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The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Two new mite species were found in a monkey's hair follicles, leading to a new genus and family proposal.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

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pCLCA2 protein may help maintain skin structure and function.

ELF5 is essential for skin cell growth and maintenance.

Nod factor can trigger changes in legume root hairs with just one molecule.

Aromatase gene variation may increase female hair loss risk.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

ERULUS is crucial for root hair growth by controlling calcium levels.

Overactive Wnt5a disrupts hair follicle orientation in mice.

Lack of cystatin M/E causes thin hair and dry skin.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A mutation in the KRT74 gene causes tightly curled hair.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Methamphetamine affects gene expression in rat whisker follicles, with key genes linked to addiction.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Two main types of fibroblasts with unique functions and additional subtypes were identified in human skin.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.