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A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Testing for the NUDT 15 variant is crucial before starting azathioprine, especially in Asians.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

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Certain miRNAs are linked to Cashmere goat hair quality.

MK-0773 safely increased muscle mass but did not improve muscle strength or function in elderly women with sarcopenia.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

The fragrance cyclohexyl salicylate helps promote hair growth and increase hair stem cell numbers.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

Leporacarus gibbus mite was found in a domestic rabbit in Espírito Santo, Brazil, for the first time.

A gene mutation causes curly hair and hair loss in rats.

Recognizing IPPP is crucial to prevent misdiagnosis and unnecessary treatments.

AgK114 protein helps in hamster skin injury recovery.

The thulium laser and PDRN injections effectively improved hair thickness in patients with pattern hair loss.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

PLA2R1 overexpression harms kidney cells by stopping their growth cycle.

AH-001 could be a safer and more effective treatment for hair loss.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Exosomal miR-222-3p reduces melanin production in rabbits by targeting the SOX10 gene.

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Polygoni Cuspidati Rhizoma et Radix contains compounds that inhibit certain enzymes.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

Don't combine abiraterone and spironolactone for prostate cancer treatment as it may worsen the disease.

TH07 is a topical combination of finasteride, latanoprost, and minoxidil, and shows promise.

A rare skin condition in a 17-year-old was diagnosed late, stressing the need for careful evaluation and genetic testing.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.