The purpose of this experiment was to simulate PKU in rats and to determine if there were a critical period during which an increase of PA in the system has its most detrimental effect. Fifty-one Sprague-Dawley rats were paired at birth with a litter mate of the same sex and randomly assigned to one of three feeding conditions for administering the PA and control diets: beginning at birth (E-l, C-l), beginning at 18 days of age (E-2, C-2) and beginning at 36 days of age (E-3, C-3). Until weaning, E-l and C-l were fed by intubation. After weaning experimental animals were fed a 7% PA diet
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
Untreated phenylketonuria (PKU) results in severe neurodevelopmental disorders, which can be partial...
Keonate rats were intubated dally from 0-29 days of age with 1-phenylalanlne plus dl-parachloropheny...
Phenylketonuria (PKU) is a metabolic disorder that results in significant brain dysfunction if untre...
Results of a longitudinal study of children treated early and continuously for phenylketonuria (PKU)...
Phenylketonuria (PKU) is a genetic disorder that is characterized by an inability of the body to uti...
Existing phenylalanine hydroxylase (PAH)-deficient mice strains are useful models of untreated or la...
Phenylketonuria (PKU) is a genetic disorder that is characterized by an inability of the body to uti...
Phenylketonuria (PKU) is a genetic disorder that is characterized by an inability of the body to uti...
The metabolism of phenylalanine-C14 was studied in three different groups of rats: normal animals, p...
Phenylketonuria (PKU) is an inherited metabolic disease characterized by abnormally high concentrati...
The mechanism of the depletion of several plasma amino acids in PKU has remained unexplained. In the...
Background: In phenylketonuria (PKU), treatment monitoring is based on frequent blood phenylalanine ...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
Untreated phenylketonuria (PKU) results in severe neurodevelopmental disorders, which can be partial...
Keonate rats were intubated dally from 0-29 days of age with 1-phenylalanlne plus dl-parachloropheny...
Phenylketonuria (PKU) is a metabolic disorder that results in significant brain dysfunction if untre...
Results of a longitudinal study of children treated early and continuously for phenylketonuria (PKU)...
Phenylketonuria (PKU) is a genetic disorder that is characterized by an inability of the body to uti...
Existing phenylalanine hydroxylase (PAH)-deficient mice strains are useful models of untreated or la...
Phenylketonuria (PKU) is a genetic disorder that is characterized by an inability of the body to uti...
Phenylketonuria (PKU) is a genetic disorder that is characterized by an inability of the body to uti...
The metabolism of phenylalanine-C14 was studied in three different groups of rats: normal animals, p...
Phenylketonuria (PKU) is an inherited metabolic disease characterized by abnormally high concentrati...
The mechanism of the depletion of several plasma amino acids in PKU has remained unexplained. In the...
Background: In phenylketonuria (PKU), treatment monitoring is based on frequent blood phenylalanine ...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
Untreated phenylketonuria (PKU) results in severe neurodevelopmental disorders, which can be partial...