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Living matter remains the quintessential puzzle of biological sciences, a question that embodies the intricate complexity and stunning diversity of life forms. A new study suggests that one viable approach to address this extreme complexity is to conceptualize living matter as a cascade of machines producing machines.

This cascade illustrates how cells are composed of smaller submachines, reaching down to the where molecular machines, such as ion pumps and enzymes, operate. In the other direction, it explains how cells self-organize into larger systems, such as tissues, organs, and populations, cumulating into the biosphere.

This new conceptual framework is a fruit of collaboration between Professors Tsvi Tlusty from the Department of Physics at Ulsan National Institute of Science and Technology (UNIST), South Korea, and Albert Libchaber from the Center for Physics and Biology at Rockefeller University, New York. The study was inspired by the seventeenth-century polymath Gottfried Leibniz, who noted that “the machines of nature, that is living bodies, are still machines in their smallest parts, to infinity.”

Panzeri et al. use a Trim28 +/D9 mouse model with intrinsic developmental heterogeneity to show that ‘heavy’ and ‘light’ developmental morphs exhibit different timing, type and severity of cancer, linked to a relevant DNA hypomethylation signature.

After more than a decade of work, researchers have reached a major milestone in their efforts to re-engineer life in the lab, putting together the final chromosome in a synthetic yeast (Saccharomyces cerevisiae) genome.

The researchers, led by a team from Macquarie University in Australia, chose yeast as a way to demonstrate the potential for producing foodstuffs that could survive the rigors of a changing climate or widespread disease.

It’s the first time a synthetic eukaryotic genome has been constructed in full, following on from successes with simpler bacteria organisms. It’s a proof-of-concept for how more complex organisms, like food crops, could be synthesized by scientists.

How could CRISPR help cure diseases? Feng Zhang, Professor of Biological Engineering at MIT, describes how CRISPR works like a search box for DNA. Using matching RNA proteins, it can find specific spots on the DNA where a gene needs to be edited or repaired. Through this method, it might be possible to go into the human genome and fix the genes that cause sickle cell disease, blindness, or neurodegeneration! How Does CRISPR Work? With Feng Zhang: https://youtu.be/ylgg7yZMJSs Among the world’s largest science centers, the Museum of Science engages millions of people each year to the wonders of science and technology through interactive exhibitions, digital programs, giant screen productions, and preK – 12 EiE® STEM curricula through the William and Charlotte Bloomberg Science Education Center. Established in 1830, the Museum is home to such iconic experiences as the Theater of Electricity, the Charles Hayden Planetarium, and the Mugar Omni Theater. Around the world, the Museum is known for digital experiences such as Mission: Mars on Roblox, and traveling exhibitions such as the Science Behind Pixar.

Key cells in the brain, neurons, form networks by exchanging signals, enabling the brain to learn and adapt at incredible speed. Researchers at the Delft University of Technology in The Netherlands (TU Delft) have developed a 3D-printed brain-like environment where neurons grow similarly to a real brain.

Using tiny nanopillars, they mimic the soft neural tissue and the brain extracellular matrix fibers. This model provides new insights into how neurons form networks, as well as a novel tool to understand in future how this process may change in neurological disorders such as Alzheimer’s, Parkinson’s disease, and autism spectrum disorders.

The work is published in the journal Advanced Functional Materials.

Researchers are paving the way for the design of bionic limbs that feel natural to users. They demonstrate the connection between hand movement patterns and motoneuron control patterns. The study, published in Science Robotics, also reports the application of these findings to a soft prosthetic hand, which was successfully tested by individuals with physical impairments.

The research study sees the collaboration of two research teams, one at Istituto Italiano di Tecnologia (Italian Institute of Technology) in Genova, Italy, led by Antonio Bicchi, and Imperial College London, UK led by Dario Farina. It is the outcome of the project “Natural BionicS” whose goal is to move beyond the model of current prosthetic limbs, which are often abandoned by patients because they do not respond in a “natural” way to their movement and control needs.

For the central nervous system to recognize the bionic limb as “natural,” it is essential for the prosthesis to interact with the environment in the same way a real limb would. For this reason, researchers believe that the prostheses should be designed based on the theory of sensorimotor synergies and soft robotics technologies, first proposed by Antonio Bicchi’s group at IIT, such as the Soft-Hand robotic hand.

Recent technological advances have opened new possibilities for the development of assistive and medical tools, including prosthetic limbs. While these limbs used to be hard objects with the same shape as limbs, prosthetics are now softer and look more realistic, with some also integrating robotic components that considerably broaden their functions.

Despite these developments, most commercially available robotic limbs cannot be easily and intuitively controlled by users. This significantly limits their effectiveness and the extent to which they can improve people’s quality of life.

Researchers at the Italian Institute of Technology (IIT) and Imperial College London recently developed a new soft prosthetic hand that could be easier for users to control. This system, presented in a Science Robotics paper, leverages a new control approach that integrates the coordination patterns of multiple fingers (i.e., postural synergies) with the decoding of the activity of motoneurons in people’s spinal column.