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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.

Mitochondrial genes help predict breast cancer outcomes and spread.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

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

Researchers found a new mutation causing total hair loss from birth.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

A specific genetic deletion in goats affects cashmere yield and thickness.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The article's correction clarifies scientific and methodological concerns about miR-200c-3p's role in alopecia areata.

A gene mutation in mice causes permanent hair loss and skin issues.

Understanding snoRNA regulation may help slow skin aging.

Precise objectives can improve student achievement in health education.

TEDAR is crucial for skin cell differentiation and barrier formation.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.

miR-146b-5p may help treat hair loss by promoting hair growth and reducing inflammation.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A compound from Calophyllum inophyllum L. leaf may help treat non-small cell lung cancer.

miR-144 affects hair growth by interacting with Lhx2.