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Tofacitinib effectively treated a woman's complex autoimmune and autoinflammatory disorders.

Belimumab may cause hair loss in lupus patients.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

The new therapy using specific stem cells from umbilical cords speeds up healing of chronic skin wounds.

Enhancing Tregs can protect against alopecia areata.

Targeting IL-15 may help treat Alopecia Areata.

Disrupting Bcl-xL in mice reduces skin cancer risk.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Different types of cells in the eye express specific keratins at various stages of development.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

A mouse gene mutation increases the risk of skin cancer.

Anifrolumab significantly improved skin lesions and hair regrowth in severe discoid lupus.

JunB is crucial for maintaining healthy skin and hair follicles.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

FOL-026 peptide can help repair blood vessels and promote growth, offering potential treatment for vascular diseases.

TLR2 is important for hair growth and can be targeted to treat hair loss.

Genetic differences affect COVID-19 severity and treatment effectiveness.

Keratin 19 expression in certain skin cells is temporary and not a reliable stem cell marker.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

CS12192 effectively treats alopecia areata with better safety than current options.

Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

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

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

TIP39 and PTH2R help control calcium levels and skin cell development.