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 ...

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

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

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.

People with certain forms of the MC4R gene have lower cholesterol levels than do other individuals with a high body-mass ...

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 ...