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Genes, Chromosomes & Cancer|October 18, 2016
Genomic landscape of retinoblastoma in Rb-/- p130-/- mice resembles human retinoblastomaIrsan E Kooi, Saskia E van Mil, David MacPherson, et al.Plos Genetics|May 23, 2017
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicityHellen Houlleberghs, Anne Goverde, Jarnick Lusseveld, et al.Nucleic Acids Research|August 27, 2024
ADARp150 counteracts whole genome duplicationFrank van Gemert, Alexandra Drakaki, Isabel Morales Lozano, et al.Journal of the National Cancer Institute|October 7, 2010
Azathioprine-induced carcinogenesis in mice according to Msh2 genotypeAlexandra Chalastanis, Virginie Penard-Lacronique, Magali Svrcek, et al.Gut Microbes|February 21, 2022
Pro-mutagenic effects of the gut microbiota in a Lynch syndrome mouse modelWietske Pieters, Floor Hugenholtz, Kevin Kos, et al.Cancer Research|July 25, 2014
RB family tumor suppressor activity may not relate to active silencing of E2F target genesTinke L Vormer, Kamila Wojciechowicz, Marleen Dekker, et al.Scientific Reports|January 27, 2019
Effective CRISPR/Cas9-mediated correction of a Fanconi anemia defect by error-prone end joining or templated repairHenri J van de Vrugt, Tim Harmsen, Joey Riepsaame, et al.Human Molecular Genetics|June 30, 2009
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group MSietske T Bakker, Henri J van de Vrugt, Martin A Rooimans, et al.The Journal of Biological Chemistry|September 8, 2005
Characterization of the condensin component Cnap1 and protein kinase Melk as novel E2F target genes down-regulated by 1,25-dihydroxyvitamin D3Lieve Verlinden, Guy Eelen, Ine Beullens, et al.Proceedings of the National Academy of Sciences of the United States of America|January 16, 2026
An accurate cellular assay to determine pathogenicity of coding and noncoding variants in Lynch syndrome genesIris E Glykofridis, Marleen Dekker, Chantal Stoepker, et al.Pageof 9