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Young patients are more likely to develop autoimmune diseases, while elderly patients are more prone to organ failure after DRESS.

A certain medication improved severe itching in a boy with liver and bowel disease by reducing histamine levels, suggesting a new treatment target.

Echinops echinatus and Tridax procumbens have compounds that fight bacteria.

The B2C promoter works in sheep cells but not in mouse embryos.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Microneedle arrays deliver botulinum toxin effectively for sweat suppression, similar to injections.

EMS and EF both show similar skin and fascia changes, but EMS has more severe symptoms and nerve inflammation.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Cholesteatoma shows abnormal and increased EGF receptor expression, indicating its rapid growth.

Dermal EZH2 controls skin cell growth and differentiation in mice.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Epiduo® is an effective first-line acne treatment that reduces inflammation and combats antibiotic resistance.

Calancardin B may help reduce inflammation in immune cells.

S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

Fibronectin-attached cell sheets improve wound healing and are safe and effective.

Henna ointment may help reduce itching and improve wound healing in patients with epidermolysis bullosa.

VEGFR-2 is active in hair follicles, sebaceous glands, sweat glands, and skin on the human scalp.

Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

A young boy with Netherton syndrome improved significantly using IVIG, dupilumab, and dietary changes.

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.

Tph cells are linked to the severity of systemic lupus erythematosus.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

EGFR is crucial for preventing hair follicle inflammation and hair loss.

Cepharanthine shows promise as a COVID-19 treatment.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.