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No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

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

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

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

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

Defective nuclear transport may cause gene expression changes in Progeria.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

A specific gene variant may increase the risk of developing Alopecia Areata.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

In STSD patients, the body compensates for low androgen levels by increasing another enzyme's activity.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

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

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Mice without certain skin proteins had abnormal skin and hair development.

A gene mutation causes curly hair and hair loss in rats.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

Hsc70 protein may influence hair growth by responding to androgens.

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

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

Blocking CXCR4 may help treat hidradenitis suppurativa.