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Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

A mutation in the KRT74 gene causes tightly curled hair.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Certain variations in the vitamin D receptor gene are linked to an increased risk of polycystic ovary syndrome.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Vitamin D receptor helps prevent skin tumors.

Sebum helps protect human skin from microbes.

Type XIX Collagen is present in specific skin and hair cells during development.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

New genetic mutations causing hair loss were found in a Chinese family.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

Dkk genes evolved faster in birds and reptiles, affecting hair development functions.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

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

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

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

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

Aging-related changes in hair follicle stem cells can be partially reversed with a specific treatment.