Primary hyperoxaluria type 1 (PH 1), an inborn error of glyoxylate metabolism characterized by excessive synthesis of oxalate and glycolate, is caused by a defect in ...
Background: Alanine (Ala), a nonessential amino acid, is present in normal brain at a concentration of ∼0.5 mmol/kg. During acute hypoxia-ischaemia (HI) Ala increases due to decreased flux of pyruvate ...
Journal of Experimental Botany, Vol. 57, No. 12 (2006), pp. 3079-3089 (11 pages) Four alanine aminotransferases (AlaATs) are expressed in Medicago truncatula. In adult plants, two genes encoding ...
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