Acylglycines
National Institutes of Health
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Inborn defects in fatty acid β-oxidation are a complex group of diseases in which 16 different entities are recognized. These are…
BALB/cByJ mice have an autosomal recessive deficiency of short-chain acyl-CoA dehydrogenase (SCAD) and show elevated excretion of…
The dynamic of glycine conjugates excretion in riboflavin deficient (RFD) rats was studied. The excretion of isovaleryl-, n…
Long-chain fatty acids (LCFA) are oxidized by muscle mitochondria after transport in the cytosol by fatty-acid-binding protein(s…