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Scientists found a gene in mice that causes early hearing loss.

Hair cell loss usually happens after hearing loss starts.

Hearing decline in SAMP8 mice starts before outer hair cell loss and may be linked to other changes.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Using CD123 to detect certain immune cells helps diagnose a type of hair loss condition.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

CDH3-related disease causes worsening eye and hair issues.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

The document concludes that new methods improve the accuracy of diagnosing scalp alopecia and challenges the old way of classifying it.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

A new genetic mutation was found causing hair and eye issues in a boy.

The study found a link between the severity of Lichen Planopilaris seen by doctors and the details seen under a microscope, and created a new way to measure this severity.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.