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The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

The document explains hair growth, hair loss types, and other hair-related terms.

Hair changes could indicate neurological diseases and help monitor treatment.

Mutant mice help researchers understand hair growth and related genetic factors.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

The document concludes that immune system abnormalities cause alopecia areata, but the exact process is still not completely understood.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Leontopodium alpinum extract may help reduce hair shedding by keeping hair in the growth phase longer.

OCT can effectively examine and reveal details about human hair and scalp conditions.

Cathepsin L is essential for normal hair growth and development.

Prolactin affects hair growth cycles and can cause early hair follicle regression.

Blocking Rab27a slows hair growth, while blocking Rab27b encourages it.

CDP is crucial for lung and hair follicle cell development.

The p75 neurotrophin receptor is important for hair follicle regression by controlling cell death.

Hair growth can be induced by certain cells found at the base of hair follicles, and these cells may also influence hair development and regeneration.

Notch-related genes play a key role in the development and cycling of hair follicles.

Vitamin D receptor is crucial for starting hair growth after birth.

People with late-stage HIV-1 often experience a specific type of hair loss linked to multiple factors, including nutritional issues and immune responses.

Hair breakage may be an early sign of a hair loss condition called CCCA in African American women.

Human hair has a protective lipid layer that can be damaged by moisture and treatments, affecting hair growth and health.

Dihydrotestosterone (DHT) stops hair growth in mice by lowering a growth factor important for hair.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Many elderly women experience unwanted facial hair and various hair loss conditions, with treatments available for each condition.

The genes OVOL1 and OVOL2 are important for hair growth and may be involved in a type of skin tumor.

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

Rac1 is essential for proper hair structure and color.

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