Researchers at Rice University have developed a new way to activate treatments only in the right places, using an inert virus, magnetic nanoparticles and the gene-editing tool CRISPR-Cas9.
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In a remarkable proof-of-concept study, scientists from the University of Pennsylvania and the Children’s Hospital of Philadelphia have, for the first time, successfully used CRISPR gene-editing technology on mice in utero, to prevent the animals being born with a lethal metabolic disorder.
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A team of researchers has been investigating ways to speed up our often long-winded crop domestication process using the latest CRISPR gene-editing technology. A study has outlined how a crop known as a groundcherry could be effectively modified to be better suited to large-scale farming.
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A novel form of treatment could help cut back on a person’s desire for cocaine and reduce its damaging effect in the body. The method involves removing a small patch of skin, introducing genes that produce cocaine-degrading enzymes, and then grafting it back onto the patient.
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Things are heating up in the world of CRISPR gene editing. Following a series of controversial studies suggesting the process is not as safe or accurate as previously thought, a team of scientists claims a simple enzyme change could help increase the precision and safety of the process.
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A new research paper has again raised doubts over the safety and accuracy of the CRISPR-Cas9 gene editing technique. The study suggests that the gene editing process can cause extensive unforeseen and unpredictable alterations to DNA sequences outside of the intended targets.
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The CRISPR gene editing revolution is less than a decade old and scientists are still learning how best to deploy this ground-breaking technique. A team has recently discovered why the technique sometimes fails, uncovering a novel insight that will hopefully make future research more efficient.
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In one of the first examples of gene-editing technology being effectively used to knock out the expression of a gene in non-human primates, researchers have lowered the blood cholesterol in monkeys by disabling a single gene in the liver.
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A remarkable new study has successfully used the CRISPR gene editing system to edit a specific gene in mice engineered to have fragile X syndrome, a disorder often related to autism. The single gene edit in the live mice resulted in significant improvements in repetitive and obsessive behaviors.
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A team of Chinese scientists has conducted the first full assessment of the effects of CRISPR on non-human primates. The study set out to study whether the CRISPR-Cas9 genome editing technique results in off-target mutations in rhesus macaque monkeys.
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