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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

PDRN is effective and safe for healing wounds and skin issues.

A new DSG4 gene mutation causes hair defects in a young girl.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

The PP2A-B55α protein is essential for brain and skin development in embryos.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A unique enzyme in guinea pig hair follicles helps form protein cross-links in hair.

A new method using gold nanoshells and infrared light effectively delivers siRNA to cancer and stem cells with precision and minimal damage.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

Syndecan-1 is essential for maintaining skin fat and preventing cold stress.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Gasdermin A3 causes hair follicle stem cells to activate too early, leading to hair loss.

The KAP13-3 gene in sheep affects wool quality by influencing keratin assembly.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Hair plucking quickly increases antizyme, reducing a specific enzyme activity in rats.

Balanced protease activity is crucial for healthy skin and hair development.

Mutations in the SNRPE gene cause hereditary hair loss.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

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

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Sciellin is a protein that helps form protective layers in skin, hair, and nails.