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Cyclohexyl salicylate promotes human hair growth and increases certain hair follicle stem cell progeny.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

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Mutations in hKAP1 genes may cause hereditary hair disorders.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

High beta-hydroxybutyrate levels may worsen hair loss in alopecia areata.

A herbal extract may help treat certain types of hair loss by reducing a specific gene's activity.

Hydrogen peroxide can affect wound healing.

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Hairless gene not strongly linked to baldness.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

New method, hair distribution width (HDW), improves accuracy in diagnosing androgenetic alopecia (AGA).

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A father and son in Yemen have a genetic condition causing hair loss and nail problems.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

New mutations in the hairless gene may cause hair loss and affect bone development.

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A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

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Caspase-7 has functions in skin and hair that are not related to cell death.

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

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

The UHS promoter is specific to mouse hair follicles.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

3-Hydroxypropionic acid may help treat hair loss by promoting hair growth in cells.