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Activating TLR3 may help produce retinoic acid, important for tissue regeneration.

TRPV3 in skin cells causes inflammation and cell death.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Certain genes control the color of human hair by affecting pigment production.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.

Mrp3 may aid in wound healing and hair growth.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

A new genetic mutation was found causing hair and eye issues in a boy.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

CDH3-related disease causes worsening eye and hair issues.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

RORA may help regulate hair growth by affecting hair follicle stem cells.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Mrp3 helps in wound healing and hair growth.

Inhibiting ODC can prevent UV-induced skin cancer.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Activating TLR3 boosts autophagy gene expression in skin cells.