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The FDA approved Casgevy and Lyfgenia in December 2023, including the first FDA-approved CRISPR/Cas9 therapy for sickle cell disease in patients 12 and older.
New findings suggest environmental toxic exposures can shift epigenetic aging markers.
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Researchers report secondary social and health harms from drug deaths extending beyond mortality counts.
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An antibody candidate was reported against two EBV entry antigens.
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Antibody repertoires varied by age, sex, and genetics in a February 2026 release.
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Neuroimaging data indicated additional structural adaptation in second pregnancy.
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