Survivin Polyclonal Antibody, 20ul[BT-AP14595] Serum & Sample Tubes Defects in MEF2A could be

Defects in MEF2A could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

Ephrin receptors and their ligands| the ephrins| mediate numerous developmental processes| particularly in the nervous system

OAS2 encodes a member of the 2-5A synthetase family

resulting in the creation of an N-terminal chain and the corresponding C-terminal chain

SIAH2 encodes E3 ubiquitin-protein ligase SIAH2 that is a member of the seven in absentia homolog (SIAH) family

Survivin Polyclonal Antibody, 20ul[BT-AP14595] Serum & Sample Tubes Defects in MEF2A could beThis gene is a member of the inhibitor of apoptosis (IAP) gene family, which encode negative regulatory proteins that prevent apoptotic cell death. IAP family members usually contain multiple baculovirus IAP repeat (BIR) domains, but this gene encodes proteins with only a single BIR domain. The encoded proteins also lack a C terminus RING finger domain. Gene expression is high during fetal development and in most tumors, yet low in adult tissues.