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The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

Low ferritin and high Anti TPO levels are linked to early hair greying.

Certain proteins can either protect against or increase the risk of hypertrophic scars.

Growth hormone-releasing hormone (GHRH) boosts hair growth and human scalp hair follicles have their own growth hormone system.

A 308 nm excimer laser successfully treated a boy with a rare skin condition after about a year of weekly sessions.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

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

Genetics affect early female hair loss, severity depends on duration, and low ferritin levels not significant.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.

Early skin biopsy is crucial for diagnosing Conradi-Hünermann-Happle syndrome.

A KRT32 gene variant causes loose anagen hair syndrome.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

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

A specific gene change in APCDD1 increases the risk of hair loss.

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

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

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

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

The study found new details about human hair growth and suggests that preventing a specific biological pathway could potentially treat hair graying.

Hair follicle stem cell research has advanced in understanding and using these cells for hair growth and skin repair.

A gene mutation causes woolly hair in a Syrian patient.

Red blood cell folate levels are reliable indicators of long-term folate status in alopecia areata patients.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

New markers help understand and use hair follicle stem cells for regeneration.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.