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TRIM, an integrated genome engineering platform that combines prime editing, gene knockouts, and large-scale chromosome engineering, enabled efficient stacking of multiple benefici...
June 05, 2026 | Source: Nature.com | by Mohana Basu, Edward Chen, and Heidi Ledford Researchers say that they have used a precise genome-editing technique called base editing to a...
Researchers developed PRINCE, a small-molecule-controlled CRISPR system enabling precise, long-term regulation of gene editing. Its compact version, Little Prince, showed therapeut...
As genome editing therapies move through clinical trials to regulatory approval, scientists continue the quest for the holy grail of large-scale DNA editing.. The post The Quest fo...
by Emma Källstig, Evelyne Ruchti, Medha Raman, Jamshid Asadzadeh, Bernard L. Schneider, Brian D. McCabe CRISPR/Cas9 based genome editing employing Homology Directed Repair (HDR) f...
This GEN Live show will bring together a panel of leading experts to break down the latest advances, innovations, and challenges shaping genome editing. The post Genome Editing at...
Successfully treating Baby KJ with a personalized CRISPR gene-editing therapy is spurring the industry to investigate how to develop standardized manufacturing platforms as well as...
Silver nanoparticles provide a more efficient way to cut and assemble DNA, improving recovery rates and boosting DNA joining efficiency for future gene engineering applications. DN...
“Guardian of the genome,” p53 is now therapeutically accessible using CRISPR-based technology from Jennifer Doudna’s lab. The approach uses RNA signatures to identify and destroy t...
Scientists have, for the first time, used an extremely precise genome editing technique called base editing to study gene function in human embryos.
June 04, 2026 | Source: The New York Times | by Carl Zimmer Scientists at Columbia University have edited the DNA of early human embryos with unprecedented accuracy, an achievemen...
A team in the US has reported promising results after using an improved form of CRISPR to gene-edit human embryos, but a major issue remains unsolved
Researchers relied on a newer gene-editing technique that may make it possible to engineer embryos, a prospect that has long alarmed bioethicists.
In a groundbreaking advance poised to reshape gene therapy and molecular medicine, researchers have unveiled a novel strategy for precise gene regulation via RNA splicing modulatio...
Fertility specialists, biotech companies and ethicists are divided over whether progress in early gene editing would wipe out diseases or trigger a rush toward enhancement.
June 05, 2026 | Source: NewsNation | by Josie Fischels (NewsNation) — Scientists at Columbia University have edited the DNA of human embryos with greater precision than ever befor...
Ученые из Колумбийского университета отредактировали ДНК на ранних стадиях развития человеческих эмбрионов с беспрецедентной точностью; это достижение может открыть путь к рождению...
A handful of start-up firms are testing therapies that target specific epigenetic markers to treat everything from high cholesterol to a rare muscular disorder
The technology, still far from clinical use, could one day prevent devastating diseases. But critics warn that even these early results may also fuel interest in commercial embryo...
Gene-editing human embryos may now be a reality.
D&D‑seq uses a base editor–nanobody fusion to record DNA–protein contacts at single‑cell resolution. The method maps transcription factor and chromatin-remodeling proteins. The...
In a groundbreaking advancement that sets a new paradigm in genetic medicine, researchers at Amsterdam University Medical Center (Amsterdam UMC), collaborating with several interna...
Scientists have devised a CRISPR-based tool that can kill cells carrying a specific strand of RNA. The tested targets include cancerous and virus-infected cells [1]. Targeted assas...
Scientists unveiled a reaction that swaps key carbon groups in complex compounds, offering a faster route to test new medicine candidates.
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