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Category Archives: Transhuman News

Bioengineers Close To Creating Painkillers Without Using Opium From Poppies

Posted: September 1, 2014 at 3:45 am

By Tom Abate, Stanford School of Engineering

A decade-long effort in genetic engineering is close to creating yeast that makes palliative medicines in stainless steel vats.

For centuries poppy plants have been grown to provide opium, the compound from which morphine and other important medicines such as oxycodone are derived.

Now bioengineers at Stanford have hacked the DNA of yeast, reprograming these simple cells to make opioid-based medicines via a sophisticated extension of the basic brewing process that makes beer.

Led by Associate Professor of Bioengineering Christina Smolke, the Stanford team has already spent a decade genetically engineering yeast cells to reproduce the biochemistry of poppies with the ultimate goal of producing opium-based medicines, from start to finish, in fermentation vats.

We are now very close to replicating the entire opioid production process in a way that eliminates the need to grow poppies, allowing us to reliably manufacture essential medicines while mitigating the potential for diversion to illegal use, said Smolke, who outlines her work in the August 24th edition of Nature Chemical Biology.

In the new report Smolke and her collaborators, Kate Thodey, a post-doctoral scholar in bioengineering, and Stephanie Galanie, a doctoral student in chemistry, detail how they added five genes from two different organisms to yeast cells. Three of these genes came from the poppy itself, and the others from a bacterium that lives on poppy plant stalks.

This multi-species gene mashup was required to turn yeast into cellular factories that replicate two, now-separate processes: how nature produces opium in poppies, and then how pharmacologists use chemical processes to further refine opium derivatives into modern opioid drugs such as hydrocodone.

From Plants to Pills Today

Plant-derived opium has been used and abused for centuries, but a good place to begin the modern story is with the use of morphine during World War II.

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ALJASSAR: The merits of GMOs

Posted: at 3:45 am

Genetically modified foods should not require distinguishing labels by Nazar Aljassar | Aug 28 2014 | 08/28/14 10:57pm

A new brand of Luddism has erupted in America. In spite of ample scientific evidence that corroborates the biosafety of genetic modification of crops, over half of Americans believe genetically modified foods are unsafe, with 93 percent in favor of mandatory labels on genetically modified food.

Part of the objection to genetically modified crops stems from a belief that natural foods are superior to unnatural foods a naturalistic fallacy. Nothing is intrinsically virtuous about consuming food crops that are grown naturally. Unfortunately, appeals to nature and tradition have hijacked the discourse surrounding genetic modification.

Its important to note that all agriculture is unnatural. Any claim about the extent to which food crops are natural is meaningless. Agriculture is the largest and most enduring human intervention into the natural world. Through selective breeding, farmers have artificially created several crops for human consumption. Kale and kohlrabi were developed from wild mustard after decades of careful heredity manipulation. Artificial selection has given rise to high-quality strains of soybeans, wheat and corn, all of which have been a boon to civilization. Artificial selection and artificial mutation through genetic engineering both alter food crops on the same microbiological level. The primary distinction is that the latter method can be used to obtain desired traits with greater speed and efficiency.

Genetic modification of organisms is not a novel concept. We have been doing it for thousands of years. Genetic modification through DNA extraction, gene cloning, gene design, transformation and backcross breeding is simply a faster, better way to achieve the results sought through traditional artificial selection.

Despite left-wing insistence that the right wing is anti-science, some of the most strident opposition to genetic modification of food crops comes from progressives. Although liberals are often stalwart supporters of clean energy laws and evolution education, many are fervently in favor of mandating labels on genetically modified foods. Vermont became the first state to enact such legislation, and pressure currently mounts for similar laws in liberal states such as New York, California, Oregon and Massachusetts.

Vermont Governor Peter Shumlin defended his states GMO labeling law, maintaining that consumers have the right to know what they buy. The problem with this line of thought lies in the fact that it suggests dangers immanent in genetically modified food. The scientific consensus, according to the American Association for the Advancement of Science, is that crop improvement by the modern molecular techniques of biotechnology is safe. After allocating over 300 million to research, the European Union revealed in a report its findings on the safety of genetically modified crops: the main conclusion to be drawn from the efforts of more than 130 research projectsis that biotechnology, and in particular GMOs, are not per se more risky than e.g. conventional plant breeding technologies. Among other organizations that have affirmed the biosafety of genetically modified crops are the World Health Organization, the American Medical Association, the U.S. National Academy of Sciences and the British Royal Society.

