The use of liver extract in dermatology.
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Dermatology↗
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Results for “Liver Extracts”
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[Standardization of liver extracts in animals].
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Animals↗
[Polarographic determination of riboflavin in liver extracts].
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Humans↗
[Enzymic deamination of 5'-desoxycytidylic acid and 5-methyl-5'-desoxycytidylic acid in the presence of rabbit liver extracts].
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Animals↗
Growth retardant properties of liver extract.
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Animals↗
[The behavior of the sulfobromophthalein chromoelimination curves subjects with ethylic hepatopathy treated with a liver extract enriched with nucleosides of the pyrimidine series and ith cyanocobalamine].
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Alcoholism↗
Inhibition of DNA synthesis in ascites hepatoma cells by normal liver extract.
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Animals↗
[Protection of liver by a cortico-vitamin-liver extract combination and cobamamide].
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Adrenal Glands↗
[Presence of an activator of glycolysis in liver extracts; its relation to vitamin B13].
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Glycolysis↗
[Some factors effecting the microbiological titration of vitamin B 12 in medicinal solutions and liver extracts].
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Corrinoids↗
Axenic cultivation of the parasitic nematode, Neoaplectana glaseri, in a fluid medium containing raw liver extract.
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Animals↗
[Vitamin complex with antianemic action in liver extracts].
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Corrinoids↗
[Influence of liver extract on the development of hepatoma in rats fed butter yellow].
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Animals↗
Relapse during treatment of pernicious anaemia with refined liver extract.
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Anemia↗
Maintenance treatment of pernicious anaemia by injections of liver extract.
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Anemia↗
[Treatment of severe alcoholic cirrhosis with lyophilized liver extract].
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Alcoholism↗
Microbiological assay of vitamin B 12 and its role in evaluation of liver extracts.
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Biological Assay↗
The mechanisms of the inhibitory effects of liver extract on lymphocyte proliferation. III. The effects of arginase on DNA polymerase activities.
The incorporation of labeled precursors into DNA, RNA and protein in phytohaemagglutinin (PHA)-prestimulated human lymphocytes was maximally inhibited by liver extract (LEx) or arginase at 24 h. The activities of DNA polymerase alpha, beta and gamma were less inhibitable by these agents than was [3H]thymidine incorporation. The inhibition of DNA, RNA and protein syntheses by either LEx or arginase is probably due to arginine depletion by arginase activity, since their syntheses were similarly inhibited when cultured in an arginine-free medium in the absence of arginase. These results indicate that arginase nonspecifically inhibits the activities of DNA polymerase. The inhibition is probably due to arginine depletion.
Animals↗