Monthly Archives: January 2015

COD AW: "LIVE" "DNA Bomb" + "53 GUN Streak" On Recovery! (Advanced Warfare DNA Bomb Gameplay) – Video

Posted: January 13, 2015 at 4:48 pm


COD AW: "LIVE" "DNA Bomb" + "53 GUN Streak" On Recovery! (Advanced Warfare DNA Bomb Gameplay)
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COD AW: "LIVE" "DNA Bomb" + "53 GUN Streak" On Recovery! (Advanced Warfare DNA Bomb Gameplay) - Video

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INSANE DNA w/BAL on HORIZON – Video

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INSANE DNA w/BAL on HORIZON
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'Junk' virus genes in our DNA may have helped our brain cells evolve

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Endogenous retroviruses have three common genes - gag, env and pol Scientists believe retrovirus DNA makes up around 5% of human genome For years, they were considered junk DNA and a side-effect of evolution New research indicates that, over the course of evolution, the viruses took an increasingly firm hold on cellular control During which time, they may have made brain cells 'active and dynamic'

By Victoria Woollaston for MailOnline

Published: 05:22 EST, 13 January 2015 | Updated: 05:46 EST, 13 January 2015

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Its long been known that DNA from so-called retroviruses make up around five per cent of our genetic makeup.

But for years, this was dubbed junk DNA with no real use, and was considered to be a side-effect of evolution - until now.

New research suggests that, over the course of evolution, the viruses took an 'increasingly firm hold' on how cells work, and they may have made brain cells in particular more active and dynamic, ultimately making us smarter.

DNA from retroviruses (HIV pictured) make up around five per cent of our genetic makeup, but for years, this was considered to be a side-effect of evolution. New research suggests that, over the course of evolution, the viruses took hold of how cells work, and may have made brain cells in particular more active and dynamic

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DNA Spectrum Defines Benefits of DNA Storage in Latest Article "Genetic Storage: Cord Blood vs. DNA"

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Chicago, IL (PRWEB) January 13, 2015

DNA Spectrum, a leading consumer genomics company, constantly updates the public with original content designed to inform the public about this constantly changing field. In its latest article "Genetic Storage: Cord Blood vs. DNA", the company compares and contrasts two current genetic storage methods: umbilical blood banking and DNA sample collection. While both methods have merit, DNA collection has proven to be an increasingly cost-effective and efficient option for the common consumer.

DNA storage has proven itself to be advantageous over cord blood banking for a number of reasons. First, the sample harvesting process is relatively simple. Most DNA stored samples are collected via cheek swabs, which is an easy and non-intrusive method versus attempting to collect umbilical cord blood immediately after birth. Second, the preservation costs are dramatically reduced. DNA Spectrum provides DNA storage plans that cost $2 per month.

Advances in genetic sequencing continue at a rapid pace leading to continuous medical breakthroughs. Research now shows that 90 percent of cancers are primarily caused by genetic mutations. By isolating the causes of such diseases to their genetic components, the opportunities to cure them are likely around the corner. An individuals human DNA will change over time, often due to environmental damage. People are able to safely store intact copies of their genomes are beneficially positioned for these future treatment advances. This insurance is the primary impetus behind DNA storage.

Stored DNA samples may also be useful for genetic disorder treatment or delaying the onset of age-related diseases. Genetic information is not only important for the sample-providing individual. Future generations may also be able to use DNA samples from family members to determine illness predispositions and other purposes which have not yet been developed. Having this information readily available could facilitate early treatment for these individuals in order to avoid complications related to serious illness or disease and the potential for customized therapies.

Many parents consider storing their childrens umbilical cord blood as a means to harvest still-generative stem cells for future usage as a means of ensuring the childs future health. Cord blood stem cells have already been used to successfully treat over seventy different diseases including leukemia, aplastic anemia, and non-Hodgkins lymphoma. Given stem cells ability to transform into virtually any other cell within the human body, they are valued for their regenerative properties and the hope of staving off future life-threatening diseases. However, despite their medical value, cord blood stems cannot be considered magic bullets that fix all genetic conditions.

