Amino Acid Metabolism A person with phenylketonuria is advised not to consume which of the following products? Aspartame Fat containing food Glycine containing foods Glucose Aspartame Fat containing food Glycine containing foods Glucose ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to fumarate tyrosine phenylpuruvate lysine fumarate tyrosine phenylpuruvate lysine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a keto-gluco amino acid ketogenic and glucogenic amino acid glucogenic amino acid ketogenic amino acid keto-gluco amino acid ketogenic and glucogenic amino acid glucogenic amino acid ketogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria cannot convert phenylalanine to lysine phenol into ketones phenylalanine to tyrosine phenylalanine to isoleucine phenylalanine to lysine phenol into ketones phenylalanine to tyrosine phenylalanine to isoleucine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A ketogenic amino acid is one which degrades to either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA keto-sugars either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA keto-sugars ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert phenylalanine to isoleucine phenylalanine to phenylpyruvate phenylpyruvate to phenylalanine tyrosine to phenylalanine phenylalanine to isoleucine phenylalanine to phenylpyruvate phenylpyruvate to phenylalanine tyrosine to phenylalanine ANSWER DOWNLOAD EXAMIANS APP
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