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ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Engineered bacteria can deliver antioxidants to protect skin.

Gene therapy in mice increased lifespan and improved health without causing cancer.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

PTCH gene mutations contribute to basal cell carcinoma development.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

A genetic variant in goats is linked to cashmere growth.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

Key genes are crucial for Drosophila wing development and could be insecticide targets.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

Cell membrane-coated nanoparticles could improve gene therapy by enhancing delivery and targeting of nucleic acids.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Certain gene variations may increase the risk of PCOS in South Indian women.

A new gene mutation is linked to monilethrix in the studied family.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A new therapy for a skin blistering condition has not been developed yet.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.