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On the heels of my latest New York Times OpEd, which is in print today on page 4 of the NYT Sunday Review, I’m excited to share my brand new book: The Futuresist Cure: Notes From the Front Lines of #Transhumanism. It’s a collection of my best essays on the future, many re-adapted, and many which have helped shape our movement. It’s #FREE today on Amazon in #Kindle. Or get the paperback version. There’s a foreword by the late Jacque Fresco. Download the book for FREE today!


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On Wednesday, we wrote about a database of mutations that could give people superhuman characteristics or medical benefits.

The database, which reads like a real-life skill tree from a video game, is housed on the website of famed Harvard geneticist George Church. Now Church has opened up, telling Futurism why he assembled the list and how he hopes others will use it as gene-hacking technology develops.

It’s not everyday that you see some of the worlds leading cancer scientists attending a scientific forum put on by a hospital from Mexico. But CHIPSA hospital isn’t your average hospital and the scientists showed presenting their research, much of which they are working on with CHIPSA.

CHIPSA
Take for instance Dr. Franco Marincola. The fa med former chief of immunogenetics for the NIH, editor of 9 peer reviewed publications and co-author of the textbook mosts oncologists use for immunotherapy reference. Dr. Marincola joined the CHIPSA Scientific advisory board in June and speaks highly of their work and passion for translational science.

Or Dr. Vijay Mahant, who did his post doctorate at MD Anderson in 1985 and invented the prostate cancer test that is widely used today. He also co-founded auto-genomics a leading liquid biopsy company that is studying diagnosing cancer through the blood.

I’m excited to share my new Op-Ed for The New York Times on the pro-life versus pro-choice debate of the artificial womb. Could this change the abortion divide forever? Conservatives may need to step up and embrace ectogenesis. Liberals should let them. The transhumanism tech will be here in a few years.


The technology would allow fetuses to develop outside the female womb so women would no longer have be pregnant.

Get your Eternal Sunshine of the Spotless Mind references ready, because scientists have just figured out a way to erase bad memories using—you guessed it—electroshock therapy. Get ready for on-demand forgetting. It’s a real thing now.

A team of Dutch neuroscientists recently devised an electroconvulsive therapy (ECT) to “target and disrupt patients’ memory of a disturbing episode.” Nature explains how patients were showed two traumatic narratives in a slideshow and then subjected to the new technique:

The team later prompted patients to recall only one of the stories by replaying part of that slide show. Immediately afterwards, when the reactivated memory is thought to be vulnerable, the patients received electroconvulsive therapy.

One day later, when given a multiple-choice memory test, patients were significantly worse at remembering details from the reactivated story, performing near chance. Patients’ memory of the other story, however, remained largely unscathed.

Researchers from North Carolina State University and Elon University have developed a technique that allows them to remotely control the movement of soft robots, lock them into position for as long as needed and later reconfigure the robots into new shapes. The technique relies on light and magnetic fields.

“We’re particularly excited about the reconfigurability,” says Joe Tracy, a professor of materials science and engineering at NC State and corresponding author of a paper on the work. “By engineering the properties of the material, we can control the ’s movement remotely; we can get it to hold a given shape; we can then return the robot to its original shape or further modify its movement; and we can do this repeatedly. All of those things are valuable, in terms of this technology’s utility in biomedical or aerospace applications.”

For this work, the researchers used soft robots made of a embedded with magnetic iron microparticles. Under normal conditions, the material is relatively stiff and holds its shape. However, researchers can heat up the material using light from a light-emitting diode (LED), which makes the polymer pliable. Once pliable, researchers demonstrated that they could control the shape of the robot remotely by applying a . After forming the desired shape, researchers could remove the LED light, allowing the robot to resume its original stiffness—effectively locking the shape in place.

Over 4000 patients in the United States alone are waiting for a heart transplant, while millions of others worldwide need hearts but are ineligible for the waitlist. The need for replacement organs is immense, and new approaches are needed to engineer artificial organs that are capable of repairing, supplementing, or replacing long-term organ function.


A team of researchers from Carnegie Mellon University has published a paper in Science that details a new technique allowing anyone to 3D bioprint tissue scaffolds out of collagen, the major structural protein in the human body. This first-of-its-kind method brings the field of tissue engineering one step closer to being able to 3D print a full-sized, adult human heart.

The technique, known as Freeform Reversible Embedding of Suspended Hydrogels (FRESH), has allowed the researchers to overcome many challenges associated with existing 3D bioprinting methods, and to achieve unprecedented resolution and fidelity using soft and living materials.

Each of the organs in the , such as the heart, is built from specialized cells that are held together by a biological scaffold called the extracellular matrix (ECM). This network of ECM proteins provides the structure and biochemical signals that cells need to carry out their normal function. However, until now it has not been possible to rebuild this complex ECM architecture using traditional biofabrication methods.

Shift Bioscience is a company aiming to solve the problem of mitochondrial dysfunction, one of the hallmarks of aging, by repairing the aging mitochondria in our cells so that they work as if they were younger.

Mitochondrial dysfunction is at the heart of aging

The mitochondria are often called the powerhouses of cells, and they convert the food we eat into usable energy in the form of a chemical called adenosine triphosphate (ATP). ATP supplies energy for many cellular processes, such as muscle contraction, nerve impulse propagation, and protein synthesis. ATP is found in all forms of life and is often referred to as the “molecular unit of currency” of intracellular energy transfer.

In a paper published in the July 31 issue of Science Translational Medicine, researchers at Fred Hutchinson Cancer Research Center used CRISPR-Cas9 to edit long-lived blood stem cells to reverse the clinical symptoms observed with several blood disorders, including sickle cell disease and beta-thalassemia.

It’s the first time that scientists have specifically edited the genetic makeup of a specialized subset of adult blood stem cells that are the source of all cells in the blood and immune system.

The proof-of-principle study suggests that efficient modification of targeted stem cells could reduce the costs of gene-editing treatments for blood disorders and other diseases while decreasing the risks of unwanted effects that can occur with a less discriminating approach.