New Developments in Fatty Acid Oxidation

Inbunden, Engelska, 1992

Del 158 i serien Progress in Clinical and Biological Research

7 402 kr

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Beskrivning

Reflects the rapid development of research in this area of intermediary metabolism. Comprehensive and up-to-date, it brings together recent clinical, biochemical and molecular advances in mitochondrial and peroxisomal fatty acid oxidation. Coverage includes novel enzymes, molecular control of fatty acid oxidation in both normal and disease states, treatment of inherited fatty acid oxidation defects and much more.

Produktinformation

Utgivningsdatum:1992-09-16
Mått:160 x 235 x 40 mm
Vikt:1 191 g
Format:Inbunden
Språk:Engelska
Serie:Progress in Clinical and Biological Research
Antal sidor:600
Förlag:John Wiley & Sons Inc
ISBN:9780471561446

Utforska kategorier

Mer om författaren

Paul M. Coates is director of the Office of State and Local Government Programs and associate professor of public policy and administration in the Department of Political Science at Iowa State University.

Innehållsförteckning

Biogenesis of Enzymes and Organelles. Enzymology of Beta Oxidation. Molecular Biology of Mitochondrial and Peroxisomal Beta OxidationEnzymes. Metabolic Pathways. Clinical Aspects of Mitochondrial and Peroxisomal Beta OxidationDefects. Genetics and Molecular Basis of MCAD Deficiency. Molecular Defects of Peroxisomal and Mitochondrial Beta OxidationEnzymes.

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Results that Matter

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New Developments in Fatty Acid Oxidation

AvPaul M. Coates,Kay Tanaka

Inbunden, Engelska, 1992

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Produktinformation

Utgivningsdatum:1992-09-16
Mått:160 x 235 x 40 mm
Vikt:1 191 g
Format:Inbunden
Språk:Engelska
Serie:Progress in Clinical and Biological Research
Antal sidor:600
Förlag:John Wiley & Sons Inc
ISBN:9780471561446

Utforska kategorier

Mer om författaren

Innehållsförteckning

Biogenesis of Enzymes and Organelles. Enzymology of Beta Oxidation. Molecular Biology of Mitochondrial and Peroxisomal Beta OxidationEnzymes. Metabolic Pathways. Clinical Aspects of Mitochondrial and Peroxisomal Beta OxidationDefects. Genetics and Molecular Basis of MCAD Deficiency. Molecular Defects of Peroxisomal and Mitochondrial Beta OxidationEnzymes.