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A new, efficient method has been developed to detect darolutamide and thalidomide, drugs used for certain hair loss and prostate cancer treatments, in pharmaceuticals and body fluids.

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DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

Activated ras can protect kidney cells from a certain substance that causes cell death.

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

SPET-085 effectively inhibits an enzyme linked to prostate issues, similar to finasteride.

The method effectively detects MeT and TP in dried blood spots after cream application.

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

Biofeedback treatment for dysfunctional voiding in adults showed no symptom improvement.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

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The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

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ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

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Method measures tamsulosin and finasteride in medicine accurately.

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The method is effective and suitable for testing finasteride tablets.

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A reliable method was developed to measure dutasteride in tablets accurately and consistently.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

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Two methods can measure finasteride and tamsulosin hydrochloride; HPLC is more advantageous, while TLC offers better separation.