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Mefloquine, an antimalarial drug, is effective in killing melanoma cells resistant to other treatments by causing lethal stress in the cells.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

UDCA reduces inflammation and joint damage in rheumatoid arthritis.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

GnRH analogue can help diagnose ovarian causes of high testosterone in postmenopausal women when scans don't show the cause.

Ruxolitinib treatment led to unexpected hair regrowth in a patient with alopecia universalis.

A new mouse mutation causes skin and hair defects due to a gene change.

A girl with rickets and hair loss was found to have a rare condition where her body didn't respond to vitamin D treatment.

The activity of a specific rat enzyme in the prostate and epididymis is highly dependent on the acidity level.

Targeting amphiregulin may improve treatment for fibrotic diseases and cancer.

Runx1 affects hair growth, cancer development, and autoimmune diseases in epithelial tissues.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

Aged Julia Creek dunnarts suffer from reproductive and hormonal issues, aiding conservation efforts.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Ritlecitinib improves emotional well-being and activity levels in alopecia areata patients.

Gene linked to common hair loss found, may lead to new treatments.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

A man's rare adrenal tumor caused feminization and white hair, was removed surgically, and improved after treatment.

Erdr1 could be a new marker for diagnosing hair loss.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Mutations in the SNRPE gene cause hereditary hair loss.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Male infertility often lacks thorough investigation, potentially missing reversible causes.

Two gene areas linked to male pattern baldness found, more research needed.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Researchers found 15 new genetic links to skin traits in Japanese women.

The combination therapy significantly improved Riehl’s melanosis in patients without serious side effects.

Zinc supplements effectively treat acrodermatitis enteropathica.