Biomedical subjects
F O Simpson
Publications and source records attributed to F O Simpson.
The use of p-phenylenediamine in the block to enhance osmium staining for electron microscopy.
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Tricyclic antidepressants and the vascular system.
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Practolol treatment in asthmatics.
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Surface features of smooth muscle cells from the mesenteric artery and vas deferens.
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Freeze-etch studies on the innervation of mesenteric arteries and vas deferens.
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Combination antihypertensive therapy.
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Hypertension and depression: interrelated problems in therapy.
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Freeze-etch studies on fish skeletal muscle.
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Intensification of osmium staining by p-phenylenediamine: paraffin and epon embedding; lipid granules in renal medulla.
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Renal vasculature and hypertensive mechanisms. Histological aspects.
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Fenfluramine in obese patients on various antihypertensive drugs. Double-blind controlled trial.
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Ultrastructure of desmosomes in mammalian intercalated disc; appearances after lanthanum treatment.
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Myofilaments in frozen-etched muscle.
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The relationship between the transverse tubular system and other tubules at the Z disc levels of myocardial cells in the ferret.
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Localization of tritiated norepinephrine in vascular sympathetic axons of the rat intestine and mesentery by electron microscope radioautography.
The distribution of infused tritiated norepinephrine (NE-(3)H) in small mesenteric arteries and intestinal arterioles in rats was investigated with electron microscopic radioautography. Silver grains, indicating the presence of the tritium label on the sections, were found lying mainly over axon bundles, but some were present over collagen and smooth muscle cells. Axons with the highest concentrations of silver grains had been sectioned at points where they were naked of Schwann cell sheath, were dilated into varicosities, and contained small granular vesicles. This finding was taken as confirmatory circumstantial evidence that the small granular vesicles were the sites of uptake and storage of NE. The short interval between the start of infusion and the fixation of the tissue appeared to rule out any process other than a direct uptake of NE by the peripheral axons. If axonal sites of uptake of NE-(3)H correspond to sites of release of NE, then the evidence suggests that such sites of release are widespread over the terminal part of the axon and are not confined to those parts of the axon which are in close contact with smooth muscle cells. Since the fixation and embedding procedures will remove NE which is not strongly bound to tissues, the localization of NE-(3)H in the radioautographs does not necessarily correspond to the distribution of all the NE present in vivo.
Surface features of striated muscle. I. Guinea-pig cardiac muscle.
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Surface features of striated muscle. II. Guinea-pig skeletal muscle.
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