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Fibroblast Growth Factor-9 (FGF-9) can help improve heart function in diabetic mice after a heart attack by reducing inflammation and harmful changes to the heart's structure.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Researchers created a new mouse model for studying scleroderma.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

Fox genes are important for hair growth and development in cashmere goats.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

The study identified key genes and pathways linked to hair disorders, aiding precision medicine.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Activating c-Myc in skin causes rapid cell growth and changes, but these effects are reversible.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

The protein EZH2 blocks microRNA-22, increasing STK40 protein, which helps hair follicle stem cells change and grow hair.

miR-148a and miR-10a affect hair growth in Hu sheep.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Gene mutations can cause problems in male genital development.

A girl inherited excessive body hair from her mother and grandmother.

miR-144 affects hair growth by interacting with Lhx2.

miR-181a-5p helps hair growth by activating a specific signaling pathway.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.