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

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

The article concludes that creating a detailed map of normal human skin at the single-cell level is important.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Scientists discovered two versions of a new human hair keratin gene.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

The hair follicle dermal sheath is essential for hair shedding and needs to communicate with the outer root sheath for normal hair growth cycles.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Stem cell therapy affects 15 key genes in rats with diabetes-related erectile dysfunction.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

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

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Activating the sonic hedgehog pathway in chicken embryos can permanently change scales to feathers.

People with Hidradenitis Suppurativa have less diverse skin bacteria and different bacterial metabolism than healthy individuals.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A unique gene mutation was found in a family with monilethrix.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Proinflammatory fibroblasts and vascular endothelial cells are key in keloid development.

Deleting part of a gene in mice causes wavy hair and high pup loss.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Sebaceous glands can regenerate after injury using stem cells from hair follicles.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

The research suggests that the ZP4 gene is linked to egg development in women with PCOS but requires more study to understand its role in infertility.