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The dense fine speckled pattern in ANA tests is common in autoimmune diseases, challenging previous beliefs that it was unrelated.

Nelfb is essential for dermal fat development and survival.

Genetic marker rs12558842 strongly linked to male hair loss.

DORN1 receptor affects eATP-induced stomatal changes but not eADP in Arabidopsis thaliana.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

New compounds show promise for treating benign prostate hyperplasia with fewer side effects.

Adding dutasteride to therapy may improve treatment for advanced salivary duct cancer.

Human amniotic membrane helps heal skin wounds faster and with less scarring.

AD198 is more effective than doxorubicin in stopping certain dog cancer cells.

5alpha-DHP may be a safe, effective treatment for certain seizures without causing sedation.

DHEA therapy improves pubic hair growth and psychological well-being in girls with central adrenal insufficiency.

The over-the-counter supplement DHEA could make COVID-19 worse, especially in diabetics and people with G6PD deficiency.

5α-reductase deficiency can cause ambiguous genitalia and gender dysphoria, treatable with testosterone.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

Vaccines work well in Netherton syndrome patients, similar to healthy people.

The drug was successfully released into hair follicles using nanocarriers.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

The nature of the side chain in RU 58841 derivatives greatly affects its AR affinity, with the N-(iodopropenyl) derivative 13 showing the highest AR binding affinity, suggesting its potential for developing high-affinity radioiodinated AR radioligands.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Metformin/dopamine-derived carbon dots help heal bacteria-infected wounds faster.

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

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Haloperidol decanoate can cause alopecia areata.

Certain enzymes react strongly with some hormones in rat skin during hair growth, mainly in sebaceous glands and hair sheaths.

Desonide is more effective than niacinamide for reducing underarm darkening.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.