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Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

HLD10 can include increased body hair and Mongolian spots.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

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

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

Activating liver X receptors can reduce fibrosis by stopping certain immune cells from releasing harmful proteins.

Hoxc13 is essential for hair growth and follicle development.

Pax9 is crucial for proper tongue surface development and preventing skin-like changes.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

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

Hox genes control hair follicle stem cell regeneration in different body regions.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

ASH2L is essential for skin and hair development.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Hoxc genes control hair growth through Wnt signaling.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

ISX9 helps regrow hair by activating a specific cell signaling pathway.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.