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Researchers found two enzymes in Avicennia marina that help produce maslinic acid and corosolic acid, which have medicinal benefits.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

CYP154C7 enzyme can effectively modify steroids and is promising for commercial use.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

Researchers developed a method to identify and analyze cyclosporin compounds and their structures effectively.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

A new patch can deliver stable antibodies over time for potential HIV treatment.

The new skin patch with human matrix and antibiotic improves wound healing.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

The method accurately measures cyproterone acetate in plasma, showing no significant difference between two formulations.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

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A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

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Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Certain genetic markers may increase or decrease prostate cancer risk.

ALRN-6924 may prevent hair loss caused by chemotherapy.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.