Step forward in gene therapy to treat cause of sudden cardiac arrest
Using gene therapy, the researchers corrected abnormal heart rhythms by restoring a protein that heart cells need to establish connections with one another.
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Using gene therapy, the researchers corrected abnormal heart rhythms by restoring a protein that heart cells need to establish connections with one another.
New urine gene test presented at EAU identified mutations across 10 genes, that were able to predict bladder cancer.
The scientists revealed in mice models that endogenous retrovirus activation increases a foetus’s susceptibility to autism.
US researchers evaluate an experimental gene therapy in the first ever nonhuman primate model for Usher Syndrome.
US researchers found that serotonin impacts the mitral valve in the heart which can lead to heart valve disease.
US researchers outline the development of a new system for testing and developing CRISPR-based gene drives in the laboratory, and safely converting them into tools for potential real-world applications.
Using lung basal cell organoids, researchers identify a gene that directs the development of lung cancer and offers a better understanding of its disease treatment.
Researchers found that proteins made by stem cells that regenerate the cornea could be new targets for treating dry eye disease.
The scientists argue the technique enables the creation of complex, data-rich “maps” of organs, including diseased organs and tumours, which could be widely useful in pre-clinical research.
Researchers have genetically profiled nearly 200,000 cells from lungs, mapping their precise locations in tissue to discover an unexpected new immune niche in our airways.
Researchers have presented comprehensive multi-omic profiles to identify genes, non-coding RNAs, proteins, and plasma metabolites involved in NAFLD-to-NASH progression.
US researchers identified that those with ADHD have differences in gene activity in the brain.
Scientists have generated polygenic risk scores for developing paediatric steroid sensitive nephrotic syndrome (pSSNS), a kidney disease in children.
MIT researchers have developed a technique that could help the production of monoclonal antibodies and other useful proteins.
The study’s findings have important implications for better understanding the neurological basis for ASD and developing effective therapies for patients.