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Struggling with your diet? Your microbiota could be to blame.


Your microbiota may not be on your side as you try improving your diet this New Year’s. In a study published December 29 in Cell Host & Microbe, researchers explore why mice that switch from an unrestricted American diet to a healthy, calorie-restricted, plant-based diet don’t have an immediate response to their new program. They found that certain human gut bacteria need to be lost for a diet plan to be successful.

“If we are to prescribe a to improve someone’s health, it’s important that we understand what help control those beneficial effects,” says Jeffrey Gordon, Director of the Center for Genome Sciences and Systems Biology at Washington University in St. Louis and senior author of the paper. “And we’ve found a way to mine the gut microbial communities of different humans to identify the organisms that help promote the effects of a particular diet in ways that might be beneficial.”

In order to study how human dietary practices influence the and how a microbiota conditioned with one dietary lifestyle responds to a new prescribed diet, Gordon and his collaborators first took fecal samples from people who followed a calorie-restricted, plant-rich diet and samples from people who followed a typical, unrestricted American diet. The researchers found that people who followed the restricted, plant-rich diet had a more diverse microbiota.

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For a few lucky patients, 2016 was the year when gene therapy turned from promises to cures. The technology, long contemplated as a way to erase disease by revising people’s DNA, made big advances and began turning into a real business offering some of the world’s most expensive and revolutionary medicines.

So what is gene therapy, anyway? The US Food and Drug Administration says it’s any treatment in which a replacement gene is added to a person’s body or a disease-causing one is inactivated. That’s usually done by adding­­­­­­ new instructions to cells via billions of viruses stuffed with correct DNA strands.

It sounds complicated, and it is. Gene therapy was first tested in a person in 1990, but scary side effects turned the gene-fix idea into a scientific backwater. And the field hasn’t conquered all its problems. We started the year with the tale of Glybera, heralded as the first gene treatment ever approved that sought to correct an inherited gene error. Yet the drug came with an eye-popping price tag of $1 million and, dogged by questions over how well it works, has turned into a medical and commercial flop.

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Researchers have discovered a technique that could block the effects of a powerful gene-editing tool to protect adjacent genes against accidental alteration. The breakthrough could be the beginning of a major step forward for genetic engineering.

Scientists at the University of California (UC) in San Francisco researchers have discovered how to switch off the effects of the CRISPR gene editing system. CRISPR has been a major advance for gene editing, but there are difficulties in limiting its effects on adjacent genes. So far this has militated against its use in research, most obviously, into the human genome.

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The Sino-Israeli Robotics Institute (SIRI) was inaugurated in mid-December when a delegation of nine Israeli companies — led by Ariel University Prof. Zvi Shiller, chair of the Israeli Robotics Association, and Technion Prof. Moshe Shoham, founder of Mazor Robotics and a world leader in medical robotics — participated in the second Sino-Israeli Robotics Innovation Conference in Guangzhou, China.

Intended as “home base” for Israeli robotics companies entering the Chinese market, SIRI is located at the Guangzhou International Robotics Center (ROBOHUB), a government-supported, 4,800-square-meter robotics incubator and demonstration center including a large exhibition and demo area, innovation lab, training center, and corporate offices.

“This is an exciting time for the Israeli robotics industry,” Shiller said. “We are committed to establishing a true partnership with SIRI and ROBOHUB, and we look forward to broadening this strategic cooperation, which will serve as a fast track for transforming ideas into products and for moving products into the Chinese market.”

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Cancer research is an area of medical science that, rightfully, gets considerable attention.

There are nearly 14.5 million Americans with a history of cancer and with more than 13 million estimated new cancer cases each year.

It’s no wonder even artificial intelligence (AI) has gotten into the field. Researchers from the University of Michigan are not getting left behind, with a groundbreaking method that has the potential to eliminate tumours.

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My infomercial of the day — “just ad water and Ta-dah, you have a vaccine!”

http://thejerseytomatopress.com/stories/To-produce-biopharmaceuticals-on-demand-just-add-water,1851


Researchers at MIT and other institutions have created tiny freeze-dried pellets that include all of the molecular machinery needed to translate DNA into proteins, which could form the basis for on-demand production of drugs and vaccines. Image: Christine Daniloff/MIT. Antimicrobial peptide illustration by Ymahn/Wikimedia Commons.

Anne Trafton | MIT

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Nice.


Stem cell treatments involve some serious health risks for the patients and are very expensive. A new alternative developed for patients with health problems may be a game-changer as a team of researchers has developed synthetic stem cells, which prove to be as efficient as the regular ones. ( NC State University )

A team of researchers made a significant breakthrough which will help patients with heart problems all over the world. The scientists managed to create synthetic stem cells, which can help the heart tissue regenerate just as well as normal stem cells, while also avoiding the complications associated with them.

Promising Results

A team of American and Chinese researchers joined efforts in order to provide a better treatment solution for people with heart problems.

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