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Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

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

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

Men with male pattern baldness may have a higher risk of heart disease due to increased levels of a specific lipid in their blood.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Diagonal earlobe and preauricular creases may indicate higher coronary artery disease risk in men.

Laminin-511 is essential for proper melanocyte movement and development in mice.

Retinoic acid affects male and female muscle energy use and function differently.

New genes and pathways are important for testosterone production and male sexual development.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

The Hairless gene is crucial for healthy skin and hair growth.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Lipedematous scalp may be underdiagnosed and doesn't improve with finasteride.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

EAAT4 decreases with age, harming skin function and calcium balance.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.