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The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

JAM-A helps hair regrowth in alopecia areata by protecting VCAN in skin cells.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Scientists improved an enzyme to better produce a hair growth-promoting chemical from an immunosuppressant.

ECM1-modified stem cells can effectively treat liver cirrhosis.

FLCN helps control iron levels in cells.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Trichohyalin, a protein from pig tongue, was purified and found to have a filamentous structure.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Black women with CCCA are more likely to have uterine fibroids.

The new formulation improved the skin absorption of the drug Thiocolchicoside.

Stat3 helps skin heal but can also cause skin diseases if overactive.

CCCA can appear as patchy hair loss in younger men, not just the usual pattern.

NKCC1 transporters help control neuron excitability and inhibition.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

The scaffold improves wound healing and tissue regeneration.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Higher Galectin-3 levels are linked to insulin resistance and may predict androgenetic alopecia severity.

Elderly patients with CCCA were all African American with low vitamin D, but no iron or zinc deficiencies, and no hormonal imbalances compared to younger patients.

CCCA causes progressive hair loss in Black women, starting from a central scalp patch.

Cholesterol transport in hair follicles decreases from growth to regression phase.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

An antibiotic called co-trimoxazole can effectively treat autoimmune diseases.