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Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Cyclohexyl salicylate promotes human hair growth and increases certain hair follicle stem cell progeny.

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

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

New mouse models help study melanocytic cells for melanoma research.

Stat3 influences keratinocyte stem cell behavior, affecting differentiation and migration.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A new gene mutation linked to a skin condition was found in a Spanish family.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Basal cell carcinomas and squamous cell carcinomas have different gene activity patterns, suggesting unique treatment approaches.

Ustekinumab treatment may reveal a genetic tendency for steatocystoma multiplex in psoriasis patients.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

A nonviral method was developed to label and culture human hair follicle stem cells.

Desmocollin 1 and 3 have distinct patterns in human tissues, with Dsc1 in specific skin and hair layers and Dsc3 in various epithelial layers.

Higher doses of Tribulus terrestris extract increase MC-1R expression in mouse hair follicles.

Skin-associated cartilage cells can influence hair growth by altering specific signaling pathways.

Lhx2 helps retinal cells respond to signals for eye development.

Keratin 33A is a key protein in goat winter coats, especially in high-producing breeds.

The UHS promoter is specific to mouse hair follicles.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Foxc1 helps keep hair follicle stem cells inactive, preventing hair loss.

MITF and WNT3A are key in Dun Mongolian horse pigmentation.

RXR-alpha is strongly expressed in both normal and psoriatic skin and may help in skin cell differentiation and hair growth.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.