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Colorectal cancer (CRC), a type of cancer that affects the large intestine and rectum, is one of the leading causes of cancer-related deaths worldwide. The mutational landscape of CRC is ...
Researchers from the Department of Pathology, School of Clinical Medicine at the LKS Faculty of Medicine of the University of ...
Researchers have identified mutations in the non-coding gene RNU2-2 as a cause of a newly defined neurodevelopmental disorder ...
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News Medical on MSNInherited mutations in healthy cells may contribute to cancer developmentMost cancer genome studies have focused on mutations in the tumor itself and how such gene variants allow a tumor to grow unchecked.
Most cancer genome studies have focused on mutations in the tumor itself and how such gene variants allow a tumor to grow unchecked. A new study takes a deep dive into inherited cancer mutations ...
Researchers have uncovered a surprising mechanism by which a single genetic mutation in the BCL11B gene causes both immune dysfunction and brain development issues.
A seminal study has uncovered a new genetic cause of neurodevelopmental disorders (NDDs). The discovery offers both closure and hope to potentially thousands of families worldwide who have long been ...
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News-Medical.Net on MSNInherited genetic variants play crucial role in cancer development and behaviorA new multicenter study by researchers at the Icahn School of Medicine at Mount Sinai, in collaboration with the National Cancer Institute-funded Clinical Proteomic Tumor Analysis Consortium (CPTAC) ...
Gene therapy for cystic fibrosis is advancing fast. Explore key biotech players, clinical progress, and its potential to ...
UD researchers extracted the DNA from the samples and worked to amplify the MDV meq oncogene, a gene essential for MDV’s ability to cause cancer, to look at its mutations. Parcells identified ...
Discover how an emerging technology called tRNA therapy could become the next big thing in genetic disease treatment.
UD researchers extracted the DNA from the samples and worked to amplify the MDV meq oncogene, a gene essential for MDV's ability to cause cancer, to look at its mutations. Parcells identified ...
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