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β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

IL-1 receptor absence in mice leads to skin cysts and changes in immune response after UVB exposure.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

Scientists found a gene in mice that causes early hearing loss.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Blocking certain receptors in the lungs might help treat a specific type of asthma.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

CS12192 effectively treats alopecia areata with better safety than current options.

A unique gene mutation was found in a family with monilethrix.

WNT10B affects hair growth by altering gene activity in hair cells.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

ABCG2 protein marks stem-like skin cells in human epidermis.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Tph cells are linked to the severity of systemic lupus erythematosus.

Transcutaneous vaccination using nanoparticles can enhance immune responses and reduce basal cell carcinomas.

A specific genetic deletion in goats affects cashmere yield and thickness.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

The PROCLIPI study found markers that help predict outcomes in skin lymphoma patients.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Brepocitinib improves cicatricial alopecia and reduces key immune markers.