9 Matching Annotations
  1. Last 7 days
  2. rupress.org rupress.org
    A heterozygous USB1 variant linked to immunodeficiency
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    rupress.org/jhi/article/1/4/e20250110/278387/A-heterozygous-USB1-variant-linked-to
  3. Mar 2023
  4. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Tumor-independent Detection of Inherited Mismatch Repair Deficiency for the Diagnosis of Lynch Syndrome with High Specificity and Sensitivity
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    ncbi.nlm.nih.gov/pmc/articles/PMC9979712/
  5. Jan 2022
  6. bpspubs.onlinelibrary.wiley.com bpspubs.onlinelibrary.wiley.com
    BPS Publications
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    bpspubs.onlinelibrary.wiley.com/doi/10.1111/bph.15722
  7. Jul 2021
  8. www.pnas.org www.pnas.org
    Identifying roles for peptidergic signaling in mice
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    pnas.org/content/early/2019/08/26/1910495116
  9. Nov 2017
  10. elifesciences.org elifesciences.org
    Lineage commitment of embryonic cells involves MEK1-dependent clearance of pluripotency regulator Ventx2
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    elifesciences.org/articles/21526
  11. elifesciences.org elifesciences.org
    MPI depletion enhances O-GlcNAcylation of p53 and suppresses the Warburg effect
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    elifesciences.org/articles/22477
  12. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Prostaglandin E2 promotes neural proliferation and differentiation and regulates Wnt target gene expression
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    onlinelibrary.wiley.com/doi/10.1002/jnr.23759/full
  13. link.springer.com link.springer.com
    The Ubiquitin Receptor ADRM1 Modulates HAP40-Induced Proteasome Activity
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    link.springer.com/article/10.1007/s12035-016-0247-y
  14. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia
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    ncbi.nlm.nih.gov/pmc/articles/PMC5005467/