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Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

ILC1-like cells can cause alopecia areata by affecting hair follicles.

COVID-19 infection rates were low in patients with immune diseases, regardless of their treatment type.

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A specific gene variation in goats is linked to better growth traits.

The study found that combining different databases gives a better estimate of drug side effects in hospitals.

The authors agree they didn't follow the original criteria strictly but found the Ottawa rule effective in all tested patients and suggest it might have wider use.

The XBB lineage of the Omicron variant spread rapidly in Southeastern Wisconsin.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Hair loss can occur in the area where hair was taken for a transplant.

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.

Sulfur-35 can be used to track hair growth and past exposure.

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Referral rates for anaphylaxis patients improved significantly after implementing guidelines.

Ticagrelor works better than clopidogrel in reducing platelet activity in elderly patients with acute coronary syndrome.

The DNS FUE technique offers discreet hair transplants with high satisfaction and low damage rates.

CD44 variant changes start alopecia areata, but don't maintain it.

The assay effectively identifies compounds that affect immune cell activation.

Most cats in Bangladesh have flea infestations, especially kittens and females.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

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

Iron infusions can help improve hair loss in patients who can't take oral iron supplements.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.