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ACVR2BActivin A Receptor, Type IIB
References in periodicals archive ?
Some studies have demonstrated that human orthologue of the Nodal signaling genes, ACVR2B (12), LEFTYA (13) and CFC1 (14), were mutated in patients with heterotaxia.
Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB.
ACVR2B inhibitor (Muscle Activation) - Patients with many serious diseases including diabetes, HIV, cancer and chronic heart failure are prone to develop cachexia, a disorder characterized by muscle atrophy.