CRISPR

Curing disease by repairing faulty genes with CRISPR

New delivery method boosts efficiency of CRISPR genome-editing system The genome-editing technique known as CRISPR

Sensing the future of living detectors and bioproduction

Plant, yeast, even mammalian cells could be engineered into living detectors of virtually any molecule

CRISPR Used to Repair Blindness-causing Genetic Defect in Patient-derived Stem Cells – Retinitis Pigmentosa

A potential precision medicine approach for treating vision loss Columbia University Medical Center (CUMC) and

High-fidelity CRISPR-Cas9 nucleases have no detectable off-target mutations

Mass. General team develops improved version of important gene-editing tool A new engineered version of

Gene-editing technique successfully stops progression of Duchenne muscular dystrophy

If efficiently and safely scaled up in DMD patients, this technique could lead to one

CRISPR-Cas9 helps uncover genetics of exotic organisms

The simplicity of CRISPR-Cas9 gene editing will soon make studying the genes of any organism,

Broad, MIT scientists overcome key CRISPR-Cas9 genome editing hurdle

Researchers at the Broad Institute of MIT and Harvard and the McGovern Institute for Brain

Mini-kidney organoids re-create disease in lab dishes

Stem-cell biology and gene editing advances offer hope for kidney regeneration, drug discovery Mini-kidney organoids