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Tiny particles from 3D-grown skin cells speed up wound healing by promoting blood vessel growth.

Finding functions for unknown GPCRs is hard but key for making new drugs.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

Human skin can make serotonin and melatonin, which help protect and maintain it.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

Human skin can make serotonin and melatonin.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Melatonin is important for skin health and protection, and can be made by the skin or applied to it.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Too much Smad7 changes skin and hair development by breaking down a protein called β-catenin, leading to more oil glands and fewer hair follicles.

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

Finasteride effectively blocks rat enzymes, but with varying methods and strength.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Androgens block hair growth by disrupting cell signals; targeting GSK-3 may help treat hair loss.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Blocking β-catenin in skin cells improves hair growth during wound healing.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Noncoding dsRNA boosts hair growth by activating TLR3 and increasing retinoic acid.