By John Barranger
Organized into six sections constructed from 29 chapters, this ebook starts with an summary of enzymes, activator proteins, and stabilizers that underlie lysosomal garage problems. It then discusses a few advancements in enzyme purification, receptors for glycoprotein enzymes, elements 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 cellphone hybridization, chromosome localization, phenotype discrimination, and cloning of genes for human lysosomal enzymes.
This e-book is beneficial to biochemists, physiologists, pathologists, geneticists, medical investigators, and practising physicians fascinated by the research, care, and remedy of sufferers with hereditary metabolic problems, in addition to undergraduate and graduate point scholars all for study during this discipline.
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