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 ...
The field of dermatology has witnessed remarkable progress in the prevention and treatment of skin diseases over the past ...
This year, gene-editing technology was customized to fix mutations in a single patient’s genes for the first time.
Syntax Bio, a synthetic biology company programming the next generation of cell therapies, today announced the publication of ...
7don MSN
EAM Jaishankar warns, ‘Bioterrorism is a serious concern,’ urges BWC framework modernization
External Affairs Minister S. Jaishankar on December 1 warned that the threat of biological weapons and bioterrorism is no longer theoretical. Speaking at a conference on 50 years of the Biological ...
A new study describes a key molecular mechanism that explains how cells exchange information through extracellular vesicles ...
Highlighting 10 innovative late-stage BioPharma drugs with the potential to reshape treatment paradigms and industry dynamics ...
Utilizing the gene-editing technology CRISPR, researchers have found a way to combat chemoresistance in lung cancer cells, restoring hope for patients. Shannon Horning/ SciTech Editor For patients ...
In the published article, in the author list, the fifth author's name was erroneously spelled as “Khzuin Dinislam” instead of the correctly spelt version “Khuzin Dinislam”. The original version of ...
Scientists used CRISPR to disable the NRF2 gene, restoring chemotherapy sensitivity in lung cancer cells and slowing tumor growth. The technique worked even when only a fraction of tumor cells were ...
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