Researchers have identified a new genetic cause of hereditary optic atrophy—a condition that leads to gradual vision loss—by discovering a previously unknown mutation in the PPIB gene. T ...

Researchers have understood for decades that some forms of deafness are inherited, yet until now, few of those genetic clues ...

Mutations in a gene known as CPD play a crucial role in a rare form of congenital hearing loss, an international team of ...

A Nature study shows sperm from older fathers carry more disease-linked mutations, revealing how age and cell competition ...

A research team from the Medical University of Vienna and the Medical University of Graz has discovered a previously unknown ...

Researchers employed a programmable DNA base editing technology to introduce a knockout mutation in the ND5 mitochondria gene, aiming to investigate the resulting genotypic and phenotypic changes.

Scientists have discovered a method to induce human endothelial cells from a small biopsy sample to multiply in the ...

In a recent perspective published in the journal Cell Death and Differentiation, researchers in France, Germany, and Sweden discussed the unique mutational spectrum of the transformation-related ...

Autologous T-Cell Therapies in Solid Tumor Malignancies: Current Landscape and Future Opportunities Histology-agnostic therapies: by focusing on common mutations across various cancers, this approach ...