Interplay Between Drugs And Metabolism als von - 5 Angebote vergleichen

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Von Händler/Antiquariat, AHA-BUCH GmbH [51283250], Einbeck, Germany.
Neuware - Predicting the fate of a drug in a particular patient and the subsequent response is still a vision and far away from application in routine clinical practice .Drug metabolism was defined as the main process responsible for biotransformation of xenobiotics in the body to make them more water soluble and thus more readily excreted in the urine or bile. CYP450s are a major source of variability in drug metabolism. Of 57 attributive functional human CYPs only about a dozen enzymes, belonging to the CYP1, 2, and 3 families, are responsible for the biotransformation of most foreign substances including 70-80% of all drugs in clinical use. The current work was designed to pore over the effect of dexamethasone and fluconazole as CYP-450 inducer and inhibitor respectively, on the metabolism of some endogenous steroidal hormones. Furthermore, highlighting their reflection on the concerning parameters and investigating their effects on an exogenously administered steroid hormone. 164 pp. Englisch.

Lieferung aus: Deutschland, Versandkosten nach: Deutschland, Versandkostenfrei.
Von Händler/Antiquariat, Buchhandlung Hoffmann, [3174608].
Neuware - Predicting the fate of a drug in a particular patient and the subsequent response is still a vision and far away from application in routine clinical practice .Drug metabolism was defined as the main process responsible for biotransformation of xenobiotics in the body to make them more water soluble and thus more readily excreted in the urine or bile. CYP450s are a major source of variability in drug metabolism. Of 57 attributive functional human CYPs only about a dozen enzymes, belonging to the CYP1, 2, and 3 families, are responsible for the biotransformation of most foreign substances including 70-80% of all drugs in clinical use. The current work was designed to pore over the effect of dexamethasone and fluconazole as CYP-450 inducer and inhibitor respectively, on the metabolism of some endogenous steroidal hormones. Furthermore, highlighting their reflection on the concerning parameters and investigating their effects on an exogenously administered steroid hormone. 13.06.2017, Taschenbuch, Neuware, 220x150x10 mm, 261g, 164, Internationaler Versand, offene Rechnung (Vorkasse vorbehalten), sofortueberweisung.de, Selbstabholung und Barzahlung, Skrill/Moneybookers, PayPal, Lastschrift, Banküberweisung.

Lieferung aus: Deutschland, Versandkostenfrei.
Von Händler/Antiquariat, European-Media-Service Mannheim [1048135], Mannheim, Germany.
Publisher/Verlag: Noor Publishing | Predicting the fate of a drug in a particular patient and the subsequent response is still a vision and far away from application in routine clinical practice .Drug metabolism was defined as the main process responsible for biotransformation of xenobiotics in the body to make them more water soluble and thus more readily excreted in the urine or bile. CYP450s are a major source of variability in drug metabolism. Of 57 attributive functional human CYPs only about a dozen enzymes, belonging to the CYP1, 2, and 3 families, are responsible for the biotransformation of most foreign substances including 70-80% of all drugs in clinical use. The current work was designed to pore over the effect of dexamethasone and fluconazole as CYP-450 inducer and inhibitor respectively, on the metabolism of some endogenous steroidal hormones. Furthermore, highlighting their reflection on the concerning parameters and investigating their effects on an exogenously administered steroid hormone. | Format: Paperback | Language/Sprache: english | 164 pp.

Lieferung aus: Deutschland, Versandkosten nach: Deutschland, Versandkostenfrei.
Von Händler/Antiquariat, Syndikat Buchdienst, [4235284].
Predicting the fate of a drug in a particular patient and the subsequent response is still a vision and far away from application in routine clinical practice .Drug metabolism was defined as the main process responsible for biotransformation of xenobiotics in the body to make them more water soluble and thus more readily excreted in the urine or bile. CYP450s are a major source of variability in drug metabolism. Of 57 attributive functional human CYPs only about a dozen enzymes, belonging to the CYP1, 2, and 3 families, are responsible for the biotransformation of most foreign substances including 70-80% of all drugs in clinical use. The current work was designed to pore over the effect of dexamethasone and fluconazole as CYP-450 inducer and inhibitor respectively, on the metabolism of some endogenous steroidal hormones. Furthermore, highlighting their reflection on the concerning parameters and investigating their effects on an exogenously administered steroid hormone. 2017, Taschenbuch / Paperback, Neuware, H: 220mm, B: 150mm, 164, Internationaler Versand, Selbstabholung und Barzahlung, PayPal, offene Rechnung, Banküberweisung.

Lieferung aus: Deutschland, Versandfertig in 1 - 2 Werktagen, Versandkostenfrei.
Von Händler/Antiquariat, dodax-shop-eu.
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