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The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

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

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The Foxn1 gene is essential for normal nail and hair development.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Personality affects stress response more than social rank in zebrafish.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

A patch with curcumin-zinc can improve hair growth and health by delivering beneficial particles to the skin, increasing hair follicles, and reversing effects of a hair loss hormone.

iNKT cells help develop and maintain healthy skin in young mice.

Zinc pyrithione dissolves quickly on the skin and in hair follicles, especially in smaller particles.

Mutations in the KRT85 gene cause hair and nail problems.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

The new zinc peroxide hydrogel speeds up wound healing and tissue regeneration effectively.

Many infants in Northern Ethiopia have zinc deficiency.

Haplogroup X found in Altaian population supports Amerindian origin.

Mutations in the HOXC13 gene cause hair and nail development issues.

Growth hormone therapy can improve growth in Netherton syndrome patients with growth hormone deficiency.

Wnt10b promotes hair growth, while SFRP2 inhibits it in Wanxi Angora rabbits.

Nicastrin deficiency may cause skin cell damage and pigmentation disorders in humans, similar to effects seen in fish.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

Dermal EZH2 controls skin cell development and hair growth in mice.

Benzo[c]quinolizin-3-ones are effective nonsteroidal inhibitors of human steroid 5α-reductase 1.

Dermal EZH2 controls skin cell growth and differentiation in mice.

FOXN1 gene variants cause low T cells and immune issues from birth.