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Citrin/Mitochondrial glycerol-3-phosphate dehydrogenase double knock-out mice recapitulate features of human citrin deficiencyJOURNAL OF BIOLOGICAL CHEMISTRYIF3.92007-08-0175OAAI
Prolonged effect of single carnitine administration on fasted carnitine-deficient JVS mice regarding their locomotor activity and energy expenditureBIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDSIF3.32006-10-015PREAI
Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient miceJOURNAL OF HEPATOLOGYIF332006-05-0136PREAI
Reduced N-acetylaspartate levels in mice lacking aralar, a brain- and muscle-type mitochondrial aspartate-glutamate carrierJOURNAL OF BIOLOGICAL CHEMISTRYIF3.92005-09-01139OAAI
Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycleMOLECULAR GENETICS AND METABOLISMIF3.52004-04-0193PREAI
Hyperammonemia in carnitine-deficient adult JVS mice caused by starvationMETABOLIC BRAIN DISEASEIF3.52002-01-012PREAI
Pathogenesis and pathophysiology of citrin (a mitochondrial aspartate glutamate carrier) deficiencyMETABOLIC BRAIN DISEASEIF3.52002-01-0171PREAI
Antagonizing effect of AP-1 on glucocorticoid induction of urea cycle enzymes: A study of hyperammonemia in carnitine-deficient, juvenile visceral steatosis miceMOLECULAR GENETICS AND METABOLISMIF3.52000-12-0114PREAI
Identification of two novel mutations in the SLC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinemiaHUMAN GENETICSIF3.62000-12-01132PREAI
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