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The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

Dual TCR Treg cells are common in mouse tissues and vary by location.

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

Lack of functional CYLD in mice leads to early aging and cancer.

S100A3 protein is crucial for hair shaft formation in mice.

Id2 gene helps keep hair follicle stem cells inactive.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

SSO helps in skin protection and keratinization.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

Discoid lupus erythematosus involves immune activation and fibrosis around hair follicles, with shared pathways across humans, dogs, and mice, suggesting potential treatments for both humans and animals.

CD2 might be a new treatment target for patchy alopecia areata.

A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

PCOS involves immune and genetic factors, with key roles for T cells and specific genes.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

A specific gene mutation causes a severe skin disorder in a family.

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

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

SQSTM1 is linked to increased risk of alopecia areata.

Scalp hair follicle cells help protect and heal skin in certain skin conditions.

Human scalp fat stem cells showed improved cartilage-like development on a special scaffold with freeze-thaw treatment.

PCOS involves genetic and immune factors, especially T cells, affecting its development.