Zobrazeno 1 - 10
of 51
pro vyhledávání: '"ALA synthetase"'
Publikováno v:
Anesthesia & Analgesia. 80:591-599
Four hereditary types of porphyria are now classified as acute porphyrias. Enzymatic defects result in accumulation of porphyrin precursors (usually ALA and PGB). The quantity of these precursors may be normal or slightly increased in latent periods
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Publikováno v:
Archives of Biochemistry and Biophysics. 138:155-159
Two types of ALA synthetase, Fraction I and Fraction II, were estimated in the cells of R. spheroides 2 which were incubated at several different environmental conditions. ALA synthetase activity in the light-anaerobically grown cells was about three
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Autor:
Arthur Rosenberg, O. Marcus
Publikováno v:
British Journal of Haematology. 26:79-83
Summary. Δ-aminolaevulinic acid (ALA) synthetase activity was determined in reticulocyte mitochondria of rabbits before and while receiving 30–40 mg of chloramphenicol per kilogram per day. Maintenance of chloramphenicol at this dosage caused a 50
Publikováno v:
American Journal of Hematology. 12:63-67
A female infant with congenital refractory sideroblastic anemia is described. A marked reduction of delta-aminolevulinic acid (ALA) synthetase activity of erythroblasts was noticed with and without treatment of pyridoxal phosphate. Mitochondrial neut
Autor:
Robert A. Neal, Takemi Yoshida
Publikováno v:
Biochemical Pharmacology. 27:2095-2098
Thiocetamide and one of its metabolites, thioacetamide- S -oxide, were shown to inhibit δ-aminolevulinic acid (ALA) synthetase when administered in vivo to adult male mice. Thioacetamide and thioacetamide- S -oxide also inhibited the 3,5-dicarboetho
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 60:212-215
N-Methylprotoporphyrin has been shown to markedly inhibit ferrochelatase activity in chick embryo liver cell culture without inducing δ-aminoievulinic acid (ALA) synthetase activity. This result supports the idea that the effects of 3,5-diethoxycarb
Publikováno v:
Toxicology Letters. 2:123-128
Effect of host-mediating anti-tumor drugs, OK-432 and PSK, on hepatic δ-aminolevulinic acid synthetase (ALA synthetase) and heme oxy genase activity was examined. Both OK-432 and PSK were shown to inhibit ALA synthetase activity when administered in
Autor:
Jenny D. Clement-Metral
Publikováno v:
FEBS Letters. 101:116-120