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Researchers at the University of Colorado School of Medicine have found that a unique bacteria found in the gut may be responsible for causing rheumatoid arthritis (RA) in patients who are already predisposed to the autoimmune disease.

A group of researchers from the Division of Rheumatology worked on the study under the leadership of Kristine Kuhn, MD, Ph.D., an associate professor of rheumatology. The study was recently published in the journal Science Translational Medicine. Meagan Chriswell, a medical student at CU, is the paper’s lead author.

“Work led by co-authors Drs. Kevin Deane, Kristen Demoruelle, and Mike Holers here at CU helped establish that we can identify people who are at risk for RA based on serologic markers, and that these markers can be present in the blood for many years before diagnosis,” Kuhn says. “When they looked at those antibodies, one is the normal class of antibody we normally see in circulation, but the other is an antibody that we usually associate with our mucosa, whether it be the oral mucosa, the gut mucosa, or the lung mucosa. We started to wonder, ‘Could there be something at a mucosal barrier site that could be driving RA?’”

Check out the on-demand sessions from the Low-Code/No-Code Summit to learn how to successfully innovate and achieve efficiency by upskilling and scaling citizen developers. Watch now.

Effects from the COVID-19 pandemic and the resulting economic disruption still loom large over businesses around the world.

Digital-native organizations (DNOs) already using cloud infrastructures and mobile apps to conduct business with customers adapted quickly to the new digital normal. However, despite their best efforts, some established enterprises remain stuck in their digital transformations and cloud adoption journeys. Companies that have struggled to adapt face a huge — and perhaps existential — challenge on how to remain relevant in this new digitally-oriented world.

The world’s first artificial womb facility, EctoLife, will be able to grow 30,000 babies a year. It’s based on over 50 years of groundbreaking scientific research conducted by researchers worldwide.

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Using new machine learning techniques, researchers at UC San Francisco (UCSF), in collaboration with a team at IBM Research, have developed a virtual molecular library of thousands of “command sentences” for cells, based on combinations of “words” that guided engineered immune cells to seek out and tirelessly kill cancer cells.

The work, published online Dec. 8, 2022, in Science, represents the first time such sophisticated computational approaches have been applied to a field that until now has progressed largely through ad hoc tinkering and engineering cells with existing—rather than synthesized—molecules.

The advance allows scientists to predict which elements—natural or synthesized—they should include in a cell to give it the precise behaviors required to respond effectively to complex diseases.

Earlier research by Dr. Li-Huei Tsai of the Massachusetts Institute of Technology and others found that APOE4 might raise Alzheimer’s risk by altering lipid metabolism in certain brain cells. But the underlying details of the process remained unclear.

To build on these findings, the team conducted a multi-pronged study that assessed gene activity of all major cell types in post-mortem human brain tissue from 32 men and women who had one, two, or no copies of the APOE4 gene. Results were published in Nature on November 24, 2022.

The researchers found that APOE4 affected gene expression across all measured cell types. The team then took a closer look at genes related to cholesterol and other lipids. Cholesterol-manufacturing genes were overly expressed, and cholesterol-transporting genes dysregulated, in brain cells called oligodendrocytes with the APOE4 gene. Oligodendrocytes are found in the brain and spinal cord. They make and maintain a fatty substance called myelin that surrounds and insulates long nerve fibers. The abnormalities were more extreme in oligodendrocytes with two copies of APOE4 rather than one.

The risk of complications in assisted reproduction is higher when two embryos are transferred, instead of one embryo. This has been shown in a study published in the journal JAMA Pediatrics, which included all births in Sweden 2007–2017.

Fertility treatments using assisted reproduction in Sweden are among the safest in the world regarding risks for the mother and children. A national recommendation to only transfer one embryo in assisted reproduction was introduced in 2003, aiming to decrease the risk of multiple pregnancies and their related complications during and delivery.

In certain cases, two are still transferred in order to increase the chance of pregnancy while the risk of multiple pregnancy remains low. Thus, many of the treatments with double embryo transfer result in single pregnancies. Many patients wish to have two embryos transferred to increase their chances of pregnancy, but there is a lack of data on potential risks with transferring two embryos when the treatment results in the of a single child.

Cancer, caused by abnormal overgrowth of cells, is the second-leading cause of death in the world. Researchers from the Salk Institute have zeroed in on specific mechanisms that activate oncogenes, which are altered genes that can cause normal cells to become cancer cells.

Cancer can be caused by , yet the impact of specific types such as structural variants that break and rejoin DNA, can vary widely. The findings, published in Nature on December 7, 2022, show that the activity of those mutations depends on the distance between a particular gene and the sequences that regulate the gene, as well as on the level of activity of the regulatory sequences involved.

This work advances the ability to predict and interpret which genetic mutations found in cancer genomes are causing the disease.

Combustion engines, propellers, and hydraulic pumps are examples of fluidic devices—instruments that utilize fluids to perform certain functions, such as generating power or transporting water.

Because fluidic devices are so complex, they are typically developed by experienced engineers who manually design, prototype, and test each apparatus through an iterative process that is expensive, time-consuming, and labor-intensive. But with a new system, users only need to specify the locations and speeds at which fluid enters and exits the device. The computational pipeline then automatically generates an optimal design that achieves those objectives.

The system could make it faster and cheaper to design fluidic devices for all sorts of applications, such as microfluidic labs-on-a-chip that can diagnose disease from a few drops of blood or artificial hearts that could save the lives of transplant patients.

Latent diffusion models (LDMs), a subclass of denoising diffusion models, have recently acquired prominence because they make generating images with high fidelity, diversity, and resolution possible. These models enable fine-grained control of the image production process at inference time (e.g., by utilizing text prompts) when combined with a conditioning mechanism. Large, multi-modal datasets like LAION5B, which contain billions of real image-text pairs, are frequently used to train such models. Given the proper pre-training, LDMs can be used for many downstream activities and are sometimes referred to as foundation models (FM).

LDMs can be deployed to end users more easily because their denoising process operates in a relatively low-dimensional latent space and requires only modest hardware resources. As a result of these models’ exceptional generating capabilities, high-fidelity synthetic datasets can be produced and added to conventional supervised machine learning pipelines in situations where training data is scarce. This offers a potential solution to the shortage of carefully curated, highly annotated medical imaging datasets. Such datasets require disciplined preparation and considerable work from skilled medical professionals who can decipher minor but semantically significant visual elements.

Despite the shortage of sizable, carefully maintained, publicly accessible medical imaging datasets, a text-based radiology report often thoroughly explains the pertinent medical data contained in the imaging tests. This “byproduct” of medical decision-making can be used to extract labels that can be used for downstream activities automatically. However, it still demands a more limited problem formulation than might otherwise be possible to describe in natural human language. By prompting pertinent medical terms or concepts of interest, pre-trained text conditional LDMs could be used to synthesize synthetic medical imaging data intuitively.