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Pediatric patients with dystrophic epidermolysis bullosa face more hospital admissions, procedures, and complications than others.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Eyelid cells share signaling components but differ in pathway activity.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

mIGF-1 in skin cells speeds up wound healing and hair growth in mice without harmful effects.

The enzyme from human skin can cross-link proteins and needs calcium to work.

Sericin hydrogels heal skin wounds well, regrowing hair and glands with less scarring.

Cell adhesion molecules are important in the development of certain skin diseases.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

Without keratin 10, there's more growth and development of oil-producing skin cells.

Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

Myc activation reduces skin stem cells by affecting cell adhesion.

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

Sciellin is a protein that helps form protective layers in skin, hair, and nails.

A unique skin cell similar to hair bulb melanocytes was identified, with better preservation using permanganate fixation.

The ZIP13 variant is linked to abnormal hair quality.

The hydrogel helps heal diabetic wounds quickly and effectively.

The hydrogel speeds up diabetic wound healing and reduces scarring.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

N-WASP is essential for healthy skin and preventing inflammation.

The newborn's skin blisters healed without scarring, leaving some light spots, and stopped forming after four months.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

Turning off a specific gene in stem cells speeds up skin healing by helping cells move better.

Proper skin care and dermocosmetics improve skin issues in diabetes patients.