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EGF aids skin development and healing, while bFGF absence in embryos may allow scar-free healing.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Nelfb is essential for dermal fat development and survival.

ARHGEF3 is essential for proper hair follicle development in mice.

Dermal EZH2 controls skin cell growth and differentiation in mice.

PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Dlx3 is essential for hair growth and regeneration.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

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

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

SFRP2 boosts Wnt3a/β-catenin signals in hair growth cells, with stronger effects in beard cells than scalp cells.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

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

NIPP1 is important for healthy skin and could help treat skin inflammation.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

LPA 4 helps control blood and lymph vessel development in zebrafish.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

A rare skin condition causes red and dark patches on the face and limbs.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

DPP4-positive fibroblasts play a major role in producing proteins that lead to skin fibrosis.

PIEZO1 helps keep hair follicle stem cells inactive, affecting hair growth.

Mutations in the SNRPE gene cause hereditary hair loss.