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Early and late matrix progenitors in hair follicles create different cell layers, with early ones forming the companion layer and later ones forming the inner root sheath and hair shaft.

Dermal Wnt/β-catenin signaling is important for the proper size and development of hair follicles.

Mammary stem cells drive mammary gland growth by branching and cell mixing.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

EDA2R gene linked to hair loss.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A gene variation is linked to hair thickness in Asians.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.