New CRISPR method efficiently corrects DMD defect in heart tissue

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 at strategic points along the patient's ...

New proton 'starter' for optogenetics

Scientists have examined a protein that will find application in optogenetics and could be used to control muscle and neuronal cells. The paper on the light-sensitive NsXeRprotein of the xenorhodopsin class was published ...

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