The GM Barnyard

Allergen-free cows milk and pigs with hardened arteries illustrate how the accuracy of genetic engineering has improved.

Two unsuspecting farm animals have helped to demonstrate the increasing accuracy of genetic engineering techniques. The first is a cow that produced hypoallergenic milk after researchers used RNA interference to block the production of an allergy-inducing protein, as reported this week (October 2) in Proceedings of the National Academy of Sciences. The second, reported in another paper in the same issue, is a pig that could be a model for atherosclerosis after researchers used an enzyme called a TALEN to silence a gene that helps to remove cholesterol.

Researchers have long struggled to remove cow milks allergy-inducing protein, beta-lactoglobulin, which can cause diarrhea and vomiting in children. They were previously unable to introduce foreign genes precisely enough, however, so they could never quite successfully replace the gene that codes for beta-lactoglobulin with a defective form.

But scientists at AgResearch in Hamilton, New Zealand, worked with molecules that interfere with messenger RNA (mRNA), which helps translate genes into proteins. They found microRNA (miRNA) in mice that targeted beta-lactoglobulin mRNA, so they inserted DNA encoding a version of this miRNA into the genomes of cow embryos. Out of 100 embryos, one calf produced beta-globulin-free milk. This isnt a quick process, Stefan Wagner, a molecular biologist at AgResearch, told Nature. One problem is that RNA interference cant eliminate the protein completely because some mRNA slips through.

Another technique could speed up the process. TALENs are enzymes that target and cut out a specific DNA sequence from the genome. As the break is repaired, mutations are introduced that scramble the targeted gene, leaving it unable to function.

The TALEN technology is staggeringly easy, quick, and leaves no mark in the genome, researcher Bruce Whitelaw, told Nature. Whitelaw, a molecular biologist at the Roslin Institute near Edinburgh, United Kingdom, used TALENs to disrupt genes encoding low-density lipoprotein (LDL) receptors in pigs. Without those receptors, which remove LDL from the blood, Whitelaws pigs develop atherosclerotic arteries. Such pigs could be reliable models for biomedical researchers studying human atherosclerosis.

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The GM Barnyard

Does moral decision-making in video games mirror the real world?

Public release date: 3-Oct-2012 [ | E-mail | Share ]

Contact: Vicki Cohn vcohn@liebertpub.com 914-740-2100 Mary Ann Liebert, Inc./Genetic Engineering News

New Rochelle, NY, October 3, 2012Making moral judgments is increasingly a central element of the plots of popular video games. Do players of online video games perceive the content and characters as real and thus make moral judgments to avoid feeling guilty? Or does immoral behavior such as violence and theft make the game any more or less enjoyable? The article "Mirrored Morality: An Exploration of Moral Choice in Video Games" published in Cyberpsychology, Behavior, and Social Networking, a peer-reviewed journal from Mary Ann Liebert, Inc., publishers examines these types of questions. The article is available free online on the Cyberpsychology, Behavior, and Social Networking website.

Andrew Weaver and Nicky Lewis, Indiana University, Bloomington, studied how players make moral choices in video games and what effects those choices have on their emotional responses to the games. In general, players tended to make "moral" decisions and to treat game characters as though they were actual people. Although behaving in antisocial ways was associated with greater guilt, it did not affect player enjoyment.

"Although preliminary, these results point to the utility of games as teaching and educational tools, as well as important tools for the assessment of behavior," says Brenda K. Wiederhold, PhD, MBA, BCIA, Editor-in-Chief of Cyberpsychology, Behavior, and Social Networking, from the Interactive Media Institute, San Diego, CA. "These findings indicate how real the virtual world can become when one suspends disbelief and immerses oneself in the scenario."

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About the Journal

Cyberpsychology, Behavior, and Social Networking is an authoritative peer-reviewed journal published monthly in print and online that explores the psychological and social issues surrounding the Internet and interactive technologies. Complete tables of content and a sample issue may be viewed online on the Cyberpsychology, Behavior, and Social Networking website.

About the Publisher

Mary Ann Liebert, Inc., publishers is a privately held, fully integrated media company known for establishing authoritative peer-reviewed journals in many promising areas of science and biomedical research, including Games for Health Journal, Telemedicine and e-Health, and Journal of Child and Adolescent Psychopharmacology. Its biotechnology trade magazine, Genetic Engineering & Biotechnology News (GEN), was the first in its field and is today the industry's most widely read publication worldwide. A complete list of the firm's 70 journals, books, and newsmagazines is available on the Mary Ann Liebert, Inc., publishers website.

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Does moral decision-making in video games mirror the real world?

