Cerebral protein synthesis in a genetic mouse model of phenylketonuria
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Phenylketonuria Pathophysiology: on the Role of Metabolic AlterationsBehavioral and neurochemical characterization of new mouse model of hyperphenylalaninemiaLarge Neutral Amino Acid Supplementation Exerts Its Effect through Three Synergistic Mechanisms: Proof of Principle in Phenylketonuria MiceVoxel-based estimation of kinetic model parameters of the L-[1-(11)C]leucine PET method for determination of regional rates of cerebral protein synthesis: validation and comparison with region-of-interest-based methods5-Hydroxytryptophan during critical postnatal period improves cognitive performances and promotes dendritic spine maturation in genetic mouse model of phenylketonuria.A spectral analysis approach for determination of regional rates of cerebral protein synthesis with the L-[1-(11)C]leucine PET method.Large neutral amino acids in the treatment of PKU: from theory to practice.In vivo catecholaminergic metabolism in the medial prefrontal cortex of ENU2 mice: an investigation of the cortical dopamine deficit in phenylketonuria.Increased rates of cerebral glucose metabolism in a mouse model of fragile X mental retardationPhenylketonuria: brain phenylalanine concentrations relate inversely to cerebral protein synthesisAutophagy induction by tetrahydrobiopterin deficiencyBiochemical, Metabolic, and Behavioral Characteristics of Immature Chronic Hyperphenylalanemic Rats.Use of acute hyperphenylalaninemia in rhesus monkeys to examine sensitivity and stability of the L-[1-11C]leucine method for measurement of regional rates of cerebral protein synthesis with PET.Voluntary exercise regionally augments rates of cerebral protein synthesis.Regional rates of cerebral protein synthesis measured with L-[1-11C]leucine and PET in conscious, young adult men: normal values, variability, and reproducibility.Long-term treatment of phenylketonuria with a new medical food containing large neutral amino acidsEarly-onset behavioral and neurochemical deficits in the genetic mouse model of phenylketonuriaOligodendrocyte development and myelinogenesis are not impaired by high concentrations of phenylalanine or its metabolites.Measurement of regional rates of cerebral protein synthesis with L-[1-11C]leucine and PET with correction for recycling of tissue amino acids: I. Kinetic modeling approach.Measurement of regional rates of cerebral protein synthesis with L-[1-11C]leucine and PET with correction for recycling of tissue amino acids: II. Validation in rhesus monkeys.Epilepsy in phenylketonuria: a complex dependence on serum phenylalanine levels.Tetrahydrobiopterin treatment reduces brain L-Phe but only partially improves serotonin in hyperphenylalaninemic ENU1/2 mice.Effects of shortened scanning intervals on calculated regional rates of cerebral protein synthesis determined with the L-[1-11C]leucine PET method.
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P2860
Cerebral protein synthesis in a genetic mouse model of phenylketonuria
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on September 2000
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Cerebral protein synthesis in a genetic mouse model of phenylketonuria
@en
Cerebral protein synthesis in a genetic mouse model of phenylketonuria.
@nl
type
label
Cerebral protein synthesis in a genetic mouse model of phenylketonuria
@en
Cerebral protein synthesis in a genetic mouse model of phenylketonuria.
@nl
prefLabel
Cerebral protein synthesis in a genetic mouse model of phenylketonuria
@en
Cerebral protein synthesis in a genetic mouse model of phenylketonuria.
@nl
P2860
P356
P1476
Cerebral protein synthesis in a genetic mouse model of phenylketonuria
@en
P2860
P304
11014-11019
P356
10.1073/PNAS.97.20.11014
P407
P577
2000-09-01T00:00:00Z