher CD, Antonescu CR.
    Genes Chromosomes Cancer; 2014 Jul 22; 53(7):622-33. PubMed ID: 24723486
    [Abstract] [Full Text] [Related]

  • 15. Undifferentiated sarcoma of bone with a round to epithelioid cell phenotype harboring a novel EWSR1-SSX2 fusion identified by RNA-based next-generation sequencing.
    Cordier F, Van der Meulen J, Van Gaever B, Lapeire L, Sys G, Van Dorpe J, Creytens D.
    Genes Chromosomes Cancer; 2022 Jan 22; 61(1):44-49. PubMed ID: 34538011
    [Abstract] [Full Text] [Related]

  • 16. Ewing-like sarcoma: An emerging family of round cell sarcomas.
    Renzi S, Anderson ND, Light N, Gupta A.
    J Cell Physiol; 2019 Jun 22; 234(6):7999-8007. PubMed ID: 30257034
    [Abstract] [Full Text] [Related]

  • 17. Ewing sarcoma with FEV gene rearrangements is a rare subset with predilection for extraskeletal locations and aggressive behavior.
    Tsuda Y, Dickson BC, Swanson D, Sung YS, Zhang L, Meyers P, Healey JH, Antonescu CR.
    Genes Chromosomes Cancer; 2020 May 22; 59(5):286-294. PubMed ID: 31756779
    [Abstract] [Full Text] [Related]

  • 18. Sarcomas with sclerotic epithelioid phenotype harboring novel EWSR1-SSX1 fusions.
    Antonescu CR, Rosenberg AE, Xie Z, Zhang L, Perell KA, Loya AC.
    Genes Chromosomes Cancer; 2021 Sep 22; 60(9):616-622. PubMed ID: 33987888
    [Abstract] [Full Text] [Related]

  • 19. Sarcomas With CIC-rearrangements Are a Distinct Pathologic Entity With Aggressive Outcome: A Clinicopathologic and Molecular Study of 115 Cases.
    Antonescu CR, Owosho AA, Zhang L, Chen S, Deniz K, Huryn JM, Kao YC, Huang SC, Singer S, Tap W, Schaefer IM, Fletcher CD.
    Am J Surg Pathol; 2017 Jul 22; 41(7):941-949. PubMed ID: 28346326
    [Abstract] [Full Text] [Related]

  • 20. Recurrent EWSR1::COLCA2 Fusions Define a Novel Sarcoma With Spindle/Round Cell Morphology and Strong Predilection for the Sinonasal Tract.
    Agaimy A, Baněčková M, De Almeida J, Dickson BC, Dimmler A, Hartmann W, Laé M, Pablik J, Schubart C, Skálová A, Stoehr R, Trautmann M, Wardelmann E, Wassef M, Weinreb I.
    Am J Surg Pathol; 2023 Mar 01; 47(3):361-369. PubMed ID: 36580038
    [Abstract] [Full Text] [Related]

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