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Heart attack patients who were not expected to live are fit and healthy after scientists regenerated their hearts with stem cells in a ground-breaking trial which could help millions of people with heart failure.

The research is the first to show that scarring of heart muscle, associated with a heart attack can be reversed, a feat which doctors believed was impossible, and which could eventually end the need for transplants.

Scarring of the heart stops the organ pumping blood effectively and can lead to further attacks and sudden death.

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Her computer, Karin Strauss says, contains her “digital attic”—a place where she stores that published math paper she wrote in high school, and computer science schoolwork from college.

She’d like to preserve the stuff “as long as I live, at least,” says Strauss, 37. But computers must be replaced every few years, and each time she must copy the information over, “which is a little bit of a headache.”

It would be much better, she says, if she could store it in DNA—the stuff our genes are made of.

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A new blood treatment developed by researchers in Greece reportedly has the power to reverse menopause, enabling post-menopausal women to release eggs once again.

None of this has been peer-reviewed as yet, but if the results can be verified by others in the scientific community, the treatment might allow women to have offspring later in life.

It could also provide a treatment for those suffering from early menopause, a condition that affects roughly 1 percent of all women.

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Will we live longer lives in the future? According to Ray Kurzweil, it’s only a matter of time until technology begins successfully tackling age-related disease—and life expectancy grows longer and longer. At some point, technology will annually add more than a year to our life expectancy—allowing us to indefinitely increase lifespans, and perhaps eventually live as long as we want.

“We will get to a point where our longevity, our remaining life expectancy is moving on away from us. The sands of time will run in rather than run out,” Kurzweil says.

How will this happen? We’re now learning to reprogram biology to cure disease and repair the body. This will accelerate in coming decades and be followed by the nanotechnology revolution.

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Um microrobô com controlo remoto que parece e se move como uma bactéria.

Ao contrário dos robôs convencionais, estes microroboô são suaves, flexíveis,. Elas são feitas de um hidrogel biocompatível e nanopartículas magnéticas e sem motor. Estas nanopartículas têm duas funções. Eles dão aos microrobôs sua forma durante o processo de fabricação, e torná-los mover-se e nadar quando um campo magnético é aplicado.

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(Medical Xpress)—A team of researchers at Sichuan University’s West China Hospital has announced plans to begin a clinical trial where cells modified using the CRISPR gene editing technique will be used on human beings for the very first time. They plan to edit genes in such a way as to turn off a gene that encodes for a protein that has been shown by prior research to slow an immune response and by so doing treat patients with lung cancer.

The CRISPR has been in the news a lot of late as scientists creep ever closer to using it as a means to treat diseases or to change the very nature of biological beings. China has been a leader in promoting such research on human beings—they were the first to use the technique to on human embryos.

This new effort is seen as far less controversial—a team in the U.S. is planning a similar study as soon as they can get regulators to greenlight their project. The Chinese team plans to retrieve T cells from patients that have incurable and then edit the genes in those cells. More specifically, they will be looking to disable a gene that encodes for a protein called PD-1—prior research has shown that it acts as a brake on an to help prevent attacks on healthy cells. Once the cells have been edited and inspected very carefully to make sure there were no editing errors they will be allowed to multiply and then all of the cells will be injected back into the same patient’s bloodstream. It is hoped that the edited cells will cause the immune system to mount a more aggressive attack on , killing them and curing the patient.

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The UK’s first double hand transplant operation has taken place at Leeds General Infirmary and the patient says his new hands look “tremendous”.

Chris King, from Doncaster, lost both his hands, apart from the thumbs, in an accident involving a metal pressing machine at work three years ago.

The 57-year-old received two new hands from a donor and says he already has some movement in them.

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I do love biometrics for security; however, many know that we will not only leverage biometrics alone for certifying identification given how easy it is for folks to retrieve others DNA information, etc. from commercial DNA sites, etc.


In the world of security, there are many tools at the IT Staff’s disposal which can be used to fight Cybercrimes of all types and levels. Regarding Physical Access Entry, Smart Cards and FOB’s are available to help alleviate the probability of a Social Engineering attack. Regarding Logical Access Entry, Network Intrusion Devices, Firewalls, Routers, etc. are also all ready to be installed and used.

But, there is one problem with all of these tools above: To some degree or another, all of them can be hijacked, stolen, or even spoofed so that a real Cyber hacker can find their way into a corporation very quickly and easily. For instance, a Smart Card can be easily lost or stolen; or even malformed data packets can be sent to a router and tricking it that it is a legitimate employee trying to gain access.

But, there is one Security technology out there which, for the most part, cannot be spoofed or tricked. As a result, it can provide 100% proof positive of the identity of an end user. This technology is known as Biometrics.

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Like Botox; another bacteria found a new usage in healthcare.


Researchers at MIT and the University of California at San Diego (UCSD) have recruited some new soldiers in the fight against cancer—bacteria.

In a study appearing in the July 20 of Nature, the scientists programmed harmless strains of bacteria to deliver toxic payloads. When deployed together with a traditional cancer drug, the bacteria shrank aggressive liver tumors in mice much more effectively than either treatment alone.

The new approach exploits bacteria’s natural tendency to accumulate at disease sites. Certain strains of bacteria thrive in low-oxygen environments such as tumors, and suppression of the host’s immune system also creates favorable conditions for bacteria to flourish.

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Wanted to share because I found this extremely interesting in what we’re discovery on implants and cells. I predict we are going to find out that in the next 7 to 10 years that we had some key things wrong as well as learned some new amazing things about cells especially with the synthetic cell & cell circuitry work that is happening for bio computing.


By Bikramjit Basu & his group Indian Institute of Science, Bangalore

For a variety of medical treatments these days, artificial, synthetic materials are inserted into the human body. Common examples include treatment for artery blockage and orthopaedic surgeries, like hip and knee replacements. Human bodies are not very receptive to foreign objects; most synthetic materials are rejected by the body. The choice of material that can be inserted, therefore, has to be very specific.

We do not yet have a material that is easily accepted inside the human body. A variety of materials are used for the different kinds of functions they are intended to perform once inserted inside. At our group, we have been trying to develop a comprehensive understanding of how biological cells in human bodies interact with a material surface. The idea is to recreate conditions that allow human cells to grow and function normally on a synthetic material. If we are able to do that, these materials, or biomaterials as we like to call them, can be used as various implants.

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