Cellectis Publishes Results Paving the Way for New Therapeutic Approaches against Cancer and Genetic Diseases

PARIS--(BUSINESS WIRE)--

Regulatory News:

Cellectis (ALCLS.PA), the French genome engineering specialist, announces in the Journal of Biological Chemistry, one of the most respected scientific journals in the world, the publication of a new approach regarding the targeted modification of DNA2. The manuscript unmasks novel perspectives and broadens the scope of TALENsTM technology to new therapeutic approaches to fight against cancer and genetic diseases. Until now, TALENsTM, the molecular scissors created by Cellectis Group, were only able to target certain parts of the genome. A team of the Groups researchers, led by Julien Valton and Philippe Duchateau, was able to overcome this constraint, opening the way to a wider range of applications, especially in the therapeutic field.

This study, the first to be published on TALENsTM, was awarded by the selection committee of the JBC as Paper of the Week.

Since their identification in 2009, TALEs have quickly emerged as the new generation of DNA-binding domain with programmable specificity and have been successfully used to generate the molecular scissors known as TALENsTM. However, their sensitivity to methylation, a ubiquitous modification of DNA, represents a major bottleneck for their widespread utilization in the genome engineering and therapeutic fields. Using a combination of biochemical, structural and cellular approaches, the R&D department of Cellectis was able to identify the basis of such sensitivity and more importantly, to propose an efficient and universal method to overcome it.

These results are proof of the scientific creativity and quality of our research teams, as well as the power of our genome engineering tools. This new publication strengthens the relevance of our investment in TALEstechnology, and confirms our strategy within the therapeutic field, declared Andr Choulika, Chief Executive Officer of Cellectis Group.

2) Overcoming TALE DNA Binding Domain Sensitivity to Cytosine Methylation Julien Valton, Aurelie Dupuy, Fayza Daboussi, Severine Thomas, Alan Marechal, Rachel Macmaster, Kevin Melliand, Alexandre Juillerat and Philippe Duchateau J. Biol. Chem. jbc.C112.408864. First Published on September 26, 2012, doi:10.1074/jbc.C112.408864

About Cellectis

Founded in France in 1999, the Cellectis Group is based on a highly specific DNA engineering technology. Its application sectors are human health, agriculture and bio-energies. Co-created by Andr Choulika, its Chief Executive Officer, Cellectis is today one of the world leading companies in the field of genome engineering. The Group has a workforce of 230 employees working on 5 sites worldwide: Paris & Evry in France, Gothenburg in Sweden, St Paul (Minnesota) & Cambridge (Massachusetts) in the United States. Cellectis achieved in 2011 16M revenues and has signed more than 80 industrial agreements with pharmaceutical laboratories, agrochemical and biotechnology companies since its inception. AFM, Dupont, BASF, Bayer, Total, Limagrain, Novo Nordisk are some of the Groups clients and partners.

Since 2007, Cellectis has been listed on NYSE-Euronext Alternext market (ALCLS.PA) in Paris.

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Cellectis Publishes Results Paving the Way for New Therapeutic Approaches against Cancer and Genetic Diseases

Animals engineered with pinpoint accuracy

A cow in New Zealand has been genetically modified to produce hypoallergenic milk.

AgResearch

Two genetically engineered farm animals reported today illustrate how far from Frankensteins stitched-together monster animal biotechnology has come. One of those animals, a cow, secretes milk that lacks an allergy-inducing protein because researchers accurately blocked its production using the technique of RNA interference1. And in pigs, scientists have used an enzyme called a TALEN2 to scramble a gene that would normally help remove cholesterol.

RNA interference (RNAi) and TALENs are more accurate at targeting the gene in question than are earlier genetic engineering techniques. For years, researchers tried to remove the allergy-inducing milk protein beta-lactoglobulin from cow's milk, which can cause diarrhea and vomiting in some toddlers. They tried replacing the gene encoding beta-lactoglobulin with a defective form, but this proved nearly impossible because the techniques available to introduce foreign genes into animal genomes were not precise, and misplaced genes failed to express themselves correctly.

In 2006, scientists at AgResearch in Hamilton, New Zealand began to experiment with molecules that interfere with the messenger RNA go-between that enables translation of a gene into protein. In mice, they discovered a short chunk of RNA, called a microRNA, that targeted beta-lactoglobulin messenger RNA directly to prevent its translation. They inserted DNA encoding a version of this microRNA into the genome to create genetically modified cow embryos that they hoped would grow into cows without the allergen in their milk. Out of 100 embryos, one calf yielded beta-globulin-free milk. This isnt a quick process, says Stefan Wagner, a molecular biologist at AgResearch. That's why it has taken so long to succeed in making an allergen-free cow, he says.

Wagner says that TALENs, which were not readily available when he began his research, might speed up the process, and that the team plans to use them to eliminate beta-lactoglobulin. RNAi cannot eliminate the protein completely because some messenger RNA slips past the blockade, but each TALEN targets a specific DNA sequence in the genome and cuts it. As the body repairs the break, mutations are often introduced that render the targeted gene non-functional. The TALEN technology is staggeringly easy, quick, and leaves no mark in the genome, says Bruce Whitelaw, a molecular biologist at the Roslin Institute near Edinburgh in the United Kingdom, who contributed to the work in pigs. In essence, we are just mimicking an evolutionary process with precise, man-made editors.

