Medscape2d
Not So Rare: Errors of Metabolism During the Neonatal Period
Steiner, MD Neonates with profound and prolonged hyperammonemia with coma due to urea cycle defect will have ... synthetase deficiency; OTC, ornithine transcarbamylase deficiency; PCD, pyruvate ...
BMJ5d
Neurological outcome of patients with ornithine carbamoyltransferase deficiency
ich.ucl.ac.uk Background: Ornithine carbamoyltransferase (OCT) deficiency is the commonest of the inherited urea cycle disorders. Aims: To determine the long term neurological and cognitive outcome of ...
Frontiers5d
Lactylation, an emerging hallmark of metabolic reprogramming: Current progress and open challenges
Lactate, the end product of glycolysis, efficiently functions as the carbon source, signaling molecules and immune regulators. Lactylation, being regulated by lactate, has recently been confirmed as a ...
Frontiers5d
CRISPR/Cas9 System as a Valuable Genome Editing Tool for Wine Yeasts with Application to Decrease Urea Production
An extensive repertoire of molecular tools is available for genetic analysis in laboratory strains of S. cerevisiae. Although this has widely contributed to the interpretation of gene functionality ...
C&EN4d
Dysregulated Neurotransmission and the Role of Viruses in Alzheimer’s Disease
Division of Evolution, Infection & Genomic Sciences, University of Manchester, Manchester M13 9PL, U.K. Division of Evolution, Infection & Genomic Sciences, University of Manchester, Manchester M13 ...