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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Engineering strategies improve stem cells' ability to heal wounds effectively.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

The availability of certain hormones and specific stimulation patterns affect long-term synaptic changes in the male rat brain.

A special clotrimazole varnish cured a siamang's persistent skin infection after 3 months.

Topical putrescine and spermine increased DNA synthesis in hairless mouse skin.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Chitosan hydrogels are promising for repairing blood vessels but need improvements in strength and compatibility.

Potassium changes lead root hair growth, with calcium and other factors regulating the process.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Mummy hair from the Taklamakan desert has calcium and phosphorus inside.

New cancer treatments aim to reduce side effects and improve effectiveness.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A brain-produced steroid causes increased scratching in mice with a skin condition similar to eczema.

Women with hair loss have more androgen receptors in certain hair follicles.

Normal skin results from interactions between EGF and the Tabby mutation.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

Dihydrotestosterone (DHT) mainly affects nearby cells, doesn't significantly change prostate hormonal environment or cancer risk, and doesn't play a main role in causing hair loss or acne. More research is needed on its effects on heart health, sexual function, and bone health.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

High calcium levels hinder wheat root growth, but not root hair formation.

Regenerative medicine may offer long-lasting relief for chronic pain and neuro-degenerative conditions.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Finasteride treatment changes Cx43 in rat testes, possibly causing fertility issues.

A Rathke's cleft cyst caused hormonal imbalances and symptoms in a 68-year-old woman.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.