[Experimental oxalic lithiases in rats. Influence of certain Krebs cycle intermediates]. 1973

J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon

UI MeSH Term Description Entries
D007274 Injections, Intraperitoneal Forceful administration into the peritoneal cavity of liquid medication, nutrient, or other fluid through a hollow needle piercing the abdominal wall. Intraperitoneal Injections,Injection, Intraperitoneal,Intraperitoneal Injection
D007669 Kidney Calculi Stones in the KIDNEY, usually formed in the urine-collecting area of the kidney (KIDNEY PELVIS). Their sizes vary and most contains CALCIUM OXALATE. Kidney Stones,Renal Calculi,Nephrolith,Renal Calculus,Calculi, Kidney,Calculi, Renal,Calculus, Kidney,Calculus, Renal,Kidney Calculus,Kidney Stone,Stone, Kidney,Stones, Kidney
D008293 Malates Derivatives of malic acid (the structural formula: (COO-)2CH2CHOH), including its salts and esters.
D010070 Oxalates Derivatives of OXALIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that are derived from the ethanedioic acid structure. Oxalate,Ethanedioic Acids,Oxalic Acids,Acids, Ethanedioic,Acids, Oxalic
D010071 Oxaloacetates Derivatives of OXALOACETIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that include a 2-keto-1,4-carboxy aliphatic structure. Ketosuccinates,Oxosuccinates,Oxaloacetic Acids
D002951 Citrates Derivatives of CITRIC ACID.
D002952 Citric Acid Cycle A series of oxidative reactions in the breakdown of acetyl units derived from GLUCOSE; FATTY ACIDS; or AMINO ACIDS by means of tricarboxylic acid intermediates. The end products are CARBON DIOXIDE, water, and energy in the form of phosphate bonds. Krebs Cycle,Tricarboxylic Acid Cycle,Citric Acid Cycles,Cycle, Citric Acid,Cycle, Krebs,Cycle, Tricarboxylic Acid,Cycles, Citric Acid,Cycles, Tricarboxylic Acid,Tricarboxylic Acid Cycles
D004195 Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. Animal Disease Model,Animal Disease Models,Disease Model, Animal
D005026 Ethylene Glycols An ethylene compound with two hydroxy groups (-OH) located on adjacent carbons. They are viscous and colorless liquids. Some are used as anesthetics or hypnotics. However, the class is best known for their use as a coolant or antifreeze. Dihydroxyethanes,Ethanediols,Glycols, Ethylene
D006038 Glyoxylates Derivatives of glyoxylic acid (the structural formula C2H2O3), including its salts and esters.

Related Publications

J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
November 1968, The American journal of physiology,
J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
July 1964, Journal of bacteriology,
J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
October 1957, Journal of cellular and comparative physiology,
J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
August 1971, Comparative biochemistry and physiology. B, Comparative biochemistry,
J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
May 1958, The Journal of laboratory and clinical medicine,
J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
January 1999, Annual review of physiology,
J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
January 2016, Cell communication and signaling : CCS,
J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
January 2020, Journal of clinical medicine,
J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
September 1955, Gan,
J Thomas, and E Thomas, and M T Duburque, and J M Melon, and A Monsaingeon
December 1982, Proceedings of the National Academy of Sciences of the United States of America,
Copied contents to your clipboard!