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Research published in The American Journal of Human Genetics has identified a previously unknown genetic link to autism spectrum disorder (ASD). The study found that variants in the DDX53 gene contribute to ASD, providing new insights into the genetic underpinnings of the condition.

ASD, which affects more males than females, encompasses a group of neurodevelopmental conditions that result in challenges related to communication, social understanding and behavior. While DDX53, located on the X chromosome, is known to play a role in brain development and function, it was not previously definitively associated with autism.

In the study, researchers from The Hospital for Sick Children (SickKids) in Canada and the Istituto Giannina Gaslini in Italy clinically tested 10 individuals with ASD from eight different families and found that variants in the DDX53 gene were maternally inherited and present in these individuals. Notably, the majority were male, highlighting the gene’s potential role in the male predominance observed in ASD.

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“High-Speed Sequential DNA Computing Using a Solid-State DNA Origami Register” ACS Central Science

DNA stores the instructions for life and, along with enzymes and other molecules, computes everything from hair color to risk of developing diseases. Harnessing that prowess and immense storage capacity could lead to DNA-based computers that are faster and smaller than today’s silicon-based versions. As a step toward that goal, researchers report in ACS Central Science a fast, sequential DNA computing method that is also rewritable — just like current computers.

Penn Engineers have modified lipid nanoparticles (LNPs)—the revolutionary technology behind the COVID-19 mRNA vaccines—to not only cross the blood-brain barrier (BBB) but also to target specific types of cells, including neurons. This breakthrough marks a significant step toward potential next-generation treatments for neurological diseases like Alzheimer’s and Parkinson’s.

In a new paper in Nano Letters, the researchers demonstrate how —short strings of —can serve as precise targeting molecules, enabling LNPs to deliver mRNA specifically to the that line the blood vessels of the brain, as well as neurons.

This represents an important advance in delivering mRNA to the cell types that would be key in treating neurodegenerative diseases; any such treatments will need to ensure that mRNA arrives at the correct location. Previous work by the same researchers proved that LNPs can cross the BBB and deliver mRNA to the brain, but did not attempt to control which cells the LNPs targeted.

To create cultured LMNs that replicate ALS neuron physiology and function, the Japanese team combined a small molecule-based approach with transcription factor transduction. The researchers achieved 80% induction efficiency of LMNs within just two weeks compared with conventional methods.

The resulting LMNs were found to have replicated ALS-specific pathologies, such as the abnormal aggregation of TDP-43 and FUS proteins. The team confirmed functionality of the LMNs using a multi-electrode array (MEA) system to measure firing activity and network activity, which were found to be similar to mature neurons.

Further analysis of the cultured LMNs showed that in addition to maintaining ALS cellular markers, the LMNs had reduced survival rates compared with healthy cells, mimicking ALS motor neuron responses.

All 3D models created with Meshy AI
https://www.meshy.ai/?utm_source=youtube&utm_medium=fimcrux.

The sublime is an emotion described as equal parts awe and terror; a perfect description of our universe.

We created this short film concept showcasing a future vision of how humans might continue exploring that universe.

We used Meshy AI to generate all the 3D models in this film, like the ships, space probes and asteroids.

If all the world’s a stage and all the species merely players, then their exits and entrances can be found in the rock record. Fossilized skeletons and shells clearly show how evolution and extinction unfolded over the past half a billion years, but a Virginia Tech analysis extends the chart of life to nearly 2 billion years ago. The study is published in the journal Science.

The chart shows the relative ups and downs in species counts, telling scientists about the origin, diversification, and extinction of ancient life.

With this new study, the chart of life now includes life forms from the Proterozoic Eon, 2,500 million to 539 million years ago. Proterozoic life was generally smaller and squishier—like sea sponges that didn’t develop mineral skeletons —and left fewer traces to fossilize in the first place.