MeSH tree: C16.320.447
Organoids are miniature, simplified versions of an organ. Over the past two decades, scientists have developed them for the gut, lung, liver, mammary gland, brain, and more. Now, researchers at Yale School of Medicine (YSM) ...
Apr 8, 2026
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Researchers have demonstrated a new class of low-cost, scalable sensors that can be used to monitor electrical activity in human cerebral organoids. Because electrical signals are key to understanding brain function, this ...
Apr 2, 2026
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New research from the University of East Anglia (UK) reveals the hidden struggles experienced by the brothers and sisters of people with Prader–Willi syndrome.
Jan 6, 2026
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Nancy Brady has been gratified to see the tool she and colleagues pioneered over a decade ago to measure the growth of infants' pre-speech communication skills translated into several languages and referenced in more than ...
Nov 10, 2025
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In a new study, researchers at The Ohio State University used artificial intelligence (AI) tools to predict seizure outcomes in mouse models.
Oct 3, 2025
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Researchers from Brain Research Institute, Niigata University, Japan, have revealed that environment influences social behaviors in autism. By using zebrafish that have a mutation in ube3a, a gene linked to Angelman syndrome ...
Sep 5, 2025
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Ali Foley Shenk still remembers the panic when her 10-year-old son, Dean, finished a 20-ounce box of raisins in the seconds the cupboard was left unlocked. They rushed to the emergency room, fearing a dangerous bowel impaction.
Jun 18, 2025
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A new review sheds light on the complex molecular mechanisms behind Angelman syndrome (AS), a rare neurogenetic disorder, and explores how cutting-edge gene-targeting therapies may offer more effective treatment options in ...
Jun 3, 2025
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Evidence is mounting that clinicians can treat serious genetic disorders prenatally by injecting medicine into the amniotic fluid, thus preventing damage that begins in utero.
May 14, 2025
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Biomedical engineers at Duke University have demonstrated a promising new approach that could be used to treat a rare and complex class of genetic diseases caused by defects in a relatively large region of the genome.
Feb 13, 2025
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