Lack of oxygen is sensed directly by a prolyl
hydroxylase known as EGL - 9 in worms and EGLN2 in mammals.
Not exact matches
Woo's technique may one day be used to treat the metabolic disorder phenylketonuria (PKU), in which the gene for the hepatic enzyme
known as phenylalanine
hydroxylase (PAH) is defective.
Phenylketonuria: Phenylketonuria (PKU) is a genetic metabolic disorder in which a baby is born without an important enzyme
known as phenylalanine
hydroxylase (PAH).
The activity of HIF is therefore strictly regulated by a set of oxygen sensors
known as the HIF - prolyl
hydroxylases (PHDs).