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The meeting highlighted major advances in skin research, including new findings on skin microbes, genetic links to skin diseases, and improved treatments for various conditions.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Disrupting natural body clocks increases the risk of developing type 2 diabetes.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

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

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Birth control pills slightly increase the risk of breast cancer, especially if used before the first full-term pregnancy.

Basal cell carcinoma mostly starts from cells in the upper skin layers, not hair follicle stem cells.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

Prominin-1 expressing cells in the dermal papilla help regulate hair follicle size and communication but don't aid in skin repair.

Most clinicians follow discharge guidelines, many lupus patients don't use sunscreen regularly, dithranol is effective for psoriasis, biopsy methods should be based on lesion type, voriconazole may raise skin cancer risk, a new scale can help diagnose female hair loss early, and most melanomas may develop from existing moles.

Significant progress was made in understanding PXE, but effective treatments are still needed.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Enzymes called PADIs play a key role in hair growth and loss.

Scalp melanoma, a deadly skin cancer, is often found late due to its hard-to-see location, especially in older men. Early detection, possible treatments, and the role of hairdressers in spotting it early are discussed. More research is needed to improve detection and treatment.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Human hair loss may have evolved to help increase brain size.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Moles may stop growing due to cell cooperation, not just because of individual cell aging.

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

Hair follicles in mutant mice self-organize into ordered patterns within a week.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Researchers found that hair follicle stem cells can become squamous cell carcinoma due to Ras activation, which could lead to new treatments.

Haircuts and medical growth factors do not cause cancer.

Wnt signaling is crucial for skin development and hair growth.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.