Proceedings: Alterations of the level of cyclic AMP in mouse epidermis after stimulation with tumor-promoting phorbol esters.
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Animals↗
Biomedical subjects
F Marks
Publications and source records attributed to F Marks.
Proceedings: Effect of fetal calf serum and epidermal growth factor on DNA synthesis in explants of chick embryo epidermis.
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Animals↗
The second messenger system of mouse epidermis. 3. Guanyl cyclase.
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Animals↗
A tissue-specific factor inhibiting DNA synthesis in mouse epidermis.
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Animals↗
Diurnal fluctuation and -adrenergic elevation of cyclic AMP in mouse epidermis in vivo.
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Adenylyl Cyclases↗
The second messenger system of mouse epidermis. I. Properties and -adrenergic activation of adenylate cyclase in vitro.
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Adenylyl Cyclase Inhibitors↗
Cyclic 3', 5'-AMP and theophylline inhibit epidermal mitosis in G2-phase.
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Animals↗
[Chalonic inhibitors of epidermal DNA synthesis].
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Animals↗
[Circadian variation and -adrenergic increase of cAMP level in the mouse epidermis].
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Animals↗
[Influence of the phorbol ester TPA on the beta adrenergic activation of epidermal adenylcyclase and the cAMP level in the mouse epidermis].
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Adenylyl Cyclases↗
Disturbance by tumor promotors of epidermal growth control (chalone mechanism).
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Alcohols↗
Direct evidence of two tissue-specific chalone-like factors regulating mitosis and DNA synthesis in mouse epidermis.
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Animals↗
Isotope content of oligonucleotides of nuclear and nucleolar RNA of rat liver.
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Animals↗
[Biochemistry and cancer. Molecular biologic attempts of understanding malignant growth].
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Carcinogens↗
Metabolism and mechanism of action of oestrogens. XII. Structure and mechanism of formation of water-soluble and protein-bound metabolites of oestrone in rat-liver microsomes in vitro and in vivo.
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Amines↗
[Metabolism and mechanism of action of estrogens. XI. Metabolism of (4-14C)2-hydroxy-estrone in rat liver microsomes].
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Air↗
[Metabolism and mechanism of action of estrogens. X. Relations between estrogen metabolism and lipid peroxidation in rat liver microsomes].
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Animals↗
[Preparation of biochemically interesting thioethers of estrogens. I. 2- and 4-(carboxymethylmercapto)estrone-3-methyl ether].
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Alkylation↗