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

RXRα is crucial for hair growth and skin cell function.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

Human bone cells mainly produce a type 1 enzyme that may help regulate bone health.

Arteannuin might work against cancer and Alzheimer's by targeting neprilysin.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

Finasteride changes androgen receptor location in rat epididymis without altering tissue structure.

A new method effectively predicts estrogen-related health effects for early screening.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

The research gives new understanding on how human steroid 5α-reductases work and how drugs like finasteride inhibit them, which could help in creating new drugs.

Necl2 affects skin cell behavior and slows wound healing.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

The ZIP13 variant is linked to abnormal hair quality.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

RDW is a useful, cost-effective tool for diagnosing and monitoring various diseases.

The drug enzalutamide may reduce the ability of the virus causing COVID-19 to enter lung cells.

The HR protein's role as a repressor is essential for controlling hair growth.

Vitamin D receptor actions without binding are crucial for healthy skin and hair.

A new gene variant causes curly coats in some dog breeds.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.