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Compounds from Pterocarpus indicus may help treat benign prostatic hyperplasia by stopping cell growth.

A20 protein is crucial for normal skin and hair development.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

People with PCOS have higher levels of PAI-1, which may increase their risk of heart disease and fertility issues.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

ERK activation spreads between cells, influencing cell division and wound healing.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Blocking the Wnt/β‐catenin pathway can speed up wound healing, reduce scarring, and improve cartilage repair.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Pig skin cells can turn into mesodermal cells but lose their ability to become neural cells.

A specific gene mutation causes a severe skin disorder in a family.

Poromas are related to sweat duct cells, and CK patterns help distinguish apocrine poromas from other neoplasms.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

Certain genes may promote longer root hairs in plants when phosphorus is low.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Lack of functional CYLD in mice leads to early aging and cancer.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

BMI1 is essential for preventing hair greying and maintaining hair color.