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

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Heparanase is essential for hair follicle health and inner root sheath differentiation.

Scientists discovered two versions of a new human hair keratin gene.

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

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Mutations in the HOXC13 gene cause hair and nail development issues.

K6hf is a unique protein found only in a specific layer of hair follicles.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Inhibiting HSP90 increases cell adaptability and survival under stress.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

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

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

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

KRTAP10 proteins help form the hair shaft's tough outer layer by interacting with specific hair keratins.