Titlebook: Inflammatory Diseases and Copper; The Metabolic and Th John R. J. Sorenson Book 1982 The Humana Press Inc. 1982 Amino acid.Arthritis.Lipid.

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Wilson’s Diseaseefect in copper metabolism. This defect which is inherited in autosomal recessive fashion, results in the accumulation of excessive amounts of copper, first in the liver and subsequently in the brain, kidneys, eyes, erythrocytes and other tissues where toxic concentrations of copper cause pathologic

膽汁

dragon

Intestinal Content of the Copper-Binding Protein in Brindled, Blotchy and Crinkled Mice and Cellularf an equilibrated chromatographic column procedure. Brindled (Mo.) mice exhibited higher CuBP content when very young (2-3 days); thereafter their CuBP dropped below that of the controls, perhaps because of diminished growth and development prior to death at 11 days. Blotchy (Mo.) mice also exhibite

Veneer

平靜生活

An Appraisal of Current Human Copper Nutriturer incomprehensible. The comprehensible class was divided further into toxic, hereditary, infectious and deficiency diseases. I stated that.I think this statement applies equally well to some of the diseases under consideration in this symposium. Further consideration and contemplation have led me to

愛國(guó)者

Hormonal Regulation of Copper and Zinc Metabolism in Isolated Rat Liver Parenchymal Cellslic processes. Since the liver plays such a critical role in the metabolism of trace elements, some years ago we initiated a project wherein the metabolism of trace elements was examined at the level of the isolated rat liver parenchymal cell. This approach has proved to be of immense importance in

Peristalsis

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Lysyl Oxidase, a Molecular Target of Copper afflicted tissues. One such enzyme is lysyl oxidase. This copper-metalloenzyme plays a key role in the maturation of connective tissue proteins. The enzyme catalyzes formation of the crosslinking compounds that bind together the peptide chains of collagen and elastin and in so doing impart both sup

拱墻

Cu-Zn Superoxide Dismutasee, EC 1.15.1.1) is believed to be present in all oxygen metabolizing cells. Each type is distinguished by its amino acid sequence and each contains different prosthetic metals, Cu, Zn-, Fe-, and Mn-enzyme (2-5). This enzyme catalyzes the reaction . (6). There is considerable evidence that this enzym