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Biotransformation is the metabolic conversion of endogenous and xenobiotic chemicals to more water-soluble compounds. Xenobiotic biotransformation is accomplished by a limited number of enzymes with broad substrate specificities. Liver is considered to be the main center of detoxification. The result of biotransformation in most cases is detoxification; nevertheless, metabolism of some xenobiotics produces metabolites more reactive than their substrate compound and leads to harmful changes. The biotransformation system involves several enzyme systems that are commonly divided into two phases. Phase I enzymes are responsible for oxidation, reduction or hydrolysis and can be either detoxifying or activating. Phase II enzymes exert mainly detoxifying potential by conjugation. The cytochrome P450 enzyme superfamily, including CYP1A1 and CYP2E1 constitutes the majority of Phase I enzymes, while the microsomal epoxide hydrolase (mEH), N-acetyl transferases (NATs) and Glutathione S-Transferases are phase II enzymes primarily responsible for detoxification of xenobiotics. Accumulating data suggest that genetic polymorphisms in genes controlling carcinogen metabolism is responsible for the individual variations in cancer risk. From the broad literature available, the current book project summarizes the role specific polymorphisms in genes encoding xenobiotic metabolism, in predisposing the individuals to various cancers.

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Dr.L.V.K.S. Bhaskar, born on August 16, 1974, at Nellore district of the Indian state of Andhra Predesh, it was dedication, hard work and intelligence which rose Dr Bhaskar to a level of the Senior Scientist in Sickle Cell Institute Chhattisgarh, Raipur. Dr. Bhaskar has obtained his Bachelor’s Degree in Sciences (B.Sc.) in 1994 and Masters degree (M.Sc. Zoology) in 1996. He was a Junior Research Fellowship (JRF) of U.G.C. in 1998 and Senior Research Fellowship (SRF) of DST in 2000. Dr.Bhaskar was awarded Ph.D. in 2002 by the Sri Venkateswara University or his work in the area of comparative animal Physiology.

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Paperback. Condizione: new. Paperback. Biotransformation is the metabolic conversion of endogenous and xenobiotic chemicals to more water-soluble compounds. Xenobiotic biotransformation is accomplished by a limited number of enzymes with broad substrate specificities. Liver is considered to be the main center of detoxification. The result of biotransformation in most cases is detoxification; nevertheless, metabolism of some xenobiotics produces metabolites more reactive than their substrate compound and leads to harmful changes. The biotransformation system involves several enzyme systems that are commonly divided into two phases. Phase I enzymes are responsible for oxidation, reduction or hydrolysis and can be either detoxifying or activating. Phase II enzymes exert mainly detoxifying potential by conjugation. The cytochrome P450 enzyme superfamily, including CYP1A1 and CYP2E1 constitutes the majority of Phase I enzymes, while the microsomal epoxide hydrolase (mEH), N-acetyl transferases (NATs) and Glutathione S-Transferases are phase II enzymes primarily responsible for detoxification of xenobiotics. Accumulating data suggest that genetic polymorphisms in genes controlling carcinogen metabolism is responsible for the individual variations in cancer risk. From the broad literature available, the current book project summarizes the role specific polymorphisms in genes encoding xenobiotic metabolism, in predisposing the individuals to various cancers. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. Codice articolo 9781534786523

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