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CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

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

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Vitamin D receptor gene changes don't affect alopecia areata risk.

RCVS should be considered in thunderclap headaches, and MRA and DSA are better for diagnosis than CT angiogram.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Avacopan may cause unexpected side effects, so early monitoring is important.

VR1 signaling can inhibit hair growth by affecting cell processes and increasing hair growth inhibitors.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

A specific gene change is linked to severe hair loss.

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

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Activin A helps heal skin wounds and protects the brain after injury.

Removing the VDR gene in skin cells reduces their growth and affects hair-related genes.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

TRPV3 channels are involved in skin processes and are affected by shear stress, influencing itch and mechanotransduction.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

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

A new gene mutation linked to a skin condition was found in a Spanish family.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

Precise objectives can improve student achievement in health education.

Three siblings with a genetic form of rickets showed different symptoms of the disease.