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Balding hair follicles have reduced growth factors and increased inhibitory factors, suggesting new treatment paths for hair loss.

Lack of cystatin M/E causes thin hair and dry skin.

Dlx3 is essential for hair growth and regeneration.

S100A3 protein is mainly found in specific parts of human hair cells.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Inhibiting certain proteins harms hair follicle immunity and increases IL-33, affecting hair health.

Family members have similar hair protein patterns, which could be useful for genetic studies.

Activating PPAR-γ signalling can protect hair follicle stem cells from damage caused by chemotherapy.

FOXC1 is essential for keeping hair follicle stem cells inactive and maintaining their environment for healthy hair growth.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

HPT axis hormones boost mitochondrial function and growth in hair follicles, potentially aiding hair health.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

Nestin identifies specific progenitor cells in hair follicles that can become outer root sheath cells.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Specialized ribosomes affect aging in human skin cells.

Cyclic ADP-ribose helps regulate calcium and signals that promote hair growth in hair follicle cells.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

Keratin gene regulation was emerging, with a key transcription factor found to influence hair growth and gene expression.

Hair follicle stem cells change states with age, affecting hair growth and aging.

Monilethrix is linked to a gene cluster on chromosome 12.

Sox13 is a new marker for early hair follicle development and differentiation.

A high-fat diet may weaken tongue structure by reducing certain protein genes.

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

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

Stopping S100A3 activity slows down hair growth in mice.