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Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Formyl-peptide receptor agonists could be new anti-inflammatory drugs.

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

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

The article concludes that while we understand a lot about how melanocytes age and how this can prevent cancer, there are still unanswered questions about certain pathways and genes involved.

Follistatin helps hair growth and cycling, while activin prevents it.

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

New butyric acid prodrugs show promise for cancer treatment, anemia management, and protecting hair from chemotherapy damage.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Anti-TNF-α therapy may increase the risk of developing alopecia areata, especially in those with a history of autoimmune disease.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Antiandrogen therapy helped increase hair growth in women with hormonal imbalances related to baldness.

Plant-based ingredients are effective and safe for modern skincare products.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.

Early onset hair loss linked to genetics and androgen levels.

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

Traditional healers in Namibia use 70 different plants to treat AIDS-related diseases, and more research is needed to test these plants' effectiveness against HIV.

A patient had skin tissue death at the hair removal site after a hair transplant, which was treated with surgery.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Increasing Wnt5a in mice skin delays hair growth but doesn't stop it.

Researchers found a new mutation causing total hair loss from birth.