His team used TALENs to disrupt genes encoding low-density lipoprotein (LDL) receptors. Without these receptor proteins to remove cholesterol-containing LDLs from the blood, LDLs build-up and lead to atherosclerosis. Pigs with this condition may be reliable models of human atheroscelerosis in biomedical research.

The TALEN-modified pig is not the first model of human heart disease (see Model pigs face a messy path), but the technique makes genetic engineering less costly and more efficient. Id be exaggerating if I said that pigs and cows can now be thought of as big mice, but we are moving in that direction, says Heiner Niemann, a bioengineer at the Institute of Farm Animal Genetics in Neustadt, Germany.

The excitement surrounding these technological advances is bittersweet, however. Originally, engineered animals were produced with the aim of making food safer, healthier and more abundant. Yet despite years of investment, almost no animal has been approved by regulatory agencies around the world. Wagner says he has not tasted the milk from his special cow because hes not permitted to under New Zealand law. We must restrict our research to scientific analysis, he says. The current climate for animal biotech is not very good, and therefore, we are nowhere near getting this to the consumer."

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Animals engineered with pinpoint accuracy

Just another GE mirage

The announcement about scientists producing GE milk will damage New Zealands brand on which our more than $10 billion a year dairy exports rely, the Green Party said today.

Today AgResearch scientists announced they have used genetic engineering (GE) technology to breed the first cow in the world that produces high protein milk that may be hypo-allergenic.

"This is just another GE mirage; another announcement from GE proponents about a potential product which we do not need and has no market," Green Party GE Steffan Browning said today.

"Its not right for these scientists to be touting their finding as a solution to milk allergies in babies as some sort of justification for the huge amount of resources that have been invested into GE research.

"We see this over and over again with GE scientists; this new product or that new product that will have apparent amazing results but it never actually meets our real needs for a safe, healthy food supply.

"The Royal Commission into GE recommended that wherever possible animals that are a common source of food should not be used for GE but that recommendation has been ignored.

"Field trials in New Zealand need to be closed down and GE research needs to be kept in the lab.

"Our export markets want safe food grown in a natural environment but the production of GE milk puts those markets at risk.

"Putting at $10 billion a year industry at risk for half a glass of milk is not something to be celebrating," said Mr Browning.

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Just another GE mirage

Ballot Watch: Labeling genetically engineered foods

Proposition 37, pushed by organic food companies and Joseph Mercola, an osteopath and owner of an alternative health website, is the second attempt nationwide to ask voters to require labeling of genetically engineered foods.

Genetic engineering, also known as genetic modifying, happens when scientists change the DNA of a plant or animal to achieve new characteristics. Common genetically engineered crops in the United States include corn mixed with pesticide so it is resistant to bugs, and soybeans bred to tolerate weed-killers such as Round-Up. Cross breeding techniques, such as mixing a plum and an apricot to make a pluot, do not meet the definition of genetic engineering under Proposition 37.

As biotech innovations have expanded in recent years, the percentage of crops made from genetic engineering has increased dramatically. Today, about 90 percent of corn and soybeans are genetically engineered, according to the USDA. That's a concern to proponents of organic farming, but a boon to producers who can grow greater quantities at lower cost.

Advocates concerned about potential health and environmental impacts of genetic engineering have been trying for years to get states and the federal government to label such foods. They have unsuccessfully pushed for food labeling laws in 19 state legislatures and submitted a petition to the federal Food and Drug Administration earlier this year. Ten years ago Oregon voters rejected a ballot measure that would have required labeling genetically engineered food.

WHAT IT WOULD DO

Require that food containing genetically engineered ingredients be labeled "Partially produced with genetic engineering" or "May be partially produced with genetic engineering."

Exempt most meat, dairy and alcohol, as well as food that is organic or sold in restaurants.

Prohibit labeling or advertising genetically engineered food as "natural," "naturally made," "naturally grown" or "all natural." May also prohibit those terms on other processed foods.

Allow people to sue food manufacturers who violate labeling rules.

SUPPORTERS

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Ballot Watch: Labeling genetically engineered foods

3D Biomatrix’s Perfecta3D® Hanging Drop Plates Featured in Prominent Life Science Journals

3D Biomatrix’s Perfecta3D Hanging Drop Plates, which are easy-to-use 96- and 384-well plates for controllable three-dimensional (3D) spheroid culture, were recently featured in several prominent life science and biotechnology journals and websites: Bioscience Technology, The Scientist, Biocompare, and Genetic Engineering and Biotechnology News.Ann Arbor, MI (PRWEB) September 25, 2012 3D ...

