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Dexamethasone increases the activity of androgen receptors in human skin cells, which may link it to certain types of hair loss.

Beta-HPV and MCPyV are linked to certain skin cancers, with ongoing research and vaccine development.

TRPV4 helps cells repair tissue and reduce scarring by controlling calcium levels.

Regulating cell death in hair follicles can help prevent hair loss and promote hair growth.

Exosomes could be a promising way to help repair skin and treat skin disorders.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

RORA may help regulate hair growth by affecting hair follicle stem cells.

Basement membrane changes are crucial for hair follicle development.

A fragment of human type XVII collagen shows great potential for skin health and wound healing.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Human hair keratin might be good for filtering out harmful substances from water.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

A patient with both bullous lichen planus and systemic lupus erythematosus showed improvement with treatment.

Sansevieria trifasciata Prain shows promise for treating hair loss by inhibiting androgen receptors.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A compound from Calophyllum inophyllum L. leaf may help treat non-small cell lung cancer.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Pannexin 3 is important for bone formation and the development of bone cells.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Bone Morphogenetic Proteins (BMPs) help control skin health, hair growth, and color, and could potentially be used to treat skin and hair disorders.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.