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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.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

The HCR gene contributes to psoriasis risk.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

UC.145 may be a new biomarker for predicting gastric cancer.

Spt4 and Spt6 are essential for fat cell development.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Cathepsin L deficiency causes hair and skin issues in mice.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

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.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

The RAS pathway affects hair growth differently in CFCS and CS.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

The Celsr1 gene is crucial for normal hair patterning in mice.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

Unique genes in hair follicle cells help tissue regeneration.

Phospholipase C-δ1 is crucial for normal hair development.

CCN1 may aid wound healing, but more research with larger samples is needed.