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3D Biomatrix’s Perfecta3D® Hanging Drop Plates Featured in Prominent Life Science Journals

NZ out of step on GE

The New Zealand Government needs to follow the lead of Austria and France who are taking action around their approval processes for genetic engineering (GE), the Green Party said today.

In response to a study finding that rats grew tumours and died after being fed GE Roundup ready corn, Austrias Minister for agriculture and the environment has asked the European Commission to review its approval processes. Frances Government have also ordered an investigation into the findings and are signalling that they may suspend imports of the corn.

"New Zealand needs to do the same but successive Governments seem too closely tied with the GE industry to be trusted to do so," Green Party genetic engineering spokesperson Steffan Browning said today.

"The National Government funded the recent biotech conference to the tune of $100,000 from the Ministry of Business, Innovation and Employment plus additional significant contributions from other departments; these are not the actions of a Government with their eyes open about GE.

"The New Zealand public want to know that the food approved for sale in this country is safe.

"Without changing the GE approval process and actually enforcing our labelling laws we cant be confident in that.

"We fought hard for proper labelling laws but they are not enforced, so New Zealanders cant actually show their opposition to GE through their purchasing.

"The fact is that this study shows we are right to be concerned and we need better approval processes that prove safety over the long term, instead of the short term feeding studies that decisions have been made on to date.

"This study has already started a strong discussion because people are really worried about the effects of these foods that have been approved to be in our stores now for a decade or longer.

"Of course this research is being described by some as controversial because there is big, big money involved in GE.

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NZ out of step on GE

Immediate withdrawal of unsafe GE corn vital

20 September 2012

Immediate withdrawal of unsafe GE corn vital

Research released yesterday shows the Governments lax policy on genetic engineering is putting the health of New Zealanders at risk, the Green Party said today.

The peer-reviewed research, published in the Journal of Food and Toxicology, shows disturbing results about the health effects of eating a genetically engineered corn that has been approved for human consumption in New Zealand for the last 10 years.

The rats in this study, fed with Roundup ready corn with levels of Roundup that are within approved limits, developed mutations and tumours at a hugely alarming rate.

There are now huge concerns over the safety of this corn. Eating this corn has now been proven to cause the growth of tumours, so why was it approved a decade ago without the necessary evidence that it was safe to eat? Green Party genetic engineering spokesperson Steffan Browning asked today.

New Zealand has more than 70 GE foods approved for sale in New Zealand to date, and these approvals were mostly based on health studies that were 90 days long or less. This new research recorded effects for two years and the tumours and deaths showed up after that previous 90 day cut off point.

We now know that eating this corn, called NK603, causes tumours and we cant be sure that any products containing these GE foods currently out there being eaten by New Zealanders are safe either.

FSANZ must immediately recall any products that have this strain of GE corn as an ingredient and reassess all previous approvals for long term eating safety.

New Zealanders dont want to be part of a science experiment. They rely on the Government to make sure these products are safe before they are released for human consumption.

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Immediate withdrawal of unsafe GE corn vital

Immediate withdrawal of unsafe GE corn vital – Greens

Research released yesterday shows the Governments lax policy on genetic engineering is putting the health of New Zealanders at risk, the Green Party said today.

The peer-reviewed research, published in the Journal of Food and Toxicology, shows disturbing results about the health effects of eating a genetically engineered corn that has been approved for human consumption in New Zealand for the last 10 years.

The rats in this study, fed with Roundup ready corn with levels of Roundup that are within approved limits, developed mutations and tumours at a hugely alarming rate.

"There are now huge concerns over the safety of this corn. Eating this corn has now been proven to cause the growth of tumours, so why was it approved a decade ago without the necessary evidence that it was safe to eat?" Green Party genetic engineering spokesperson Steffan Browning asked today.

"New Zealand has more than 70 GE foods approved for sale in New Zealand to date, and these approvals were mostly based on health studies that were 90 days long or less. This new research recorded effects for two years and the tumours and deaths showed up after that previous 90 day cut off point.

"We now know that eating this corn, called NK603, causes tumours and we cant be sure that any products containing these GE foods currently out there being eaten by New Zealanders are safe either.

"FSANZ must immediately recall any products that have this strain of GE corn as an ingredient and reassess all previous approvals for long term eating safety.

"New Zealanders dont want to be part of a science experiment. They rely on the Government to make sure these products are safe before they are released for human consumption.

"Despite legal requirements, most GE foods are unlabelled so New Zealanders cant even choose to avoid them.

"I am hopeful that this study is on the top of the Minister for Food Safetys reading list this morning and that she will take immediate action to protect the health of New Zealanders.

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Immediate withdrawal of unsafe GE corn vital - Greens

Genetic test predicts risk for Autism

Professor Stan Skafidas, Director, Centre for Neural Engineering, University of Melbourne

A team of Australian researchers, led by The University of Melbourne has developed a genetic test that is able to predict the risk of developing Autism Spectrum Disorder, ASD.

