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WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

DRDE-07 shows promise for treating skin diseases due to its favorable properties.

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

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Finasteride helps female-pattern hair loss.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Different parts of the nail express different keratins, showing unique patterns of differentiation.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

DHEA therapy improved pubic hair growth and psychological well-being in young females with adrenal insufficiency.

New genes and pathways are important for testosterone production and male sexual development.

The inhibitor DPP can promote hair growth.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

The treatments stopped hair regrowth in mice.

DPR can cause skin, hair, and nail issues, sometimes appearing later in life.

A reliable method was created to measure dutasteride and related molecules in capsules.

High doses of dihydroartemisinin caused reversible liver toxicity in rats, with females more affected than males.

The Shaven mutation in mice affects hair growth and causes a greasy coat due to abnormal lipid content.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

The Greek DCQ is a reliable and valid tool for assessing dysmorphic concern.

A new platinum complex was made and studied, which might help fight cancer better.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.