CRISPR Tool Targets Neuron Gene Repair

15 сентября 2025 Сообщено ИИ

Stanford researchers have created a CRISPR-based technology to target RNA in neurons, enabling repair processes for genetic diseases. The method addresses key challenges in Cas9 delivery and DNA repair. It reveals unique genome editing rules in neurons, paving the way for targeted therapies.

First mRNA Therapy for ISG15 Deficiency Developed

Researchers developed the first experimental mRNA-based therapy for ISG15 deficiency, a rare genetic mutation providing near-universal viral immunity, as reported on September 9, 2025.

Gene mutation raises disease risk by 50 percent

30 сентября 2025 Сообщено ИИ

A new study has identified a specific gene mutation that increases the risk of type 2 diabetes by 50 percent. Led by researchers at the University of California, Berkeley, the findings come from a five-year analysis of 1,000 participants. The discovery highlights potential pathways for early detection and treatment.

Illumina AI Tool for Rare Diseases

11 сентября 2025 Сообщено ИИ

Illumina introduced an AI tool aiding in the diagnosis of rare diseases. This innovation enhances genetic analysis for complex conditions. It was highlighted in biotech news updates.

Study identifies potential genetic subtypes of autism

Researchers have proposed that autism spectrum disorder may consist of genetically distinct subtypes, based on an analysis of large-scale genetic data. This finding could lead to more personalized approaches to diagnosis and treatment. The study highlights variations in genetic markers among individuals with autism.