The current chances that a family member will actually end up using this biological material for serious disease treatment is one in 2,700. What compounds the issue are the storage costs associated with umbilical cord blood. Private banking costs can approach $2000 USD in the first year alone. While public banks are an alternative, in which cord blood is made available via a national registry, few U.S. hospitals actively collect it for storage. In essence, most families are forced to pay exorbitant fees for genetic material that statistically-speaking is virtually unused.

Compared to simple DNA storage, private cord blood banking costs approximately 83 times the amount for that same first year. Additionally, DNA storage can be deployed in cases of missing children or identification in criminal cases; having a complete genome sample readily available in times of emergency is not only invaluable but proven desirable. In a BBC-commissioned opinion poll, 66 percent of participants stated they would voluntarily submit their own DNA samples if said samples were used to aid crime detection and prevention.

In essence, companies like DNA Spectrum, are creating the future now and make it affordable for every family. DNA storage provides parents with a stable and cost-effective means to store a genetic profile from their childs young age as a benchmark or snapshot. Compared against cord bloods helpful yet cost-prohibitive benefits, DNA storage is where future generations will migrate to in preserving their health and history.

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Photonic Crystal Nanolaser Biosensor Simplifies DNA Detection

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Newswise WASHINGTON, D.C., January 13, 2015 A simple method to sense DNA, as well as potential biomarker proteins of cancer or other diseases such as Alzheimers, may soon be within reach thanks to the work of a team of Yokohama National University researchers in Japan.

As the team reports in Applied Physics Letters, from AIP Publishing, they created a photonic crystal nanolaser biosensor capable of detecting the adsorption of biomolecules based on the lasers wavelength shift.

Equally impressive, the nanolaser biosensor enables detection of the surface charge from its laser emission intensity, which in turn can also be used to sense the adsorption of biomolecules. Using laser intensity to detect biomolecules is potentially less expensive than the fluorescent tagging or spectroscopy techniques typically used in biosensors because it is a simpler procedure.

When the team first set out to explore photonic crystal nanolaser sensors, they werent focusing on the intensity of the laser emission because its sensitive to the quality of the fabricated laser and, frankly, they didnt expect it to show sensing signals.

In the beginning we focused on wavelength behavior, but quickly noticed that [the laser emission] intensity is influenced by both pH and polymers, noted Toshihiko Baba, a professor in Yokohama National Universitys Department of Electrical and Computer Engineering. Our results were very reproducible and, interestingly, we found that the behaviors of the wavelength and intensity are independent.

The team was surprised by these results, which they discovered when they deposited a protective film of thin zirconium dioxide (ZrO2) over the device using atomic layer deposition, and then tried sensing in liquids of high or low pH and liquids containing charged polymers. The coating was necessary to protect the nanolaser from damage and unwanted wavelength drift.

The nanolaser device can sense surface charge because the surface charge changes the occupancy rate of electrons at the surface states in the semiconductor of the nanolaser, Baba explained. This modifies the semiconductors emission efficiency.

So far, the teams work is the first report of the detection of surface charges using such photonic sensors. It enables detection of the adsorption of biomolecules from the nanolaser biosensor both in terms of wavelength and intensity, Baba said. Since it involves different physical parameters, the researchers can examine the details of the biomolecules.

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Stoke with Genome – Video

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Stoke with Genome
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Our Global Human Genome – Video

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Our Global Human Genome
In order to create a comprehensive genomic cancer database, scientists have to reach out to the entire world. Starting with the underserved populations in South Chicago, oncologist Olufunmilayo...

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Yourgenome website from Wellcome Genome Campus to unravel mysteries of DNA

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A WEBSITE has been relaunched in a bid to take genetics to a wider audience and unravel the mysteries of DNA.

Relaunched last week to coincide with Association for Science Education's Annual Conference, yourgenome.org has been developed by public engagement professionals at the Wellcome Genome Campus at Hinxton.

The site aims to provide accessible, entertaining and thought-provoking guides to an area of science that is revolutionising diagnosis and treatment.

