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Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

GLI2 increases follistatin production in human skin cells.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Ginkgo biloba polysaccharides may reduce inflammation and promote hair growth in mice with hair loss.

Lgr6+ cells are important for tissue repair and could be a target for treating cancer and other diseases.

Higher anxiety symptoms and social behavior affect stress levels in hair.

Editing the FGF5 gene in sheep increases fine wool growth.

Few dermatology programs mention gender-affirming care, highlighting a need for better training and visibility.

Thymosin beta 4 protects cells from damage by blocking a harmful microRNA and boosting a protective gene.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Galectin-1 helps in RNA processing in cell nuclei.

Targeting Sirt1 can reduce androgen levels and slow glioblastoma growth.

Ginsenoside compound K shows promise for treating metabolic diseases like diabetes and obesity.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

TSPO might help treat anxiety and depression.

Social isolation makes rats more sensitive to alcohol's effects on the brain.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

GLP-1 receptor agonists may help manage and prevent diabetic foot ulcers.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A 44-year-old woman with Down's syndrome was diagnosed with both rheumatoid and gouty arthritis and treated with multiple medications.

G-1 promotes hair growth in female mice by activating specific signaling pathways.