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On May 12, 2025, the U.S. Court of Appeals for the Federal Circuit issued a long-awaited decision in Regents of the University of California v.
Successful trial results in the next few years could save thousands of lives and generate billions in new annual revenue for ...
The personalized CRISPR treatment could be the future of gene therapy, but hurdles remain before everyone has access.
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AZoLifeSciences on MSNEpigenome Editing: Enhancing Endonuclease Protein Design for In Vivo ApplicationsBy Pooja Toshniwal PahariaIn a study published in Nature Biotechnology, researchers have enhanced the genome editing ...
With gene therapy offering new hope for thalassemia, experts urge Indian govt to invest in early diagnosis, genetic testing, ...
Beginning a chain of events that will presumably lead to the origin of our universe's Spider-Man, researchers in Germany have ...
Scientists have used personalised gene-editing therapy to successfully treat a baby with a rare genetic condition. Could this ...
In 2012, scientists Jennifer Doudna and Emmanuelle Charpentier replicated this mechanism found in microbes to develop a ...
Manufacturing CAR T cells in the laboratory is expensive and time-consuming. An in vivo approach could get the powerful ...
The CRISPR gene editing tool has been revolionary for the research lab, and it has also been used to transform the lives ... | Genetics And Genomics ...
KJ Muldoon came into the world with a genetic time bomb ticking inside him.
Progressive multifocal leukoencephalopathy (PML) is a fatal demyelinating disease of the central nervous system caused by lytic infection of oligodendrocytes by pathogenic strains of the JC ...
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