Lead researcher Stan Skafidas, Director of the Centre for Neural Engineering and Professor of Electrical and Electronic Engineering at the University of Melbourne, said the test could be used to assess the risk for developing the disorder.

This test could assist in the early detection of the condition in babies and children and help in the early management of those who become diagnosed, he said.

It would be particularly relevant for families who have a history of Autism or related conditions such as Aspergers Syndrome, he said.

Autism affects around one in 150 births and is characterised by abnormal social interaction, impaired communication and repetitive behaviours.

The test correctly predicted ASD with more than 70 per cent accuracy in people of central European descent. Ongoing validation tests are continuing including the development of accurate testing for other ethnic groups.

Clinical neuropsychologist, Dr Renee Testa from the University of Melbourne and Monash University, said the test would allow clinicians to provide early interventions that may reduce behavioural and cognitive difficulties that children and adults with ASD experience.

Early identification of risk means we can provide interventions to improve overall functioning for those affected, including families, she said.

A genetic cause has been long sought with many genes implicated in the condition, but no single gene has been adequate for determining risk.

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Genetic test predicts risk for Autism

Prop. 37: Another example of the perils of the initiative process

Love it or hate it, the one thing you can say for sure about California's ballot initiative process is that it's the absolute worst way to craft policy dealing with complex scientific issues.

That doesn't stop advocates on one side or another from constantly trying, with the result that the public's understanding of the underlying facts plummets faster than you can say, well, "Proposition 37."

Proposition 37 is on November's ballot. The measure would require some, but not all, food sold in California and produced via genetic engineering to be labeled as such. (There are exemptions for milk, restaurant food and other products.)

Genetic engineering, or genetic modification, which involves manipulating DNA or transferring it from one species to another, is increasingly common in agriculture and food processing, and wouldn't be banned or even regulated by the measure. Genetic engineering has pluses and minuses. It can increase crop yields and pest resistance. But it can also affect the environment in negative ways pollen or seeds from genetically engineered crops can be spread by wind, birds or insects to territory where they're unwanted, for example.

Once you've said that, you've said pretty much everything that's known to be relevant to Proposition 37. The rest is baloney, of the non-genetically engineered variety.

So what does this mean for you? It means that between now and election day your airwaves are likely to be filled with steaming piles of fatuous nonsense about genetically engineered foods (which will be depicted as horrifically perilous or absolutely safe), about trial lawyers, about struggling mom-and-pop grocery stores, about the evils of multinational agribusinesses and federal regulators. You'll be presented with learned scientific and economic studies on both sides, and they'll almost certainly be misleading, incomplete or irrelevant, though they'll sound pretty danged convincing.

This will all come to you courtesy of war chests that are already in the neighborhood of $30 million, total.

Great initiative system we have here in the Golden State. As a procedure for producing rational law, it could only be designed by a mad scientist working with rogue DNA.

Let's start with the Yes on 37 campaign. It describes its bottom line as your right to know what's in your food; so what's wrong with mandating explicit labeling? That's fair as far as it goes, but it doesn't go very far. The danger in enacting rules like this is that while they sound perfectly reasonable, they distract from the need for thoughtful and effective regulation and for action at the Legislature, not the ballot box.

"All consumers should have a right to know how their food is produced," observes Gregory Jaffe, head of the biotechnology project at the Center for Science in the Public Interest, which is no crony of the food industry. "But that includes not merely genetic engineering, but irradiated foods and those produced from cloning."

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Prop. 37: Another example of the perils of the initiative process

GEN reports on ocular therapeutics targeting the retina

Public release date: 10-Sep-2012 [ | E-mail | Share ]

Contact: John Sterling jsterling@genengnews.com 914-740-2196 Mary Ann Liebert, Inc./Genetic Engineering News

New Rochelle, NY, September 10, 2012-- Therapies for retinal diseases are expected to overtake those for glaucoma by 2014, reports Genetic Engineering & Biotechnology News (GEN). Because current retinal disease treatments only improve vision for six to eight weeks, there is a critical need for new remedies, according to a recent issue of GEN.

"As increasing numbers of baby-boomers continue to grow older, many will have to deal with eye diseases such as age-related macular degeneration," said John Sterling, Editor-in-Chief of GEN. "Some estimates put the current AMD and diabetic retinopathy drug segment of the market at $3 billion, and this is expected to increase to about $5 billion in two years."

Standard therapy has been Genentech's VEGF inhibitors Lucentis and the off-label use of Avastin. Regeneron, in collaboration with Bayer HealthCare, is challenging these drugs with a similar VEGF inhibitor, Eyela. The FDA approved the drug last November for wet AMD.

