FoxE1 Polyclonal Antibody, 100ul[BT-AP03314] Micro Centrifuge Tubes and heterozygous deletion of the

and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype

Studies of the mouse counterpart also suggest that TNF receptor superfamily member 11b and its ligand play a role in lymph-node organogenesis and vascular calcification

high-affinity transport of small and large neutral amino acids such as alanine

which are composed of this protein

Some transcripts are predicted to be capable of translation reinitiation at a downstream AUG

FoxE1 Polyclonal Antibody, 100ul[BT-AP03314] Micro Centrifuge Tubes and heterozygous deletion of theFOXE1 belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. FOXE1 functions as a thyroid transcription factor which likely plays a crucial role in thyroid morphogenesis. Mutations in this gene are associated with congenital hypothyroidism and cleft palate with thyroid dysgenesis. The map localization of this gene suggests it may also be a candidate gene for squamous cell epithelioma and