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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

The HDDPiW-jSB solution may prevent hair loss caused by docetaxel in rats when applied regularly.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

SHPro® improved urinary symptoms and erectile function in men and is safe.

Ritlecitinib effectively reduces severe hair loss in alopecia areata over 24 months.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

The triple-wavelength diode laser effectively and safely reduces hair and improves skin appearance in people with darker skin.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

RUM-loaded SLN shows promise for treating acne and hair loss topically.

The new ELISA method is reliable and eco-friendly for checking the quality of Pueraria candollei.

CD101 is highly effective in treating dermatophytosis in guinea pigs.

Ritlecitinib is being tested for safety and effectiveness in young children with severe alopecia areata.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

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The research found that the properties of solid-state Electronic Circular Dichroism (ss-ECD) are influenced by the orientation of local crystals, which could help in examining and mapping chiral materials like pharmaceutical ingredients.