Genomics has been catapulted into the public conciousness in recent months, with the Government having pledged to understand the genomes of 100,000 people. In December, website 23andMe launched a UK version, enabling people in this country to to have their DNA screened for genes associated heridetary conditions such as cystic fibrosis or sickle cell anaemia. Regular readers of Ideas will also know that Cambridge is home to a number of firms specialising in genomics, such as start-up GeneAdviser which is aiming to provide accurate testing for patients with rare genetic diseases.

"Genomics is constantly in the news but, for many, DNA and its role in our biology is still something of a mystery," says Dr Julia Willingale-Theune, manager of public engagement at the Wellcome Genome Campus. "With yourgenome.org, we want to share what scientists know about the genome already and what they are trying to find out, helping everyone to understand and engage with a topic that's likely to have a huge impact on their future health."

The website provides key facts about genomics and bioinformatics with the help of videos and 3D animations. It also features posts by experts looking at advances in research and applications in healthcare. There are also debates that give readers a balanced view of the more controversial aspects of genomics, such as data security, animal research and gene therapy.

Content on the website is driven by an editorial board comprised of expert researchers and specialists in science education and communication from the Wellcome Genome Campus and beyond. This editorial board will ensure that the website remains up-to-date, relevant and accurate.

The Wellcome Genome Campus is home to the Wellcome Trust Sanger Institute, which made the greatest single contribution to the Human Genome Project in 2003 and has remained at the forefront of genetic research ever since. It is also home to the European Bioinformatics Institute, which goes by the catchy acronym of EMBL-EBI. This is a global leader in the storage, analysis and dissemination of large biological datasets, and helps scientists realise the potential of 'big data', enhancing their ability to exploit complex information to make discoveries that benefit mankind. Experts from both institutes have contributed to the site.

"During our lifetimes, the way we experience healthcare will change; in the next decade many aspects of care, from diagnosis to medication, and many lifestyle choices will depend on the information encoded in our genome," said Jon Kudlick, director of membership, marketing and communications at the Society of Biology.

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UC Santa Cruz to lead effort to build a new map of human genetic variation

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Simons Foundation awards up to $1 million to UC Santa Cruz Genomics Institute to develop a comprehensive Human Genome Variation Map for scientific and medical research

VIDEO:Benedict Paten discusses work on the Human Genome Variation Map at the University of California Santa Cruz Genomics Institute. view more

Researchers at the UC Santa Cruz Genomics Institute have received a grant for up to $1 million from the Simons Foundation to develop a comprehensive map of human genetic variation. The Human Genome Variation Map will be a critical new resource for both medical research and basic research in the life sciences.

The one-year pilot project aims to overcome the limitations of the current model for analyzing human genome data, which is based on the use of a single reference sequence for the human genome. Essentially, all novel sequencing data is analyzed by mapping new genome sequences to this one reference set of 24 human chromosomes to identify variants. But this approach leads to biases and mapping ambiguities, and some variants simply cannot be described with respect to the reference genome, according to David Haussler, professor of biomolecular engineering and director of the Genomics Institute at UC Santa Cruz.

"One exemplary human genome cannot represent humanity as a whole, and the scientific community has not been able to agree on a single precise method to refer to and represent human genome variants. There is a great deal we still don't know about human genetic variation because of these problems," said Haussler, who will lead the project with co-investigator Benedict Paten, a research scientist at the Genomics Institute.

According to Paten, the proliferation of different genomic databases has resulted in hundreds of specialized coordinate systems and nomenclatures for describing human genetic variation. UC Santa Cruz genomics researchers are intimately familiar with this "Tower of Babel" of databases through their work to display data from all these sources on the widely used UCSC Genome Browser. Launched in July 2000 shortly after UC Santa Cruz posted the first working draft of the human genome sequence on the Internet, the browser now serves 130,000 researchers around the world and gets more than 1 million web page requests per day.

"For now, all our browser staff can do is to serve the data from these disparate sources in their native, mutually incompatible formats," Paten said. "This lack of comprehensive integration, coupled with the over-simplicity of the reference model, seriously impedes progress in the science of genomics and its use in medicine."

