The goal of gene therapy is to permanently cure hereditary diseases. One of the most promising technologies for this is the ...

CRISPR-edited insulin cells restore natural insulin in a Type 1 diabetes patient without rejection or immunosuppressants, ...

Importantly, the researchers at Boston Children's Hospital utilized the Nabsys OhmX Platform to identify a ...

Since 2019, MIT researchers have published a new concept called prime editing, which is more precise than regular CRISPR-Cas9 gene editing. As a result, it has fewer off-target effects and less chance ...

BRENTFORD, ENGLAND, UNITED KINGDOM, October 14, 2025 / EINPresswire.com / -- The global CRISPR gene-editing market is expected to witness significant growth, projected to rise from a valuation of US$ ...

MIT scientists have found a way to make gene editing far safer and more accurate — a breakthrough that could reshape how we ...

Two scientists won the 2020 Nobel Prize in Chemistry on Wednesday for creating genetic 'scissors' that can rewrite the code of life, contributing to new cancer therapies and holding out the prospect ...

Conjugation is mediated by a large molecular machinery termed Type IV secretion system (T4SS), embedded within the donor cell wall. In addition, some bacteria utilise T4SS to inject effector proteins ...

Dive into this daily current affairs quiz covering everything from polity and economy to science, environment, and world affairs. Every question is fact-checked and crafted to give your prep an extra ...

The hereditary transthyretin amyloidosis market is experiencing significant growth driven by increasing disease awareness, ...

A research team at Lund University in Sweden has discovered a mechanism that helps acute myeloid leukemia cells to evade the ...