For liberal legislators to yield to the publics fears about genetic modification only advances scientific misinformation about an agricultural innovation that provides plants resistant to infectious disease, superior foods with longer shelf lives and large crop yields to permit more efficient land use.

There are legitimate criticisms of genetic modification. Economically, introducing genetically modified food to market demands significant time and cost, endangering smaller farms that cannot afford to compete with large agricultural biotechnology companies. Genetic modification also presents a few environmental risks such as reduced biodiversity through genetic homogeneity and resulting from extensive monoculture crop production.

But we shouldnt ignore its efficiency because of these few flaws. Like any scientific advancement, genetic modification will continue to improve with research for which public and political support is crucial. In the face of concerns about genetic modification, we should not jettison the benefits of genetic modification of crops, nor should we propagate the falsehoods that infect scientific discussion by encouraging labels that imply biohazards associated with genetic modification.

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ALJASSAR: The merits of GMOs

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Do closed-loop insulin delivery systems improve blood glucose control in type 1 diabetes?

Posted: at 3:45 am

PUBLIC RELEASE DATE:

25-Aug-2014

Contact: Kathryn Ryan kryan@liebertpub.com 914-740-2100 Mary Ann Liebert, Inc./Genetic Engineering News

New Rochelle, NY, August 25, 2014In a closed-loop control approach to managing type 1 diabetes, glucose sensors placed under the skin continuously monitor blood sugar levels, triggering the release of insulin from an implantable insulin pump as needed. The aim of this closed-loop insulin delivery system is improved control of blood glucose levels throughout the day and night. But a new study in adults and adolescents found that mean blood glucose levels remained at safe levels 53-82% of the time, according to the results published in Diabetes Technology & Therapeutics (DTT), a peer-reviewed journal from Mary Ann Liebert, Inc., publishers. The article is available free on the DTT website at http://online.liebertpub.com/doi/full/10.1089/dia.2014.0066 until September 25, 2014.

Howard Zisser, MD and an international team of researchers representing the Control to Range Study Group measured plasma glucose levels every 15-30 minutes in a group of individuals with type 1 diabetes who participated in the "Control to Range" multinational artificial pancreas study. They monitored the adults and teens over 22 hours, including three meals and periods of day and night. The authors describe the risks of hypo- and hyperglycemia, the variability between participants, and the differences in daytime/nighttime results, and also propose improvements needed in the design and implementation of closed-loop systems in the article "Multicenter Closed-Loop Insulin Delivery Study Points to Challenges for Keeping Blood Glucose in a Safe Range by a Control Algorithm in Adults and Adolescents with Type 1 Diabetes from Various Sites".

"It appears that we are getting closer to an Artificial Pancreas option for patients with type 1 diabetes," says DTT Editor-in-Chief Satish Garg, MD, Professor of Medicine and Pediatrics at the University of Colorado Denver. "The first version may need to be a hybrid system in which meals and exercise are announced with necessary dose adjustments along with Automatic Threshold Suspend for hypoglycemia."

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About the Journal

Diabetes Technology & Therapeutics (DTT) is a monthly peer-reviewed journal that covers new technology and new products for the treatment, monitoring, diagnosis, and prevention of diabetes and its complications. Led by Editor-in-Chief Satish Garg, MD, Professor of Medicine and Pediatrics at the University of Colorado Denver, the Journal covers topics that include noninvasive glucose monitoring, implantable continuous glucose sensors, novel routes of insulin administration, genetic engineering, the artificial pancreas, measures of long-term control, computer applications for case management, telemedicine, the Internet, and new medications. Tables of content and a sample issue may be viewed on the Diabetes Technology & Therapeutics (DTT) website at http://www.liebertpub.com/DTT. DTT is the official journal of the Advanced Technologies & Treatments for Diabetes (ATTD) Conference.

About ATTD

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Do closed-loop insulin delivery systems improve blood glucose control in type 1 diabetes?

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Human Genetics – The Complexity of Living Cells Debunks Evolution. – Video

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Human Genetics - The Complexity of Living Cells Debunks Evolution.
Dr Mark Harwood explains human genetics and the probabilities of life evolving from nothing.

