Multiple sclerosis (MS) is a chronic neurological disease characterized by nerve damage and consequent impairments in vision, ...

The startup aims to create a platform for treating extremely rare genetic mutations, armed with CRISPR advances and new regulatory pathways.

Technologies at the Advanced Rodent Transgenics Laboratory include genome editing design and implementation and transgenic ...

Scientists have discovered a new CRISPR mechanism with precise activity, expanding the potential applications of the existing ...

SCD gene therapy approaches using CRISPR, gene therapy, and base editing show different stem cell outcomes in a mouse study.

Researchers have unveiled a way to flip genes back on without slicing into the genome, a shift that could make CRISPR far ...

Researchers say discoveries could expand the CRISPR toolbox and lead to more efficient, rapid diagnostic tools for detecting COVID-19, influenza, and RSV.

A genome-wide CRISPR study maps 331 genes essential for early brain development, identifying PEDS1 as a new ...

CHANGE-seq-BE was developed to enable scientists to better understand base editors, an important class of CRISPR precise genome editors.

A new CRISPR breakthrough shows scientists can turn genes back on without cutting DNA, by removing chemical tags that act ...

Abu Dhabi introduces a revolutionary gene therapy for hemoglobinopathies, utilizing CRISPR-Cas9 technology. Explore how this ...

Scientists and physicians can better assess precision genome editing technology using a new method made public today by St.