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Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.

Rubbing seborrheic keratoses causes specific skin changes and may link them to hair follicles.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

A form of vitamin E promotes hair growth by activating a specific skin pathway.

Skin stem cells are maintained by signals from nearby cells and vary in their ability to renew and mature.

Researchers identified key cell types and genes involved in hair and skin diseases.

Mice with extra sheep genes had hair that fell out and regrew in cycles.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

CK 19 expression is higher in more severe skin cancers.

CD4+ skin cells may be precursors to basal cell carcinoma.

Trypsin slows hair growth and affects color by causing cell death in hair follicles.

Thorough hair examination is crucial for accurate diagnosis and treatment.

Keratoacanthoma and some squamous cell carcinomas are linked to hair follicles, while others are not.

Twist1 is crucial for UVB-induced skin cancer development.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Basal cell carcinoma behaves like hair follicles and targeting specific pathways may help treat it.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Hair follicle stem cells have significant potential for treating various disorders.

Trichoscopy effectively diagnoses and assesses hair loss severity in androgenetic alopecia and alopecia areata.

Onychomatricoma is a unique nail tumor, not related to other hair-related tumors.

Hair repigmentation can indicate malignancy and should be investigated.

Wnt and SHH pathways help form hair follicles by coordinating cell processes.

Genetic testing can identify causes of rare hair loss disorders in children, but no treatments exist.

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.

KRT72 gene helps form hair.

Trichoscopy helps diagnose and assess the severity of two types of hair loss diseases, androgenetic alopecia and alopecia areata.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.