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Custom software found that common allergy drugs might have new uses for various conditions and could improve survival in some cancers.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

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Using existing drugs for new purposes could be a cost-effective way to treat chest pain and non-clogged heart arteries, with some drugs for lung blood pressure showing promise but needing more testing.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Machine learning identified three unique subtypes of androgen excess in women with PCOS, each with different metabolic risks.

The combination therapy is effective and well-tolerated for treating esophageal cancer.

Recent selection on immune response genes was identified across seven ethnicities.

The document concludes that PK/PD modeling is important for determining the safe and effective dosages of drugs.

Polish medical societies recommend personalized treatment for PCOS based on the patient's specific symptoms and use the Rotterdam criteria for diagnosis.

Enriching the French health care database with external data greatly improved its usefulness.

PPCM microspheres can effectively release finasteride over 42 days.

The lotion CG428 did not show effectiveness in treating permanent hair loss in breast cancer survivors.

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PPCM microspheres allow controlled finasteride release over 24 hours.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

MEGA PROTAC improves prediction and ranking of protein complexes better than existing methods.

The flexible fixed-sequence testing method allows for more effective evaluation of multiple goals in a clinical trial while controlling the risk of false positives.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Forensic DNA phenotyping faces challenges due to inconsistent terminology, limited genetic understanding, and debates over technology and models.

Combining glucocorticoids with immunosuppressants like cyclophosphamide improves remission and reduces relapse in pemphigus patients.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.