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TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Mice without the p21 gene can fully regenerate injured ears due to reduced Sdf1 increase and leukocyte recruitment, suggesting new ways to induce tissue regeneration in mammals.

A substance called epidermal growth factor helps increase the growth of important hair follicle cells by activating a specific cell communication route.

Two main types of fibroblasts with unique functions and additional subtypes were identified in human skin.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

p63 controls Satb1 to help skin develop properly.

ASH2L is essential for skin and hair development.

GLI2 increases follistatin production in human skin cells.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Hemidesmosomes and Notch signaling help skin cells mature by moving them to the outer layer.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Abnormal growth factors can cause hair and skin issues.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

EGFR deficiency in skin causes hair follicle issues and inflammation.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

RhoA helps skin stem cells grow, aiding wound healing.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.