Ten years ago, scientists put DNA barcodes in AAV vectors, creating an approach that simplified, expedited, and streamlined AAV screening. 

A 3D variation of pooled CRISPR screens could connect the dots between autism spectrum disorder genetics and cell fate pathways in the developing brain.

Animals with human cells could provide donor organs or help us understand neuropsychiatric disorders.

With the help of directed evolution, scientists inch closer to developing viral vectors that can cross the human blood-brain barrier to deliver gene therapy.

The common fluorescent marker GFP traveled a long road to take its popular place in molecular biology today.

Paola Arlotta seeks to understand the complex symphony of brain development in vitro by using organoid models.

p53 is possibly the most important protein for maintaining cellular function. Losing it is synonymous with cancer.

Researchers find that UBQLN2 gene dysfunction causes a virus-like protein to accumulate in cells, which changes gene expression and may contribute to disease progression in amyotrophic lateral sclerosis (ALS).

George Church is at it again, this time using multiplex gene editing to create virus-proof cells, improve organ transplant success, and protect elephants.