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A new compound shows promise as a topical treatment for hair loss.

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

GIANT improves brain imaging by using genetics to better map brain regions.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Tofacitinib significantly improved symptoms in a patient with overlapping autoimmune disorders.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Tofacitinib significantly improved hair loss and lesions in a patient with overlapping autoimmune disorders.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

New mutations in the DSG4 gene cause a rare hair condition.

The K14 promoter is more active in skin cells than the K5 promoter.

Changes in certain RNA and protein levels may contribute to alopecia areata and could be treatment targets.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

A synthetic octapeptide may help promote hair growth and counteract hair loss.

Treatment restored normal sexual characteristics and blood condition in a patient with testicular cancer.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

The scraggly mutation causes hair loss and skin defects in mice.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

t-Flavanone may help hair growth by reducing a specific protein's activity in skin cells.

A genetic variant in the KRT25 gene causes tightly curled hair.

Tislelizumab can cause cutaneous lupus erythematosus.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

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

β-Catenin signaling is involved in brain cell growth after injury and could be a therapy target.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

A child was initially wrongly diagnosed with a fungal scalp infection but actually had a non-scarring hair loss condition called Temporal Triangular Alopecia.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Low Level Laser Therapy can promote hair growth.