By: Max Bauer

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Human Genetics - The Complexity of Living Cells Debunks Evolution. - Video

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MARC travel awards announced for: American Society of Human Genetics 2014 Annual Meeting

Posted: at 3:45 am

PUBLIC RELEASE DATE:

28-Aug-2014

Contact: Kelly Husser khusser@faseb.org 301-634-7109 Federation of American Societies for Experimental Biology

Bethesda, MD FASEB MARC (Maximizing Access to Research Careers) Program has announced the travel award recipients for the American Society of Human Genetics from October 18 22, 2014 in San Diego, California. These awards are meant to promote the entry of students, post doctorates and scientists from underrepresented groups into the mainstream of the basic science community and to encourage the participation of young scientists at the American Society of Human Genetics. This year MARC conferred 16 awards totaling $29,600.

The FASEB MARC Program is funded by a grant from the National Institute of General Medical Sciences, National Institutes of Health. A primary goal of the MARC Program is to increase the number and competitiveness of underrepresented groups engaged in biomedical and behavioral research. The following participants have been selected to receive a FASEB MARC Travel Award:

POSTER/ORAL PRESENTER (FASEB MARC PROGRAM)

FACULTY/MENTOR & STUDENT/MENTEE (FASEB MARC PROGRAM)

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FASEB is composed of 27 societies with more than 120,000 members, making it the largest coalition of biomedical research associations in the United States. Our mission is to advance health and welfare by promoting progress and education in biological and biomedical sciences through service to our member societies and collaborative advocacy.

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MARC travel awards announced for: American Society of Human Genetics 2014 Annual Meeting

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GSK/NIAID Ebola Vaccines To Enter US, UK Human Safety Trials

Posted: at 3:45 am

The Wellcome Trust, the Medical Research Council (MRC), and the UK Department for International Development (DFID) have announced this morning that an Ebola vaccine developed in the U.S. will enter human safety trials in the UK as early as September. The consortium is devoting 2.8 million to the effort.

Anthony S. Fauci, M.D., director of the National Institute of Allergy and Infectious Diseases (NIAID), an arm of the U.S. National Institutes of Health, held a press conference this morning to discuss the specifics about the U.S. vaccine. The FDA has given the green light to begin testing here.

The vaccine was designed by Nancy J. Sullivan, Ph.D., chief of the Biodefense Research Section in NIAIDs Vaccine Research Center (VRC). She worked with other collaborators in the U.S. Army Medical Research Institute for Infectious Diseases (USAMRIID) and scientists at the Swiss-Italian biotechnology company,Okairos, acquired byGlaxoSmithKlinein May, 2013.

Ebola virus particles, colored digitally, emerging from a type of monkey epithelial cell line (Vero) grown in the laboratory. Credit: CDC Public Health Image Library

The GSK/NIAID vaccine has been designed to produce a protective immune reaction toward the surface protein on the Zaire Ebola and Sudan Ebola viruses, a protein required for the virus to normally infect humans. Because its directed at two versions of the viral protein, its called a bivalent vaccine.

In science, you never know

While the vaccine has proven to protect non-human primates from Ebola infection and produced high levels of immunogenic responses, the phase 1 trials are being conducted to ensure that any untoward reactions in humans are detected and the production of protective antibodies proceeds as observed in non-human primates.

NIAID will be starting with typical caution for the first time a vaccine is tested in healthy human volunteers. The trial, termed VRC 207, will ultimately enroll 20 healthy, adult human volunteers (age 18 to 50 years) and evaluate the safety of the virus nine times over a 48-week period and, said Fauci, whether it generates an immune response in healthy adults that, based on our animal studies, could predict effectiveness in preventing the acquisition of Ebola infection.

The volunteers will be split into two groups to receive a high or low dose of the vaccine. The trial will be staged so that small groups of volunteers receive the vaccine at a time, with the first three volunteers to be dosed starting next week at the NIH Clinical Research Center in Bethesda, Maryland. Those three volunteers will be followed for three days before any other volunteers are injected.

We expect to be able to report initial safety and immunogenicity data from this study by the end of this calendar year, said Dr. Fauci.

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Shared biology in human, fly and worm genomes: Powerful commonalities in biological activity, regulation

Posted: at 3:45 am

Researchers analyzing human, fly, and worm genomes have found that these species have a number of key genomic processes in common, reflecting their shared ancestry. The findings, appearing Aug. 28, 2014, in the journal Nature, offer insights into embryonic development, gene regulation and other biological processes vital to understanding human biology and disease.

