Neu Monoclonal Antibody, 50ul[BT-MCA0942] RNA Tools Defects in TRPS1 are a

Defects in TRPS1 are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III

and other cellular activities

Regulation of aurora B kinase is key in the regulation of the CPC

Among its related pathways are Cell cycle

The encoded secretory protein also shares similarities with the secretogranin/chromogranin family

Neu Monoclonal Antibody, 50ul[BT-MCA0942] RNA Tools Defects in TRPS1 are aThis gene encodes a member of the epidermal growth factor (EGF) receptor family of receptor tyrosine kinases. This protein has no ligand binding domain of its own and therefore cannot bind growth factors. However, it does bind tightly to other ligand bound EGF receptor family members to form a heterodimer, stabilizing ligand binding and enhancing kinase mediated activation of downstream signalling pathways, such as those involving mitogen activated