CRISPR is being significantly enhanced thanks to DNA-coated nanostructures, which improve the delivery and precision of gene editing, paving the way for safer genetic medicine. Scientists from Northwestern University (USA)…
Magazines
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The following review from Gene Therapy of Nature presents the advances and future prospects of gene editing in relation to collagen disorders. Collagen disorders include a broad spectrum of inherited…
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A research group funded by the National Institutes of Health (NIH) has successfully created and delivered a personalized gene-editing therapy to treat an infant suffering from a life-threatening, previously untreatable…
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A large research group led by Dr. Jeff Vierstra, a researcher at the Altius Institute for Biomedical Sciences in Seattle (USA), and Dr. Nikoletta Psatha, Assistant Professor in the Department…
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This selection of influential and fascinating gene therapy research has been hand-picked by the editors of Cell Stem Cell and Cell Reports Medicine. These are only a few of the…
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In a historic medical breakthrough, a child diagnosed with a rare genetic disorder was successfully treated with a personalized CRISPR gene-editing therapy by a group from the Children’s Hospital of…
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In a major medical breakthrough, India has successfully completed its first human gene therapy for severe hemophilia-A using a lentiviral vector, resulting in zero bleeding rates in patients. Hemophilia, a…
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A very interesting news article was published on the website of the journal Nature which comments on the whole course of CRISPR genetic modification technology. In this article, all the…
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The Laboratory of Physiology of the Department of Medicine of the University of Patras led by Professor Stavros Taraviras has published a new paper in the journal EMBO Molecular…
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A very interesting study showed that treatment with CART cells that target the urokinase plasminogen activator receptor (uPAR), which is associated with aging, improves exercise capacity in normal aging and…
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