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Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

BMP signaling is essential for the development of touch domes.

A new drug, abrocitinib, helped a child with severe hair loss regrow hair.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Extracellular ATP promotes growth, while adenosine inhibits it in Arabidopsis plants.

Deucravacitinib helped a man regrow hair and improve psoriasis.

Activating cAMP and ATP improves hair growth and strength.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

dAR-6–1 is a promising new treatment for hair loss that works better than minoxidil.

Genetic insights can lead to personalized treatments for acne, androgenetic alopecia, and alopecia areata.

Reduced SIRT1 in hair cells may cause alopecia areata by triggering immune responses.

MARCKSL1 is important for wound healing and could be a target to reduce scarring.

Different keratins have unique expression patterns in mouse skin cells.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

Upadacitinib may effectively treat both alopecia universalis and Crohn's disease.

The new rabbit model better mimics human acne symptoms.

Neuroactive steroids affect cocaine's rewarding effects through the ς₁ receptor.

Stress in hair follicle cells increases certain immune-related proteins, which might contribute to hair loss conditions.

Nephronectin helps attach muscle cells to hair follicles.

Removing Mediator 1 causes teeth cells to turn into hair cells.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Human keratinocytes do not naturally respond to androgens.

New genetic mutations linked to rare skin disorders were found in three newborns.