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The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

Poodles' hair changes aren't always linked to calcium, and special staining is needed to detect true calcium deposits.

A young cat had a rare fungal infection caused by Microsporum gypseum.

Larger nail cavity sizes suggest benign tumors, while smaller ones may need further biopsy to rule out cancer.

Dogs have a skin condition like human pseudopelade, causing hair loss that doesn't improve with treatment.

Sox9 is crucial for hair follicle stem cells to become melanocytes instead of glial cells.

Keratoacanthoma changes as it grows, showing different hair follicle characteristics at each stage.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

A 69-year-old smoker was wrongly diagnosed with lung cancer but actually had a rare lymphatic system disorder.

A rare skin condition causes red and dark patches on the face and limbs.

Dogs with skin lesions often have blood abnormalities and damaged hair.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

High Demodex mite density may be linked to sebaceous hyperplasia.

Mogamulizumab can cause hair loss, often linked to a better treatment response.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

A man had a rare pigmented nodule on his scalp that developed from birthmarks.

Breast cancer skin metastases are rare, look different, and can be confused with other skin issues, so a biopsy is needed for accurate diagnosis.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

A gene mutation in mice causes skin defects and early death.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.

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

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.