Metabolism/Related Articles: Difference between revisions
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imported>Chris Day |
imported>Chris Day |
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{{r|Metabolic network modelling}} | {{r|Metabolic network modelling}} | ||
{{r|dynamic energy budget}} | {{r|dynamic energy budget}} | ||
{r|Newborn screening}} | |||
{{r|3-Meth{ylcrotonyl-CoA carboxylase deficiency||**}} | |||
{{r|Argininosuccinic acidemia||**}} | |||
{{r|Beta-Ketothiolase deficiency||**}} | |||
{{r|Biotinidase deficiency||**}} | |||
{{r|Carnitine uptake defect||**}} | |||
{{r|Citrullinemia||**}} | |||
{{r|Classical galactosemia||**}} | |||
{{r|Congenital adrenal hyperplasia||**}} | |||
{{r|Congenital hypothyroidism||**}} | |||
{{r|Cystic fibrosis||**}} | |||
{{r|Glutaric acidemia type I||**}} | |||
{{r|Hb S/Beta-Thalassemia||**}} | |||
{{r|Homocystinuria||**}} | |||
{{r|HMG-CoA lyase deficiency||**}} | |||
{{r|Isovaleric acidemia||**}} | |||
{{r|Long-chain 3-OH acyl-CoA dehydrogenase deficiency||**}} | |||
{{r|Maple syrup urine disease||**}} | |||
{{r|Medium-chain acyl-CoA dehydrogenase deficiency||**}} | |||
{{r|Methylmalonic acidemia (CBLAB)||**}} | |||
{{r|Methylmalonic acidemia (MUT)||**}} | |||
{{r|Multiple carboxylase deficiency||**}} | |||
{{r|Phenylketonuria||**}} | |||
{{r|Propionic acidemia||**}} | |||
{{r|Sickle cell anemia||**}} | |||
{{r|Trifunctional protein deficiency||**}} | |||
{{r|Tyrosinemia type I||**}} | |||
{{r|Very long-chain acyl-CoA dehydrogenase deficiency||**}} | |||
Revision as of 21:03, 25 September 2008
- See also changes related to Metabolism, or pages that link to Metabolism or to this page or whose text contains "Metabolism".
Parent topics
- Biology [r]: The science of life — of complex, self-organizing, information-processing systems living in the past, present or future. [e]
- Biochemistry [r]: The chemistry of living things; a field of both biology and chemistry. [e]
Subtopics
General pathways
- Carbohydrate metabolism [r]: The various biochemical processes responsible for the formation, breakdown and interconversion of carbohydrates in living organisms. [e]
- Fatty acid metabolism [r]: Oxidative degradation of saturated fatty acids in which two-carbon units are sequentially removed from the molecule with each turn of the cycle, and metabolized so that it can be used as a source of energy in aerobic respiration. [e]
- Protein synthesis [r]: "a certain kind of natural production (or biosynthesis) of polypeptides for protein molecules according to a nucleic acid code" [e]
- Nucleic acid metabolism [r]: Process by which nucleotides are synthesized and degraded, using an anabolic mechanism generally involving chemical reaction of phosphate, pentose sugar, and a nitrogenous base. [e]
- Central metabolism [r]: Add brief definition or description
Anabolism
- Anabolic [r]: Biological processes that build larger molecules from smaller ones, and increase the size of bones, organs and muscles. [e]
- Biosynthesis [r]: The production of chemical metabolites by living systems. [e]
- Glycogenesis [r]: Add brief definition or description
- Gluconeogenesis [r]: Formation of glucose, especially by the liver, from noncarbohydrate precursors, such as amino acids, lactate, pyruvate, and the glycerol portion of fats. [e]
- Porphyrin [r]: Class of cyclic compounds in which the parent macrocycle consists of four pyrrole-type units interconnected at their α carbon atoms via a methine bridge, and functioning as a metal-binding cofactor in haemoglobin, chlorophyll, and certain enzymes. [e]
- HMG-CoA reductase pathway [r]: Add brief definition or description
- Secondary metabolism [r]: Add brief definition or description
- Photosynthesis [r]: The process by which an organism captures and stores energy from sunlight, energy it uses to power its cellular activities. [e]
