Tag: Gene editing

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CAR T-Cell Therapy Linked to Rare T-Cell Lymphoma Cases, FDA Investigates

CAR T-Cell Therapy under FDA investigation for potential link to rare T-Cell lymphoma. Experts weigh in on risks and benefits of groundbreaking cancer treatment.

Scientists Discover 188 New CRISPR Systems in Microorganisms, Revolutionizing Gene Editing

Scientists uncover 188 new CRISPR systems in microorganisms, advancing gene editing and revolutionizing genetic research. A game-changing discovery!

Rare CRISPR Systems Discovered: Revolutionizing Gene Editing and Diagnostics

Revolutionize gene editing and diagnostics with the discovery of thousands of rare CRISPR systems. A breakthrough in molecular biology with far-reaching implications.

FDA Grants RMAT Designation to Editas Medicine’s EDIT-301 for Severe Sickle Cell Disease, US

The FDA grants RMAT designation to Editas Medicine's EDIT-301 for severe sickle cell disease. Learn about the potential life-changing benefits of this innovative gene editing medicine.

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Breakthrough in Xenotransplantation: Pig Kidneys Provide Life-Sustaining Function in Human Patient, US

Discover a breakthrough in xenotransplantation as pig kidneys show promising results in human patients, offering hope for the organ shortage crisis. Learn more!

Breakthrough: Pig Kidney Transplants Provide Life-Sustaining Function in Humans, Offering Hope for Organ Shortage Crisis, US

Discover the groundbreaking breakthrough in pig kidney transplants, offering hope for the organ shortage crisis and a potential cure for end-stage kidney disease.

FDA Grants RMAT Designation to Editas Medicine’s EDIT-301 for Severe Sickle Cell Disease, US

The FDA grants RMAT designation to Editas Medicine's EDIT-301 for severe sickle cell disease. Learn about the potential life-changing benefits of this innovative gene editing medicine.

Researchers Develop New Technique for Gene Editing in Bone Marrow, Potentially Eliminating the Need for Transplants

Revolutionary gene editing technique in bone marrow may eliminate need for transplants. Promising breakthrough in treating blood cell disorders.

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