Results 141 to 150 of about 2,031 (187)
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Triose phosphate isomerase deficiency

Biochemical Medicine, 1977
Abstract Three patients with triose phosphate isomerase deficiency have been studied. 1. (a) A profound deficiency was found in red blood cells, white blood cells, and fibroblasts of the patients. 2. (b) Extracts from leukocytes and fibroblasts showed a marked decrease in thermal stability. 3. (c) The electrophoretic mobility of the major
H, Skala   +4 more
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Lacto‐N‐triose I und Lacto‐N‐triose II

Chemische Berichte, 1956
AbstractDie beiden N‐haltigen Trisaccharide, die bei partieller Säurehydrolyse des Tetrasaccharids der Frauenmilch gebildet werden, ließen sich kristallisiert gewinnen und durch schöne Phenylosazone kennzeichnen. Ihr Verhalten gegen Enzyme und gegen verd. Alkali steht in Übereinstimmung mit den bereits ermittelten Konstitutionsformeln.
Kuhn, R., Gauhe, A., Baer, H.
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Kinetic study of aldolization reactions of trioses

Collection of Czechoslovak Chemical Communications, 1975
J. Königstein, M. Fedoroňko
exaly   +2 more sources

Versuche mit Triose‐Redukton

Chemische Berichte, 1955
AbstractDas Triose‐Redukton OCH‐C(OH)CH(OH) verhält sich gegen aromatische primäre und sekundäre Amine als α‐Oxy‐malondialdehyd, indem es je nach den Reaktionsbedingungen Monoanile, Dianilbasen oder Dianilsalze bildet. Die Konstitution und die wechselseitigen Umwandlungen dieser “Anile” werden besprochen.
Bernd Eistert   +2 more
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Isolation of triose phosphate isomerase from the lens

Experimental Eye Research, 1968
The glycolytic enzyme, triose phosphate isomerase, has been purified and crystallized from bovine lens. The lens enzyme resembles the enzyme from rabbit muscle in its catalytic activity, and in its crystalline form. The electrophoretic mobility of the enzyme from bovine lens differs from that of the enzyme from rabbit muscle.
P M, Burton, S G, Waley
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Triose phosphate isomerase deficiency: Prenatal diagnosis

The Journal of Pediatrics, 1985
A child with triose phosphate isomerase deficiency has congenital nonspherocytic hemolytic anemia, mental subnormality, motor impairment, growth failure, and cardiac failure. The deficiency state is characterized by moderately reduced red cell triose phosphate isomerase activity and marked instability of the abnormal enzyme to heat.
A C, Clark, M A, Szobolotzky
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Purification and properties of liver triose phosphate isomerase

Biochimica et Biophysica Acta (BBA) - Enzymology, 1971
Abstract Triose phosphate isomerase ( d -glyceraldehyde-3-phosphate ketol-isomerase, EC 5.3.1.1) was prepared from horse and human livers with specific activities of 3 183 and 2 397 I.U./mg, respectively. The molecular weights of the human liver isomerase and the corresponding rabbit muscle enzyme were not significantly different.
E W, Lee   +3 more
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Triose phosphate isomerase deficiency: Report of a family

Journal of Paediatrics and Child Health, 1986
AbstractTriose phosphate isomerase (TPI) deficiency is associated with a syndrome of congenital non‐spherocytic haemolytic anaemia, mental subnormality, motor impairment, growth failure and cardiac failure. The deficiency state is characterized by moderately reduced red cell TPI activity, and marked instability of the abnormal enzyme to heat.
A C, Clark, M A, Szobolotzky
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Pea seed triose phosphate isomerase

Phytochemistry, 1979
Abstract Triose phosphate isomerase was purified ca 250-fold from pea seed extracts. The k m for D -glyceraldehyde-3-P was 0.44 mM and for dihydroxyacetone-P, 0.88 mM. P-enolpyruvate, 2-P-glycerate, 3-P-glycerate and 2-P-glycolate were strongly inhibitory. Pi and arsenate also inhibited pea seed triose phosphate isomerase.
J.David Tomlinson, John F. Turner
openaire   +1 more source

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