Keonate rats were intubated dally from 0-29 days of age with 1-phenylalanlne plus dl-parachlorophenylalanlne in order to produce an animal model of phenylketonuria (PKU). On the 29th day of intubation, the PKU group had elevated plasma phenylalanine and tyrosine levels and reduced body and brain weights as compared to an agar control group. At 85 days of age the PKU animals made significantly fewer bar presses than the agar controls, with the largest difference occurring when the subjects were shifted from a CRF to a DRL-5" schedule of reinforcement. The rats were decapitated at 330 days of age and the PKU animals had significantly less DNA and wet brain weight than the agar controls in the cerebellum only. Early drug treatment of the PKU a...
Phenylketonuria (PKU) is a metabolic disorder accumulating phenylalanine (Phe) and its metabolites i...
Mothers with untreated phenylketonuria (PKU) have an increased risk of bearing children with congeni...
and phenylethylamine, were measured in the urine of PKU patients. In general correlation was found b...
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 one of the most common human inborn errors of metabolism, caused by phenyla...
The purpose of this experiment was to simulate PKU in rats and to determine if there were a critical...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
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...
To unravel the role of gene mutations in the healthy and the diseased state, countless studies have ...
Habituation and classical conditioning were investigated during the cortical developmental period in...
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...
Central nervous system (CNS) deficiencies of the monoamine neurotransmitters dopamine and serotonin ...
Phenylketonuria (PKU) is a metabolic disorder accumulating phenylalanine (Phe) and its metabolites i...
Mothers with untreated phenylketonuria (PKU) have an increased risk of bearing children with congeni...
and phenylethylamine, were measured in the urine of PKU patients. In general correlation was found b...
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 one of the most common human inborn errors of metabolism, caused by phenyla...
The purpose of this experiment was to simulate PKU in rats and to determine if there were a critical...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
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...
To unravel the role of gene mutations in the healthy and the diseased state, countless studies have ...
Habituation and classical conditioning were investigated during the cortical developmental period in...
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...
Central nervous system (CNS) deficiencies of the monoamine neurotransmitters dopamine and serotonin ...
Phenylketonuria (PKU) is a metabolic disorder accumulating phenylalanine (Phe) and its metabolites i...
Mothers with untreated phenylketonuria (PKU) have an increased risk of bearing children with congeni...
and phenylethylamine, were measured in the urine of PKU patients. In general correlation was found b...