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A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

A 532 nm laser helps tendon stem cells grow and become tendon-like by increasing Nr4a1 activity, which may speed up tendon repair.

EZH2 is essential for hair growth and skin cell development.

Tcf3 and Lef1 are key in deciding skin stem cell roles.

Hair loss gene found on chromosome 3q26.

A mutation in the human hairless gene causes alopecia universalis.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

Activating TLR3 boosts autophagy gene expression in skin cells.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

A mouse gene mutation increases the risk of skin cancer.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

The lncRNA LOXL1-AS1 may help diagnose and treat androgenic alopecia.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

Using special RNA to target a mutant gene fixed hair problems in mice.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

KLF4 is important for keeping hair follicle stem cells inactive.

Mutations in the KRT16 gene can cause skin and nail disorders.

A new gene mutation causes insulin resistance in a girl and her mother.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Researchers created a new mouse model for studying scleroderma.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Egfl6 is not needed for zebrafish face development.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.