A prosthodontic digital guide for reproducing lip–instrument positioning for wind instruments
Peer-Reviewed Publication
Updates every hour. Last Updated: 21-Oct-2026 06:16 ET (21-Oct-2026 10:16 GMT/UTC)
Excess fat accumulation in the liver can contribute to the development and progression of metabolic dysfunction-associated steatotic liver disease (MASLD), highlighting the need for new approaches to manage the condition. Now, researchers have found that hyodeoxycholic acid (HDCA), a bile acid, can reduce liver fat in mice while also identifying the biological pathways involved. The findings suggest that HDCA could help inform the development of new approaches to managing MASLD.
How deep is the deepest ocean—and how precisely can we actually measure it? A Japanese research team has mapped the Challenger Deep in the Mariana Trench using the EM124 multibeam echosounder aboard the research vessel Hakuho-maru.
Osaka Metropolitan University researchers developed an AI-driven transfer-learning method that refines volume size factor predictions from first-principles calculations, enabling more reliable prediction of properties in previously unexplored alloy systems.
Researchers at the Nano Life Science Institute (WPI-NanoLSI) at Kanazawa University, Kyoto University, SOKENDAI, and the National Institute for Physiological Sciences have revealed how CaMKIIα—a key brain protein involved in learning and memory—organizes itself into chain-like structures. Their study, published in Science Advances, shows how activation causes these protein structures to grow and how a mutation associated with neurodevelopmental disorders changes their organization, findings that could deepen our understanding of memory formation and neurological disease.
As new memories form the connections between brain cells can become stronger. A protein called CaMKIIα plays an important part in this process and is found in especially large amounts at the points where brain cells communicate. Scientists have long known that more of this protein gathers at active connections, but they have not been able to see clearly how the individual protein molecules come together.
In the new study, a team led by Mikihiro Shibata, used high-speed atomic force microscopy, a technique that can visualize individual molecules at very high resolution, to observe how CaMKIIα molecules move and interact in real time. The researchers discovered that, under crowded conditions similar to those inside brain-cell connections, the molecules join together to form chain-like structures.