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A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

Tofacitinib may help treat nail dystrophy, especially when other treatments fail.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

Keratin 14 is uniquely found in a specific group of placental cells.

DA-9401 protects against hair loss, improves organ function, and prevents infertility caused by finasteride.

HOXC13 is essential for hair and nail development by regulating Foxn1.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

MicroRNA-21 could help diagnose and treat skin fibrosis.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Mutations in hKAP1 genes may cause hereditary hair disorders.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

AMPK activation may reduce melanoma risk in red-haired individuals.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

The prototype for analyzing skin aging works technically and clinically.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

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