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The new delivery system improves Alzheimer's symptoms by releasing Huperzine A slowly and effectively.

Baicalin nanocapsules greatly enhance its anticancer effects on breast cancer cells.

Desmoglein 3 organization in cell connections changes without calcium, affecting cell adhesion.

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

Nail stem cells help nail and finger regeneration through BMP signaling.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

Increasing XIAP and DDRGK1 can help prevent hearing loss from loud noise.

Activating the hexosamine pathway can improve skin health and increase hair follicle stem cells.

A rigid compound with a common structural motif was successfully synthesized.

The hydrogel is versatile and easy to make.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

High TSPEAR levels in colorectal cancer predict worse outcomes.

A certain gene variation can affect protein production and is linked to male pattern baldness.

A natural compound called VB-1 can help promote hair growth by boosting a specific cell signal in human skin cells.

BMP signaling controls hair growth and skin color.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

PCA hydrogel promotes hair growth by enhancing blood vessel formation and hair follicle stem cell activity.

A new mouse mutation causes skin and hair defects due to a gene change.

Mouse skin cells can become sperm-like cells in the lab.

Coal tar shampoo increases enzyme activity in hair follicles, enhancing carcinogen binding to DNA.

A new compound effectively inhibits human 5α-reductase 1.

Keratin 17 is crucial for cell growth in wound healing by aiding protein synthesis.

Finasteride helps female-pattern hair loss.

Microneedle arrays deliver botulinum toxin effectively for sweat suppression, similar to injections.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Mutations in the SNRPE gene cause hereditary hair loss.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.