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Dermatologists can help detect and manage eating disorders by recognizing skin changes.

Immune cells are essential for early hair and skin development and healing.

Hair growth is influenced by factors like genetics and nutrition, and more research is needed to understand hair loss and growth mechanisms.

The document provides 70 multiple choice questions to improve haematology skills.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Geriatric Julia Creek dunnarts often suffer from reproductive and skin diseases, impacting conservation efforts.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

The document tests knowledge and decision-making in hematology through multiple-choice questions.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

Lung and liver macrophages protect our tissues and their dysfunction can cause various diseases.

The project created a standardized system for classifying skin lesions in lab rats and mice.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

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

The skin is the largest organ, protecting the body, regulating temperature, and producing hormones.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Umbilical cord blood is a valuable source of stem cells for medical treatments, but its use is less common than other transplants, and there are ethical issues to consider.

Gene mutations can cause problems in male genital development.

Topical Imiquimod may fight vascular tumors by affecting blood vessels or the immune system, low iron might be linked to some hair loss, removing the top skin layer helps vitamin C get in, genetic testing helps diagnose skin conditions, and too much iron could worsen skin inflammation.

The gene Prss53 affects hair shape and bone development in rabbits.

Some therapies using stem cells and platelet-rich plasma may help treat osteoarthritis, but more research is needed to ensure they are safe and effective.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Understanding how cells die in the skin is important for treating skin diseases and preventing hair loss.

Potassium levels affect blood sugar and insulin during dialysis, and malnutrition changes children's hair roots.