11 Matching Annotations
  1. Oct 2025
  2. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    RAS pathway inhibitors combined with targeted agents are active in patient-derived spheroids with oncogenic KRAS variants from multiple cancer types
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    pmc.ncbi.nlm.nih.gov/articles/PMC12505081/
  3. Sep 2025
  4. www.sciencedirect.com www.sciencedirect.com
    HT SpaceM: A high-throughput and reproducible method for small-molecule single-cell metabolomics
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    sciencedirect.com/science/article/pii/S0092867425009298
  5. Aug 2024
  6. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    HTS384 NCI60: The Next Phase of the NCI60 Screen
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    ncbi.nlm.nih.gov/pmc/articles/PMC11292194/
  7. May 2024
  8. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Synergy of EGFR and AURKA Inhibitors in KRAS-mutated Non–small Cell Lung Cancers
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    ncbi.nlm.nih.gov/pmc/articles/PMC11078142/
  9. Sep 2023
  10. 52.53.155.43 52.53.155.43
    British J Pharmacology - 2023 - Kleszcz-html.html
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    52.53.155.43/bda5ca2ff5fc6352261b5aa6b5327e2f6367b095/British J Pharmacology - 2023 - Kleszcz-html.html
  11. Apr 2023
  12. www.mdpi.com www.mdpi.com
    TEAD Inhibitors Sensitize KRASG12C Inhibitors via Dual Cell Cycle Arrest in KRASG12C-Mutant NSCLC
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    mdpi.com/1424-8247/16/4/553
  13. Aug 2022
  14. www.sciencedirect.com www.sciencedirect.com
    Chromatin-bound RB targets promoters, enhancers, and CTCF-bound loci and is redistributed by cell-cycle progression
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    sciencedirect.com/science/article/pii/S1097276522007109
  15. May 2021
  16. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Urinary malate dehydrogenase 2 is a new biomarker for early detection of non-small-cell lung cancer
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    onlinelibrary.wiley.com/doi/10.1111/cas.14845
  17. Jan 2020
  18. www.sciencedirect.com www.sciencedirect.com
    RUVBL1/RUVBL2 ATPase Activity Drives PAQosome Maturation, DNA Replication and Radioresistance in Lung Cancer
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    sciencedirect.com/science/article/pii/S2451945619304015
  19. Nov 2017
  20. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    TP53 exon-6 truncating mutations produce separation of function isoforms with pro-tumorigenic functions
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    pmc.ncbi.nlm.nih.gov/articles/PMC5092050/