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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Calcium channels are vital for normal skin function and their dysfunction can lead to skin issues.

FER and TOR signaling help root hair growth in low temperature and low nitrate conditions.

The Hairless gene is crucial for healthy skin and hair growth.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

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These gene variations are not linked to alopecia areata in Egyptians.

Natural α-hydroxyl acids cause skin exfoliation by activating TRPV3 channels.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A new DSG4 gene mutation causes hair defects in a young girl.

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.

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Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

CD101 is highly effective in treating dermatophytosis in guinea pigs.

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

The 755 nm laser is more effective and safer for hair removal than the dual-wavelength laser.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

The B2 genes are crucial for hair growth in rats.

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Introducing the rat OTC gene partially corrected OTC deficiency in mice.

A protein called PLC2 is important for the growth and development of plant roots influenced by auxin.

Alopecia areata patients have higher levels of certain immune receptors, suggesting new treatment possibilities.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.