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Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

In 1995, international medical graduates did better than U.S. graduates on a medical exam.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Certain medications and smaller pupil size increase the risk of intraoperative floppy iris syndrome during eye surgery.

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The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

The treatment was not recommended due to limited effectiveness and significant side effects.

Certain medications and conditions increase the risk of intraoperative floppy-iris syndrome.

Tamsulosin increases the risk of floppy iris during eye surgery.

IL-18 signaling helps mature Tregs move into the thymus.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Prophylactic pilocarpine may not prevent angle closure in the other eye.

CD8+ T cells re-expressing CD45RA may predict treatment resistance in severe alopecia areata.

Increased TEMRA cells can predict treatment outcomes in rapidly progressive alopecia areata.

The T allele of the PTPN22 gene may increase the risk of alopecia areata.

It's not possible to get unlimited hair for transplants from the same donor area.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A chemical called 5-Bromo-2′-deoxyuridine caused rapid hair loss in mice by killing certain skin cells through a specific cell death pathway.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Asian immigrant mothers in Leicestershire need better obstetric care to reduce higher perinatal mortality risks.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

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The CD44-CD49d complex boosts T cell activation and survival in autoimmune disease.

Certain medications, hypertension, and short eye length increase the risk of Intraoperative Floppy Iris Syndrome during cataract surgery.

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Early stage bald spots are linked to skin inflammation and damage to the upper part of the hair follicle.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.