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Ezh2 controls skin development by balancing signals for dermal and epidermal growth.

The PML protein helps prevent skin cancer in mice.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

Notch/CSL signaling controls hair follicle differentiation through Wnt5a and FoxN1.

Poromas are related to sweat duct cells, and CK patterns help distinguish apocrine poromas from other neoplasms.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

Hox genes control hair growth patterns in mammals by regulating stem cell activity in the skin.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

Blocking mTORC1 reduces skin tumor growth in mice.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

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

The type of tumor suppressor gene lost affects the behavior of skin cancer.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

Overexpressing ornithine decarboxylase and v-Ha-ras in keratinocytes leads to invasiveness and malignancy.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.