The studies highlight the data generated by the modENCODE Project and the ENCODE Project, both supported by the National Human Genome Research Institute (NHGRI), part of the National Institutes of Health. Integrating data from the three species, the model organism ENCyclopedia Of DNA Elements (modENCODE) Consortium studied how gene expression patterns and regulatory proteins that help determine cell fate often share common features. Investigators also detailed the similar ways in which the three species use protein packaging to compact DNA into the cell nucleus and to regulate genome function by controlling access to DNA.

Launched in 2007, the goal of modENCODE is to create a comprehensive catalog of functional elements in the fruit fly and roundworm genomes for use by the research community. Such elements include genes that code for proteins, non-protein-coding genes and regulatory elements that control gene expression. The current work builds on initial catalogs published in 2010. The modENCODE projects complement the work being done by the ENCyclopedia Of DNA Elements (ENCODE) Project, which is building a comprehensive catalog of functional elements in the human and mouse genomes.

"The modENCODE investigators have provided a valuable resource for researchers worldwide," said NHGRI Director Eric Green, M.D., Ph.D. "The insights gained about the workings of model organisms' genomes greatly help to inform our understanding of human biology."

"One way to describe and understand the human genome is through comparative genomics and studying model organisms," said Mark Gerstein, Ph.D., Albert L. Williams Professor of Biomedical Informatics at Yale University in New Haven, Connecticut, and the lead author on one of the papers. "The special thing about the worm and fly is that they are very distant from humans evolutionarily, so finding something conserved across all three -- human, fly and worm -- tells us it is a very ancient, fundamental process."

In one study, scientists led by Dr. Gerstein and others, analyzed human, fly and worm transcriptomes, the collection of gene transcripts (or readouts) in a genome. They used large amounts of gene expression data generated in the ENCODE and modENCODE projects -- including more than 67 billion gene sequence readouts -- to discover gene expression patterns shared by all three species, particularly for developmental genes.

Investigators showed that the ways in which DNA is packaged in the cell are similar in many respects, and, in many cases, the species share programs for turning on and off genes in a coordinated manner. More specifically, they used gene expression patterns to match the stages of worm and fly development and found sets of genes that parallel each other in their usage. They also found the genes specifically expressed in the worm and fly embryos are re-expressed in the fly pupae, the stage between larva and adult.

The researchers found that in all three organisms, the gene expression levels for both protein-coding and non-protein-coding genes could be quantitatively predicted from chromatin features at the promoters of genes. A gene's promoter tells the cell's machinery where to begin copying DNA into RNA, which can be used to make proteins. DNA is packaged into chromatin in cells, and changes in this packaging can regulate gene function.

"Our findings open whole new worlds for understanding gene expression and how we think about the role of transcription," said co-senior author Susan Celniker, Ph.D., Head, Department of Genome Dynamics, Lawrence Berkeley National Laboratory, Berkeley, California. "modENCODE has been transformative," she added. "It has helped set the standard for the types of data that should be generated and catalogued."

Another group of scientists investigated how chromatin is organized and how it influences gene regulation in the three species. Using both modENCODE and ENCODE data, scientists compared patterns of modifications in chromatin that are needed for the cell to access the DNA inside, and the changes in DNA replication patterns as a result of these modifications. The investigators discovered that many features of chromatin were similar in all three species.

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Shared biology in human, fly and worm genomes: Powerful commonalities in biological activity, regulation

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My Y-DNA Haplogroup J2 – Video

Posted: at 3:44 am


My Y-DNA Haplogroup J2
A video about my Haplogroup J2 and where it come from.

By: The Ignorant Killer

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My Y-DNA Haplogroup J2 - Video

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Smack: DNA Will Have a Classic or Lose vs. Tay Roc – Video

Posted: at 3:44 am


Smack: DNA Will Have a Classic or Lose vs. Tay Roc
http://www.vladtv.com - DNA and Smack had a fun joint interview with VladTV Battle Rap Journalist Michael Hughes, during which they debated DNA #39;s upcoming clash vs. Tay Roc at Smack/URL #39;s Summer...

By: djvlad

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Smack: DNA Will Have a Classic or Lose vs. Tay Roc - Video

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Device opens DNA testing to masses – Video

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Device opens DNA testing to masses
Device opens DNA testing to masses.

By: Niklo12912

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Device opens DNA testing to masses - Video

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