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Showing 1–18 of 18 results
Advanced filters: Author: Sebastian M B Nijman Clear advanced filters
  • Lysosomal phospholipase PLA2G15 was identified as a physiological BMP hydrolase whose activity depends on unique esterification and stereochemistry of BMP and offers a potential therapeutic target for Niemann–Pick disease type C1 and other neurodegenerative conditions.

    • Kwamina Nyame
    • Jian Xiong
    • Monther Abu-Remaileh
    ResearchOpen Access
    Nature
    Volume: 642, P: 474-483
  • ATM is a tumor suppressor often mutated in lung adenocarcinoma. In this study, the authors starting from a synthetic lethal screen, demonstrate that tumor cells with mutations in ATM exhibit increased sensitivity to MEK1/2 inhibition through the modulation of the AKT/mTOR pathway.

    • Michal Smida
    • Ferran Fece de la Cruz
    • Sebastian M. B. Nijman
    ResearchOpen Access
    Nature Communications
    Volume: 7, P: 1-13
  • The combination of a light-activated receptor tyrosine kinase and a fluorescent MAPK/ERK reporter results in the development of an optogenetics-based cell screening method to identify small-molecule inhibitors of RTK signaling.

    • Álvaro Inglés-Prieto
    • Eva Reichhart
    • Harald Janovjak
    Research
    Nature Chemical Biology
    Volume: 11, P: 952-954
    • Tony T. Huang
    • Sebastian M.B. Nijman
    • Alan D. D'Andrea
    Amendments and Corrections
    Nature Cell Biology
    Volume: 8, P: 424
  • A case–control study investigating the causes of recent cases of acute hepatitis of unknown aetiology in 32 children identifies an association between adeno-associated virus infection and host genetics in disease susceptibility.

    • Antonia Ho
    • Richard Orton
    • Emma C. Thomson
    Research
    Nature
    Volume: 617, P: 555-563
  • CRISPR-Cas9 has greatly enhanced genome engineering however gene tagging can still be cumbersome due to a requirement for homology donors. Here the authors introduce a generic system for gene tagging that does not require homology between the donor and the genomic target site.

    • Daniel H. Lackner
    • Alexia Carré
    • Tilmann Bürckstümmer
    ResearchOpen Access
    Nature Communications
    Volume: 6, P: 1-7
  • Drugs identified in high-content screens are often difficult to link to the cellular target, especially when multiple signaling pathways impinge on the phenotypic endpoint. A chemical-genetic approach in fruit fly cells now greatly improves the prioritization of drug hits by directing the screen toward a single pathway.

    • Markus K Muellner
    • Sebastian M B Nijman
    News & Views
    Nature Chemical Biology
    Volume: 6, P: 397-398
  • A chemical-genetic study predicts mechanisms of resistance to PI3K inhibitors. Activation of NOTCH signaling, which leads to c-MYC expression, can overcome cancer cell dependency on PI3K signaling for growth. NOTCH and PI3K have not previously been linked in breast cancer.

    • Markus K Muellner
    • Iris Z Uras
    • Sebastian M B Nijman
    Research
    Nature Chemical Biology
    Volume: 7, P: 787-793
  • A collection of single-gene-mutant human cells is described. This growing resource is based on gene-trap mutagenesis of a near-haploid human cell line and covers almost 3,500 human genes.

    • Tilmann Bürckstümmer
    • Carina Banning
    • Sebastian M B Nijman
    Research
    Nature Methods
    Volume: 10, P: 965-971
  • Carette et al. use a retroviral gene-trap vector to disrupt and tag >98% of all genes in a haploid human cancer cell line. Cells selected for a phenotype of interest are pooled and characterized by parallel DNA sequencing to circumvent time- and labor-intensive screening of individual clones.

    • Jan E Carette
    • Carla P Guimaraes
    • Thijn R Brummelkamp
    Research
    Nature Biotechnology
    Volume: 29, P: 542-546