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A newly found RNA in Cashmere goats may play a role in hair growth and development.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The research suggests that the ZP4 gene is linked to egg development in women with PCOS but requires more study to understand its role in infertility.

People with Inflammatory Bowel Disease often lose hair due to stress, medication side effects, or lack of nutrients, and treatment depends on the specific cause.

Hair in mammals likely evolved from glandular structures, not scales.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Dermatoscopy helps diagnose hair and scalp disorders in people with Afro-textured hair, but more research is needed for better understanding and treatment.

Hormone imbalances can cause skin diseases, and understanding these links is important for diagnosis and treatment.

Hormones and genes affect hair growth and male baldness.

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

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Some skin diseases and their treatments can negatively affect male fertility.

Troxerutin helps protect skin cells from oxidative stress and may be good for treating hair loss.

Early diagnosis and treatment of PCOS in young people is important to prevent long-term health problems.

Different combinations of human hair keratins affect how hair fibers form.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Explosions don't stop hair proteins from being used to identify people.

PSA levels could help detect illegal steroid use in female athletes but face challenges like cost and PCOS prevalence.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

Hexi cashmere goats' hair growth varies by stage, with Hoxc13 linked to hair activity.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

Apoptosis may contribute to hair loss in androgenetic alopecia.

Hair loss can be reversed or even cured using advanced hair restoration techniques, with rare complications like swelling and bleeding.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

AB+ blood group is more common in alopecia areata patients.

The conclusion is that different blood diseases cause specific oral symptoms and require varied treatments to manage these symptoms and improve patient health.