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Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

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

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

Injecting specific oligonucleotides can change hair growth and structure by altering a gene.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

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

Keratin gene regulation is similar across mammals, affecting hair follicle differentiation.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

UC.145 may be a new biomarker for predicting gastric cancer.

Certain gene variations are found in people with polycystic ovary syndrome.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

A gene mutation causes curly hair and hair loss in rats.

A new gene mutation linked to a skin condition was found in a Spanish family.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

Two new gene clusters important for hair formation were found on human chromosome 11.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

KRTAP genes evolved early in mammals, leading to diverse hair traits.

Two new gene clusters important for hair formation were found on human chromosome 11.

BRG1 is essential for skin cells to move and heal wounds properly.

Keratin mutations cause skin diseases and could lead to new treatments.

Prostaglandins and the enzyme AKR1C3 could play a role in skin cancer and hair loss, and further research is needed to understand these mechanisms.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.