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

Ac-GFFY-IGF peptide is a promising, safe, and effective treatment for hair loss, better than current options.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

LGR5 and LGR6 are expressed differently in various skin tumors, which may offer clues about their origins.

Epidermal growth factor disrupts hair and gland formation in bandicoots.

LHX2 and SOX9 identify unique hair follicle cell groups, crucial for hair maintenance.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

A dissolving microneedle patch with collagen XVII effectively promotes hair regrowth in androgenic alopecia.

Removing Lrig1-positive cells in mice leads to temporary loss of sebaceous glands.

Spiny mice have resilient, large mitochondria that help them regenerate tissue.

FGFR2 signaling controls Merkel cell formation in different skin regions.

GATA6 is important for maintaining and differentiating cells in a key area of human skin.

Sebaceous glands help study fatty acid transporters and binding proteins.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Increasing TSPO in the brain may help improve memory problems.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

FLCN helps control iron levels in cells.

FilaggrinHigh melanomas have active FGFR signaling and weak GNA14 and Th1 signatures.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

Normal skin results from interactions between EGF and the Tabby mutation.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

A gene variation is linked to hair thickness in Asians.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Blocking the HEDGEHOG-GLI1 pathway can reduce keloid growth and may be a potential treatment.