PRA20 Rabbit Polyclonal Antibody, 50ul RNA Synthesis Mutations in this gene cause

Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex| leading to epilepsy| mental retardation| subcortical band heterotopia ("double cortex" syndrome) in females and lissencephaly ("smooth brain&quo

It is expressed at high levels in ACTH-secreting pituitary adenomas as well as in bronchial carcinoids responsible for the ectopic ACTH syndrome

The isoforms lacking the transmembrane domain may negatively regulate the apoptosis mediated by the full length isoform

Serine/threonine-protein kinase MRCK beta contains a Cdc42/Rac-binding p21 binding domain resembling that of PAK kinase

SPINK5 encodes a multidomain serine protease inhibitor that contains 15 potential inhibitory domains

PRA20 Rabbit Polyclonal Antibody, 50ul RNA Synthesis Mutations in this gene cause