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anti-miR-199b is an experimental antisense oligonucleotide (antimiR) designed to selectively inhibit microRNA-199b (miR-199b). miR-199b is a microRNA that has been implicated in various pathological processes, including pressure overload-induced cardiac hypertrophy and heart failure, as well as the progression of several malignancies such as acute myeloid leukemia (AML), colorectal cancer, and ovarian cancer. In the heart, miR-199b targets the dual-specificity tyrosine-phosphorylation-regulated kinase 1A (DYRK1A), which normally acts as a negative regulator of the calcineurin/NFAT signaling pathway; thus, inhibiting miR-199b can restore DYRK1A levels and mitigate cardiac remodeling. Additionally, research has explored its role in modulating CD44 expression in lymphocytes to treat experimental autoimmune encephalomyelitis (EAE), a model for multiple sclerosis. Development has been associated with Mirabilis Therapeutics and academic institutions.
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