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A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

The flexible fixed-sequence testing method allows for more effective evaluation of multiple goals in a clinical trial while controlling the risk of false positives.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Unique genes in hair follicle cells help tissue regeneration.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

Targeting impaired Nrf2 signaling might help treat hidradenitis suppurativa early on.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A new DSG4 gene mutation causes hair defects in a young girl.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

Two new gene clusters important for hair formation were found on human chromosome 11.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

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

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A new gene mutation causes insulin resistance in a girl and her mother.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

FOL-005 peptide can reduce human hair growth by lowering FGF7 levels.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Pigs are a good model for studying human hair growth and disorders.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Two new gene clusters important for hair formation were found on human chromosome 11.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.