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Cyclohexyl salicylate promotes human hair growth and increases certain hair follicle stem cell progeny.

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

Drospirenone can hide symptoms of certain hormonal disorders, complicating diagnosis.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

The hydrogel effectively treats hair loss using light to release nitric oxide.

Hsc70 protein may influence hair growth by responding to androgens.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

NFIC helps rat dental cells grow and turn into bone-like cells.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Canine hair follicle cells show stem cell properties, aiding hair growth.

A PEG-400/oleic acid mixture best improves drug delivery monitoring through hair follicles.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

11α-Hydroxyprogesterone is changed into different substances by certain enzymes and may play a role in prostate cancer.

The study developed a reliable method to measure active ingredients in hair nourisher products using HPLC.

Human hair follicle organ culture is a useful model for hair research with potential for studying hair biology and testing treatments.

A child with rough nails also had hair loss and allergies.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

Calanthoside may help hair growth by boosting cell proliferation.

ZO-1 helps hair follicle stem cells renew better by changing their structure.

H19 may help cause PCOS by affecting CTGF levels, suggesting a new treatment target.

Hoxc13 gene is essential for hair, nail, and papilla development.

"20-nail dystrophy" can have multiple causes.

Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.