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A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

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

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Hair follicle stem cell exosomes help nerve regeneration.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Chemistry42 effectively creates and optimizes new molecules for drug discovery.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

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

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

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.