Recently, with funding from the Simons Foundation, researchers David Reich and Nick Patterson at the Broad Institute of MIT and Harvard have amassed more than 300 complete human genome sequences representing a range of ethnicities. Haussler and Paten plan to use this set of human genomes, which they say is deeper and more completely organized than any prior human data set, to build a new graph-based human reference genome structure.

"This unique data set of genome diversity gives us an opportunity to define a comprehensive reference genome structure that can be truly representative of human variation. Eventually, we will want to expand it to include many more genomes, but this pilot project will focus on building a map structure based on the Reich-Patterson data set," Paten said.

The new Human Genome Variation Map will replace the current snarl of isolated, incompatible databases of human genetic variation with a single, fundamental representation formalized as a very large mathematical graph. The clean mathematical formulation is a major strength of this new approach, Paten said.

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New Subtle Energy Pattern Research Shows Increases in Cell Growth and Viability

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White City, OR (PRWEB) January 13, 2015

Groundbreaking new results show targeted subtle energy patterns, sometimes referred to as bioenergetic patterns, have a significant positive impact on human cell growth and mitochondrial membrane potential. Three notable findings include an 83% increase in cell viability under food deprivation conditions, a 50% increase in mitochondrial longevity in the presence of toxins and third of all, that mitochondria exposed to subtle energy and under starved and poisoned conditions showed increased viability over even the non-poisoned control. These recent findings show potential long term improvement to human cell viability which can slow and reverse the breakdown of human cells.

Cell growth experiments at Beech Tree Labs tested human dermal fibroblasts (HDF) infused with one of four unique, proprietary subtle energy patterns from Vital Force Technology; Cell Longevity, Peak Performance, Stress Relief, and Anti-Cancer. The experiment compared the influence of different subtle energy patterns on cell viability and longevity. It was found that cells growing with subtle energy pattern Stress Relief had 83% more live cells remaining on the 9th day than the control group. Additionally, those groups infused with Cell Longevity and Peak Performance yielded 50% more live cells on the 9th day than found in the control.

At Rigas University in Latvia researchers looking into mitochondrial viability and longevity tested Cell Longevity, and Peak Performance energy patterns on human embryonic kidney cells. After three days, stressed cells exposed to the subtle energy patterns showed increased viability over the control groups. Meaning, the stressed cells exposed to subtle energy showed more mitochondrial longevity than the cells that were never stressed to begin with.

Ultimately both Beech Tree Labs and Rigas findings hint at new possibilities that could have major implications for human health and may be the first step towards a completely non-toxic, natural, and no side effect alternative to traditional health treatments. The full study along with other studies can be reviewed in the research section of the Vital Force Technology website at http://vitalforcetechnology.energytoolsint.com/results/research/cellular/

Vital Force Technology continues to create and explore new subtle energy patterns targeted to achieve specific wellness outcomes, such as the cell longevity and performance enhancement formulas they've already established. For more information on Vital Force Technology and the research above, visit vitalforcetechnology.com or call 800-341-7458.

About Vital Force Technologytm Founded in 2000 by Russian Radio-Physicist and Inventor Dr. Yury Kronn, and President and CEO Constance Kronn., Vital Force Technology (VFT) offers a range of innovative energetic signature formulas for wellness, personal care, animal care and agriculture markets. Headquartered in White City, Oregon, the firm is a global market leader in bio-energetic ingredients. VFT also markets numerous health and wellness energetic formulas under the same name. The company serves thousands of clinicians and practitioners in over 40 countries, as well as a growing number of leading-edge manufacturers. For more information about Vital Force Technology and its energetic formulas, visit http://www.vitalforcetechnology.com.

About Dr. Yury Kronn Dr. Yury Kronn is a world renowned authority, scientist, inventor, author, and lead scientist for Vital Force Technology, a division of Energy Tools International LLC. Educated in Russias prestigious Gorky University, Dr. Kronn earned his PhD. He was one of the leading theoreticians in high frequency electromagnetic vibrations, laser physics and nonlinear optics. He was awarded a Doctor of Sciences degree by the scientific committee of Lebedevs Institute of Physics, in Moscow, chaired at the time by N. G. Basov, Nobel Prize winner.

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New Subtle Energy Pattern Research Shows Increases in Cell Growth and Viability

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