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A new DSG4 gene mutation causes hair defects in a young girl.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

New genes linked to male pattern baldness were found on chromosome 20p11.

Deleting part of a gene in mice causes wavy hair and high pup loss.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

FPHL is a common, age-related, genetic hair loss with unclear causes and limited treatment options.

Hair follicle analysis can track body changes from high-intensity interval training.

Type II keratin genes are crucial for hair follicle differentiation and have a conserved structure and expression pattern.

FOXC1 is essential for keeping hair follicle stem cells inactive and maintaining their environment for healthy hair growth.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

Key genes linked to immune response are upregulated in hair follicles and skin tissues in chronic discoid lupus erythematosus.

K15 gene is mainly active in the basal layers of hair follicles and epithelia, aiding early skin cell development.

Hirosaki hairless rats have sparse, twisted hair due to missing hair keratin genes.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Changes in certain RNA and protein levels may contribute to alopecia areata and could be treatment targets.

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

These gene variations are not linked to alopecia areata in Egyptians.

High androgen levels can cause excessive hair growth and may indicate serious health issues, including heart disease and fertility problems.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Low androgen levels can still cause female pattern hair loss.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

A KRT32 gene variant causes loose anagen hair syndrome.

The risk of skin tumors becoming malignant depends on the specific skin cell type affected.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

Researchers created a new mouse model for studying scleroderma.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.