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

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

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

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Mutations in hKAP1 genes may cause hereditary hair disorders.

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

Whn is essential for hair growth, and its malfunction causes hair loss.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

The N gene affects the protein makeup of mouse hair.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

The enzyme PA-PLA1α is important for proper hair follicle development.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

SFRP2 and PTGDS may be key factors in female hair loss.

Targeting NMMHC IIA may help treat blood-brain barrier damage.