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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.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

FAKΔe4 helps cells sense and respond to different stiffness levels in their environment.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Overactivating Hedgehog signaling makes hair follicle cells in mice grow hair faster and create more follicles.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.

Too much Smad7 can cause serious changes in skin tissues, including problems with hair growth, thymus shrinkage, and eye development issues.

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

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A specific gene mutation causes woolly hair and hair loss.

Jag2 is essential for proper skin cell differentiation and organization.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

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