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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

Certain gene variations increase the risk of alopecia areata in Koreans.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.

The E2 protein affects gene activity in hair follicles of mice.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Certain gene variations may increase the risk of PCOS in South Indian women.

Different genes are linked to various types of hair loss.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Id2 gene helps keep hair follicle stem cells inactive.

TP0427736 may help treat hair loss by blocking a specific protein and promoting hair growth.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

Controlling transposable elements is crucial for successful tissue regeneration.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The ACE1 gene variant doesn't affect long-COVID symptoms.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

HOTTIP and miR-10b contribute to glioma therapy resistance by affecting cell behavior, suggesting they could be targets for treatment.

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

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.