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Stanford Medicine


Diseased heart muscle cells have abnormally shortened telomeres, Stanford researchers find

Researchers at Stanford University School of Medicine discovered that people with cardiomyopathy have abnormally short telomeres in their heart muscle cells. This finding opens the door to new research and drug discovery, potentially allowing for the identification of individuals at risk for heart failure due to genetic defects.

SourceStanford Medicine·JournalProceedings of the National Academy of Sciences·DateAug 27, 2018

Study solves mystery of genetic-test results for patient with suspected heart condition

Researchers have developed a technique to determine the significance of gene variants of uncertain significance in patients with suspected heart conditions. By using advanced genetic-editing tools and stem cell technology, they were able to confirm that a patient had a mild case of long QT syndrome and rule out another condition.

SourceStanford Medicine·JournalJournal of the American College of Cardiology·DateJun 26, 2018

CRISPR used to genetically edit coral, Stanford researchers report

Researchers at Stanford University School of Medicine successfully used CRISPR-Cas9 to genetically edit coral, demonstrating its potential as a resource for coral biologists. The technique allowed them to identify critical genes in coral biology and alter multiple gene copies, offering hope for conserving coral reefs.

SourceStanford Medicine·JournalProceedings of the National Academy of Sciences·DateApr 23, 2018

Altered immune cells clear childhood brain tumor in mice

Researchers at Stanford Medicine have developed a CAR-T therapy that eradicates diffuse intrinsic pontine glioma (DIPG) tumors in mice, leaving few residual cancer cells. The treatment targets the GD2 sugar molecule on DIPG tumors and has shown promising results, but side effects such as brain swelling must be carefully managed.

SourceStanford Medicine·JournalNature Medicine·DateApr 16, 2018