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Rat hair follicle stem cells have functional oxytocin receptors, useful for studying neuropsychiatric disorders.

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

Mutations in the AR gene cause hair thinning and loss.

Hirsutism in females is caused by high male hormones or sensitive hair follicles.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

HDAC1 is crucial for skin development and preventing tumors.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Scientists made a mouse that can be made to lose hair and then grow it back.

Hair stem cells produce a protein called COL17A1 that plays a key role in their development and is linked to hair thinning and baldness.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

Targeting Keratin 17 may help overcome cancer therapy resistance.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

Claudin-1 is important for the barrier function and growth of hair.

Lipase H is important for hair follicle function and shaping hair fibers.

Heat treatment increases hair loss in certain mice.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.