BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 31999033)

  • 1. A rare case of congenital spindle cell rhabdomyosarcoma with TEAD1-NCOA2 fusion: A subset of spindle cell rhabdomyosarcoma with indolent behavior.
    Tan GZL; Saminathan SN; Chang KTE; Odoño EG; Kuick CH; Chen H; Lee VKM
    Pathol Int; 2020 Apr; 70(4):234-236. PubMed ID: 31999033
    [No Abstract]   [Full Text] [Related]  

  • 2. Recurrent NCOA2 gene rearrangements in congenital/infantile spindle cell rhabdomyosarcoma.
    Mosquera JM; Sboner A; Zhang L; Kitabayashi N; Chen CL; Sung YS; Wexler LH; LaQuaglia MP; Edelman M; Sreekantaiah C; Rubin MA; Antonescu CR
    Genes Chromosomes Cancer; 2013 Jun; 52(6):538-50. PubMed ID: 23463663
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Intraosseous Spindle Cell Rhabdomyosarcoma with
    Smith BF; Doung YC; Beckett B; Corless CL; Davis LE; Davis JL
    Cancer Invest; 2023 Sep; 41(8):704-712. PubMed ID: 37668330
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Soft tissue angiofibroma: Clinicopathologic, immunohistochemical and molecular analysis of 14 cases.
    Bekers EM; Groenen PJTA; Verdijk MAJ; Raaijmakers-van Geloof WL; Roepman P; Vink R; Gilhuijs NDB; van Gorp JM; Bovée JVMG; Creytens DH; Flanagan AM; Suurmeijer AJH; Mentzel T; Arbajian E; Flucke U
    Genes Chromosomes Cancer; 2017 Oct; 56(10):750-757. PubMed ID: 28639284
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital spindle cell rhabdomyosarcoma.
    Whittle SB; Hicks MJ; Roy A; Vasudevan SA; Reddy K; Venkatramani R
    Pediatr Blood Cancer; 2019 Nov; 66(11):e27935. PubMed ID: 31339226
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel fusion genes in spindle cell rhabdomyosarcoma: The spectrum broadens.
    Montoya-Cerrillo DM; Diaz-Perez JA; Velez-Torres JM; Montgomery EA; Rosenberg AE
    Genes Chromosomes Cancer; 2021 Oct; 60(10):687-694. PubMed ID: 34184341
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spindle cell rhabdomyosarcoma of bone with FUS-TFCP2 fusion: confirmation of a very recently described rhabdomyosarcoma subtype.
    Dashti NK; Wehrs RN; Thomas BC; Nair A; Davila J; Buckner JC; Martinez AP; Sukov WR; Halling KC; Howe BM; Folpe AL
    Histopathology; 2018 Sep; 73(3):514-520. PubMed ID: 29758589
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Head and neck rhabdomyosarcoma with TFCP2 fusions and ALK overexpression: a clinicopathological and molecular analysis of 11 cases.
    Xu B; Suurmeijer AJH; Agaram NP; Zhang L; Antonescu CR
    Histopathology; 2021 Sep; 79(3):347-357. PubMed ID: 33382123
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Establishment and Characterization of a Cell Line (S-RMS1) Derived from an Infantile Spindle Cell Rhabdomyosarcoma with
    Colletti M; Galardi A; Miele E; Di Paolo V; Russo I; De Stefanis C; De Vito R; Rinelli M; Ciolfi A; De Angelis B; Zin A; Guffanti A; Digilio MC; Novelli A; Alaggio R; Milano GM; Di Giannatale A
    Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34067464
    [No Abstract]   [Full Text] [Related]  

