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The Latest
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Home CRISPR

Single injection treats hemophilia B for life, in proof-of-concept study

Single injection treats hemophilia B for life, in proof-of-concept study

The Salk approach, tested in a mouse model, points to cheaper and more effective treatments for humans For most people with hemophilia B, whose bodies can’t properly form blood clots, consta... Read more

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Breakthrough in gene editing vastly improves precision of gene-editing technology

Breakthrough in gene editing vastly improves precision of gene-editing technology

New technique developed by UAlberta researchers vastly improves precision of gene-editing technology. Imagine a future where a guided biomachine put into your body seeks out defective gene s... Read more

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Gene therapy for common blood disorders?

Gene therapy for common blood disorders?

In a landmark study, scientists have used CRISPR gene editing to introduce beneficial natural mutations into blood cells to boost their production of foetal haemoglobin. In a landmark study... Read more

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A new tool called CasRx targets RNA to correct a protein imbalance in cells from a dementia patient

A new tool called CasRx targets RNA to correct a protein imbalance in cells from a dementia patient

Salk scientists create new molecular scissors to correct protein imbalance in cellular model of dementia Most people have heard of the CRISPR/Cas9 gene-editing technology, which acts as targ... Read more

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Reducing triglycerides and cholesterol by up to 50 percent with gene editing

Reducing triglycerides and cholesterol by up to 50 percent with gene editing

CRISPR-like technique offers clues to mimic protective genetic mutations Using a variation of CRISPR gene editing may be a potential strategy for mimicking the protective effects of a geneti... Read more

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Could a new CRISPR gene-editing technique correct a majority of the 3,000 mutations that cause Duchenne muscular dystrophy?

Could a new CRISPR gene-editing technique correct a majority of the 3,000 mutations that cause Duchenne muscular dystrophy?

Scientists have developed a CRISPR gene-editing technique that can potentially correct a majority of the 3,000 mutations that cause Duchenne muscular dystrophy (DMD) by making a single cut a... Read more

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CRISPR-Cas9 and other gene editing systems may need to be customized to the patient

CRISPR-Cas9 and other gene editing systems may need to be customized to the patient

Patients’ individual genomes may affect efficacy, safety of gene editing Gene editing has begun to be tested in clinical trials, using CRISPR-Cas9 and other technologies to directly ed... Read more

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Scientists modify CRISPR to epigenetically treat diabetes, kidney disease, muscular dystrophy

Scientists modify CRISPR to epigenetically treat diabetes, kidney disease, muscular dystrophy

Approach could also be applied to reversing aging and age-related diseases such as hearing loss and macular degeneration Salk scientists have created a new version of the CRISPR/Cas9 genome... Read more

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Feeding and fueling the planet with algae via new genome engineering technique

Feeding and fueling the planet with algae via new genome engineering technique

Vast quantities of medicines and renewable fuels could be produced by algae using a new gene-editing technique, a study suggests. Scientists have devised a method that could lead to cheap, e... Read more

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Genetically engineering mosquitoes to self-destruct

Genetically engineering mosquitoes to self-destruct

UCR researchers are generating genetically engineered insects to help prevent the spread of infectious diseases Researchers at the University of California, Riverside have developed transgen... Read more

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In a world-first, CRISPR/Cas9 is used to change flower color

In a world-first, CRISPR/Cas9 is used to change flower color

What’s your story, morning glory? Scientists use CRISPR technology to change flower colour in an ornamental plant In a world-first, Japanese scientists have used the revolutionary CRISPR, or... Read more

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Genome therapy could eventually lead to a cure for sickle cell anaemia and other blood disorders

Genome therapy could eventually lead to a cure for sickle cell anaemia and other blood disorders

A UNSW Sydney-led team of scientists has made an advance that could eventually lead to a cure for sickle cell anaemia and other blood disorders. By introducing a beneficial natural mutation... Read more

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Genome engineering system transforms living cells into archival data storage devices

Genome engineering system transforms living cells into archival data storage devices

New CRISPR technology takes cells to the movies Researchers use expensive machinery to develop ways to harness DNA as a synthetic raw material to store large amounts of digital information o... Read more

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Breakthrough in CRISPR technology to improve genome editing

Breakthrough in CRISPR technology to improve genome editing

A new molecular scissors act like a GPS to improve genome editing Researchers from the University of Copenhagen (Denmark), led by the Spanish researcher Guillermo Montoya, have discovered ho... Read more

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Optimized CRISPR-Cpf1 to More Efficiently Edit Human Genome

Optimized CRISPR-Cpf1 to More Efficiently Edit Human Genome

Scientists on the Florida campus of The Scripps Research Institute (TSRI) have improved a state-of-the-art gene-editing technology to advance the system’s ability to target, cut and paste ge... Read more

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