Testing in mice suggests that rejuvenating T cells could make vaccines and some cancer therapies more effective.
Scientists at Johns Hopkins Medicine say results of a new study are advancing efforts to exploit a new target for Alzheimer’s disease: a protein that manufactures an important gas in the brain.
Experiments conducted in genetically engineered mice reinforce that the protein, Cystathionine γ-lyase, or CSE—ordinarily known for producing hydrogen sulfide gas responsible for the foul smell of rotten eggs—is critical for memory formation, says Bindu Paul, M.S., Ph.D., associate professor of pharmacology, psychiatry and neuroscience at the Johns Hopkins University School of Medicine, who led the study.
The new research, published in Proceedings of the National Academy of Sciences, was designed to better understand the basic biology of the protein, and its value as a novel target for drugs that boost the expression of CSE in people to help keep brain cells healthy and slow neurodegenerative disease.
Thousands of glaciers will vanish each year in the coming decades, leaving only a fraction standing by the end of the century unless global warming is curbed, a study showed on Monday.
Government action on climate change could determine whether the world loses 2,000 or 4,000 glaciers annually by the middle of the century, according to the research.
A few degrees could be the difference between preserving almost half of the world’s glaciers in 2100—or fewer than 10%.
A research team led by Professor Kanghyun Nam from the Department of Robotics and Mechanical Engineering at DGIST has developed a physical AI-based vehicle state estimation technology that accurately estimates the driving state of electric vehicles in real time.
This technology is viewed as a key advancement that can improve the core control performance of electric vehicles and greatly enhance the safety of autonomous vehicles. The work was conducted through international joint research with Shanghai Jiao Tong University in China and the University of Tokyo in Japan.
The work is published in the journal IEEE Transactions on Industrial Electronics.
An ultrathin ferroelectric capacitor, designed by researchers from Japan, demonstrates strong electric polarization despite being just 30 nm thick including top and bottom electrodes—making it suitable for high-density electronics. Using a scandium-doped aluminum nitride film as the ferroelectric layer, the team achieved high remanent polarization even at reduced thicknesses. This breakthrough demonstrates good compatibility with semiconductor devices combining logic circuits and memory, paving the way for compact and efficient on-chip memory for future technologies.
Modern electronic technology is rapidly advancing towards miniaturization, creating devices that are increasingly compact yet high-performing. As the devices continue to shrink in size, there is an increasing demand for ultra-small memory materials that can efficiently store data, even in smaller dimensions. Ferroelectric memory devices are promising options for future mobile and compact electronics, as they store information using switchable electric polarization, allowing data retention even without power. However, very few initiatives have reported progress in downscaling of these ferroelectric devices.
Bridging this gap, a research team led by Professor Hiroshi Funakubo from the School of Materials and Chemical Technology, Institute of Science Tokyo (Science Tokyo), Japan, in collaboration with Canon ANELVA Corporation (Canon ANELVA), successfully downscaled a total ferroelectric memory capacitor stack using scandium-substituted aluminum nitride ((Al, Sc)N) thin films with platinum electrodes, reducing the total thickness to just 30 nm including top and bottom electrodes.
An exploration of the not often considered aspect of the Alcubierre faster-than-light Drive and the terrifying implications of it.
Wagner et al. demonstrate that RNase H1 only removes a subset of R-loops in vivo. In yeast, overexpressed RNH1 acts more frequently at dysregulated R-loops and infrequently, if at all, at other RNA-DNA hybrids. Endogenous Rnh1 is induced in a Rad53-dependent manner at transcription-replication conflicts to promote replication completion.