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- Rational Design of CYP3A4 Inhibitors: a One-Atom Linker Elongation in Ritonavir-Like Compounds Leads to a Marked Improvement in the Binding Strength
- Inhibition of CYP1A2 and CYP3A4 by Oltipraz Results in Reduction of Aflatoxin B1 Metabolism in Human Hepatocytes in Primary Culture'
- Physiology of Mineralocorticoids and Regulation by the Renin-Angiotensin- Aldosterone System………………………………………………………………
- Genetic Polymorphisms of CYP2C9, CYP2C19, CYP2D6, CYP3A4, and CYP3A5 in Vietnamese-Koreans
- Pdf) and May Also Be Used to Inform Experimental Design
- 46,XX DSD Due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features
- 3 INSPRA Eplerenone Tablets DESCRIPTION INSPRA Contains Eplerenone, a Blocker of Aldosterone Binding at the Mineralocorticoi
- Clinical Role of CYP2C19 Polymorphisms in Patients With
- Analysis of Human Cyp51 Inhibitors”
- CYP450 Interactions Between Illicit Substances and Prescription Medications
- Hydroxylase Gene Transcription and Bile Acid Synthesis In
- Descriptors of Cytochrome Inhibitors and Useful Machine Learning Based Methods for the Design of Safer Drugs
- Comparison of Lanosterol-14Α-Demethylase
- A Computational Study of the Substrate Conversion and Selective Inhibition of Aldosterone Synthase
- P450-Glo™ Assays
- Pharmacogenomics of CYP2C9: Functional and Clinical Considerations†
- Effect of Dietary Flavonoids on Hepatic CYP2E1 and 3A4 Activity
- Factors Influencing the Magnitude and Clinical Significance of Drug Interactions Between Azole Antifungals and Select Immunosuppressants
- Steroid Pathways Spironolactone84, Dexamethasone85, Adrenal Gland (+) 86 84 87 Ketoconazole29, Bile Acid , St
- A Review of the Important Role of CYP2D6 in Pharmacogenomics
- Metabolism of Oral Turinabol by Human Steroid Hormone–Synthesizing Cytochrome P450 Enzymes
- Suicide, Depression, and CYP2D6: How Are They Linked?
- An Update on Vitamin D Metabolism
- 3 Overview of Vitamin D
- Steroidogenesis Enzyme Inhibitors in Cushing's Syndrome
- Cytochromes P450
- Effect of the Most Relevant CYP3A4 and CYP3A5 Polymorphisms on The
- Regulation of Vitamin D 25-Hydroxylases
- Human Lanosterol 14-Alpha Demethylase (CYP51A1) Is a Putative Target for Natural Flavonoid Luteolin 7,30-Disulfate
- Grapefruit Juice Furanocoumarins and P450 Cytochrome Cyp3a4
- Bile Acids, Nuclear Receptors and Cytochrome P450
- Inhibition of Placental CYP19A1 Activity Remains As a Valid
- CYP2R1 Is a Major, but Not Exclusive, Contributor to 25-Hydroxyvitamin D Production in Vivo
- CYP3A4 Induction by Rifampin: an Alternative Pathway for Vitamin D Inactivation in Patients with CYP24A1 Mutations
- In Vitro Inhibition of Human CYP1A2, CYP2D6, and CYP3A4 by Six Herbs Commonly Used in Pregnancy
- Role of Human Cytochrome P450 3A4 in Metabolism of Medroxyprogesterone Acetate
- Hepatic Activation and Inactivation of Clinically-Relevant Vitamin D Analogs and Prodrugs
- The Influence of Biological Sex and Sex Hormones on Bile Acid
- Screening of Human CYP1A2 and CYP3A4 Inhibitors from Seaweed in Silico and in Vitro
- CYP51) Enzyme Required for Synthesis of Antimicrobial Triterpenes in Plants