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Researchers found four genes that could help diagnose severe alopecia areata early.

A woman with severe hair loss was successfully treated with the drug adalimumab.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Sca-1+ cells in newborn mouse skin may become fat cells.

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

Congenital alopecia areata may have genetic links and topical corticosteroids are an effective treatment.

Ubiquitination of the insulin receptor regulates collagen secretion in human skin.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Targeting specific T cells may help treat alopecia areata.

IMG-007 helps regrow hair and reduce scalp inflammation in severe alopecia areata.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

CUX1 boosts sheep hair cell growth and affects curl patterns.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

Betacellulin helps blood vessel growth in wounds but delays hair growth.

CNGC14 is crucial for calcium entry needed for root hair growth in plants.

Dr. Connelly agrees that linear basal cell carcinomas might be more aggressive but highlights the study's lack of clear criteria to identify them.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

Alopecia areata involves unique activation of certain immune cells.

M-CSF-stimulated myeloid cells can cause alopecia areata in mice.

The 6-year-old Somalian girl fully recovered from her symptoms after successful surgery and treatment.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

The study found that a key immune pathway protecting hair follicles is reduced in a mouse model of scarring hair loss.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.