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Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Wnt10b promotes hair growth, while SFRP2 inhibits it in Wanxi Angora rabbits.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

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

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

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

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

The study found nine new hair protein genes in human hair follicles.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

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

Adipose-derived stem cells can be used to create cells that help grow new hair.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

Vitamin D receptor and hairless protein are essential for hair growth.

Keratin 17 is crucial for cell growth in wound healing by aiding protein synthesis.

Genetic marker rs12558842 strongly linked to male hair loss.

BSSP may help skin tumors grow and could be a marker or target for skin cancer treatment.

The Walleye dermal sarcoma virus cyclin causes excessive skin cell growth in mice.

Human dermal stem/progenitor cells can divide and differentiate more than hair follicle dermal papilla cells.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

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

Certain gene variations may increase the risk and severity of alopecia areata.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.