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Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Finasteride helps female-pattern hair loss.

A new gene mutation causes a rare type of hair loss.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

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

ANXA1 influences hair growth in mice through the EGF signaling pathway.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

TGF-β1 and 2 may play a role in hair loss in AGA.

WNT10A and EBF1 interaction affects hair growth in male-pattern baldness.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

A unique enzyme in guinea pig hair follicles helps form protein cross-links in hair.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Trps1 is essential for proper hair follicle development.

Thymosin β4 and VEGF are important for organ function and may help with blood vessel formation.

Genetic marker rs12558842 strongly linked to male hair loss.

A new DSG4 gene mutation causes hair defects in a young girl.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Wnt/β-catenin and TGF-β pathways affect hair loss, and activating Wnt/β-catenin could be a potential treatment.