'Phenylpyruvic acid' diaporamas de présentation

Inborn errors of metabolism

Inborn errors of metabolism. By : - Dr. Sanjeev. Phenylketonuria ( PKU ). It is an autosomal recessive (two copies of an abnormal gene ) genetic disorder characterized by a deficiency in the hepatic enzyme phenylalanine hydroxylase (PAH).

1.63k views • 56 slides

Enzyme Mimics (Artificial Enzymes)

5.73k views • 16 slides

Enzyme Mimics (Artificial Enzymes)

596 views • 16 slides

?. Chemical Properties

?. Chemical Properties. carboxyl, ??. amino, ??. 1. Acidity. glutamic acid, ???. monosodium glutamate ?????? (gourmet powder). ??. Chinese restaurant syndrome (CRS), ???????. Kwok, R.H.M. Chinese Restaurant Syndrome . New England Journal of Medicine , 1968, 17:796.

261 views • 10 slides

??

Effects of the Streptomyces Metabolites, Homogentisic Acid and ?-Phenylpyruvic Acid Against Oxidative Stress.

123 views • 2 slides