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

CCL5 is important for the hair growth potential of human dermal papilla cells.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

A woman's masculine features were caused by a rare ovarian tumor that produced male hormones.

Papular acantholytic dyskeratosis of the vulva is a rare, benign skin condition that can be managed conservatively.

SVpgC2a cells show abnormal growth and keratin changes, modeling early cancer development.

Researchers found a non-functional sheep keratin gene due to mutations.

Versican in dermal papilla cells is crucial for healthy hair growth.

Bullous pyoderma gangrenosum can develop on cesarean scars and may require steroids for treatment.

The Spherical Skin Model improves drug and cosmetic testing by accurately mimicking human skin for efficient compound screening.

Grasp protein helps maintain skin health after UVB exposure.

Dermoscopic and histopathological features combined can help diagnose Pityriasis versicolor.

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The 2012 criteria are better for diagnosing atypical lupus cases.

The conclusion is that using light-sheet fluorescence microscopy with a special solution can effectively create detailed 3D images of human skin for dermatological research.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A rare, non-cancerous ovarian tumor was successfully treated with surgery, improving the patient's symptoms.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

A rare form of lupus can cause severe nerve damage and other symptoms, but treatment can help.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Ganoderma lucidum can cause severe skin reactions and hair loss.

Anti-DFS70 antibodies can help identify nonsystemic autoimmune conditions in SLE patients.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

Clascoterone cream 1% is effective and well-tolerated for treating acne and other related conditions.

Cadd4 effectively reduces cholesterol levels without side effects.

Squaric acid dibutylester helps hair growth by increasing certain immune cells in the skin.