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The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

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

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

A new gene, JMJD1C, may affect testosterone levels in men.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

The conclusion is that understanding the complex relationship between allergies, autoimmunity, and psychological factors is key to treating skin disorders with itching.

Skin problems are common in Lupus patients and can indicate the disease's severity, requiring specific treatments and lifestyle changes.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Potassium channel openers show promise for treating heart disease and other conditions, but more research is needed to fully understand their effects and safety.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

Human hair protein modifications could potentially indicate heart disease risk.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Metformin improves early signs of heart disease in women with PCOS and raises apelin levels, but doesn't significantly change artery thickness.

Good nutrition is crucial for health and preventing disease, and supplements can help prevent nutrient deficiencies.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Scientists created a 3D skin model to study a chronic skin disease and test treatments.

Chronic stress in mice changes skin metabolism and gene expression, leading to hair loss.