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Gender-affirming hormone therapy changes hair growth in transgender people, with feminizing therapy reducing hair and masculinizing therapy increasing it, but sometimes additional treatment is needed.

Children with pituitary dwarfism have higher zinc and copper, lower manganese, and similar iron levels in hair compared to normal children.

High LH levels cause hair loss by damaging and aging hair follicles.

Mutations in the KRT85 gene cause hair and nail problems.

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

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

A gene mutation causes monilethrix in a Chinese family.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

CRH causes hair loss by reducing autophagy and increasing cell death in hair cells.

HGF-modified hair follicle stem cells help brain recovery after injury in rats.

hHbl gene is active in hair shaft cells and some pilomatricomas.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The modified Ferriman-Gallwey method is a useful tool for diagnosing hirsutism.

Women with PCOS have lower ghrelin levels and a weaker response to sugar, which might affect their feeling of fullness and lead to overeating.

IGFBP-rP1 could be a new treatment for a common type of hair loss.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

CRH causes hair loss by reducing cell survival in hair follicles.

CD98hc's role in skin health decreases with age.

GLP-1RA therapy may increase the risk of hair loss.

The IBHRS is now operational.

Androstanediol glucuronide is a reliable marker for hirsutism in women.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

CGF therapy may effectively treat psoriasis by reducing inflammation.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Double-stranded RNA helps regenerate hair follicles by increasing retinoic acid production and signaling.

Rushton's hyaline bodies form from hair keratin and blood substances.