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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.

The treatment improved hair growth in people with male pattern baldness.

Lef1 helps stem cells become hair cells by interacting with specific signaling pathways.

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

ULBP3 levels are higher in Tinea capitis patients and may help predict the disease's severity.

Psoriasis patients' immune response to a hair protein depends on their specific gene type.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Lactate production is important for activating hair growth stem cells.

Omega-6 fats in certain cells boost male hormone production.

BMP2 and BMP7 have opposite roles in feather formation.

Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

Dicer is crucial for hair growth in mice.

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

The treatment was ineffective in humans.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Bilateral ovarian hyperthecosis is a rare but treatable cause of increased facial hair in postmenopausal women.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Children with pituitary dwarfism have higher zinc and copper, lower manganese, and similar iron levels in hair compared to normal children.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.