In another approach, Acucela is in Phase II trials using visual cycle modulators to lighten the metabolic load on the retina by reducing the activity of the rod visual system. This protects the retina from light damage, improves retinal vasculature, and reduces the accumulation of A2E and other retinal-related toxic by-products.

GlaxoSmithKline has two drugs in Phase II trials for ocular therapy: darapladib, an oral Lp-PLA2 inhibitor for diabetic macular edema, and Votrient, a multi-kinase angiogenesis inhibitor in eye drop form for AMD. Early-stage work also is under way for neovascular AMD, dry AMD, diabetic retinopathy, diabetic macula edema, uveitis, and glaucoma, as well as for technologies for drug delivery.

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Other companies covered in the GEN article include Acucela, pSiveda, Sanofi, NeuroTech, QLT, Applied Genetic Technologies, RetroSense Therapeutics, Aerie Pharmaceuticals, Kowa Pharmaceuticals America, Novartis, Senju Pharmaceutical, Can-Fite Biopharma, Inotek Pharmaceuticals, Otsuka Pharmaceutical, and Santen Pharmaceutical.

For a copy of the September 1 issue of GEN, please call (914) 740-2146, or email: pbartell@genengnews.com

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GEN reports on ocular therapeutics targeting the retina

Mandatory GM Labeling Would Require Major Change

CPG manufacturers may be on the cusp of monumental change as voters in California contemplate a hotly contested ballot initiative to require labeling of genetically modified foods.

Food marketers will face tough choices should the measure pass, as about 70% of processed foods sold in supermarkets contain GM ingredients like corn and soy. Some estimate that 100,000 or more foods sold in California contain some level of GE ingredients and would therefore be affected.

The mandate would be limited to the Golden State, but the implications for companies that choose not to move away from GM ingredients in advance of the July 1, 2014, deadline could be as far-reaching as consumer awareness spreads.

While the government deems genetically modified organisms safe, Californians want to judge for themselves. A Pepperdine University poll found that if the election were held last month, Californians would pass the proposition by a 3-1 margin.

To avoid the partially produced with genetic engineering label and possible consumer backlash, suppliers will likely reformulate product with more costly non-GE foods or organic ingredients, just as theyve done in countries where genetic modification disclosure is required.

Read more: Prop 37 Battle Rages in California

A recent study commissioned by the No on 37, Stop the Deceptive Food Labeling Scheme campaign, of which the Grocery Manufacturers Association is a chief sponsor, bears this out.

It projects that reformulations to non-GE and organic ingredients, which by law cannot be genetically modified, will be the most likely course taken by food producers.

Read more: California GMO Bill Is Top Priority for GMA

Retailers might also adjust their sourcing policies to gain consumer favor by incorporating more organic foods and those that have been verified under the Non-GMO Project and labeled with its seal.

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Mandatory GM Labeling Would Require Major Change

Promising new drug target for inflammatory lung diseases

Public release date: 6-Sep-2012 [ | E-mail | Share ]

Contact: Cathia Falvey cfalvey@liebertpub.com 914-740-2100 Mary Ann Liebert, Inc./Genetic Engineering News

New Rochelle, NY, September 6, 2012The naturally occurring cytokine interleukin-18, or IL-18, plays a key role in inflammation and has been implicated in serious inflammatory diseases for which the prognosis is poor and there are currently limited treatment options. Therapies targeting IL-18 could prove effective against inflammatory diseases of the lung including bronchial asthma and chronic obstructive pulmonary disease (COPD), as described in a review article published in Journal of Interferon & Cytokine Research (http://www.liebertpub.com/jir), a peer-reviewed publication from Mary Ann Liebert, Inc., publishers (http://www.liebertpub.com). The article is available free online at the Journal of Interferon & Cytokine Research website. (http://www.liebertpub.com/jir)

Tomotaka Kawayama and coauthors from Kurume University School of Medicine, Fukuoka, Japan, University of Ryukyus, Okinawa, Japan, and Frederick National Laboratory for Cancer Research, Frederick, MD, review the growing evidence to support the important role IL-18 has in inflammation and how it may help to initiate and worsen inflammatory disorders such as arthritis, dermatitis and inflammatory diseases of the bowel and immune system. In the article "Interleukin-18 in Pulmonary Inflammatory Diseases" (http://online.liebertpub.com/doi/full/10.1089/jir.2012.0029) they describe the potential benefits of therapies aimed at blocking the activity of IL-18 to treat inflammatory lung disease.

"This review provides an interesting and thorough summary of the biology and potential application of IL-18 in the setting of inflammatory pulmonary disease," says Co-Editor-in-Chief Thomas A. Hamilton, PhD, Chairman, Department of Immunology, Cleveland Clinic Foundation.

