Search Results - "Vereecke, Stijn"

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    Hallmarks of ribosomopathies by Kampen, Kim R, Sulima, Sergey O, Vereecke, Stijn, De Keersmaecker, Kim

    Published in Nucleic acids research (20-02-2020)
    “…Abstract Ribosomopathies are diseases caused by defects in ribosomal constituents or in factors with a role in ribosome assembly. Intriguingly, congenital…”
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    Journal Article
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    Ribosomal Lesions Promote Oncogenic Mutagenesis by Sulima, Sergey O, Kampen, Kim R, Vereecke, Stijn, Pepe, Daniele, Fancello, Laura, Verbeeck, Jelle, Dinman, Jonathan D, De Keersmaecker, Kim

    Published in Cancer research (Chicago, Ill.) (15-01-2019)
    “…Ribosomopathies are congenital disorders caused by mutations in ribosomal proteins (RP) or assembly factors and are characterized by cellular hypoproliferation…”
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    The T-cell leukemia-associated ribosomal RPL10 R98S mutation enhances JAK-STAT signaling by Girardi, T, Vereecke, S, Sulima, S O, Khan, Y, Fancello, L, Briggs, J W, Schwab, C, de Beeck, J Op, Verbeeck, J, Royaert, J, Geerdens, E, Vicente, C, Bornschein, S, Harrison, C J, Meijerink, J P, Cools, J, Dinman, J D, Kampen, K R, De Keersmaecker, K

    Published in Leukemia (01-03-2018)
    “…Several somatic ribosome defects have recently been discovered in cancer, yet their oncogenic mechanisms remain poorly understood. Here we investigated the…”
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    Journal Article
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