Copper Transport and Its Disorders | Molecular and Cellular Aspects. Questo articolo non è disponibile.Copper Transport and Its Disorders | Molecular and Cellular Aspects

The history of biological research into copper dates from the latter half of the last century when the presence of copper as a component of living systems was first noted, but it was not until the 1920s that the essential role of copper was first recognized.

Introductory Chapter; J.F.B. Mercer, A. Leone. Copper Transport in Mammals; M.C. Linder, et al. Models to Evaluate Health Risks Derived from Copper Exposure/Intake in Humans; M. Olivares, et al. Cu Metabolism in the Liver; H.J. McArdle, et al. Multiple Forms of the Menkes Cu-ATPase; E.D. Harris, et al. The Cell Biology of the Menkes Disease Protein; M.J. Petris, et al. Functional Analysis of the Menkes Protein (MNK) Expressed from a cDNA Construct; S. La Fontaine, et al. Mutation Spectrum of ATP7A the Gene Defective in Menkes Disease; Z. Tümer, et al. Animal Models of Menkes Disease; J.F.B. Mercer, et al. Developmental Expression of the Mouse Mottled and Toxic Milk Genes; Y.-M. Kuo, et al. The Treatment of Wilson¿s Disease; G.J. Brewer. Indian Childhood Cirrhosis and Tyrolean Childhood Cirrhosis: Disorders of a Copper Transport Gene? M.S. Tanner. Animal Models of Wilson¿s Disease; J.McC. Howell. Copper-Binding Properties of the N-Terminus of the Menkes Protein; P. Cobine, et al. Expression, Purification, and Metal Binding Characteristics of the Putative Copper Binding Domain from the Wilson Disease Copper Transporting ATPase (ATP7B); M. DiDonato, et al. 9 additional chapters. Index.