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PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A new gene mutation is linked to monilethrix in the studied family.

A gene mutation in mice causes permanent hair loss and skin issues.

A father and son in Yemen have a genetic condition causing hair loss and nail problems.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Hair follicles repair 3D injuries using a 2D healing process.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Growth hormone-releasing hormone (GHRH) boosts hair growth and human scalp hair follicles have their own growth hormone system.

Netherton's disease causes multiple hair defects.

Nfib in hair follicle stem cells boosts melanocyte stem cell growth and differentiation.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Melatonin affects when and how goat hair follicle genes turn on and off during growth cycles.

Mutations in the KRT85 gene cause hair and nail problems.

NADPH oxidase 4 is key for stem cell activity and growth under low oxygen.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

S100a4 is key for hair growth in cashmere goats.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

LPA 4 helps control blood and lymph vessel development in zebrafish.

High-frequency ultrasonography helps diagnose and manage hair and nail disorders safely and effectively.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

HBCs in the olfactory epithelium can self-renew or differentiate into other cell types, with specific patterns during regeneration.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.

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

The research shows that hydrogen bonds greatly affect the crystal structure of a Finasteride derivative.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.