Potential therapeutic target for ventricular fibrillation found
A signalling mechanism for ventricular fibrillation involving the stress kinases p38γ and p38δ has been discovered.
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A signalling mechanism for ventricular fibrillation involving the stress kinases p38γ and p38δ has been discovered.
In Alzheimer’s disease patients, irritability and anxiety is likely caused by neuroinflammation, which indicates new therapeutic pathways.
Combining cancerous and non-cancerous cell patterns, the AI model evaluates breast cancer outcomes better than expert pathologists.
Method to improve sterility assurance in biopharmaceutic manufacturing will lead to better patient outcomes.
Treating C. elegans with inhibitors of small or large mitochondrial ribosomes extended their median lifespan.
Researchers have completely decoded the human Y chromosome, which may result in more effective treatment for digestive disorders.
Findings of rare CRISPR-linked gene modules and a novel CRISPR-Cas system have promising implications for genomic therapeutics.
Novel findings about the tafazzin gene offers a potential new target and drug candidate for Barth syndrome.
Discovery about the DNA of leukaemia cells suggests promising target for gene therapy in paediatric oncology.
Researchers have found a way to genetically modify stem cells so that cell and organ transplants are not rejected.
An epigenetic pathway is mediated by a certain protein that could potentially reverse vascular remodelling in pulmonary hypertension.
A living material resembling sputum from CF patients can grow biofilms, enabling scientists to assess the effectiveness of antimicrobials.
Researchers have developed a new method to study protein clumps that occur in many difficult-to-treat diseases.
Researchers have developed organoids with naturally occurring early-stage immune cells, which could lead to effective personalised treatment.
Eliminating AT1-like cells in experimental models has shown potential to improve KRAS inhibitor treatment for lung adenocarcinoma.