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Artificial Intelligence Can Identify Genetic Disorders in Embryo With Simple Blood Test

New Israeli startup aims to get product to market within two years; technology could also be used to identify early markers of cancer.

An Israeli startup is developing a non-invasive early detection method using artificial intelligence (AI) to identify genetic disorders in human embryos.

Via a simple blood test taken from the pregnant mother during the first trimester, IdentifAI Genetics can read the embryo’s entire DNA and provide in-depth analysis to detect genetic disorders.

Revolutionary ‘bionic’ pacemaker capable of reversing heart failure now set for human trials

AUCKLAND, New Zealand — We may be on the medical precipice of turning back time, or actually reversing the heart rhythm effects of cardiac events. A potentially game-changing “bionic” pacemaker capable of restoring the human heart’s naturally irregular beat is set to undergo trials involving heart patients in New Zealand this year.

“Currently, all pacemakers pace the heart metronomically, which means a very steady, even pace. But when you record heart rate in a healthy individual, you see it is constantly on the move,” says professor Julian Paton, a lead researcher and director of Manaaki Manawa, the Centre for Heart Research at the University of Auckland, in a university release.

Current pacemakers just can’t mimic the perfectly irregular pace of a naturally healthy human heart, Paton explains. This new version, though, may change everything. “If you analyze the frequencies within your heart rate, you find the heart rate is coupled to your breathing. It goes up on inspiration, and it goes down on expiration, and that is a natural phenomenon in all animals and humans. And we’re talking about very ancient animals that were on the planet 430 million years ago.”

The last century revealed our DNA’s secrets and lingering mysteries

The Human Genome Project received a lot of media attention from scientific journals and the mainstream press.

Left to right: Time July 3, 2000; Science February 16, 2001; Nature February 15, 2001.

Green: Or sloppy transcription, that our enzymes are just going off and making a bunch of RNA because they don’t know how to control themselves. And it’s just garbage. But, no. And I like your point about 20 years ago, we couldn’t imagine. I would propose that 20 years from now, we might look back at this conversation and say, ‘Oh, my goodness, think about all these other ways that the genome functions.’ There’s no reason to think we have our hands around it all in terms of all the biological complexity of DNA; I’m quite sure we don’t.

Study raises new possibilities for triggering room-temperature superconductivity with light

Much like people can learn more about themselves by stepping outside of their comfort zones, researchers can learn more about a system by giving it a jolt that makes it a little unstable—scientists call this “out of equilibrium”—and watching what happens as it settles back down into a more stable state.

In the case of a known as yttrium barium copper oxide, or YBCO, experiments have shown that under certain conditions, knocking it out of equilibrium with a laser pulse allows it to superconduct—conduct electrical current with no loss—at much closer to room than researchers expected. This could be a big deal, given that scientists have been pursuing room-temperature superconductors for more than three decades.

But do observations of this unstable state have any bearing on how high-temperature superconductors would work in the real world, where applications like power lines, maglev trains, particle accelerators and medical equipment require them to be stable?

“Mini-Brains” Grown in a Lab Provide Clues About Early Life Origins of Schizophrenia

Multiple changes in brain cells during the first month of embryonic development may contribute to schizophrenia later in life, according to a new study by Weill Cornell Medicine investigators.

The researchers, whose study was published in Molecular Psychiatry, used stem cells collected from patients with schizophrenia and people without the disease to grow 3-dimensional “mini-brains” or organoids in the laboratory. By comparing the development of both sets of organoids, they discovered that a reduced expression of two genes in the cells stymies early development and causes a shortage of brain cells in organoids grown from patient stem cells.

“This discovery fills an important gap in scientists’ understanding of schizophrenia,” said senior author Dr. Dilek Colak, assistant professor of neuroscience at the Feil Family Brain and Mind Institute and the Center for Neurogenetics at Weill Cornell Medicine. Symptoms of schizophrenia typically develop in adulthood, but postmortem studies of the brains of people with the disease found enlarged cavities called ventricles and differences in the cortical layers that likely occurred early in life.

Inspired by insects, engineers create spiky materials that could pop bacteria

Researchers have created intricately patterned materials that mimic antimicrobial, adhesive and drag reducing properties found in natural surfaces.

The team from Imperial College London found inspiration in the wavy and spiky surfaces found in insects, including on cicada and dragonfly wings, which ward off .

They hope the new could be used to create self-disinfecting surfaces and offer an alternative to chemically functionalized surfaces and cleaners, which can promote the growth of antibiotic-resistant bacteria.

New brain imaging technique suggests memories are stored in the connections between your neurons

All memory storage devices, from your brain to the RAM in your computer, store information by changing their physical qualities. Over 130 years ago, pioneering neuroscientist Santiago Ramón y Cajal first suggested that the brain stores information by rearranging the connections, or synapses, between neurons.

Since then, neuroscientists have attempted to understand the physical changes associated with memory formation. But visualizing and mapping synapses is challenging to do. For one, synapses are very small and tightly packed together. They’re roughly 10 billion times smaller than the smallest object a standard clinical MRI can visualize. Furthermore, there are approximately 1 billion synapses in the mouse brains researchers often use to study brain function, and they’re all the same opaque to translucent color as the tissue surrounding them.

A new imaging technique my colleagues and I developed, however, has allowed us to map synapses during memory formation. We found that the process of forming new memories changes how brain cells are connected to one another. While some areas of the brain create more connections, others lose them.

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