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A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

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

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Intestinal stem cells can help repair skin damage from radiation.

Keratin 16 delays skin maturation and affects skin and hair development in mice.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

SH-340 may improve skin barrier and help treat atopic dermatitis.

CD200 is not a reliable marker for identifying stem cells in all skin types.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Prostaglandins and the enzyme AKR1C3 could play a role in skin cancer and hair loss, and further research is needed to understand these mechanisms.

BMI1 is essential for preventing hair greying and maintaining hair color.

Activating TRPV4 in skin cells helps regrow hair in mice, possibly offering a treatment for hair loss.

K16 can partially replace K14 but causes hair loss and skin issues.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Increasing Smurf2 hinders hair follicle stem cell differentiation and wound healing.

Two main types of fibroblasts with unique functions and additional subtypes were identified in human skin.

Keratin 19 helps identify skin stem cells, with its presence varying by body location, age, and culture stage.

Inhibiting SFRP1 may help treat hair loss.

Sphingosine 1-phosphate helps control mechanical pain.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

Spiny keratoderma is a rare skin condition with small spines on palms and soles, possibly linked to abnormal hair formation.

Runx1 helps control the KAP5 gene in human hair follicles.