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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.

Overexpressing SIMK in alfalfa boosts root hair growth, nodule clustering, and shoot biomass.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Editing the FGF5 gene in sheep increases fine wool growth.

Disabling the FGF5 gene in sheep leads to longer wool.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

High levels of auxin increase root hair growth by activating RSL2 and producing ROS, while high phosphate levels hinder growth by repressing RSL2.

Miz1 is essential for proper hair structure and growth.

Men with less sun-sensitive skin have lower PSA levels, while men with more sun-sensitive skin have higher PSA levels.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

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

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.