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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Restoring EDA and WNT pathways early may help improve skin, hair, and teeth issues in hypohidrotic ectodermal dysplasia.

NFATc1 controls hair stem cell activity, affecting hair growth and could be a target for hair loss treatments.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Monilethrix is linked to a gene cluster on chromosome 12.

Activating TLR3 boosts autophagy gene expression in skin cells.

Blocking certain immune signals can reduce skin damage from radiation therapy.

Trps1 is essential for proper hair follicle development.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

TCDD reduces EGF receptors in the liver, affecting growth and development.

RCS-01 therapy is safe and may improve skin structure by affecting gene expression.

PKM2 is a promising target for heart repair and regeneration.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

CNGC14 is crucial for calcium entry needed for root hair growth in plants.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

JAK inhibitors help hair growth by boosting beta-catenin activity in hair root cells.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A specific gene mutation causes congenital hair loss.