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The vitamin D receptor helps control hair growth and may protect against certain skin tumors.

Vitamin D receptor is essential for adult hair growth.

Vitamin D is important for skin cell growth and health, and its active form and receptor play key roles in skin and hair processes.

Calcium supplements improved bone deformities but not skin papules or hair loss.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

The VDR gene polymorphism does not affect BDNF levels in autoimmune thyroiditis and hypothyroidism patients.

Diet can prevent bone issues but not hair loss in mice lacking vitamin D receptors.

Vitamin D and calcium are crucial for proper skin wound healing.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Two new gene mutations cause a rare hair disorder.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

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

A specific gene mutation causes congenital hair loss.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Specific keratin gene mutations can cause monilethrix.