FoxO3A(Phospho Ser253) Polyclonal Antibody, 100ul Cell Senescence Mutations in this gene have

Mutations in this gene have been associated with Andersen syndrome

Overexpression of MARK leads to hyperphosphorylation of MAPs

A rare microsatellite polymorphism in XRCC5 is associated with cancer in patients of varying radiosensitivity

including mouse Mekk2

enzyme activation

FoxO3A(Phospho Ser253) Polyclonal Antibody, 100ul Cell Senescence Mutations in this gene haveThis gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. This gene likely functions as a trigger for apoptosis through expression of genes necessary for cell death. Translocation of this gene with the MLL gene is associated with secondary acute leukemia. Alternatively spliced transcript variants encoding the same protein have been observed.