Social Media Ideas for Gene Editing

Donor-matched prime editing enables precise, library-ready kilobase DNA insertions

Editing Without Cutting: New Prime-Editing Strategy Writes Kilobase-Scale DNA Into the Genome For years, the promise of precisely writing new DNA into the genome has been constrain...

Human engineering fixes the flaws in AI-designed gene editors

Protein engineering improves AI-designed base editors, boosting precision and efficiency for more reliable nuclear and mitochondrial DNA editing.

A Newer Kind of Gene Editing Promises to Edit ‘Nurture’ Over ‘Nature’

Traditional gene editing rewrites DNA. But a new approach, called epigenome editing, aims to treat the molecular scars we collect throughout our lives.

Targeted lipid nanoparticles enable in vivo editing of human blood stem cells

A new study reports a strategy for delivering gene-editing technology directly to human haematopoietic stem cells inside the body, using targeted lipid nanoparticles rather than vi...

Rewriting Disease: Gene Editing Breakthroughs in Hawaii

Imagine being able to edit disease out of a person's DNA.

BaseMap ABE Launched for Off-Target Characterization in Base Editing Therapeutic Development

Unlike prediction-based approaches, Broken String Biosciences says BaseMap ABE generates genome-wide data directly from biologically relevant cells, providing researchers with clea...

Base Editing Strategy Alleviates Huntington’s Disease in Mice

By precisely altering the huntingtin gene rather than switching it off, an in vivo CRISPR base-editing approach reduced toxic protein fragments and disease symptoms in mouse models...

Team uses AlphaFold AI to redesign gene-editing proteins to make them safer

Google's AlphaFold can help ID what parts of a gene editing protein enable mistakes.

Gene editing gets further boost in UK

Rothamsted Research is claiming a boost for its gene editing development programmes concerning the “evolution” of new cereal varieties. This follows the granting by UK regulators o...

Editas: Slow Progress Doesn't Mean No Progress For In-Vivo Gene Editor

A New Gene Editing Technique May Reduce Some CRISPR Risks, But Raises Ethical Concerns

Learn more about the medical treatments CRISPR could improve and the ethical concerns it raises. 

Rewriting Disease: Oligonucleotides Take Aim at the Untreatable

How synthetic DNA and RNA are becoming the discovery engines behind a new generation of precision therapies. The post Rewriting Disease: Oligonucleotides Take Aim at the Untreatabl...

Gene-editing therapies not yet ready for human trials, Stanford expert says

Gene-editing therapies for the nervous system may need at least another round of studies before they are safe enough to enter human trials, according to one of the world’s most inf...

Scientists Are Designing CRISPR Gene Editors With AI

To make CRISPR better at its job, researchers are turning to algorithms like DeepMind's AlphaFold. The post Scientists Are Designing CRISPR Gene Editors With AI appeared first on S...

Gene-Editing Technology Offers New Ways to Create the Dogs of Our Dreams

Technologies like CRISPR are giving us new ways to create the dogs of our dreams — and a reason to reckon with our past mistakes.

Gene Therapy Partners Aim to Enhance Protein Expression

Avenue Biosciences´ machine learning-powered platform engineers and screens signal peptide variants to increase protein secretion from cells. Circio’s circVec technology has demons...

Genomes to bioreactors: Saudi Arabia’s gene editing oncology push

Saudi Arabia is pairing gene editing breakthroughs with new biomanufacturing capacity, from CRISPR oncology therapies to CDMOs like Lifera, as it builds a full biotech pipeline. Th...

Как нейросеть придумала белки, которых нет в природе, и обошла эволюцию

В 2012 году ученые показали, что бактериальную систему CRISPR-Cas9 можно превратить в программируемые «ножницы» для ДНК. Через восемь лет Дженнифер Дудна и Эммануэль Шарпантье полу...

Award topping $35M to fuel CHOP gene editing work in hemophilia A

Children’s Hospital of Philadelphia (CHOP) has been awarded up to $38.9 million to advance the development of personalized gene‑editing therapies for four groups of rare genetic di...

AlphaFold AI redesigns gene-editing proteins to enhance safety, and biotech investors should pay attention

ContactSeek, a new AI framework using AlphaFold3, redesigns gene-editing proteins for dramatically improved safety, with implications for biotech The post AlphaFold AI redesigns ge...

AI-Designed Synthetic CRISPR-Like Nucleases Show Activity in Cells

Scientists used artificial intelligence to design CRISPR nucleases with properties not found in nature, achieving activity that matches or exceeds natural enzymes despite the prote...

UCSD, IGI Partnership Expands CRISPR Innovation Across Health, Agriculture, and the Environment

UC San Diego has joined the Innovative Genomics Institute as its fourth UC partner, expanding collaboration to develop next-generation genome-editing technologies that address majo...

New gene-editing tool speeds regeneration of hard-to-breed perennial crops

‘CRISPR-Combo’ system cuts months off growing plants The post New gene-editing tool speeds regeneration of hard-to-breed perennial crops appeared first on AgriLife Today.

RNAV8 Bio Joins ARPA-H Team to Pioneer Programmable RNA Medicines

The PROPEL program aims to control gene expression through RNA structure, building logic-gated RNA therapies that switch on only where and when intended, without altering the genom...