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Pharmacologic or genetic ablation of maleylacetoacetate isomerase increases levels of toxic tyrosine catabolites in rodents
Authors:Ammini Chandramohan V  Fernandez-Canon Jose  Shroads Albert L  Cornett Rachel  Cheung Jang  James Margaret O  Henderson George N  Grompe Markus  Stacpoole Peter W
Affiliation:Division of Endocrinology and Metabolism, Department of Medicine, University of Florida, Gainesville, FL 32610, USA.
Abstract:
Keywords:DCA, dichloroacetate   MAAI, maleylacetoacetate isomerase   SD, Sprague-Dawley   mRNA, messenger ribonucleic acid   MAAI-KO, maleylacetoacetate isomerase knockout   SA, succinylacetone   δ-ALA, delta-aminolevulinate   CLA, congenital lactic acidosis   PDH, pyruvate dehydrogenase   GSTZ1, glutathione transferase zeta 1   MA, maleylacetone   HMG-CoA, β-hydroxy-β-methylglutaryl-CoA   NMR, nuclear magnetic resonance   PVDF, polyvinylidene fluoride   SSC, selenosemicarbazide   GC-MS, gas chromatography-mass spectrometry   SIM, selective ion monitoring   MCA, monochloroacetic acid   FA, fumarylacetone   MAA, maleylacetoacetate   FAA, fumarylacetoacetate
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