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Verteporfin reduces growth and stem cell traits in rat hair follicle cells by blocking the Hippo pathway.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Frontal fibrosing alopecia has occurred in two related male families.

Mutations in the hairless gene cause a rare form of permanent hair loss.

A new type of nerve cell involved in itch perception was discovered.

Gefitinib can cause hair loss without scarring.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

IL-9/IL-9R signaling can negatively affect human hair growth and may be a target for treating hair loss conditions.

Retinoic acid, glucocorticoids, and IGF1 increase IGFBP-3 production in human dermal papilla cells, affecting hair growth.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Dacomitinib can cause nail and skin issues, but these can be managed without stopping the drug.

Nail-matrical fibroblasts can make non-nail cells produce hard keratin, useful for nail repair.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Tofacitinib may help treat nail dystrophy, especially when other treatments fail.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

FFA can be mistaken for rosacea, requiring specific treatment for accurate diagnosis and management.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

A cancer patient's hair became permanently curly after treatment with nivolumab.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition that may respond to antiandrogen therapy.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Caspase-1 helps hair stem cells move to heal wounded or inflamed skin.

FFA patients have fewer melanocytes and thinner skin compared to others.

Four new cases confirmed the unique features of follicular porokeratosis.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

The technique allowed noninvasive tracking of hair stem cell survival and growth, showing potential for hair loss research.

Stopping nalfurafine reversed hair loss in a hemodialysis patient.