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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Reduced Stx17 expression may contribute to Alopecia Areata.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Researchers found a non-functional sheep keratin gene due to mutations.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Mutations in the KRT85 gene cause hair and nail problems.

CTIP2 may help in skin development and maintenance.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

UTX is important for skin health and its loss can lead to skin issues, especially in females.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

Krox20 is important for cell differentiation in the brain and hair follicles.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

N-WASP is essential for healthy skin and preventing inflammation.

A new tool accurately identifies human cornea cell states and key factors.

Dermal EZH2 controls skin cell development and hair growth in mice.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

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

Dkk4 protein is necessary for the proper development and arrangement of hair follicles.

Researchers found a genetic region that influences the number of coat layers in dogs.

KAP6 genes are conserved across species and active in hair follicles.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.