Role of Albumin and Simulated Gastric Fluid in Modulating Phenylalanine Ammonia Lyase Enzyme Activity
<p> Phenylketonuria (PKU) is an inborn error of metabolism characterized by a loss of phenylalanine hydroxylase activity; an enzyme that metabolizes phenylalanine to tyrosine. Phenylalanine ammonia lyase (PAL) is currently being evaluated as a possible therapy for the management of PKU. PAL ca...
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| Language: | EN |
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University of the Sciences in Philadelphia
2018
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| Online Access: | http://pqdtopen.proquest.com/#viewpdf?dispub=10904825 |