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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.

A specific gene change in APCDD1 increases the risk of hair loss.

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

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

A protein called HMGB1 helps hair grow by affecting prostaglandin metabolism.

ABCG2 protein marks stem-like skin cells in human epidermis.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Tanning ability is linked to specific DNA changes in skin genes.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

CGF treatment effectively and safely improves hair loss in androgenic alopecia patients.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

GT20029 helps regrow hair in men with hair loss and is well-tolerated.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Hair loss gene found on chromosome 3q26.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Hair testing can detect a single GHB exposure, useful for documenting sexual assault.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

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

Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.