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There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

Key genes linked to hair growth and cancer were identified in hairless mice.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

Mutations in the Whn gene affect hair keratin gene expression differently.

A new mouse mutation causes skin and hair defects due to a gene change.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

miR-199a-3p controls hair growth and is linked to alopecia areata.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

H3K4me3 helps control RSPO3 to influence hair growth and development.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

A mutation in the Sgkl gene causes defective hair growth in mice.

Keratin 17 is crucial for early hair strength and cell survival.

Low IRES/Cap translation is linked to higher stem cell potential.

Mutations in the KRT85 gene cause hair and nail problems.

Certain genetic markers may increase or decrease prostate cancer risk.

Targeting PTEN can improve healing in venous leg ulcers.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.