The following pages link to Glucogenic amino acid
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Ketogenesis (links | edit)
- Cortisol (links | edit)
- Gamma-glutamyltransferase (links | edit)
- Glycogenolysis (links | edit)
- Carbohydrate metabolism (links | edit)
- Proteinogenic amino acid (links | edit)
- Anaerobic respiration (links | edit)
- Photorespiration (links | edit)
- Phosphocreatine (links | edit)
- Methylmalonic acidemias (links | edit)
- Propionic acidemia (links | edit)
- Hyperammonemia (links | edit)
- S-Adenosyl methionine (links | edit)
- Waardenburg syndrome (links | edit)
- Mevalonate pathway (links | edit)
- Homocystinuria (links | edit)
- Biological carbon fixation (links | edit)
- Succinyl-CoA (links | edit)
- Fumaric acid (links | edit)
- Creatine kinase (links | edit)
- L-DOPA (links | edit)
- Agmatine (links | edit)
- Cystinuria (links | edit)
- Aspartate transaminase (links | edit)
- Glutamate dehydrogenase (links | edit)
- Ornithine transcarbamylase deficiency (links | edit)
- Oxaloacetic acid (links | edit)
- Inborn errors of metabolism (links | edit)
- Fatty acid metabolism (links | edit)
- Glycogenesis (links | edit)
- Pentose phosphate pathway (links | edit)
- Cysteine dioxygenase (links | edit)
- Trimethylaminuria (links | edit)
- Specific dynamic action (links | edit)
- Isovaleric acidemia (links | edit)
- Maple syrup urine disease (links | edit)
- Tyrosinase (links | edit)
- Cystinosis (links | edit)
- Citrullinemia (links | edit)
- Beta-ketothiolase deficiency (links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (links | edit)
- Tyrosinemia (links | edit)
- Beta oxidation (links | edit)
- Hartnup disease (links | edit)
- Glutaric aciduria type 1 (links | edit)
- Saccharopinuria (links | edit)
- Β-Hydroxy β-methylbutyric acid (links | edit)
- Ochronosis (links | edit)
- Glutamine synthetase (links | edit)
- Lysinuric protein intolerance (links | edit)