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Found microRNA differences in hair cells, suggesting potential treatment targets for hair loss.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

The document concludes that proper diagnosis and evidence-based treatments are crucial for managing hair diseases, and psychological support for patients is important.

Henna dye improves hair cuticle and thickness but effects vary by hair type and health.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

The document concludes that understanding hair loss and considering medical treatments like minoxidil and finasteride before surgery is important, especially for young patients with rapid hair loss, and that hairline design varies among different ethnicities.

CARI ONE helps start hair growth and makes hair follicles bigger and more numerous.

Low zinc levels might contribute to early hair graying.

Human hair keratins can self-assemble and support cell growth, useful for biomedical applications.

Keratin hydrogels from human hair show promise for tissue engineering and regenerative medicine.

Gene mutations can cause problems in male genital development.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

PRP helps with skin, hair, and wound treatments but needs more research for standard use.

Topical minoxidil helps treat hair loss in teens, but more research needed for safe options.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Prolactin affects the production of different keratins in human hair, which could lead to new treatments for skin and hair disorders.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

Telogen Effluvium is a hair loss condition where treatment involves identifying and managing its triggers.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

Hormones and genes affect hair growth and male baldness.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Hair follicles prevent NK cell attacks to avoid hair loss.

Hair strength is similar across different scalp areas, and not affected by age, gender, or hair thickness.

TTD hair brittleness is caused by multiple structural abnormalities.