BIOMAT Database Logo BIOMAT Database Logo

HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY. 1965

A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007535 Isomerases A class of enzymes that catalyze geometric or structural changes within a molecule to form a single product. The reactions do not involve a net change in the concentrations of compounds other than the substrate and the product.(from Dorland, 28th ed) EC 5. Isomerase
D007770 L-Lactate Dehydrogenase A tetrameric enzyme that, along with the coenzyme NAD+, catalyzes the interconversion of LACTATE and PYRUVATE. In vertebrates, genes for three different subunits (LDH-A, LDH-B and LDH-C) exist. Lactate Dehydrogenase,Dehydrogenase, L-Lactate,Dehydrogenase, Lactate,L Lactate Dehydrogenase
D007962 Leukocytes White blood cells. These include granular leukocytes (BASOPHILS; EOSINOPHILS; and NEUTROPHILS) as well as non-granular leukocytes (LYMPHOCYTES and MONOCYTES). Blood Cells, White,Blood Corpuscles, White,White Blood Cells,White Blood Corpuscles,Blood Cell, White,Blood Corpuscle, White,Corpuscle, White Blood,Corpuscles, White Blood,Leukocyte,White Blood Cell,White Blood Corpuscle
D010428 Pentosephosphates
D010710 Phosphates Inorganic salts of phosphoric acid. Inorganic Phosphate,Phosphates, Inorganic,Inorganic Phosphates,Orthophosphate,Phosphate,Phosphate, Inorganic
D010732 Phosphofructokinase-1 An allosteric enzyme that regulates glycolysis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-1,6-bisphosphate. D-tagatose- 6-phosphate and sedoheptulose-7-phosphate also are acceptors. UTP, CTP, and ITP also are donors. In human phosphofructokinase-1, three types of subunits have been identified. They are PHOSPHOFRUCTOKINASE-1, MUSCLE TYPE; PHOSPHOFRUCTOKINASE-1, LIVER TYPE; and PHOSPHOFRUCTOKINASE-1, TYPE C; found in platelets, brain, and other tissues. 6-Phosphofructokinase,6-Phosphofructo-1-kinase,Fructose-6-P 1-Kinase,Fructose-6-phosphate 1-Phosphotransferase,6 Phosphofructokinase,Phosphofructokinase 1
D010733 Phosphoglucomutase An enzyme that catalyzes the conversion of alpha D-glucose 1-phosphate to alpha D-glucose 6-phosphate. EC 5.4.2.2. Glucose Phosphomutase,Phosphomutase, Glucose
D010734 Phosphogluconate Dehydrogenase An enzyme of the oxidoreductase class that catalyzes the reaction 6-phospho-D-gluconate and NADP+ to yield D-ribulose 5-phosphate, carbon dioxide, and NADPH. The reaction is a step in the pentose phosphate pathway of glucose metabolism. (From Dorland, 27th ed) EC 1.1.1.43. 6-Phosphogluconate Dehydrogenase,6 Phosphogluconate Dehydrogenase,Dehydrogenase, 6-Phosphogluconate,Dehydrogenase, Phosphogluconate
D010735 Phosphoglycerate Kinase An enzyme catalyzing the transfer of a phosphate group from 3-phospho-D-glycerate in the presence of ATP to yield 3-phospho-D-glyceroyl phosphate and ADP. EC 2.7.2.3. Kinase, Phosphoglycerate

Related Publications

A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
[Congenital hemolytic anemia due to triosephosphate isomerase deficiency].
January 1975, Pediatrie,
A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
Glucose phosphate isomerase deficiency with hereditary nonspherocytic hemolytic anemia.
October 1974, The Journal of pediatrics,
A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
Hemolytic anemia and progressive neurologic impairment: think about triosephosphate isomerase deficiency.
August 2014, Fetal and pediatric pathology,
A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
Triosephosphate isomerase deficiency in a child with congenital hemolytic anemia and severe hypotonia.
January 1998, Pediatric hematology and oncology,
A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
Glucosephosphate isomerase (GPI) deficiency mutations associated with hereditary nonspherocytic hemolytic anemia (HNSHA).
December 1997, Blood cells, molecules & diseases,
A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
Molecular analysis of glucose phosphate isomerase deficiency associated with hereditary hemolytic anemia.
September 1996, Blood,
A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
[Hereditary nonspherocytic hemolytic anemia caused by deficiency of erythrocytic glucosephosphate isomerase].
January 1990, Pediatriia,
A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
Hereditary deficiency of triosephosphate isomerase in four unrelated families.
June 1979, European journal of clinical investigation,
A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia.
June 1973, Blut,
A S SCHNEIDER, and W N VALENTINE, and M HATTORI, and H L HEINS
[HEREDITARY HEMOLYTIC ANEMIA WITH PYRUVATE-KINASE DEFICIENCY].
June 1964, Minerva medica,
Copied contents to your clipboard!