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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Transglutaminase-3 is often reduced in esophageal cancer.

A specific gene variant may increase the risk of developing Alopecia Areata.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Reduced AhR signaling in HS tunnels leads to persistent inflammation and microbial imbalance.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

miR-325-3p can slow down brain tumor growth by targeting FOXM1.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Two microRNAs in stem cell exosomes help treat hair loss by targeting a specific signaling pathway.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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

Two specific genes are more active during hair growth in mice.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A new mutation in the HR gene causes hair loss in a specific family.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

Scleroderma patients have lower hair miR-29a levels.

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

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

ARHGEF3 is essential for proper hair follicle development in mice.

Certain blood miRNAs are linked to severe alopecia areata and could lead to new treatments.

miR-155 levels in blood could help identify alopecia areata.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Mrp3 helps in wound healing and hair growth.

miR-877-3p can improve cashmere quality by regulating hair growth in goats.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

Blocking CXCR4 may help treat hidradenitis suppurativa.