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Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

A genetic variant in the KRT25 gene causes tightly curled hair.

Researchers created a new mouse model for studying scleroderma.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

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

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Increased PHGDH expression causes early melanin buildup in hair follicles.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The vector successfully directed specific gene expression in hair follicles.

A mutation in the KRTHB5 gene causes hair and nail issues.

PTCH gene mutations contribute to basal cell carcinoma development.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

PmtHEE is a better model for studying pigmented skin because it includes melanocytes and shows improved cell differentiation.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Mutations in specific genes cause different types of ectodermal dysplasias.

Scientists discovered two versions of a new human hair keratin gene.

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

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.