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A specific RNA can help hair growth in baldness by boosting stem cell activity.

The alpha-helix was confirmed as a key structure in proteins.

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

Gut microbiota influences the development of alopecia areata.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Ceramide helps protect African–American hair from breakage.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

BMPs are important for hair growth and can counteract the negative effects of androgens on hair follicle stem cells.

Abrocitinib significantly improved hair regrowth in adolescents with alopecia areata without serious safety issues.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Key proteins and potential drugs for treating alopecia areata were identified.

Monoclonal antibody B72.3 selectively reacts with certain dog tissues, mainly in the gastrointestinal and respiratory tracts.

Epidermal Wnt/β-catenin signaling controls fat cell formation and hair growth.

A woman with CCCA has hair loss due to factors like straighteners and tight hairstyles, and treatments include steroids and avoiding certain hair products.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Sebaceous glands help study fatty acid transporters and binding proteins.

Specific RNA patterns are linked to alopecia areata.

JW0061 may be a new treatment for hair loss by promoting hair growth through WNT signaling.

Roots adapt to uneven environments by changing growth and gene expression.

A rare combination of hair loss and excessive fine hair growth was found in celiac disease patients.

Beard alopecia areata causes patchy beard hair loss, often treatable with janus kinase inhibitors.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Epigenetic changes in blood cells may contribute to alopecia areata.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Hair follicles play a crucial role in regulating skin barrier function.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.