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Injecting platelet-rich plasma under the skin significantly improves hair growth and quality without harmful effects.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

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

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

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

The document explains how to create detailed biological pathways using genomic data and tools, with examples of hair and breast development.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Changthangi goats have specific genes that help produce Pashmina wool.

ILK is essential for skin development, pigmentation, and healing.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

A mix of sulforaphane, L-menthol, and dexpanthenol could help increase hair growth and reduce hair loss.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Hair follicle stem cells are important for maintaining healthy skin and interact with many signals.

Disrupting Smad4 in mouse skin causes early hair follicle stem cell activity that leads to their eventual depletion.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The document explains the genetic causes and characteristics of inherited hair disorders.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Monilethrix causes fragile, patchy hair loss.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.