Zobrazeno 1 - 10
of 55
pro vyhledávání: '"R.G. Slee"'
Publikováno v:
Clinica Chimica Acta. 103:169-173
Human liver phosphofructokinase has been isolated in order to obtain antibodies against human liver phosphofructokinase. With the antiserum it could be shown in human liver that two types of phosphofructokinase exist with no subunits in common. Leuco
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 754:238-242
Peroxidized linoleic acid (13 OOH) induces lipid peroxidation, measured as malondialdehyde in erythrocyte ghosts and intact erythrocytes. This process can be inhibited by desferal, thiourea and butylated hydroxytoluene. During the lipid peroxidation
Autor:
Johan F. Koster, R.G. Slee
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 620:489-499
1. 1. The NADPH-dependent lipid peroxidation process was studied with microsomes and also the effects of addition of Superoxide dismutase, catalase and thiourea. Only catalase and thiourea were able to inhibit lipid peroxidation. It seems that the in
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 710:230-235
1. 1. The formation of malondialdehyde by intact hepatocytes, induced by ADP/Fe3+ or cumene hydroperoxide, can be inhibited by the addition of thiourea. This may indicate that hydroxyl radicals are involved in this process. 2. 2. Lipid peroxidation o
Autor:
A. Edixhoven-Bosdijk, M. A. Alleman, M.J. Kroos, Johan F. Koster, R.G. Slee, Henk G. van Eijk, J. H. P. Wilson
Publikováno v:
Biochemical Pharmacology. 34:161-166
Hexachlorobenzene (HCB) induces a porphyria characterized by a diminished activity of the enzyme uroporphyrinogen decarboxylase (URO-D), presumably due to inactivation by reactive metabolites of HCB. We studied the effect of iron on HCB porphyria in
Autor:
Johan F. Koster, R.G. Slee
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Enzymology. 482:89-97
1. Albumin activates human liver acid alpha-glucosidase (alpha-D-glucoside hydrolase, EC 3.2.1.20). From the Arrhenius plot, pH-dependence and Lineweaver-Burk plots it can be concluded that this activation is not only due to stabilisation of the enzy
Publikováno v:
Clinica Chimica Acta. 94:229-235
Three patients with myophosphorylase deficiency were investigated. Two had no detectable activity, while one had 1% residual activity. The patient with 1% residual activity had 40% of the normal amount of myophosphorylase protein. No myophosphorylase
Publikováno v:
Clinica Chimica Acta. 51:319-325
The acid maltase activities of human lymphocytes and polymorphonuclear cells from controls and patients suffering from Pompe's disease, have been investigated. The effect of antibody against human liver acid maltase on leucocyte acid maltase was stud
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 715:63-69
A biochemical study was performed in a Lapland dog suspected of glycogen storage disease type II (acid α-glucosidase deficiency, Pompe's disease). Glycogen content was substantially elevated in heart and skeletal muscle but not in the liver. Severly