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About the Journal Journal of Interferon & Cytokine Research (http://www.liebertpub.com/jir), led by Co-Editors-in-Chief Ganes C. Sen, PhD, Chairman, Department of Molecular Genetics, Cleveland Clinic Foundation, and Thomas A. Hamilton, PhD, is an authoritative peer-reviewed journal published monthly in print and online that covers all aspects of interferons and cytokines from basic science to clinical applications. Journal of Interferon & Cytokine Research is the official journal of the International Society for Interferon and Cytokine Research. Complete tables of content and a sample issue (http://online.liebertpub.com/toc/jir/31/6) may be viewed online at the Journal of Interferon & Cytokine Research website. (http://www.liebertpub.com/jir)

About the Publisher

Mary Ann Liebert, Inc., publishers (http://www.liebertpub.com) is a privately held, fully integrated media company known for establishing authoritative peer-reviewed journals in many promising areas of science and biomedical research, including Viral Immunology, AIDS Research and Human Retroviruses, and DNA and Cell Biology. Its biotechnology trade magazine, Genetic Engineering & Biotechnology News (GEN), was the first in its field and is today the industry's most widely read publication worldwide. A complete list of the firm's 70 journals, books, and newsmagazines is available at Mary Ann Liebert, Inc., publishers website. (http://www.liebertpub.com).

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Promising new drug target for inflammatory lung diseases

Why does Alzheimer's disease affect twice as many women as men?

Public release date: 5-Sep-2012 [ | E-mail | Share ]

Contact: Cathia Falvey cfalvey@liebertpub.com 914-740-2100 Mary Ann Liebert, Inc./Genetic Engineering News

New Rochelle, NY, September 5, 2012A group of experts has developed consensus recommendations for future research directions to determine why nearly two-thirds of Americans with Alzheimer's disease (AD) are women. The recommendations are published in a Roundtable discussion in Journal of Women's Health, a peer-reviewed publication from Mary Ann Liebert, Inc., publishers. The article is available free on the Journal of Women's Health website at http://www.liebertpub.com/jwh.

An estimated 5.4 million Americans are affected by AD and related dementias, and that number will likely rise to 11-16 million people by the year 2050 if no effective cures or preventive measures are developed. The main risk factors for AD are age and sex, with affected women outnumbering men 2 to 1. This may be due at least in part to the fact that women tend to live longer.

An interdisciplinary roundtable of experts convened by the Society for Women's Health Research (Washington, DC) led to a set of recommendations to help guide future AD research and make the evaluation of sex and gender differences a component of future studies. The consensus recommendations encompass seven themes, including the need to assess the link between sex and AD incidence, raise awareness of sex differences among the research community, and to take into account sex-based differences in the experimental design and data analysis of studies on disease risk, early diagnosis, and drug discovery.

"There are still major gaps in our knowledge of the role of sex and gender in the onset and progression of Alzheimer's disease, and these recommendations will provide a useful guide for future research in this area," says Susan G. Kornstein, MD, Editor-in-Chief of Journal of Women's Health, Executive Director of the Virginia Commonwealth University Institute for Women's Health, Richmond, VA, and President of the Academy of Women's Health.

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About the Journal

Journal of Women's Health, published monthly, is a core multidisciplinary journal dedicated to the diseases and conditions that hold greater risk for or are more prevalent among women, as well as diseases that present differently in women. The Journal covers the latest advances and clinical applications of new diagnostic procedures and therapeutic protocols for the prevention and management of women's healthcare issues. Tables of content and a sample issue may be viewed on the Journal of Women's Health website at http://www.liebertpub.com/jwh. Journal of Women's Health is the Official Journal of the Academy of Women's Health.

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Why does Alzheimer's disease affect twice as many women as men?

Can videogaming benefit young people with autism spectrum disorder?

Public release date: 5-Sep-2012 [ | E-mail | Share ]

Contact: Vicki Cohn vcohn@liebertpub.com 914-740-2100 x2156 Mary Ann Liebert, Inc./Genetic Engineering News

New Rochelle, NY, September 5, 2012According to the Centers for Disease Control and Prevention (CDC), 1 in 88 children in the U.S. has autism spectrum disorder (ASD), a broad group of neurodevelopmental disorders. Children and adolescents with ASD are typically fascinated by screen-based technology such as videogames and these can be used for educational and treatment purposes as described in an insightful Roundtable Discussion published in Games for Health Journal: Research Development, and Clinical Applications, a peer-reviewed publication from Mary Ann Liebert, Inc.. The article is available free on the Games for Health Journal website.

Individuals with ASD have difficulty with communication and social interaction, but they often have particularly good visual perceptual skills and respond well to visual stimuli. Videogames offer opportunities for successful learning, motivation to improve skills such as planning, organization, and self-monitoring, and reinforcement of desired behaviors without the need for direct human-to-human interaction.

