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Scientists discover how to convert the brain’s glial cells into multipotent neural stem cells.

Mechanically sensitive gut cells similar to touch sensors in the skin allow the intestine to feel and assess the physical properties of its contents.

Clinicians and researchers teamed up to investigate how inappropriate proinflammatory mechanisms contribute to the pathogenesis of drug-refractory epilepsy.

Scientists employ cutting edge tools and techniques to create artificial organs for research and disease therapeutics.

Deconstructing concepts, approaches, and data analysis in proteomics workflows.  

Researchers found that shifted sleep/wake cycles in young rats result in increased functional deficits and mortality following stroke later in life.

Researchers use blue light therapy to treat infected burn wounds.

Researchers discovered monkeypox virus in primate testicular tissues.

Researchers employ peripheral blood mononuclear cells (PBMCs) in clinical and academic applications related to the immune system and regenerative medicine.

Neurons transmit information through the body via chemical signals and electrical impulses.

Researchers show how a toxic therapy helped identify a mummy using preserved DNA.

Scientists use locust brains as living biosensors to perform cancer cell breath tests.

Researchers found that the ApoA1 protein can restore ALS epithelial cell survival in vitro.

Scientists develop cancer nutrition guidelines based on research examining how dietary patterns affect cancer risk and prevention.

High throughput sequencing is a versatile technology that revolutionized the field of genetics.

Microbes communicate with quorum sensing to coordinate their behavior in response to how many neighbors they have.

A new frontier in repairing organ damage

As alternatives to insecticides, Omar Akbari uses sophisticated genetic engineering methods to solve the world’s mosquito problems.

By packaging lipid nanoparticles with elements that decrease the fibrous nature of solid tumors, researchers can deliver CRISPR therapies in a more efficient manner.

Researchers turned to base editors to correct mutations causing the rare genetic disease Fanconi anemia without inducing double-strand DNA breaks.