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PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

A new keratin gene was found in mice, explaining hair growth.

Three genes, BMP4, POSTN, and WNT5A, may help treat keloids.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

GLI2 increases follistatin production in human skin cells.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

Gremlin proteins help regulate hair growth by balancing signals in hair follicles.

The treatment effectively promotes hair regrowth in androgenetic alopecia without causing skin irritation.

Thymosin Beta 4 helps human dental pulp cells develop into tooth-forming cells, suggesting it could aid dental regeneration.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

WWP2 is crucial for tooth development in mice.

Piezo1 helps skin grow by managing metabolism and inflammation.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

ZIP10 is crucial for skin development and maintaining healthy skin.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

H3K4me3 helps control RSPO3 to influence hair growth and development.

SOX4 is crucial for the development of melanoma.

The Wave complex controls skin growth by suppressing certain signals.

A protein called sFRP4 can partly inhibit hair growth.

ePUKs could be valuable for regenerative medicine due to their wound healing abilities.

Ceramide Synthase 4 is crucial for maintaining hair follicle stem cells and preventing hair loss.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.