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GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

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

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

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

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Overexpression of certain genes can shorten hair by disrupting the hair-growth cycle.

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

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Overexpressing the Tβ4 gene in goats can increase cashmere production.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

A protein called HMGB1 helps hair grow by affecting prostaglandin metabolism.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

Selective breeding can enhance immunity in dairy cattle.

The FRZB gene slows hair growth in rabbits.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Keratin 6A increases skin inflammation, suggesting it could be a target for treating certain skin diseases.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

The Itpr3 gene causes a specific hair pattern in mice.

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

New mutations in the hairless gene may cause hair loss and affect bone development.