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A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

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

Chi-miR-130b-3p helps develop hair follicles in goat fetuses by targeting the WNT10A gene.

A mutation in the human hairless gene causes alopecia universalis.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

The research mapped gene activity in developing mouse skin and found key markers for skin cell types and changes from fetal to early postnatal stages.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

lncRNAs may regulate hair follicle development in Hu sheep.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Targeting LGR4 may help treat cancer by reducing cancer stem cell traits and drug resistance.

Ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes and influencing hair follicle phases.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Inherited color dilution in rabbits is linked to DNA methylation changes.

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

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Integrin α6 helps identify different neural crest cell types in the skin.

HPV8 causes skin cancer by expanding specific skin stem cells.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.