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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

HPV type 56 can hide in hair follicles even without visible warts.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

HAIRCARECUBE TM (HCC) helps hair products work better by getting active ingredients deeper into the hair.

IL-26 has antimicrobial and pro-inflammatory effects in the chronic skin condition Hidradenitis Suppurativa.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Hair care products used for 4 weeks made hair smoother.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

Keratin's mechanical properties are influenced by hydrogen bonds and secondary structure, and can be improved with the SPD-2 peptide.

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

A specially designed molybdenum oxide nanozyme can treat and monitor acute kidney injury effectively.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

The study found an efficient method to extract antioxidants from Hibiscus leaves.

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YH0618 helps reduce chemotherapy-induced hair loss by targeting specific proteins and pathways.

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A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

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Ajwain seed extract improved skin healing and hair growth in a mouse skin irritation model.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Cyclohexyl salicylate may help hair growth and treat hair loss.

An 11-year-old girl with Kawasaki disease experienced hair loss that improved after treatment.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.