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Newly found stem cells in horse hooves show promise for treating a hoof disease called laminitis.

Human-induced stem cell-created skin models can help understand skin diseases by studying the skin's layers.

Skin can become dry and thick in hypothyroidism.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Cathepsin L deficiency causes hair and skin issues in mice.

Epithelial-derived Pop-Up Keratinocytes (ePUKs) may enhance wound healing in regenerative medicine.

Blood cells turned into stem cells can become skin cells similar to normal ones, potentially helping in skin therapies.

Tumor cells in calcifying epithelioma of Malherbe resemble hair follicle cells.

Hidradenitis suppurativa may be a type of autoinflammatory skin disease linked to gene mutations and immune system issues.

A specific group of slow-growing stem cells marked by Thy1 is crucial for skin maintenance and healing in mice.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Oral Acitretin effectively resolved symptoms in a child with Netherton syndrome.

The study found nine new hair protein genes in human hair follicles.

A mutation in the KRT74 gene causes tightly curled hair.

A missing mK6irs1 gene causes hair loss in mice.

Alopecia areata can show unusual red-dotted vessels and dithranol treatment may mask typical patterns.

Hirsutism and acanthosis nigricans are important for diagnosing PCOS; dermatologists play a key role in early detection and treatment.

The analyses helped identify different skin diseases in the two dogs.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Keratin proteins in hair are complex and come from multiple gene families.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

HPV8 causes skin cancer by expanding specific skin stem cells.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

A man with nevus comedonicus syndrome had multiple skin issues, including basal cell carcinomas, which improved with treatment.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.