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

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

DNMT3A is crucial for healthy skin and hair growth.

The 14-3-3σ gene is essential for preventing hair loss.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

MPZL3 protein affects hair growth cycles and could help manage hair loss.

PAD enzymes play a key role in hair growth and structure.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

MEX3A is crucial for maintaining intestinal stem cells in mice.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Certain genes help dermal papillae cells in hair follicles grow and group together.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

Pannexin 3 is important for bone formation and the development of bone cells.

The role of 5α-reductase-3 in prostate cancer is unclear and needs more research.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

SIRT3 and SIRT7 genes may play a role in hair loss.

Trichohyalin and peptidylarginine deiminase type III are found together in rat hair follicles, with trichohyalin being modified after expression.

TRPV3 channels are involved in skin processes and are affected by shear stress, influencing itch and mechanotransduction.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.