Search Results - "Mrsic, Alan"

Integrated genomics identifies five medulloblastoma subtypes with distinct genetic profiles, pathway signatures and clinicopathological features by Kool, Marcel, Koster, Jan, Bunt, Jens, Hasselt, Nancy E, Lakeman, Arjan, van Sluis, Peter, Troost, Dirk, Meeteren, Netteke Schouten-van, Caron, Huib N, Cloos, Jacqueline, Mrsić, Alan, Ylstra, Bauke, Grajkowska, Wieslawa, Hartmann, Wolfgang, Pietsch, Torsten, Ellison, David, Clifford, Steven C, Versteeg, Rogier

“…Medulloblastoma is the most common malignant brain tumor in children. Despite recent improvements in cure rates, prediction of disease outcome remains a major…”
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Across array comparative genomic hybridization: A strategy to reduce reference channel hybridizations by Buffart, Tineke E., Israeli, Daniëlle, Tijssen, Marianne, Vosse, Sjoerd J., Mršić, Alan, Meijer, Gerrit A., Ylstra, Bauke

“…Array comparative genomic hybridization (array CGH) is widely used for studying chromosomal copy number aberrations (CNAs) on a genome‐wide and high‐resolution…”
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Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations by Nellist, Mark, Brouwer, Rutger W W, Kockx, Christel E M, van Veghel-Plandsoen, Monique, Withagen-Hermans, Caroline, Prins-Bakker, Lida, Hoogeveen-Westerveld, Marianne, Mrsic, Alan, van den Berg, Mike M P, Koopmans, Anna E, de Wit, Marie-Claire, Jansen, Floor E, Maat-Kievit, Anneke J A, van den Ouweland, Ans, Halley, Dicky, de Klein, Annelies, van IJcken, Wilfred F J

“…Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutations in TSC1 and TSC2. Conventional DNA diagnostic screens identify a TSC1 or…”
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Mutation of C/EBPα predisposes to the development of myeloid leukemia in a retroviral insertional mutagenesis screen by Hasemann, Marie S., Damgaard, Inge, Schuster, Mikkel B., Theilgaard-Mönch, Kim, Sørensen, Annette B., Mršić, Alan, Krugers, Thijs, Ylstra, Bauke, Pedersen, Finn S., Nerlov, Claus, Porse, Bo T.

“…The CCAAT enhancer binding protein α (C/EBPα) is an important myeloid tumor suppressor that is frequently mutated in human acute myeloid leukemia (AML). We…”
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Mutation of C/EBPalpha predisposes to the development of myeloid leukemia in a retroviral insertional mutagenesis screen by Hasemann, Marie S, Damgaard, Inge, Schuster, Mikkel B, Theilgaard-Mönch, Kim, Sørensen, Annette B, Mrsic, Alan, Krugers, Thijs, Ylstra, Bauke, Pedersen, Finn S, Nerlov, Claus, Porse, Bo T

“…The CCAAT enhancer binding protein alpha (C/EBPalpha) is an important myeloid tumor suppressor that is frequently mutated in human acute myeloid leukemia…”
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