12 Matching Annotations
  1. Oct 2024
  2. aacrjournals.org aacrjournals.org
    Clinical Outcome–Related Mutational Signatures Identified by Integrative Genomic Analysis in Nasopharyngeal Carcinoma
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    aacrjournals.org/clincancerres/article/26/24/6494/82920/Clinical-Outcome-Related-Mutational-Signatures
  3. Aug 2024
  4. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    The GC-content at the 5′ ends of human protein-coding genes is undergoing mutational decay
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    ncbi.nlm.nih.gov/pmc/articles/PMC11323403/
  5. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    St. Jude Survivorship Portal: Sharing and Analyzing Large Clinical and Genomic Datasets from Pediatric Cancer Survivors
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    ncbi.nlm.nih.gov/pmc/articles/PMC11294819/
  6. Mar 2024
  7. www.biorxiv.org www.biorxiv.org
    The GC-content at the 5’ends of human protein-coding genes is undergoing mutational decay
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    biorxiv.org/content/10.1101/2024.03.12.584636v1
  8. Nov 2021
  9. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Pharmacogenomics characterization of the MDM2 inhibitor MI-773 reveals candidate tumours and predictive biomarkers
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    ncbi.nlm.nih.gov/pmc/articles/PMC8553758/
  10. Aug 2021
  11. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Untitled document
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    ncbi.nlm.nih.gov/pmc/articles/PMC6305932/
  12. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Gene mutations in a Han Chinese Alzheimer's disease cohort
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    ncbi.nlm.nih.gov/pmc/articles/PMC6346667/
  13. Jul 2021
  14. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Untitled document
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    onlinelibrary.wiley.com/doi/full/10.1002/brb3.1144
  15. europepmc.org europepmc.org
    A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.
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    europepmc.org/articles/PMC5764568/
  16. Jan 2020
  17. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Gene mutations in a Han Chinese Alzheimer's disease cohort
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    onlinelibrary.wiley.com/doi/full/10.1002/brb3.1180
  18. Nov 2017
  19. elifesciences.org elifesciences.org
    Recombination, meiotic expression and human codon usage
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    elifesciences.org/articles/27344