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The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Recombinant type XVII collagen may help regrow hair by activating specific cell pathways.

A specific gene mutation causes different hair defects in Indian monilethrix families.

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

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Mutations in the HOXC13 gene cause hair and nail development issues.

A new staining method shows a special area in the hair's skin layer with lots of proteoglycans.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

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

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Ptprq has multiple forms that change during inner ear development.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Inherited color dilution in rabbits is linked to DNA methylation changes.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Higher CRHR1 levels in AA patients lead to increased inflammation.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

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

Hydroxypinacolone retinoate is a potent anti-aging ingredient for skin that is more effective and less irritating than other forms of retinoids.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

ARHGEF3 is essential for proper hair follicle development in mice.

Collagen XVII is crucial for skin cell growth and nail health.