Browsing BioMed Central høstingsarkiv by Author "Panagopoulos, Ioannis"

Now showing items 1-5 of 5

  • Fusion of the HMGA2 and C9orf92 genes in myolipoma with t(9;12)(p22;q14) 
    Panagopoulos, Ioannis; Gorunova, Ludmila; Agostini, Antonio; Lobmaier, Ingvild; Bjerkehagen, Bodil; Heim, Sverre (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2016)
    Background Myolipoma of soft tissue is an extremely rare benign tumor composed of mature adipose tissue and smooth muscle cells. It is found predominantly in women. The cytogenetic and molecular genetic ...
  • Loss of chromosome 13 material in cellular angiofibromas indicates pathogenetic similarity with spindle cell lipomas 
    Panagopoulos, Ioannis; Gorunova, Ludmila; Bjerkehagen, Bodil; Andersen, Kristin; Lund-Iversen, Marius; Heim, Sverre (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2017)
    Background Cellular angiofibroma is a rare benign mesenchymal neoplasm with morphological and immunohistochemical similarities to spindle cell lipoma. Karyotypic information on cellular angiofibroma is ...
  • Novel GTF2I–PDGFRB and IKZF1–TYW1 fusions in pediatric leukemia with normal karyotype 
    Panagopoulos, Ioannis; Brunetti, Marta; Stoltenberg, Margrethe; Strandabø, Rønnaug A U; Staurseth, Julie; Andersen, Kristin; Kostolomov, Ilyá; Hveem, Tarjei S; Lorenz, Susanne; Nystad, Tove A; Flægstad, Trond; Micci, Francesca; Heim, Sverre (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2019)
    Background Many cases of acute lymphoblastic leukemia (ALL) carry visible acquired chromosomal changes of pathogenetic, diagnostic, and prognostic importance. Nevertheless, from one-fourth to half of newly ...
  • PAN3–PSMA2 fusion resulting from a novel t(7;13)(p14;q12) chromosome translocation in a myelodysplastic syndrome that evolved into acute myeloid leukemia 
    Panagopoulos, Ioannis; Gorunova, Ludmila; Andersen, Hege K; Bergrem, Astrid; Dahm, Anders; Andersen, Kristin; Micci, Francesca; Heim, Sverre (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2018)
    Background Acquired primary chromosomal changes in cancer are sometimes found as sole karyotypic abnormalities. They are specifically associated with particular types of neoplasia, essential in establishing ...
  • Rare MLL-ELL fusion transcripts in childhood acute myeloid leukemia—association with young age and myeloid sarcomas? 
    Panagopoulos, Ioannis; Gorunova, Ludmila; Kerndrup, Gitte; Spetalen, Signe; Tierens, Anne; Osnes, Liv T N; Andersen, Kristin; Müller, Lil-Sofie O; Hellebostad, Marit; Zeller, Bernward; Heim, Sverre (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2016)
    Background The chromosomal translocation t(11;19)(q23;p13) with a breakpoint within subband 19p13.1 is found mainly in acute myeloid leukemia (AML) and results in the MLL-ELL fusion gene. Variations in the ...