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- Identification of a Cyclosporine-Specific P450 Hydroxylase Gene through Targeted Cytochrome P450 Complement (CYPome) Disruption in Sebekia benihana
- A novel regio-specific cyclosporin hydroxylase gene revealed through the genome mining of <i>Pseudonocardia autotrophica</i>
- Integrating multi-omics analyses of Nonomuraea dietziae to reveal the role of soybean oil in [(4′-OH)MeLeu]4-CsA overproduction
- Functional characterization and unraveling the structural determinants of novel steroid hydroxylase CYP154C7 from Streptomyces sp. PAMC26508
- Structure-guided manipulation of the regioselectivity of the cyclosporine A hydroxylase CYP-sb21 from Sebekia benihana
- Transcriptome sequencing and identification of cytochrome P450 monooxygenases involved in the biosynthesis of maslinic acid and corosolic acid in <i>Avicennia marina</i>
- The Role of Cytochrome P-450 in Dermatology
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Baiting Proteins with C<sub>60</sub>
- Chapter 14 Principles of drug metabolism
- An Update of Congenital Adrenal Hyperplasia
- Pathways to inflammation: acne pathophysiology
- Nonclassic adrenal hyperplasia
- Enhancing 1α-Hydroxylase Activity with the 25-Hydroxyvitamin D-1α-Hydroxylase Gene in Cultured Human Keratinocytes and Mouse Skin
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- Disruptors of Androgen Action and Synthesis
- Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
- Metabolic pathways of eicosanoids—derivatives of arachidonic acid and their significance in skin
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Congenital adrenal hyperplasia
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Congenital Adrenal Hyperplasia
- Examination of Fluconazole-Induced Alopecia in an Animal Model and Human Cohort
- Epoxy Fatty Acids and Inhibition of the Soluble Epoxide Hydrolase Selectively Modulate GABA Mediated Neurotransmission to Delay Onset of Seizures
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Transcriptome sequencing reveals the key genes associated with hair follicle development in Qianhua Mutton Merino