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Colchicine can inhibit hair growth by affecting cell activity and protein expression in hair follicles.

GhPLDα1 helps thicken cotton fiber walls by boosting cellulose production.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

Apple polyphenol, especially oligomeric procyanidins, can reduce fat absorption and lower blood fat levels.

Drugs targeting EMT molecules show promise for treating lichen planopilaris.

Mrp3 may aid in wound healing and hair growth.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

The process efficiently converts α-pinene oxide to campholenic aldehyde using a special catalyst, achieving high yields quickly.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

LIPH mutations cause woolly hair in some Chinese people.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

LiPADI is a useful tool for monitoring the severity and treatment of lichen planus.

Lamins are vital for cell survival, organ development, and preventing premature aging.

Intermediate filaments are crucial for cell differentiation and stem cell function.

Cubosomes enhance antimicrobial peptide stability and effectiveness.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

Genetic variants in specific genes cause a type of hair loss.

Palmitoyl-GDPH speeds up wound healing and improves tissue regeneration without toxicity.

PIEZO1 helps keep hair follicle stem cells inactive, affecting hair growth.

Injectable platelet-rich fibrin improves hair growth and reduces hair loss in women.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

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

PAD type III enzyme is specific to rat skin and hair follicles.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.