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A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

PM-9, like finasteride, may help treat certain diseases by blocking a key enzyme.

Anti-CD19 therapy may help treat SLE and NMOSD.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

Niosomes improve aminexil's effectiveness in preventing hair loss without needing propylene glycol.

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

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

The scraggly mutation causes hair loss and skin defects in mice.

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Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Genetic profiling can improve androgenetic alopecia treatment by predicting drug response and minimizing side effects.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

Some skin medications can have harmful interactions with the COVID-19 drug nirmatrelvir-ritonavir, but not with molnupiravir.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Tamsulosin increases the risk of floppy iris during eye surgery.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Combining Ficlatuzumab and Gefitinib can cause severe hair loss.

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ASLNC168501 may help treat hair loss by boosting hair follicle stem cell activity.