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LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Male mice with FGF5 mutations grow longer hair than females.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Stat3 affects skin cancer development by altering keratinocyte stem cell behavior.

Keratinocyte growth factor significantly alters skin and tissue development.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

AQB reduces harmful skin changes in systemic sclerosis.

A comprehensive human skin cell atlas was created to better understand skin biology and disease.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Transgenic sheep cells with spider silk gene were successfully created for future sheep hair expression.

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

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

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

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

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

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.

Deep skin fibroblasts help recruit immune cells for better wound healing.