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With gene therapy offering new hope for thalassemia, experts urge Indian govt to invest in early diagnosis, genetic testing, ...
Thalassemia, a group of inherited blood disorders characterized by reduced or abnormal hemoglobin production, continues to ...
A four-year-old Pakistani girl diagnosed with severe thalassemia has been successfully treated with a Chinese-developed ...
Beam Therapeutics faces slow pipeline progress and high R&D costs despite a $500M cash boost. Learn why patience is key for ...
Further, Editas Medicine has decreased expenses and costs thanks to discontinuing the development of reni-cel and laying off ...
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ZME Science on MSNThis Baby’s One-in-a-Million Genetic Disorder Had No Cure. So Scientists Designed One Just for HimKJ Muldoon came into the world with a genetic time bomb ticking inside him.
Cell and gene therapy (C>) is set to revolutionise treatment of complex diseases, offering new possibilities for patients.
The personalized CRISPR treatment could be the future of gene therapy, but hurdles remain before everyone has access.
The death of a patient in a trial of an experimental gene therapy casts new shadows over a technology once seen as the future ...
High levels of cholesterol may gradually clog your arteries, which makes it more difficult for blood to flow. This increases the likelihood of high blood pressure, heart attack, and stroke if not ...
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