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Intense pulsed light with radiofrequency showed mixed results in improving quality of life for hidradenitis suppurativa patients, with no clinical improvements.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

LSD1 and HSP90 help heal skin wounds by changing hair follicle stem cells' metabolism.

SAHA syndrome is a condition in women involving skin and hair issues, often related to hormonal imbalances, and is treated based on the underlying cause.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

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

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

SAHA syndrome links oily skin, acne, excess hair, and hair loss in women, similar to PCOS.

A specific gene mutation causes sparse, brittle hair in a family.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

Caspase-1 helps hair stem cells move to heal wounded or inflamed skin.

Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.