Researchers at UT Southwestern Medical Center have identified a protein that causes human cell membranes to break open in a ...
Prominent companies operating in the global drug discovery services market include: • Charles River Laboratories (US) • ...
Morning Overview on MSN
Programmable CRISPR cuts stem cell timing from months to weeks
Programmable CRISPR tools are turning stem cell biology into something closer to software engineering, shrinking ...
Bedford ‘s Nicole Steele, a biochemistry and molecular biology major at Clark University, is part of a team working with the ...
AZoLifeSciences on MSN
Syntax Bio develops CRISPR technology to program stem cell gene activity
Syntax Bio, a synthetic biology company programming the next generation of cell therapies, today announced the publication of ...
A cutting-edge base-edited CAR T-cell therapy is opening a revolutionary new frontier for patients battling aggressive T-cell ...
A team of researchers at the Icahn School of Medicine at Mount Sinai has uncovered why children with the same ...
A recent study in the journal PNAS from the lab of Julie Overbaugh reveals a previously unknown antiviral function of a gene ...
This year, gene-editing technology was customized to fix mutations in a single patient’s genes for the first time.
Penn Medicine shows how sustained research investment drives innovation, economic growth, and global health breakthroughs.
A team of researchers at the Icahn School of Medicine at Mount Sinai has uncovered why children with the same ...
The problem, Zaaijer explained, is that algorithms used in precision medicine models overwhelming are built on DNA with ...
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