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A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Epiregulin can help hair grow and may be useful for treating hair loss.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Proinflammatory fibroblasts and vascular endothelial cells are key in keloid development.

A humanized IL-2 fusion protein boosts T regulatory cells and helps control hair loss in Alopecia Areata.

RAGE is a potential target for melanoma treatment, but its effectiveness is uncertain due to variable expression levels.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

The HPV type 11 region activates hair-specific gene expression in mice.

Regulatory T cells help prevent autoimmunity and have potential for treating autoimmune diseases.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

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

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

PRF lysates reduce inflammation in cancer cells and boost immune response in healthy oral cells.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

Different γδ T cell types have unique roles in causing alopecia areata.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

COX-2 levels change during the hair cycle and affect skin and hair growth.

TRPV3 in skin cells causes inflammation and cell death.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Hair loss gene linked to prostate issues.

Basal cell carcinomas have much higher levels of Vitamin D3 receptors compared to healthy skin.

Some prostate cancers have gene changes that may affect treatment with certain drugs.