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Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

Adalimumab may cause severe hair loss in some patients.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Hexahydrobenzo[f]quinolines are effective at blocking the enzyme 5α-reductase.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Cantú syndrome is caused by mutations in the ABCC9 gene.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

NFATc1 controls hair stem cell activity, affecting hair growth and could be a target for hair loss treatments.

Coenzyme Q10 may protect liver function but doesn't reduce hair loss from anthracycline antibiotics.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

IL-15 helps maintain hair growth and protects the immune status of hair follicles.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

A new gene mutation causes a rare type of hair loss.

The fuzzy gene is crucial for controlling hair growth cycles.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

Baricitinib helps regrow hair and improves quality of life and mental health in severe alopecia areata patients.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Activated protein C helps protect mice from long-term radiation damage.

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Targeting NMMHC IIA may help treat blood-brain barrier damage.

ILC1-like cells can cause alopecia areata by affecting hair follicles.