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PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

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Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

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The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Finasteride helps female-pattern hair loss.

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A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

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The compounds tested could potentially treat hair loss and alopecia.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

A mutant FERONIA gene affects root hair growth at high temperatures.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

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

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Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

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Clinical trials for hair loss in the USA show differences in participation among different races and ethnic groups.

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A new EDA gene mutation was found in a Chinese family with a specific skin disorder.