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

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

NKG2D+CD4+ T cells are higher in alopecia areata patients and may be involved in the disease.

The CD44-CD49d complex boosts T cell activation and survival in autoimmune disease.

Elf5 is important for skin stem cell growth and could help treat skin and hair problems.

Inflammation is linked to hair loss.

A missing mK6irs1 gene causes hair loss in mice.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

A specific gene mutation causes severe skin and nail issues and hair loss.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

FoxN1 overexpression in young mice harms immune cell and skin development.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Nucleic acids trigger chemokine production in skin cells, affecting skin inflammation.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A new mouse model for vitiligo helps study immune responses and potential treatments.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

miR-22 helps skin cancer grow and spread by activating specific cell signals.

Lactate production is important for activating hair growth stem cells.

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

Secukinumab reduces immune activity in hidradenitis suppurativa skin.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

A truncated protein linked to breast cancer may change cell adhesion.