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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

CARB is a strong barrier in human hair that prevents dye penetration.

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The prototype for analyzing skin aging works technically and clinically.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

CTP-543 is generally safe for treating alopecia areata.

The document concludes that DAB389-IL2 is promising for treating refractory cutaneous T-cell lymphoma, but more research is needed on its effectiveness and side effect management.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Genetic marker rs12558842 strongly linked to male hair loss.

The folate-cyclodextrin conjugate targets cancer cells more precisely, potentially reducing chemotherapy side effects.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

RU 58841 may treat acne, hair loss, and excessive hair growth.

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Two new gene mutations cause a rare hair disorder.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

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

EPC-K is stable except at very acidic pH or when exposed to sunlight, and it can decompose in low ethanol concentrations.

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TCDD speeds up skin barrier formation by increasing certain gene expressions.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.