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Alpha-Keto Acid Dehydrogenase Complexes

Alpha-Keto Acid Dehydrogenase Complexes
Author: M.S. Patel
Publisher: Birkhäuser
Total Pages: 321
Release: 2012-12-06
Genre: Science
ISBN: 303488981X

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Found in all organisms, the alpha-keto acid dehydrogenase complexes have central roles in cellular metabolism and are major sites of regulation. The understanding of the organization, function and regulation of these quintessential multienzyme complexes has been greatly advanced by studies employing molecular biology and biophysical techniques. Although these enzyme systems have some features in common, their diversity in fulfilling unique organism - or tissue - specific roles is truly amazing. These systems have medical importance in areas ranging from defects in regulation (linked to diabetes, heart disease, obesity, nutrition defects), to inherited diseases (inborn errors, maple syrup urine disease) to acquired immune diseases (primary biliary cirrhosis). This book brings together wide-ranging recent findings on the structure(function relationships, gene regulation, and genetic defects of the alpha-keto acid dehydrogenase complexes, namely the pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase and the branched-chain alpha-keto acid dehydrogenase complexes. A wide variety of experimental approaches together with new results presented in this book should serve as a resource for beginning to established investigators in the field as well as scientists who are interested in mitochondria, dehydrogenases, kinases, phosphatases, lipoic acid, thiamine pyrophosphate, and enzyme complexes.


Alpha-keto Acid Dehydrogenase Complexes

Alpha-keto Acid Dehydrogenase Complexes
Author: Thomas E. Roche
Publisher:
Total Pages: 474
Release: 1989
Genre: Alpha-keto acid dehydrogenase complexes
ISBN:

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Branched-chain Amino Acids

Branched-chain Amino Acids
Author: Robert Allison Harris
Publisher: Academic Press
Total Pages: 587
Release: 2000
Genre: Amino Acids
ISBN: 0121822257

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Volume 324 of Methods in Enzymology supplements Volume 166. It includes genetic information (cloning, gene expression) and information on human genetic diseases not available when Volume 166 was published.


Inborn Metabolic Diseases

Inborn Metabolic Diseases
Author: K. Tada
Publisher: Springer Science & Business Media
Total Pages: 421
Release: 2013-03-14
Genre: Medical
ISBN: 3662031477

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Each disease-related chapter begins with a detailed description of the patient and the delineating symptoms used for establishing the diagnosis and differential diagnosis. The highly detailed figures illustrate the metabolic derangement in a uniform way, together with essential aspects of the genetics involved, thus affording clarification and better understanding of the treatment. Topics covered range from general aspects such as the clinical approach, emergency treatment, diagnostic procedures, and psychosocial care for the child and the family, to specific discussions of new modes of treatment, including liver, bone marrow transplantation and somatic gene therapy.


Lipoic Acid

Lipoic Acid
Author: Mulchand S. Patel
Publisher: CRC Press
Total Pages: 558
Release: 2008-03-17
Genre: Medical
ISBN: 1420045393

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The recognition of oxidative stress as a major factor in health, aging, and disease has led to a surge in research aimed at uncovering effective countermeasures in the form of antioxidants. Unique in its two-fold protective function, alpha-lipoic acid has drawn unprecedented interest as a coenzyme in mitochondrial energy metabolism and as an antiox


Progressive Brain Disorders in Childhood

Progressive Brain Disorders in Childhood
Author: Juan M. Pascual
Publisher: Cambridge University Press
Total Pages: 507
Release: 2017-04-20
Genre: Medical
ISBN: 1107042054

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A review of childhood neurodegenerative and other progressive but non-degenerative disorders to guide their diagnosis and management.