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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Hoxc genes control hair growth through Wnt signaling.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

The hedgehog signaling pathway is crucial for hair growth but not for the initial creation of hair follicles.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Boosting HGF signaling could improve the creation of hair follicles in lab-made skin.

Human hair follicles can be used to create heart muscle cells.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Mutations in the HOXC13 gene cause hair and nail development issues.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

Abnormal Hedgehog signaling in blood cancers may help tumors grow and resist chemotherapy, suggesting potential for targeted treatments.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Most 46XX CAH patients have female identity, but a few identify as male and may need treatment and surgery.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

The Hairless gene is crucial for healthy skin and hair growth.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

The Hedgehog signaling pathway is important for skin and hair growth and can lead to cancer if it doesn't work right.

HEM-13HDC, a mix of 8 herbal extracts, helps hair grow and affects hair growth at a molecular level.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.