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New Approach Aims to Make CRISPR Therapy Safer and More Effective
CRISPR is a powerful gene-editing tool that holds enormous potential for treating genetic diseases by allowing scientists to ...
Correcting Genetic Spelling Errors With Next-Generation Crispr
Treatments for rare diseases are hard to create and expensive to deliver, but there is new hope for editing the software of ...
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New breakthrough could solve antibiotic resistance crisis
Recent TAU study demonstrates how a crucial but underexplored process of DNA transfer between bacteria affects its defense ...
New gene-editing treatment extends lifespan in mice with prion disease
Researchers at the Broad Institute of MIT and Harvard have developed a gene-editing treatment for prion disease that extends lifespan by about 50 percent in a mouse model of the fatal ...
Promising Developments and Strategic Partnerships Drive Crispr Therapeutics’ Growth Potential
William Blair analyst Sami Corwin has maintained their bullish stance on CRSP stock, giving a Buy rating on January 14.Stay Ahead of the ...
Scientists engineer CRISPR enzymes that evade immune system
The core components of CRISPR-based genome-editing therapies are bacterial proteins called nucleases that can stimulate ...
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Understanding the Regulatory Challenges for CRISPR Gene Editing on Crops
CRISPR gene-editing technology presents a possible solution for feeding a growing population, but incorporating CRISPR into ...
CRISPR therapy corrects muscular dystrophy mutations and regrows muscles in mice
Researchers at the Experimental and Clinical Research Center (ECRC), a joint institution of the Max Delbrück Center and ...