DDC Polyclonal Antibody, 50ul Shakers Mutations in RET are associated

Mutations in RET are associated with the disorders multiple endocrine neoplasia

infusion of this hormone in obese rodents has shown to decrease weight gain

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protein phosphatase 1

and SEC22B

DDC Polyclonal Antibody, 50ul Shakers Mutations in RET are associatedThe encoded protein catalyzes the decarboxylation of L 3,4 dihydroxyphenylalanine (DOPA) to dopamine, L 5 hydroxytryptophan to serotonin and L tryptophan to tryptamine. Defects in this gene are the cause of aromatic L amino acid decarboxylase deficiency (AADCD). AADCD deficiency is an inborn error in neurotransmitter metabolism that leads to combined serotonin and catecholamine deficiency. Multiple alternatively spliced transcript variants encoding