BHE22 Rabbit Polyclonal Antibody, 20ul Aspirating Pipets hereditary hemorrhagic telangiectasia and erythropoietic

hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18

smooth muscle relaxation and cardioprotection by mediating the effects of angiotensin-(1-7)

Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects

Mutations in GDI1 have been linked to X-linked nonspecific mental retardation

BHE22 Rabbit Polyclonal Antibody, 20ul Aspirating Pipets hereditary hemorrhagic telangiectasia and erythropoieticThis gene encodes a protein that belongs to the basic helix loop helix (bHLH) family of transcription factors that regulate cell fate determination, proliferation, and differentiation. A similar protein in mouse is required for the development of the dorsal cochlear nuclei, and is thought to play a role in in the differentiation of neurons involved in sensory input. The mouse protein also functions in retinogenesis.