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SARS-CoV-2 Human Challenge Study Provides Infection Insights
Findings from the UK's world-leading human challenge study provide new insights into mild infections with SARS-CoV-2 in healthy young adults.
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New Imaging Technique Reveals Causes of Swelling in the Brain
Cerebral oedema is a dangerous complication in many brain-related conditions such as strokes. Researchers have developed a new measurement method that enables better understanding of the cellular causes of cerebral oedema.
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RNA Sequencing Improves Diagnosis of Childhood Cancers
The use of RNA sequencing to identify fusion genes in childhood cancers has improved diagnoses and aided the use of targeted treatments.
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Novel Genetic Insights on Multiple Sclerosis Risk
Researchers have discovered that oligodendrocytes might have a different role in the development of multiple sclerosis than previously thought.
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Further Research Explores Genetic Underpinnings of COVID-19 Disease Severity
Researchers have found genetic variants in extremely ill patients with COVID-19 that may help explain the differences in how sick people get.
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Blood Test, Combined With MRI, Reduces Harm and Costs When Diagnosing Cancer
Combining a new blood test with MRI cuts the societal cost of prostate cancer screening and reduces the overdiagnosis of low-risk cancers, supporting organized prostate cancer testing in Sweden.
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Blood Tests Could Make for Easier, More Reliable ALS Diagnosis
Blood tests may enable a more accurate diagnosis of ALS at an earlier stage of the disease.
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New Approach Accelerates Cancer Biomarker Detection
Researchers have developed an approach that accelerates the detection of cancer biomarkers in samples taken at the time and place of patient care.
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The Potential of Structural Proteomics for Treating Neurodegenerative Diseases
Structural proteomics can resolve the detailed structure of protein interactions and therefore may progress understanding of neurodegenerative disease treatments.
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RNA-Based Molecule Helps Cells “Skip Over” Cystic Fibrosis Mutation
Researchers have discovered a way to modify the message containing the instruction for CFTR, forcing the protein-making machinery to skip over this “stop sign” mutation, which allows a functional version of the protein to be made.
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