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Lower levels of certain genes in hair cells improve hair loss treatment outcomes.

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

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

Higher levels of miR-1199-5p may reduce the effectiveness of certain prostate treatments.

Urotensin II increases growth and VEGF production in rat skin cells by turning on the Wnt-β-catenin pathway.

Liver enzyme helps minoxidil work better for blood vessel relaxation.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Increasing TSPO in the brain may help improve memory problems.

New LSS gene variants help understand congenital hypotrichosis 14 better.

The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

The study found that Tourette Syndrome may be linked to certain immune system processes and synaptic signaling.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

Certain gene variations increase the risk of alopecia areata in Koreans.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

The LTF gene may help predict and manage nonspecific orbital inflammation.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Researchers found a new mutation causing total hair loss from birth.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Researchers found 15 new genetic links to skin traits in Japanese women.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

A certain gene variation can affect protein production and is linked to male pattern baldness.

Inhibiting ACE2 improves skin regeneration during tissue expansion.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.