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CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Men with Kennedy disease have less chance of hair loss.

Topical diphencyprone helped regrow hair in mice and rats with a condition similar to human hair loss.

Disrupting Smad4 in mouse skin causes early hair follicle stem cell activity that leads to their eventual depletion.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

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

CDK4/6 inhibitors may cause hair loss in breast cancer patients.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

MK-5108 is safe and shows potential against tumors, especially alone.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

Prostaglandin D2 blocks new hair growth after skin injury through the Gpr44 receptor.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Delta opioid receptors help regulate touch sensation by reducing neurotransmitter release in the spinal cord.

KAP8.2 gene variations affect cashmere quality in goats.

PLDζ2 and NPC4 have different roles in lipid changes and root hair growth in Arabidopsis under low phosphate, with PLDζ2 reducing root hair growth and NPC4 promoting it.

CS12192 effectively treats alopecia areata with better safety than current options.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

Hirosaki hairless rats have sparse, twisted hair due to missing hair keratin genes.

A new method can detect mutations in mice by observing changes in hair follicle cells.

A new mouse model helps study melanocyte cells using GFP expression.

All Indian dromedary camel breeds have the same KRTAP7 gene affecting hair quality.

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

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Finasteride reduces certain behaviors caused by D1-like receptor agonists but not by D2-like receptor agonists in mice.

Ku80 is a key receptor for Thymosin β4, affecting cell migration and wound healing.

A defective gene causes hair loss and taste insensitivity in BTBR mice.