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Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Methyl jasmonate boosts tanshinone production in Salvia miltiorrhiza callus cultures.

Hemoglobin α acts as an antioxidant in skin cells, especially protecting hair follicle stem cells from UV damage.

The Brigham Eyebrow Tool for Alopecia is a simple and reliable way to measure eyebrow hair loss.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

IL-13 protein is much higher in the skin of atopic dermatitis patients than in healthy skin.

Thymosin β4 helps in cell activities, healing, and organ preservation, and treats hair loss and skin injuries.

β‐thymosins, especially thymosin β4, help in heart protection, wound healing, and hair growth by stabilizing actin in cells.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

A new gene mutation causes insulin resistance in a girl and her mother.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

Human hair follicles have their own thyroid hormone system.

Trichohyalin may trigger the immune response causing alopecia areata.

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

Abatacept may help some people with alopecia areata regrow hair.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

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

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Baricitinib is effective and safe for severe alopecia areata, working similarly with or without an atopic background.