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Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

Hair follicles help skin immune recovery after UVB exposure.

Malondialdehyde-modified DNA may trigger an immune response in alopecia areata patients.

A new patch can deliver stable antibodies over time for potential HIV treatment.

IL-17 plays a key role in severe hair loss in chronic alopecia areata.

Mutations in the LIPH gene cause woolly hair in a child.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

Lithocholic acid helps hair growth and regeneration in alopecia by activating vitamin D receptors.

A woman with lupus had blood cell destruction, treated successfully with medication.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

Vitamin D receptor FokI gene variation is not linked to alopecia areata.

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

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

People with Alopecia areata have higher levels of certain T regulatory cells in their blood.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

Blocking the CCR5 receptor may be a new way to treat hair loss from alopecia areata.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

People living with HIV in Turkey often have skin conditions, which are more common in advanced HIV stages and may help in diagnosing the infection.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.