New recyclable electronics could be critical to curbing e-waste, scientists argue, especially because these circuit boards can be repaired or reconfigured by simply applying heat.

Learning “universal representations” of life’s fundamental unit

A new hypothesis called the “quantum memory matrix” could solve long-standing physics questions, including the Black Hole Information Paradox and dark matter.

Mark Hersam is a nanotechnologist who believes that understanding materials at the shortest of length scales can provide solutions to the world’s largest problems. Using an interdisciplinary approach at the intersection of neuroscience and nanoelectronics, Hersam presents a solution to the greatest societal threat posed by AI.

Dr. Mark C. Hersam, the Walter P. Murphy Professor of Materials Science and Engineering, Director of the Materials Research Center, and Chair of the Materials Science and Engineering Department at Northwestern University, has made major breakthroughs in the field of nanotechnology. His research interests include nanomaterials, additive manufacturing, nanoelectronics, scanning probe microscopy, renewable energy, and quantum information science. Dr. Hersam has received several honors including the Marshall Scholarship, Presidential Early Career Award for Scientists and Engineers, American Vacuum Society Medard Welch Award, U.S. Science Envoy, and MacArthur Fellowship. In addition, he is an elected member of the American Academy of Arts and Sciences, National Academy of Engineering, and National Academy of Inventors and has founded two companies, NanoIntegris and Volexion, which are suppliers of nanoelectronic and battery materials, respectively.

This talk was given at a TEDx event using the TED conference format but independently organized by a local community.

Join Mari in rationally understanding and accepting humanity’s transition to AI superintelligence.

Scientists start a controversial project to create the building blocks of human life, in what is thought to be a world first.

Gene therapy—once something out of science fiction—is now being used in real hospitals to treat real people. Gene editing has become a conversation of not only treating rare diseases but also about access, fairness, and how much control we should have over our biology.

Genes are sections of DNA that act like instruction manuals telling our cells how to build proteins. Proteins perform vital function like energy use, cellular communications, immunity and cell repair. So when people say “We are what our genes make us,” it’s because these gene-coded proteins guide our growth, health, and behaviour.

Sometimes, typos appear in these instruction manuals. They are called genetic mutations. While many mutations are harmless, some affect the protein made from the mutated gene and disrupt how the cell functions. Some cause serious diseases like cystic fibrosis, muscular atrophy or certain cancers.

Join us for an exclusive 1-hour conversation with Dr. Eriona Hysolli, the visionary scientist bridging de-extinction technology and the future of human reproduction. Recognized by Time100 Next for her groundbreaking work reviving the woolly mammoth, Dr. Hysolli brings a unique perspective to reproductive biotechnology that you won’t find anywhere else.

In this informal Q&A session, we’ll explore how cutting-edge technologies originally developed for species conservation are now revolutionizing human fertility treatments. Dr. Hysolli will share insights on:
The latest breakthroughs in synthetic embryos and artificial wombs.
How in vitro gametogenesis could transform infertility treatment.
Lessons from mammoth de-extinction that apply to human reproductive health.
The intersection of genome engineering and fertility solutions.
Near-term commercial applications in reproductive biotechnology.

Drawing from her pioneering work at Yale, George Church’s lab at Harvard, and as Head of Biological Sciences at Colossal Biosciences, Dr. Hysolli offers a rare glimpse into technologies that could redefine human reproduction within the next decade.

The session will feature a moderated discussion followed by audience Q&A. Whether you’re an investor, entrepreneur, healthcare professional, or simply fascinated by the future of fertility, this conversation will provide essential insights into one of biotechnology’s most promising frontiers.

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Could we replace the brain with computer chips? Reality is much more complex and the brain seems to be much more than just a biological computer.

Introducing a new, unifying DNA sequence model that advances regulatory variant-effect prediction and promises to shed new light on genome function — now available via API.

The genome is our cellular instruction manual. It’s the complete set of DNA which guides nearly every part of a living organism, from appearance and function to growth and reproduction. Small variations in a genome’s DNA sequence can alter an organism’s response to its environment or its susceptibility to disease. But deciphering how the genome’s instructions are read at the molecular level — and what happens when a small DNA variation occurs — is still one of biology’s greatest mysteries.

Today, we introduce AlphaGenome, a new artificial intelligence (AI) tool that more comprehensively and accurately predicts how single variants or mutations in human DNA sequences impact a wide range of biological processes regulating genes. This was enabled, among other factors, by technical advances allowing the model to process long DNA sequences and output high-resolution predictions.