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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

New treatments targeting specific genes show promise for treating keratin disorders.

Wnt3a activates certain genes in hair follicle cells, including a newly discovered one, EP2, which may affect hair growth.

TGF-beta 1 and IGF-II mRNA have specific patterns in pig subcutaneous tissue, affecting fat and muscle development.

Epiprofin helps cells grow in developing teeth, hair, and limbs.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Antizyme slows skin tumor growth by reducing cell growth in mice.

Mrp3 helps in wound healing and hair growth.

A special receptor in sensory nerve endings helps control how they respond to stretching.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

BAF200 is essential for proper heart and coronary artery formation.

Sonic hedgehog signaling is needed for the development of touch-receptor cells in the skin, and the loss of Polycomb repressive complex 2 can lead to more of these cells.

Glypicans help hair follicle stem cells differentiate by interacting with specific receptors, influencing hair growth.

Activated ras can protect kidney cells from a certain substance that causes cell death.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Blocking hair follicle development stops key gene signals needed for hair growth in mice.

Only two of the four keratin genes are expressed in wool fibers.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

The man has a genetic skin condition called pachyonychia congenita.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.