Phenylalanine hydroxylase (PAH) is an allosteric enzyme that maintains phenylalanine (Phe)
below neurotoxic levels; its failure results in phenylketonuria, an inborn error of amino acid …

Objective The objective of this study is to examine radiologic occult injury screening
performance/yield among contacts presenting for precautionary medical assessments and assess …

Phenylalanine hydroxylase (PAH) is an allosteric enzyme responsible for maintaining
phenylalanine (Phe) below neurotoxic levels; its failure results in phenylketonuria. Wild type (WT) …

Objective: The goal of this study was to simulate the application of the dietary recommendations
to increase dietary fiber (DF)-containing foods. Methods: This study used 24-hour dietary …

Evidence-based design (EBD) of hospitals could significantly improve patient safety and make
patient, staff and family environments healthier. This systematic review aims to determine …

Objective: The goal of this study was to simulate the application of the dietary recommendations
to increase dietary fiber (DF)-containing foods. Methods: This study used 24-hour dietary …

Phenylketonuria (PKU), a genetic disorder characterized by phenylalanine hydroxylase (PAH)
deficiency and phenylalanine (Phe) accumulation, is primarily managed with a protein-…

The evolution of large vultures linked to mountainous habitats was accompanied by extreme
physiological and behavioral specializations for energetically efficient flights. However, little …

Peer review is the driving force of journal development, and reviewers are gatekeepers who
ensure that Genes maintains its standards for the high quality of its published papers. …

Much of the US population fails to achieve the dietary reference intakes (DRI) for key nutrients,
including vitamins A, D & calcium. This study evaluated the contribution of micronutrient …