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Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

Dual TCR Treg cells are common in mouse tissues and vary by location.

Hair follicles can be used to study gene expression and understand conditions like COPD.

Hair samples can be used to create stem cells easily and non-invasively.

A new gene mutation causes a rare type of hair loss.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

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

The antibody created from BCC tissues reacts similarly to both BCC and hair follicles, suggesting BCC may come from hair follicle cells.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

The immune processes causing VKH and vitiligo are similar in dogs and humans.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.

Hair follicles in mutant mice self-organize into ordered patterns within a week.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

MTS24 marks a new type of skin cell that helps hair growth and repair.

M2 macrophages help hair regrowth in wounds by making growth factors.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Sox2 controls hair color by affecting pigment production in hair follicles.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

The Shaven mutation in mice affects hair growth and causes a greasy coat due to abnormal lipid content.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.