9 Matching Annotations
  1. Mar 2024
  2. www.biorxiv.org www.biorxiv.org
    The GC-content at the 5’ends of human protein-coding genes is undergoing mutational decay
    1
    1. scibot 19 Mar 2024
      RRID:SCR_002846

      DOI: 10.1101/2024.03.12.584636

      Resource: International HapMap Project (RRID:SCR_002846)

      Curator: @scibot

      SciCrunch record: RRID:SCR_002846

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      RRID:SCR_002846
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    biorxiv.org/content/10.1101/2024.03.12.584636v1
  3. Nov 2021
  4. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Pharmacogenomics characterization of the MDM2 inhibitor MI-773 reveals candidate tumours and predictive biomarkers
    1
    1. scibot 05 Nov 2021
      RRID:SCR_002846

      DOI: 10.1038/s41698-021-00235-7

      Resource: International HapMap Project (RRID:SCR_002846)

      Curator: @scibot

      SciCrunch record: RRID:SCR_002846

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      RRID:SCR_002846
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    ncbi.nlm.nih.gov/pmc/articles/PMC8553758/
  5. Aug 2021
  6. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Untitled document
    1
    1. scibot 11 Aug 2021
      RRID:SCR_002846

      DOI: 10.1002/brb3.1144

      Resource: International HapMap Project (RRID:SCR_002846)

      Curator: @scibot

      SciCrunch record: RRID:SCR_002846

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      RRID:SCR_002846
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    ncbi.nlm.nih.gov/pmc/articles/PMC6305932/
  7. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Gene mutations in a Han Chinese Alzheimer's disease cohort
    1
    1. scibot 11 Aug 2021
      RRID:SCR_002846

      DOI: 10.1002/brb3.1180

      Resource: International HapMap Project (RRID:SCR_002846)

      Curator: @scibot

      SciCrunch record: RRID:SCR_002846

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      RRID:SCR_002846
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    ncbi.nlm.nih.gov/pmc/articles/PMC6346667/
  8. Jul 2021
  9. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Untitled document
    1
    1. scibot 30 Jul 2021
      RRID:SCR_002846

      DOI: 10.1002/brb3.1144

      Resource: International HapMap Project (RRID:SCR_002846)

      Curator: @scibot

      SciCrunch record: RRID:SCR_002846

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      RRID:SCR_002846
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    onlinelibrary.wiley.com/doi/full/10.1002/brb3.1144
  10. europepmc.org europepmc.org
    A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.
    2
    1. scibot 29 Jul 2021
      RRID:SCR_002846

      DOI: 10.7554/eLife.30490

      Resource: International HapMap Project (RRID:SCR_002846)

      Curator: @evieth

      SciCrunch record: RRID:SCR_002846

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      RRIDCUR:Validated RRID:SCR_002846
    2. scibot 27 Jul 2021
      RRID:SCR_002846

      DOI: 10.7554/eLife.30490

      Resource: International HapMap Project (RRID:SCR_002846)

      Curator: @evieth

      SciCrunch record: RRID:SCR_002846

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      RRID:SCR_002846 RRIDCUR:Unrecognized
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    europepmc.org/articles/PMC5764568/
  11. Jan 2020
  12. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Gene mutations in a Han Chinese Alzheimer's disease cohort
    1
    1. scibot 13 Jan 2020
      RRID:SCR_002846

      DOI: 10.1002/brb3.1180

      Resource: International HapMap Project (RRID:SCR_002846)

      Curator: @evieth

      SciCrunch record: RRID:SCR_002846

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      RRID:SCR_002846 RRIDCUR:Validated
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    onlinelibrary.wiley.com/doi/full/10.1002/brb3.1180
  13. Nov 2017
  14. elifesciences.org elifesciences.org
    Recombination, meiotic expression and human codon usage
    1
    1. scibot 08 Nov 2017
      RRID:SCR_002846

      Curator: @kaitlinsung

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      (International HapMap Project, RRID:SCR_002846)

      SciCrunch record: RRID:SCR_002846

      Alternate resolvers: SciCrunch xml N2T identifiers.org

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      RRID:SCR_002846 RRIDCUR:Validated
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    elifesciences.org/articles/27344