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Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Proper cell death regulation is crucial for normal hair follicle regeneration and skin remodeling.

Wnt ligands, produced by dermal papilla cells, are essential for adult hair growth and regeneration.

Certain inflammatory factors may increase or decrease the risk of developing PCOS.

Lower MC2R expression may contribute to alopecia areata.

ILC1-like cells can cause alopecia areata by affecting hair follicles.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Keratin 15 helps maintain tissue integrity and is reduced in activated keratinocytes.

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

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

MicroRNA-181a slows sheep hair growth by targeting GNAI2 and affecting a key growth pathway.

Smad2 and Smad3 are essential for normal skin development, and their absence causes severe skin issues and cancer.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

BMP signaling prevents hair growth by stopping stem cell activation.

Hair follicle cells help protect against immune attacks by regulating T-cell activity.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

New mutations in the hairless gene may cause hair loss and affect bone development.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Targeting NETs may help reduce fibrosis in Crohn's disease.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

Secreted inhibitors of Wnt and IGF signaling control hair and tooth development, creating species-specific patterns.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

BMP signaling helps prevent skin tumors by blocking cancer-promoting pathways.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.