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Melasma is now considered a skin aging disorder caused by sun exposure in people with a genetic tendency, which impacts treatment and prevention approaches.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

Scientists found genes linked to the growth of high-quality brush hair in Chinese Haimen goats.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Fat cells in the skin help start healing and form important repair cells after injury.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

Auxin and ethylene hormones both work together and against each other to control plant growth.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

Spironolactone may make some cancer treatments more effective by blocking a protein that helps cancer cells survive.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

Implanting hair-follicle stem cells in mice brains helped repair brain bleeding and reduced brain inflammation.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

Hashimoto thyroiditis is an autoimmune disease that can lead to an underactive thyroid and is treated with medication and sometimes diet changes or surgery.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Scarless healing is complex and influenced by genetics and environment, while better understanding could improve scar treatment.

Losing weight, fixing varicoceles, and using advanced sperm selection methods improve male infertility treatment outcomes.

Two-photon microscopy effectively tracks live stem cell activity in mouse skin with minimal harm and clear images.

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

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

Blocking certain immune signals can reduce skin damage from radiation therapy.

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