  • 10. ZFP64::NCOA3 gene fusion defines a novel subset of spindle cell rhabdomyosarcoma.
    Han R; Dermawan JK; Demicco EG; Ferguson PC; Griffin AM; Swanson D; Antonescu CR; Dickson BC
    Genes Chromosomes Cancer; 2022 Nov; 61(11):645-652. PubMed ID: 35521817
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expanding the Spectrum of Intraosseous Rhabdomyosarcoma: Correlation Between 2 Distinct Gene Fusions and Phenotype.
    Agaram NP; Zhang L; Sung YS; Cavalcanti MS; Torrence D; Wexler L; Francis G; Sommerville S; Swanson D; Dickson BC; Suurmeijer AJH; Williamson R; Antonescu CR
    Am J Surg Pathol; 2019 May; 43(5):695-702. PubMed ID: 30720533
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosomal imbalances in pleomorphic rhabdomyosarcomas and identification of the alveolar rhabdomyosarcoma-associated PAX3-FOXO1A fusion gene in one case.
    Gordon A; McManus A; Anderson J; Fisher C; Abe S; Nojima T; Pritchard-Jones K; Shipley J
    Cancer Genet Cytogenet; 2003 Jan; 140(1):73-7. PubMed ID: 12550764
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Molecular Study of Pediatric Spindle and Sclerosing Rhabdomyosarcoma: Identification of Novel and Recurrent VGLL2-related Fusions in Infantile Cases.
    Alaggio R; Zhang L; Sung YS; Huang SC; Chen CL; Bisogno G; Zin A; Agaram NP; LaQuaglia MP; Wexler LH; Antonescu CR
    Am J Surg Pathol; 2016 Feb; 40(2):224-35. PubMed ID: 26501226
    [TBL] [Abstract][Full Text] [Related]  

  • 14. PAX3-NCOA2 fusion gene has a dual role in promoting the proliferation and inhibiting the myogenic differentiation of rhabdomyosarcoma cells.
    Yoshida H; Miyachi M; Sakamoto K; Ouchi K; Yagyu S; Kikuchi K; Kuwahara Y; Tsuchiya K; Imamura T; Iehara T; Kakazu N; Hojo H; Hosoi H
    Oncogene; 2014 Dec; 33(49):5601-8. PubMed ID: 24213582
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genes.
    Jin Y; Möller E; Nord KH; Mandahl N; Von Steyern FV; Domanski HA; Mariño-Enríquez A; Magnusson L; Nilsson J; Sciot R; Fletcher CD; Debiec-Rychter M; Mertens F
    Genes Chromosomes Cancer; 2012 May; 51(5):510-20. PubMed ID: 22337624
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Histological spectrum of angiofibroma of soft tissue: histological and genetic analysis of 13 cases.
    Yamada Y; Yamamoto H; Kohashi K; Ishii T; Iura K; Maekawa A; Bekki H; Otsuka H; Yamashita K; Tanaka H; Hiraki T; Mukai M; Shirakawa A; Shinnou Y; Jinno M; Yanai H; Taguchi K; Maehara Y; Iwamoto Y; Oda Y
    Histopathology; 2016 Sep; 69(3):459-69. PubMed ID: 26845637
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Congenital spindle cell/sclerosing rhabdomyosarcoma: a clinicopathological analysis].
    Xu JT; Fu LB; Yao XF; Jia C; Guan XX; Zhang M; He LJ
    Zhonghua Bing Li Xue Za Zhi; 2024 Apr; 53(4):344-350. PubMed ID: 38556817
    [No Abstract]   [Full Text] [Related]  

  • 18. ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations.
    Strehl S; Nebral K; König M; Harbott J; Strobl H; Ratei R; Struski S; Bielorai B; Lessard M; Zimmermann M; Haas OA; Izraeli S
    Clin Cancer Res; 2008 Feb; 14(4):977-83. PubMed ID: 18281529
    [TBL] [Abstract][Full Text] [Related]  

  • 19. VGLL2-NCOA2 leverages developmental programs for pediatric sarcomagenesis.
    Watson S; LaVigne CA; Xu L; Surdez D; Cyrta J; Calderon D; Cannon MV; Kent MR; Silvius KM; Kucinski JP; Harrison EN; Murchison W; Rakheja D; Tirode F; Delattre O; Amatruda JF; Kendall GC
    Cell Rep; 2023 Jan; 42(1):112013. PubMed ID: 36656711
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rhabdomyosarcoma and other soft tissue sarcomas of childhood.
    Pappo AS
    Curr Opin Oncol; 1994 Jul; 6(4):397-402. PubMed ID: 7803541
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.