檢索結果 - Roel Janssen

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  1. 1
    MutationalPatterns: comprehensive genome-wide analysis of mutational processes

    MutationalPatterns: comprehensive genome-wide analysis of mutational processes 由 Francis Blokzijl, Roel Janssen, Ruben van Boxtel, Edwin Cuppen

    出版 2018
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    Artigo
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  2. 2
    Twenty Years of Ferroportin Disease: A Review or An Update of Published Clinical, Biochemical, Molecular, and Functional Features

    Twenty Years of Ferroportin Disease: A Review or An Update of Published Clinical, Biochemical, Molecular, and Functional Features 由 L. Tom Vlasveld, Roel Janssen, Edouard Bardou‐Jacquet, Hanka Venselaar, Houda Hamdi‐Rozé, Hal Drakesmith, Dorine W. Swinkels

    出版 2019
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    Revisão
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  3. 3
    GRIDSS2: comprehensive characterisation of somatic structural variation using single breakend variants and structural variant phasing

    GRIDSS2: comprehensive characterisation of somatic structural variation using single breakend variants and structural variant phasing 由 Daniel Cameron, Jonathan Baber, Charles Shale, Jose Espejo Valle-Inclán, Nicolle Besselink, Arne van Hoeck, Roel Janssen, Edwin Cuppen, Peter Priestley, Anthony T. Papenfuss

    出版 2021
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    Artigo
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  4. 4
    The mutational impact of culturing human pluripotent and adult stem cells

    The mutational impact of culturing human pluripotent and adult stem cells 由 Ewart Kuijk, Myrthe Jager, Bastiaan van der Roest, Mauro D. Locati, Arne van Hoeck, Jerome Korzelius, Roel Janssen, Nicolle Besselink, Sander Boymans, Ruben van Boxtel, Edwin Cuppen

    出版 2020
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    Artigo
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    5-Fluorouracil treatment induces characteristic T>G mutations in human cancer

    5-Fluorouracil treatment induces characteristic T>G mutations in human cancer 由 Sharon Christensen, Bastiaan van der Roest, Nicolle Besselink, Roel Janssen, Sander Boymans, John W.M. Martens, Marie‐Laure Yaspo, Peter Priestley, Ewart Kuijk, Edwin Cuppen, Arne van Hoeck

    出版 2019
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    Artigo
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  6. 6
    Deficiency of nucleotide excision repair is associated with mutational signature observed in cancer

    Deficiency of nucleotide excision repair is associated with mutational signature observed in cancer 由 Myrthe Jager, Francis Blokzijl, Ewart Kuijk, Johanna Bertl, Maria Vougioukalaki, Roel Janssen, Nicolle Besselink, Sander Boymans, Joep de Ligt, Jakob Skou Pedersen, Jan H.J. Hoeijmakers, Joris Pothof, Ruben van Boxtel, Edwin Cuppen

    出版 2019
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    Artigo
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