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The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

The vitamin D receptor can work without its usual activating molecule.

Disitamab vedotin and gemcitabine effectively treated bladder cancer without major side effects.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

CTIP2 may help in skin development and maintenance.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Mutations in the SNRPE gene cause hereditary hair loss.

The research found a way to develop hair growth materials by targeting a specific signaling pathway.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

The drug TGU was ineffective against small cell lung cancer and caused significant bone marrow suppression.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Treg cells help repair and regenerate tissues by interacting with local cells.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Genetically modified cells improved skin wound healing in rats.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

ROR2 is essential for hair follicle stem cell renewal and maintenance.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

Rizatriptan benzoate-loaded dissolving microneedles are effective and convenient for treating acute migraines.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

PTHrP and its receptor can control blood vessel growth and hair development in mouse skin.

Activin A helps heal skin wounds and protects the brain after injury.

A mutation in the KRT25 gene causes a rare hair disorder with thin, woolly hair.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

Vitexin Compound 1 may help reduce skin aging caused by UVA light.