Autism is a growing area of interest for the gamification community, and Games for Health Journal continues to explore various aspects of how videogame technology can be beneficial in treating this complex spectrum of disorders. In a previous issue of the Journal, the article "Comparing Energy Expenditure in Adolescents with and without Autism while Playing Nintendo Wii Games" described how gaming might help individuals with ASD increase their daily physical activity to prevent obesity.

"Children and young adults with ASD have unique opportunities to capitalize on their interest and aptitude in videogames as a resource to develop desired social behaviors and life skills and to increase their physical activity," says Games for Health Journal Editor-in-Chief Bill Ferguson, PhD, who moderated the Roundtable.

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About the Journal

Games for Health Journal (http://www.liebertpub.com/g4h) breaks new ground as the first journal to address this emerging and increasingly important area of health care. The Journal provides a bimonthly forum in print and online for academic and clinical researchers, game designers and developers, health care providers, insurers, and information technology leaders. Articles explore the use of game technology in a variety of clinical applications. These include disease prevention and monitoring, nutrition, weight management, and medication adherence. Gaming can play an important role in the care of patients with diabetes, post-traumatic stress disorder, Alzheimer's disease, and cognitive, mental, emotional, and behavioral health disorders.

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Can videogaming benefit young people with autism spectrum disorder?

Why does Alzheimer’s disease affect twice as many women as men?

Public release date: 5-Sep-2012 [ | E-mail | Share ]

Contact: Cathia Falvey cfalvey@liebertpub.com 914-740-2100 Mary Ann Liebert, Inc./Genetic Engineering News

New Rochelle, NY, September 5, 2012A group of experts has developed consensus recommendations for future research directions to determine why nearly two-thirds of Americans with Alzheimer's disease (AD) are women. The recommendations are published in a Roundtable discussion in Journal of Women's Health, a peer-reviewed publication from Mary Ann Liebert, Inc., publishers. The article is available free on the Journal of Women's Health website at http://www.liebertpub.com/jwh.

An estimated 5.4 million Americans are affected by AD and related dementias, and that number will likely rise to 11-16 million people by the year 2050 if no effective cures or preventive measures are developed. The main risk factors for AD are age and sex, with affected women outnumbering men 2 to 1. This may be due at least in part to the fact that women tend to live longer.

An interdisciplinary roundtable of experts convened by the Society for Women's Health Research (Washington, DC) led to a set of recommendations to help guide future AD research and make the evaluation of sex and gender differences a component of future studies. The consensus recommendations encompass seven themes, including the need to assess the link between sex and AD incidence, raise awareness of sex differences among the research community, and to take into account sex-based differences in the experimental design and data analysis of studies on disease risk, early diagnosis, and drug discovery.

"There are still major gaps in our knowledge of the role of sex and gender in the onset and progression of Alzheimer's disease, and these recommendations will provide a useful guide for future research in this area," says Susan G. Kornstein, MD, Editor-in-Chief of Journal of Women's Health, Executive Director of the Virginia Commonwealth University Institute for Women's Health, Richmond, VA, and President of the Academy of Women's Health.

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About the Journal

Journal of Women's Health, published monthly, is a core multidisciplinary journal dedicated to the diseases and conditions that hold greater risk for or are more prevalent among women, as well as diseases that present differently in women. The Journal covers the latest advances and clinical applications of new diagnostic procedures and therapeutic protocols for the prevention and management of women's healthcare issues. Tables of content and a sample issue may be viewed on the Journal of Women's Health website at http://www.liebertpub.com/jwh. Journal of Women's Health is the Official Journal of the Academy of Women's Health.

About the Academy

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Why does Alzheimer's disease affect twice as many women as men?

Author argues U.S. must lead way on bioengineering

Greg Stock wrote a book about the future of human genetic engineering. (Photo courtesy of Greg Stock.)

While perhaps not yet a majority many parents says they would bioengineer their children if they could, to create the perfect, or more perfect child. Now, that parental dream is closer to reality, but no one is quite sure what the implications may be.

Nearly a decade after the human genome was decoded, scientists are only now beginning to understand its implications.

One of the leading thinkers in this field is the biotech entrepreneurGregory Stock. A biophysicist by training, his 2002 bookRedesigning Humans: Our Inevitable Genetic Futuremakes the case that full-scale genetic engineering is on the way whether we like it or not.

And, Stock believes, if the U.S. doesnt lead the way in developing those advances, other nations will.

Between a third and two-thirds of the population and even higher if you look at China or Thailand and other eastern cultures of parents say if they could enhance the genetics of their children, enhance their either cognitive or physical capabilities, they would absolutely do it," he said.

But engineering traits to improve people remains a thorny issue.

It sounds so compelling, take out a little bit of this, that, its going to be the best of you, Stock said. But actually, we don't have a clue what creates exceptional capabilities."

While Stocks attitude is full-speed ahead, he admits, its going to get weird."

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Author argues U.S. must lead way on bioengineering