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Ivarmacitinib significantly improved hair regrowth in severe alopecia areata after tofacitinib was less effective.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

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Infants with severe KID syndrome may be more prone to serious infections and need close monitoring.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

Finasteride's polymorphic form affects capsule quality and drug effect, requiring strict control.

4-octyl itaconate may prevent hearing loss caused by the drug cisplatin by activating certain cell protection pathways.

New itaconate prodrugs improve its absorption and effectiveness for treating inflammation.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Isoalantolactone promotes hair growth by activating specific cell pathways.

The hair tonic with cinnamon oil and coconut oil was stable and caused very mild irritation.

A new gene mutation causes insulin resistance in a girl and her mother.

Certain eye surgery complications can be managed effectively, especially in patients who have used specific prostate medications.

The prototype for analyzing skin aging works technically and clinically.

The gel with icariin speeds up wound healing, reduces scarring, and helps hair growth by controlling BMP4 signaling. It also reduces inflammation and improves wound quality in mice, adapts to different wound shapes, and gradually releases icariin to aid healing. It also prevents too much collagen and myofibroblast formation during skin healing.

Myo-inositol and D-chiro-inositol improve hormonal and physical symptoms in teenage girls with PCOS.

ICAM-1 helps regulate hair growth cycles and skin remodeling.

ILC1-like cells can cause alopecia areata by affecting hair follicles.

The right balance of Myo-Inositol to D-Chiro-Inositol in follicular fluid is crucial for good egg and embryo quality.

A patient developed a blister at the injection site after hepatitis C treatment.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.