{
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  "affiliations": [
    "Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095, USA.",
    "Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511, USA.",
    "Department of Biological Chemistry and Institute of Genomics and Proteomics, University of California, Los Angeles, CA 90095, USA.",
    "Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06511, USA.",
    "Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.",
    "Department of Chemistry, Yale University, New Haven, CT 06511, USA.",
    "Molecular Biology Institute, University of California, Los Angeles, CA 90095, USA.",
    "Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, University of California, Los Angeles, CA 90095, USA.",
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  "pmcid": "PMC13666002",
  "pmid": "42873854",
  "published": "2026-10-14",
  "publisher": "American Association for the Advancement of Science (AAAS)",
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  "title": "A B1 SINE element within the mouse Malat1 long noncoding RNA acts as an internal ribosome entry site mediating micropeptide translation",
  "title_text": "A B1 SINE element within the mouse Malat1 long noncoding RNA acts as an internal ribosome entry site mediating micropeptide translation",
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  "venue": "Science Advances",
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