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Women with more 3α,17β-androstanediol glucuronide compared to sex hormone binding globulin are more likely to have female pattern baldness.

Women with more body hair tend to have thicker belly fat and more metabolic health issues.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Hirsutism is excessive male-pattern hair growth mainly caused by ovarian hormones, and severe cases may require costly treatment with side effects.

Researchers found that bulge cells from human hair can grow quickly in culture and have properties of hair follicle stem cells, which could be useful for skin treatments.

3D microenvironments in microwells improve hair follicle stem cell behavior and hair regeneration.

Human skin cell byproducts can potentially be used to treat hair loss and promote hair growth.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

A new gene mutation causes a rare type of hair loss.

MYB83 limits root hair growth and helps plants tolerate nutrient deficiencies.

Japanese infants fed hydrolysate formula may have low biotin levels.

Bisphenol-A (BPA) increases connections between brain cells and boosts their activity, but it blocks the effects of a male hormone on brain cell plasticity.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

Hidradenitis suppurativa may mainly affect vellus hair follicles, not terminal ones.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

The method can measure vitamin B3 levels in human hair accurately.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

A new genetic mutation was found causing hair and eye issues in a boy.

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

PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Gasdermin A3 causes hair follicle stem cells to activate too early, leading to hair loss.