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People who inherit pathogenic mutations in either one of these genes have an increased risk of developing certain cancers.
Understanding the genetics of an infectious tumor in Tasmanian devils could point toward new treatment targets.
This gene is fused to many partner genes in different tumors. Now, scientists know it causes cancer — and how they might intervene.
Tumors known as gliomas generally don’t respond to the immunotherapy drugs even when the tumor cells are “hypermutated."
One finding of the project was that, on average, the genome of cancer cells contains four or five “driver” mutations.
The crowd-sourced effort has yielded unexpected findings about angiosarcoma, a disease that’s been difficult to study because it is so rare.
In support of precision medicine, a new method enables scientists to separate cancer-driving mutations from passengers.
This finding could lead to very early cancer interventions.
New site-agnostic therapies highlight the importance of genetic testing.
Task force recommends BRCA screening for women at increased cancer risk
To take advantage of these new therapies, people must first learn whether their cancer harbors targetable mutations.
High-tech approach solves ‘real mystery’ in many cancers.
While most gene mutations are harmless, others are not and can spur the formation of cancer.
Dana-Farber researchers have shown that the mutated copy of the gene TP53 sabotages the normal, healthy copy.
First KRAS targeted therapy shows promise for lung and colon cancer
Both have tested positive for the BRCA2 gene mutation.
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