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Researchers found 15 new genetic links to skin traits in Japanese women.

MicroRNAs are crucial in controlling cell signaling, affecting cancer and tissue regeneration.

The androgen receptor is a promising target for breast cancer treatment, especially in triple-negative cases, but more research is needed for personalized therapies.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

Temporary ROS production in cultured human hair follicles promotes growth and stem cell activation.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Skin aging is due to impaired stem cell mobilization or fewer responsive stem cells.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

Lung and liver macrophages protect our tissues and their dysfunction can cause various diseases.

Dermal EZH2 controls skin cell growth and differentiation in mice.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Endoglin is crucial for proper hair growth cycles and stem cell activation in mice.

Male pattern baldness involves genetics, hormones, and needs better treatments.

Cell polarity signaling controls tissue mechanics and cell fate, with complex interactions and varying pathways across species.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

Cell aging can be both good and bad for tissue repair.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

The document concludes that better targeted treatments are needed for wound healing, and single-cell technologies may improve cell-based therapies.

TGF-β signaling is crucial for stem cell maintenance, differentiation, and has implications for cancer treatment.

New genes found linked to balding, may help develop future treatments.

The research showed how melanocytes develop, move, and respond to UV light, and their stem cells' role in hair color and skin cancer risk.