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TCDD changes skin cell growth and keratin production in mice.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Lower GATA3 levels in mice help hair regrow by changing certain immune cells.

Activating TLR3 may help produce retinoic acid, important for tissue regeneration.

MLPH helps hair grow by activating IGF-1 signaling in hair cells.

Insulin-dependent diabetes alters hair's molecular structure, making it useful for studying diabetes effects.

Lipin-1 is important for skin cell differentiation and skin barrier function.

IL-3 worsens lupus nephritis and blocking it improves kidney health.

Krtap11-1 is important for hair strength and structure.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Targeting DKK3–CKAP4 can help reverse hair loss in androgenetic alopecia.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

Interleukin‐1 α reduces androgen receptor levels and increases certain cytokines in human scalp cells.

Desmocollin 1 and 3 have distinct patterns in human tissues, with Dsc1 in specific skin and hair layers and Dsc3 in various epithelial layers.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

The vitamin D receptor can work without its usual activating molecule.

Mutations in the hairless protein gene cause hair loss.

ILK is essential for skin development, pigmentation, and healing.

A specific DNA region controls skin cell gene expression by working with certain proteins.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

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

New vitamin D3 forms need the vitamin D receptor to reduce fibrosis in human cells.

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

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.