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CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Two patients with stubborn hair loss grew hair after PDRN injections.

NXC736 significantly reduced hair loss in mice with alopecia areata.

Changes in genes FGA, VWF, and ACTG1 may contribute to pemphigus vulgaris.

Advanced platelet-rich fibrin improves healing and reduces pain in oral surgery.

PP2Acα is essential for proper hair and skin development.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Blocking a protein called prostaglandin D2 might help treat hair loss.

PCA hydrogel promotes hair growth by enhancing blood vessel formation and hair follicle stem cell activity.

Apremilast may help treat hair loss in alopecia areata.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition that may respond to antiandrogen therapy.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

Daprodustat, combined with PAβN, could be a new antibacterial treatment.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

A mutant FERONIA gene affects root hair growth at high temperatures.

Fatp4 is crucial for healthy skin development and function.

A new microneedle patch effectively treats hair loss by delivering growth factors to the skin.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

17β-estradiol lowers polyamine oxidase levels in breast cancer cells through estrogen receptor 2.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

The androgen receptor's shape-changing ability helps it function but can lead to cancer treatment resistance.

Fibrosing alopecia in a pattern distribution is a new type of scarring hair loss that resembles common baldness and an autoimmune skin disease.

Longer CAG repeats in gene linked to more severe hair loss in females.

Sphingosine 1-phosphate helps control mechanical pain.

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

The new wound dressing speeds up healing of infected wounds safely and effectively.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.