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The conclusion is that effectively treating hair disorders is difficult due to the complex factors affecting hair growth and more research is needed to improve treatments.

Human skin cells produce proenkephalin, which changes with environmental factors and skin diseases.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

Epigenetic mechanisms control skin development by regulating gene expression.

Adult hair follicle cells can create new hair follicles from corneal cells with the right support.

The document concludes that for hair and feather growth, it's better to target the environment around stem cells than the cells themselves.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

The skin has different types of stem cells that can repair and regenerate tissue.

A gluten-free diet significantly improves skin and health issues in people with dermatitis herpetiformis, a skin condition linked to celiac disease.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Minoxidil boosts hair growth by triggering growth factor release from specific stem cells.

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

Patients with mycosis fungoides have a higher risk of heart disease.

Guilu Erxian Glue may help reduce chemotherapy side effects like weight loss and heart stress.

The document suggests a possible link between Crohn's disease and Johne's disease and calls for more research.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Wnt signaling is crucial for skin development and hair growth.

Different species and human skin models vary in their skin enzyme activities, with pig skin and some models closely matching human skin, useful for safety assessments and understanding the skin's protective roles.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

The document concludes that managing female hyperandrogenism requires a combination of identifying the cause, lifestyle changes, medication, and cosmetic treatments.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Some chemicals absorbed through the skin can cause serious health problems.

Adrenal disorders can cause lasting brain and behavior issues in children.

Two women with very high androgen levels had only slight skin issues, one due to a non-classical adrenal disorder and the other due to an adrenal tumor.