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A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Researchers isolated and identified structural components of human hair follicles, providing a model for studying hair formation.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Chromosomal changes, including those in the WRN gene and rDNA, may significantly contribute to aging.

A mutation in the KRT74 gene causes tightly curled hair.

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

A new staining method shows a special area in the hair's skin layer with lots of proteoglycans.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

BMI1 is essential for preventing hair greying and maintaining hair color.

Heterotypic cell contacts likely help hair matrix cells differentiate during mouse hair follicle development.

Low oxygen levels help hair follicle stem cells turn into heart muscle cells faster.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

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

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

MOF controls skin development by regulating genes for mitochondria and cilia.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Keratinous tissues have multiple structural layers, including ordered keratin and lipid granules.

Different Myc family proteins are located in various parts of the hair follicle and may affect stem cell behavior.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

The human scalp has different types of pigment cells in hair follicles with varying abilities to produce pigment.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Mice with the naked gene have missing or abnormal hair cells.

HB24 helps convert IBA to IAA, promoting root hair growth.