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A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Ivacaftor can protect against noise-induced hearing loss by reducing oxidative stress.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

The AVET system effectively delivers genes to human keratinocytes and may help treat skin diseases.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A vitamin D receptor mutation causes rickets and affects immune responses.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

The vitamin D receptor is involved in multiple body functions beyond calcium regulation, including immune response and rapid reactions not related to gene activity.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

Controlling transposable elements is crucial for successful tissue regeneration.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

IL-18 signaling helps mature Tregs move into the thymus.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

Osthole inhibits the TRPV3 channel by binding to specific sites, potentially aiding drug development for skin diseases and cancers.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

Lentiviral vector effectiveness in skin is influenced by external factors, not receptor availability.