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- Plasma Metabolomic and Lipidomic Alterations Associated with COVID-19
- Differential Effects of Post-Weaning Diet and Maternal Obesity
- Direct Quantification of Amino Acids in Plasma by Liquid Chromatography-Tandem Mass Spectrometry for Clinical Research
- Saccharopinuria 0
- Organic Acids Support Guide
- Organic Acid Disorders
- AASS Gene Aminoadipate-Semialdehyde Synthase
- University of Oklahoma
- Alanine, Aspartate and Glutamate Metabolism Alcohols and Polyols
- Biomarkers Identified in Inborn Errors for Lysine, Arginine, and Ornithine
- Biochemical Pathways Supporting Beta-Lactam Biosynthesis in the Springtail Folsomia Candida Wouter Suring, Janine Mariën, Rhody Broekman, Nico M
- Pathways of Amino Acid Degradation in Nilaparvata Lugens (Stål) with Special Reference to Lysine-Ketoglutarate Reductase/Saccharopine Dehydrogenase (LKR/SDH)
- Lysine Degradation Through the Saccharopine Pathway in Bacteria: LKR and SDH in Bacteria and Its Relationship to the Plant and Animal Enzymes
- LKR/SDH Plays Important Roles Throughout the Tick Life Cycle Including a Long Starvation Period
- Lysine Metabolism in Mammals by FLORENCE C
- The Regulation of the Sulfur Amino Acid Biosynthetic Pathway In
- Advances in Biotechnology and Biochemistry
- Nutritionalrich and Stresstolerant Crops by Saccharopine Pathway Manipulation
- Saccharopinuria Accompanied by Hyperammonemia and Hypercitrullinemia Presented with Elderly-Onset Epilepsy, Progressive Cognitive Decline, and Gait Ataxia
- Hyperornithinemia, Hyperammonernia, and Homocitrullinuria Associated with Decreased Carbamyl Phosphate Synthetase I Activity
- Genetic Basis of Hyperlysinemia
- Simultaneous Detection of Lysine Metabolites by a Single LC–MS/MS Method: Monitoring Lysine Degradation in Mouse Plasma Izabella A
- Comprehensive Preterm Breast Milk Metabotype Associated with Optimal Infant Early Growth Pattern
- Lysine Intolerance in a Variant Form of Citrullinemia
- Hyperlysinemia
- Anaplerotic Therapy in Propionic Acidemia