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Cellular Mechanism That Drives Blood Stem Cell Aging Discovered
Age-related changes in blood stem cells are linked to decreased platelet factor 4, marking a critical finding for treating immune aging.
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“Structure Never Goes Away” – New Insight Into Mitosis
MIT scientists have overturned the belief that genome structure vanishes during cell division. Using high-resolution genome mapping, they found that small 3D DNA loops, or “microcompartments,” persist and even strengthen during mitosis.
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Nasal Organoids Reveal How Good Bacteria May Prevent Infections
Discover how human nasal organoids reveal bacterial interactions in noses, influencing immune responses and health.
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Brain Organoids Bring Insights to Lissencephaly Development and Treatment
New research has developed a brain organoid model to study lissencephaly, a rare genetic disorder.
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Study Reveals How Brain Cells Route Supplies To Build Memories
When we form a memory, brain cells need to deliver supplies to strengthen specific neural connections. A new study from MPFI and Weill Cornell Medicine has revealed how two cellular switches, Rab4 and Rab10, direct supplies to where they are needed.
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Bacteriophage Discovery Could Provide Insights for Microbiome Health
Research on bacteriophages in the human gut reveals their dormant nature and potential to impact gut microbiome health significantly.
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95% of RNA Differs Between Living and Postmortem Human Brains
Two new studies from Mount Sinai’s Living Brain Project reveal that living human brain tissue shows major molecular differences compared to postmortem samples, the current research standard.
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How Childhood Trauma Leaves Lasting Epigenetic Marks
A recent study by researchers from the University of Fukui and Hiroshima University in Japan shows that child maltreatment leaves measurable biological “scars” on children’s DNA.
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Stressors Damage Kidneys by Mutating Mitochondrial DNA
New findings in chronic kidney disease research highlight mitochondrial DNA mutations as a key factor in kidney health decline.
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CPD Gene Mutation Reveals New Therapeutic Target for Rare Hearing Loss
Researchers have identified that mutations in the CPD gene are a key factor in a rare type of congenital hearing loss.
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