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PUBMED FOR HANDHELDS

Journal Abstract Search


207 related items for PubMed ID: 33850302

  • 1. Novel BRAF gene fusions and activating point mutations in spindle cell sarcomas with histologic overlap with infantile fibrosarcoma.
    Penning AJ, Al-Ibraheemi A, Michal M, Larsen BT, Cho SJ, Lockwood CM, Paulson VA, Liu YJ, Plank L, Fritchie K, Beadling C, Neff TL, Corless CL, Rudzinski ER, Davis JL.
    Mod Pathol; 2021 Aug; 34(8):1530-1540. PubMed ID: 33850302
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  • 3. ALK rearrangements in infantile fibrosarcoma-like spindle cell tumours of soft tissue and kidney.
    Tan SY, Al-Ibraheemi A, Ahrens WA, Oesterheld JE, Fanburg-Smith JC, Liu YJ, Spunt SL, Rudzinski ER, Coffin C, Davis JL.
    Histopathology; 2022 Mar; 80(4):698-707. PubMed ID: 34843129
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  • 5. A novel group of spindle cell tumors defined by S100 and CD34 co-expression shows recurrent fusions involving RAF1, BRAF, and NTRK1/2 genes.
    Suurmeijer AJH, Dickson BC, Swanson D, Zhang L, Sung YS, Cotzia P, Fletcher CDM, Antonescu CR.
    Genes Chromosomes Cancer; 2018 Dec; 57(12):611-621. PubMed ID: 30276917
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  • 6. Second Report of PDE10A-BRAF Fusion in Pediatric Spindle Cell Sarcoma With Infantile Fibrosarcoma-Like Morphology Suggesting PDE10A-BRAF Fusion Is a Recurrent Event.
    Hughes CE, Correa H, Benedetti DJ, Smith B, Sumegi J, Bridge J.
    Pediatr Dev Pathol; 2021 Dec; 24(6):554-558. PubMed ID: 34120511
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  • 7. CD34/S100 protein-positive, NTRK1-rearranged infantile fibrosarcoma-like tumors in genitourinary system: two cases expanding the clinicopathologic spectrum and illustrating the diagnostic dilemma.
    Zhao M, Xu J, Wang J.
    Virchows Arch; 2024 Sep; 485(3):575-581. PubMed ID: 38801436
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  • 9. RAF1 gene fusions are recurrent driver events in infantile fibrosarcoma-like mesenchymal tumors.
    Motta M, Barresi S, Pizzi S, Bifano D, Lopez Marti J, Garrido-Pontnou M, Flex E, Bruselles A, Giovannoni I, Rotundo G, Fragale A, Tirelli V, Vallese S, Ciolfi A, Bisogno G, Alaggio R, Tartaglia M.
    J Pathol; 2024 Jun; 263(2):166-177. PubMed ID: 38629245
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  • 11. Clinicopathological findings of pediatric NTRK fusion mesenchymal tumors.
    Kang J, Park JW, Won JK, Bae JM, Koh J, Yim J, Yun H, Kim SK, Choi JY, Kang HJ, Kim WS, Shin JH, Park SH.
    Diagn Pathol; 2020 Sep 21; 15(1):114. PubMed ID: 32957984
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  • 12. Spindle cell sarcoma with KIAA1549-BRAF resembling infantile fibrosarcoma morphologically: A case report and literature review.
    Fujikawa T, Uemura S, Yoshida M, Hyodo S, Kozaki A, Saito A, Kishimoto K, Ishida T, Mori T, Uematsu A, Morita K, Hatakeyama T, Tamura A, Yamamoto N, Komatsu M, Soejima T, Hasegawa D, Kosaka Y.
    Oncol Lett; 2022 Dec 21; 24(6):452. PubMed ID: 36380878
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  • 13. Recurrent RET gene fusions in paediatric spindle mesenchymal neoplasms.
    Davis JL, Vargas SO, Rudzinski ER, López Marti JM, Janeway K, Forrest S, Winsnes K, Pinto N, Yang SE, VanSandt M, Boyd TK, Corless CL, Liu YJ, Surrey LF, Harris MH, Church A, Al-Ibraheemi A.
    Histopathology; 2020 Jun 21; 76(7):1032-1041. PubMed ID: 31994201
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  • 16. Pan-sarcoma genomic analysis of KMT2A rearrangements reveals distinct subtypes defined by YAP1-KMT2A-YAP1 and VIM-KMT2A fusions.
    Massoth LR, Hung YP, Nardi V, Nielsen GP, Hasserjian RP, Louissaint A, Fisch AS, Deshpande V, Zukerberg LR, Lennerz JK, Selig M, Glomski K, Patel PJ, Williams KJ, Sokol ES, Alexander BM, Vergilio JA, Ross JS, Pavlick DC, Chebib I, Williams EA.
    Mod Pathol; 2020 Nov 21; 33(11):2307-2317. PubMed ID: 32461620
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  • 18. Molecular detection of the ETV6-NTRK3 gene fusion differentiates congenital fibrosarcoma from other childhood spindle cell tumors.
    Bourgeois JM, Knezevich SR, Mathers JA, Sorensen PH.
    Am J Surg Pathol; 2000 Jul 21; 24(7):937-46. PubMed ID: 10895816
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  • 19. Neurofibrosarcoma Revisited: An Institutional Case Series of Uterine Sarcomas Harboring Kinase-related Fusions With Report of a Novel FGFR1-TACC1 Fusion.
    Devereaux KA, Weiel JJ, Mills AM, Kunder CA, Longacre TA.
    Am J Surg Pathol; 2021 May 01; 45(5):638-652. PubMed ID: 33481389
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