When the monkeys were single-celled embryos, scientists had used CRISPR editing tools to silence, or “knock out”, a gene that ...
2024 — Researchers have used gene editing to restore hearing in adult mice with a type of inherited hearing loss. They showed that shutting down a damaged copy of a gene called a microRNA (miRNA ...
Researchers developed a new gene-editing strategy that dramatically boosts the effectiveness of gene therapies in the liver, a breakthrough that could lead to new treatments for about 700 genetic ...
A vast search of natural diversity has led scientists at MIT's McGovern Institute and the Broad Institute of MIT and Harvard ...
Live Science on MSN13d
'Speech gene' seen only in modern humans may have helped us evolve to talkIn a new study, published Tuesday (Feb. 18) in the journal Nature Communications, researchers used CRISPR gene editing to ...
A £1.65 million treatment has been approved for use for some NHS patients, offering some with an inherited blood disorder hope of a cure. Campaigners reacted with joy as health officials approved ...
The Associated Press on MSN14d
Scientists link gene to emergence of spoken languageA new study links a particular gene to the origins of spoken language, proposing that a protein variant found only in humans may have helped us develop speech.
In a shift away from GMOS, aka genetically modified organisms, important research is continuing in gene editing, sometimes referred to as “the next big thing in agriculture.” The important ...
PRGN-2012—which Precigen has begun to call by its generic name of zopapogene imadenovec—is a gene therapy designed to elicit immune responses directed against cells infected with human papillomavirus ...
Agans is doing cutting-edge research in experimental genetics as a lab assistant and honors student in Jack Bateman’s lab.
Verve offered few details on the early end of a collaboration the companies inked in 2022, saying only that Vertex cited “changing priorities.” ...
One innovative aspect of this study is the methodology used: the team employed CRISPR-Cas9 gene editing to label the MFN1 and MFN2 proteins within the cell, without resorting to artificial ...
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