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The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

New mutations in the DSG4 gene cause a rare hair condition.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

Keratin-associated proteins are crucial for hair strength and structure.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Deleting Twist1 in skin cells reduces UVB-induced skin cancer risk.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Keratin proteins in hair are complex and come from multiple gene families.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Somatic BHD mutations are rare in Japanese renal tumors.

The KDM1 gene helps Venus flytraps close by managing potassium ions.

Ribonucleotide excision repair is crucial to prevent skin cancer.

K31 can identify clear secretory cells in human sweat glands.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

A gene mutation in mice causes permanent hair loss and skin issues.

New genetic mutations causing hair loss were found in a Chinese family.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Certain genetic variations in camels affect hair coarseness.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

New genetic mutations linked to rare skin disorders were found in three newborns.

Blue-light activation of TrkA improves hair-follicle stem cells' ability to become neurons and glial cells.

Gene expression regulates keratin production for normal hair growth.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

ABCG2 protein marks stem-like skin cells in human epidermis.