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A novel UPLC-MS/MS based method to determine the activity of N-acetylglutamate synthase in liver tissue.
Dercksen, Marli; Duran, Marinus; IJlst, Lodewijk; Kulik, Wim; Ruiter, Jos P N; van Cruchten, Arno; Tuchman, Mendel; Wanders, Ronald J A.
Affiliation
  • Dercksen M; Laboratory Genetic Metabolic Diseases, Departments of Pediatrics and Clinical Chemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands; Human Metabonomics, North-West University, Potchefstroom Campus, South Africa. Electronic address: marli.dercksen@nwu.ac.za.
  • Duran M; Laboratory Genetic Metabolic Diseases, Departments of Pediatrics and Clinical Chemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • IJlst L; Laboratory Genetic Metabolic Diseases, Departments of Pediatrics and Clinical Chemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Kulik W; Laboratory Genetic Metabolic Diseases, Departments of Pediatrics and Clinical Chemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Ruiter JP; Laboratory Genetic Metabolic Diseases, Departments of Pediatrics and Clinical Chemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • van Cruchten A; Laboratory Genetic Metabolic Diseases, Departments of Pediatrics and Clinical Chemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Tuchman M; Children's National Medical Center, The George Washington University, Washington, DC, USA.
  • Wanders RJ; Laboratory Genetic Metabolic Diseases, Departments of Pediatrics and Clinical Chemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Mol Genet Metab ; 119(4): 307-310, 2016 12.
Article in En | MEDLINE | ID: mdl-27771289

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carbamoyl-Phosphate Synthase (Ammonia) / Hyperammonemia / Amino-Acid N-Acetyltransferase / Urea Cycle Disorders, Inborn Limits: Animals / Humans Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2016 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carbamoyl-Phosphate Synthase (Ammonia) / Hyperammonemia / Amino-Acid N-Acetyltransferase / Urea Cycle Disorders, Inborn Limits: Animals / Humans Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2016 Document type: Article Country of publication: