The launch of BIRSA 101 marks a major breakthrough in CRISPR gene-editing technology, positioning India to deliver affordable cures for Sickle Cell...
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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 [...]
The launch of BIRSA 101 marks a major breakthrough in CRISPR gene-editing technology, positioning India to deliver affordable cures for Sickle Cell...
by Christopher Outcalt | Colorado State University SOURCE Researchers at Colorado State University have developed an innovative new cancer...
by Christopher Outcalt | Colorado State University SOURCE Researchers at Colorado State University have developed an innovative new cancer...
The immune system faces a delicate balancing act: it must be aggressive enough to fight infections and cancer, yet restrained enough to avoid...
A major breakthrough in cancer research has shown that using CRISPR gene editing technology to turn off a specific gene can help fight chemotherapy...
Highlights: India unveils its first indigenous CRISPR based gene therapy for Sickle Cell Disease BIRSA 101 a
In clinical medicine, five core missions have been identified: cell therapy (stem cells, immune cells), cell-based products for chronic and...
Setting a new milestone in Atmanirbhar Bharat, the government on Wednesday launched an indigenous CRISPR-based gene therapy for Sickle Cell Disease,...
Setting a new milestone in Atmanirbhar Bharat, the government on Wednesday launched an indigenous CRISPR-based gene therapy for Sickle Cell Disease,...
A team of scientists in Japan has developed a new way to treat cancer that does not rely on the body’s immune system. This is important because many...