By John Barranger
Organized into six sections constructed from 29 chapters, this ebook starts off with an outline of enzymes, activator proteins, and stabilizers that underlie lysosomal garage issues. It then discusses a few advancements in enzyme purification, receptors for glycoprotein enzymes, components that regulate endocytosis, and the intracellular destiny of lysosomal hydrolases. a few chapters clarify the enzyme biosynthesis, bone marrow transplantation, and enzyme substitute, in addition to mobile hybridization, chromosome localization, phenotype discrimination, and cloning of genes for human lysosomal enzymes.
This e-book is beneficial to biochemists, physiologists, pathologists, geneticists, scientific investigators, and working towards physicians occupied with the research, care, and remedy of sufferers with hereditary metabolic problems, in addition to undergraduate and graduate point scholars all in favour of examine during this discipline.
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Extra info for Molecular Basis of Lysosomal Storage Disorders
Molecular Basis of Lysosomal Storage Disorders by John Barranger