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Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A specific gene mutation causes sparse, brittle hair in a family.

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

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.

KLF4 is important for keeping hair follicle stem cells inactive.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Nonpalmoplantar skin cells can be made to express keratin 9 by interacting with palmoplantar fibroblasts.

K16 can partially replace K14 but causes hair loss and skin issues.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Dickkopf-related Protein 2 can help hair grow by activating a specific cell pathway.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

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

HSD11b1 affects skin nerves and increases non-histaminergic itch.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Hair root sheaths can be used to accurately analyze genetic markers.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

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

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

A mutation in the Sgkl gene causes defective hair growth in mice.

Activating Kras in mouse skin causes excess skin and hair loss.

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.