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OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

Changes in certain RNA and protein levels may contribute to alopecia areata and could be treatment targets.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

CD2 might be a new treatment target for patchy alopecia areata.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

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

Alopecia areata shows a unique type 1 interferon signature, suggesting potential treatment by targeting this pathway.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

JAM-A helps hair regrowth in alopecia areata by protecting VCAN in skin cells.

MLO proteins help regulate calcium and ROS levels, promoting root hair growth in Arabidopsis.

PP2Acα is essential for proper hair and skin development.

A rabbit gene important for hair development was identified and detailed.

Human prostate cells produce more WISP1/CCN4 when there's not enough oxygen.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

A peptide from hair follicle stem cells can boost hair growth.

CYP11A1 is crucial for skin health and disease by producing important steroids.

A specific gene mutation causes complete hair loss without other health issues.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Amino acid storage proteins are essential for maintaining stem cells in female fruit flies.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

ILC1 cells contribute to hair loss in alopecia areata.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.