- Calvin cycle [r]: A metabolic cycle, discovered by Melvin Calvin, that is responsible for the reduction of carbon dioxide to sugar in the stroma of chloroplasts. [e]
- Carbon fixation [r]: Add brief definition or description
- Glyoxylate cycle [r]: Metabolic pathway in some orgnaisms which uses acetyl CoAs to synthesize carbohydrates. [e]
Catabolism
- Glycolysis [r]: Add brief definition or description
- Glycogenolysis [r]: Add brief definition or description
- Citric acid cycle [r]: Add brief definition or description
- Beta-oxidation [r]: Add brief definition or description
Drug metabolism
- Drug metabolism [r]: Add brief definition or description
- Cytochrome P450 oxidase [r]: Add brief definition or description
- Flavin-containing monooxygenase system [r]: Add brief definition or description
- Alcohol metabolism [r]: Add brief definition or description
Nitrogen metabolism
- Nitrogen cycle [r]: Add brief definition or description:
- Urea cycle [r]: Add brief definition or description
- Nitrogen assimilation [r]: Add brief definition or description
- Nitrification [r]: Add brief definition or description
- Denitrification [r]: Add brief definition or description
Other
- Metabolomics [r]: Add brief definition or description
- Metabolome [r]: Add brief definition or description
- Metabolite [r]: Add brief definition or description
- Basal metabolic rate [r]: Add brief definition or description
- Thermic effect of food [r]: Add brief definition or description
- Iron-sulfur world theory [r]: Add brief definition or description
- Biodegradation [r]: Add brief definition or description
- Calorimetry [r]: Add brief definition or description
- Respirometry [r]: Add brief definition or description
- Microbial metabolism [r]: Add brief definition or description
- Metabolic network modelling [r]: Add brief definition or description
- Dynamic energy budget [r]: Add brief definition or description
{r|Newborn screening}}
- [[3-Meth{ylcrotonyl-CoA carboxylase deficiency]] [r]: [{{fullurl:3-Meth{ylcrotonyl-CoA carboxylase deficiency/Definition|action=edit&preload=Template%3ADef_preload}} Add brief definition or description]
- Argininosuccinic acidemia [r]: Add brief definition or description
- Beta-Ketothiolase deficiency [r]: Add brief definition or description
- Biotinidase deficiency [r]: Add brief definition or description
- Carnitine uptake defect [r]: Add brief definition or description
- Citrullinemia [r]: Add brief definition or description
- Classical galactosemia [r]: Add brief definition or description
- Congenital adrenal hyperplasia [r]: Add brief definition or description
- Congenital hypothyroidism [r]: Add brief definition or description
- Cystic fibrosis [r]: Add brief definition or description
- Glutaric acidemia type I [r]: Add brief definition or description
- Hb S/Beta-Thalassemia [r]: Add brief definition or description
- Homocystinuria [r]: Add brief definition or description
- HMG-CoA lyase deficiency [r]: Add brief definition or description
- Isovaleric acidemia [r]: Add brief definition or description
- Long-chain 3-OH acyl-CoA dehydrogenase deficiency [r]: Add brief definition or description
- Maple syrup urine disease [r]: Add brief definition or description
- Medium-chain acyl-CoA dehydrogenase deficiency [r]: Add brief definition or description
- Methylmalonic acidemia (CBLAB) [r]: Add brief definition or description
- Methylmalonic acidemia (MUT) [r]: Add brief definition or description
- Multiple carboxylase deficiency [r]: Add brief definition or description
- Phenylketonuria [r]: Add brief definition or description
- Propionic acidemia [r]: Add brief definition or description
- Sickle cell anemia [r]: Add brief definition or description
- Trifunctional protein deficiency [r]: Add brief definition or description
- Tyrosinemia type I [r]: Add brief definition or description
- Very long-chain acyl-CoA dehydrogenase deficiency [r]: Add brief definition or description