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A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

Eyebrow follicles are best for accurate genetic testing after stem cell transplants.

Some postmenopausal women with frontal fibrosing alopecia stopped losing hair with finasteride treatment, hinting at a possible hormonal cause.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Bcl-2 affects hair growth and pigmentation by controlling cell death.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Four genes affect hair follicle density in goats.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Different types of fibroblasts play various roles in both healthy and diseased tissues, and understanding them better could improve treatments for fibrotic diseases.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Sex steroids affect the MafB gene differently in male and female hamsters.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Compound 6 is a promising candidate for better wound healing.

Stressed fibroblasts greatly increase melanin production in hair, skin, and eye cells, mainly due to a growth factor called bFGF.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Frontal fibrosing alopecia often occurs after menopause, with delayed diagnosis and possible links to certain medications and conditions.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

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

Scalp hair follicle cells help protect and heal skin in certain skin conditions.

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

Finasteride may affect female fertility by altering gene activity.