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

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

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

The protein p21 is more abundant in normal skin cells than in melanoma cells and may help protect against melanoma, with UVB light affecting its levels.

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

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

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

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Modulating Cytochrome P450 activity could help develop new skin disease treatments.

A new method accurately measures clobetasol propionate in hair and skin.

The prototype for analyzing skin aging works technically and clinically.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

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

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Lack of functional CYLD in mice leads to early aging and cancer.

Foreskin keratinocytes and SVK14 cells express certain cytochrome P450 enzymes, unlike hair follicle keratinocytes.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

CTIP2 may help in skin development and maintenance.

CTCF protein is essential for skin and hair follicle development in mice.

Scientists made two new chemicals that might help treat diseases caused by male hormones.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Vitamin C derivative may promote hair growth by activating specific genes.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Certain gene changes and hormone levels are linked to female hair loss.

Scientists made all eight versions of a compound called cyoctol, but found it's not an anti-androgen and it fully breaks down in the skin.

Aromatase gene variation may increase female hair loss risk.

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

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

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