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Department Of Molecular Metabolism And Biochemical Genetics Kagoshima University Graduate School Of | 論文
- Fasting-induced reduction in locomotor activity and reduced response of orexin neurons in carnitine-deficient mice
- Conventional Diet Therapy for Hyperammonemia is Risky in the Treatment of Hepatic Encephalopathy Associated with Citrin Deficiency
- Metabolic derangements in deficiency of citrin, a liver-type mitochondrial aspartate-glutamate carrier
- Risk of Worsened Encephalopathy after Intravenous Glycerol Therapy in Patients with Adult-onset Type II Citrullinemia (CTLN2)
- Hepatocellular Carcinoma in a Case of Adult-onset Type II Citrullinemia
- Early neonatal onset carbamoyl-phosphate synthase 1 deficiency treated with continuous hemodiafiltration and early living-related liver transplantation
- A possible mechanism of neonatal intrahepatic cholestasis caused by citrin deficiency
- A pregnant patient with fulminant hepatic failure was found to carry a novel missense mutation in the argininosuccinate synthetase gene
- MRI of adult-onset type II citrullinemia
- Histological findings in the livers of patients with neonatal intrahepatic cholestasis caused by citrin deficiency
- Attenuation of Cardiac Hypertrophy in Carnitine-Deficient Juvenile Visceral Steatosis (JVS) Mice Achieved by Lowering Dietary Lipid
- Detection of candidate chromosome for cleft lip with palate in A/WySn mice
- The mutation spectrum of the SLC25A13 gene in Chinese infants with intrahepatic cholestasis and aminoacidemia
- Candidate Genes for Cleft Lip and for Cleft Lip with Cleft Palate in the A/WySn Mouse Strain