People with phenylketonuria cannot break down a substance in food called phenylalanine. Following a phenylketonuria diet is the main treatment for preventing serious symptoms. People with ...

The research published recently online on 《Science China-Life Sciences》 led by Prof. Sheng Yang from the Key Laboratory of Synthetic Biology, Chinese Academy of Sciences and a collaborating company, ...

Hyperphenylalaninemia is a common inherited metabolic disease that is due to phenylalanine hydroxylase deficiency, and at least half the affected patients have mild clinical phenotypes. Treatment with ...

The latest short science news items from C&EN. Most folks never need to think about their phenylalanine levels. But about 1 in 16,000 people in the US are born with a faulty phenylalanine hydroxylase ...

This is a preview. Log in through your library . Abstract Phenylalanine ammonia lyase (PAL) activity was studied in different genotypes of pearl millet with varying degrees of susceptibility to downy ...