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Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Nrf-2-modified stem cells from hair follicles significantly improve ulcerative colitis in rats.

Zinc is crucial for health, and its transporters are linked to various diseases.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

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.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

Paeoniflorin protects brain cells by involving a specific protein and neurosteroids.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Gene variations may increase oxidative stress in male pattern baldness.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Targeting specific metabolic and ionic pathways may improve alopecia areata treatment.

Raltitrexed conjugates are less potent than the free drug but more effective at high concentrations.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.

Peptide-based PROTACs show promise in targeting hard-to-treat proteins, especially for cancer therapy.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

The new minoxidil formulation could better promote hair growth for treating androgenic alopecia.

Testosterone changes how certain channels work in male rat reproductive tracts, affecting fertility-related fluid balance.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

Inositol prevents hair loss and improves health in rats.

Targeting SOX proteins may improve cancer treatment by restoring immune function.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

DGAT1 enzyme helps make diacylglycerols, waxes, and retinyl esters.