Cell and gene therapies, or CGT, have come a long way since they were first introduced. In the last few decades, both cell therapy -- the...
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Maroc - ONCOLOGYNEWS.COM.AU - A La Une - 19/11/2024 13:53
In recent years, scientists have created a range of new methods based on CRISPR-Cas technology for precisely editing the genetic material of living organisms. One application is in cell therapy: a patient’s immune cells can be specifically reprogrammed to fight cancer more effectively. Researchers in the Department of Biosystems Science and Engineering at ETH Zurich [...]
Cell and gene therapies, or CGT, have come a long way since they were first introduced. In the last few decades, both cell therapy -- the...
Creative Biolabs provides end-to-end scientific support—from liposomal formulation design to next-generation LNP platforms tailored for CRISPR-Cas9,...
Creative Biolabs provides end-to-end scientific support—from liposomal formulation design to next-generation LNP platforms tailored for CRISPR-Cas9,...
A team led by investigators at Mass General Brigham and Dana-Farber Cancer Institute, USA, has shown that a single injection of an oncolytic virus—a...
A team led by investigators at Mass General Brigham and Dana-Farber Cancer Institute, USA, has shown that a single injection of an oncolytic virus—a...
Over the years, cell biology has built a detailed picture of how cells compartmentalize their internal functions. Central to this organization is the...
Scientists have uncovered an elegant biophysical trick that tuberculosis-causing bacteria use to survive inside human cells, a discovery that could...
India has the ptoential to become a global leader in equitable gene therapy ......
India has the ptoential to become a global leader in equitable gene therapy ......
UCLA researchers have developed a lipid nanoparticle-based gene-editing approach capable of inserting an entire healthy gene into human airway cells,...