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Skin grafts from related donors significantly healed chronic wounds in patients with a severe skin condition over a year.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

The discovery of 5α-reductase deficiency in guevedoces led to the development of important urologic medications.

A unique gene mutation was found in a family with monilethrix.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

Using a call center to collect data in a trial for eye disease in diabetics led to high response rates and very little missing information.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Trichoepithelioma and desmoplastic trichoepithelioma have distinct features that can be identified using reflectance confocal microscopy.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

HSPC016 gene is important for hair growth.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

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Keratin 17 is important for skin development and may help define skin cell types.

ARHGEF3 is essential for proper hair follicle development in mice.

Rare earth elements are crucial in medical imaging and cancer treatment.

The gene GJA1 is important for regulating coarse hair density in goats.

EGFR helps protect hair follicles from damage and scarring.

Eyelid cells share signaling components but differ in pathway activity.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

EGFR helps hair follicles transition properly by controlling Stathmin levels.

Gynostemma pentaphyllum extract may help grow hair and prevent graying.

A dissolving microneedle patch with collagen XVII effectively promotes hair regrowth in androgenic alopecia.

XEDAR triggers a specific signaling pathway in cells.

EGFR inhibitors often cause dry, brittle hair and eyebrow/eyelash changes.

cGEL hydrogel improves melanin production in skin cells, making it a promising option for skin treatments.

Rose stem cell exosomes can significantly improve hair growth in androgenetic alopecia.

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.