Sunday, March 31, 2013

Tech firms bumping up perks to recruit, retain

Apple's ring-shaped, gleaming "Spaceship Headquarters" will include a world class auditorium and an orchard for engineers to wander. Google's new Bay View campus will feature walkways angled to force accidental encounters. Facebook, while putting final touches on a Disney-inspired campus including a Main Street with a B-B-Q shack, sushi house and bike shop, is already planning an even larger, more exciting new campus.

More than ever before, Silicon Valley firms want their workers at work.

Yahoo CEO Marissa Mayer has gone so far as to ban working from home, and many more offer prodigious incentives for coming in to the office, such as free meals, massages and gyms.

This spring, as the tech industry is soaring out of the Great Recession, plans are in the works for a flurry of massive, perk-laden headquarters.

"We're seeing the mature technology companies trying to energize their work environments, getting rid of cube farms and investing in facilities to compete for talent," said Kevin Schaeffer, a principal at architecture and design firm Gensler in San Jose. "That's caused a huge transition in the way offices are laid out."

New Silicon Valley headquarters or expansions are under way at most of the area's major firms, including eBay, Intel, LinkedIn, Microsoft, Netflix, Nvidia and Oracle. Many will be huge: Apple Corp.'s 176-acre campus will be one of the world's largest workplaces. On the outside, many of the new buildings boast striking architectural designs and will collectively be among the most environmentally friendly in the country. Inside, there are walls you can draw on, ping pong tables, Lego stations, gaming arcades and free haircuts.

Critics say that while some workplace perks and benefits are a good thing, the large, multibillion dollar corporate headquarters are colossal wastes of money that snub the pioneering technology these firms actually create.

"Companies led by older management tend to be very controlling, but when I look at people in the 20s or 30s, they're totally capable of working on their own and being productive," said Kevin Wheeler, whose Future of Talent Institute researches and consults on human resources for Silicon Valley businesses. "To have artificial structures that require everybody to be in the office at certain hours of the day is simply asinine."

Wheeler said he thinks Yahoo called everyone back to work "because they had gotten into a culture of laziness," and that the firm will likely loosen the restrictions soon.

Yahoo was, in fact, an early model of Silicon Valley's happy workplace culture, touting their espresso bar and inspirational speakers as a method of inspiring passion and originality. Today yoga, cardio-kickboxing and golf classes at the office, as well as discounts to ski resorts and theme parks, help it receive top ratings as one of America's happiest workplaces.

Companies say extraordinary campuses are necessary to recruit and retain top talent and to spark innovation and creativity.

And there are business benefits and financial results for companies that keep their workers happy. The publicly traded 100 Best Companies To Work For in America consistently outperform major stock indices and have more qualified job applicants and higher productivity, according to the San Francisco-based Great Place to Work Institute. That may not always be obvious, however.

"People do work really, really hard here," Facebook spokesman Slater Tow said as an engineer glided past a row of second floor conference rooms on a skateboard. "They have to be passionate about what they do. If they're not, we would rather someone who is."

He points out the Jumbotron frame for outdoor movies, the Nacho Royale taqueria, a bank branch with tellers standing by, an artist in residence. Traditional benefits are part of the Silicon Valley packages as well. Facebook offers free train passes, a shuttle to work, a month of paid vacation, full health care and stock options.

Facebook staffers are welcome to stop by and play in Ben Barry's Analog Research Laboratory, a large, sunlit studio with laser cutters, woodworking tools, a letter press machine and silk screening supplies.

"I believe if people feel they can control their environment, that leads to a greater sense of ownership over the product," says Barry, who makes posters for the campus walls with mantras like "What would you do if you weren't afraid?" and "Move fast and break things."

About six miles north at Google's headquarters, workers on one of more than 1,000 Google-designed bikes rolled from one building to another. Others stepped into electric cars, available for free check outs if someone has an errand. In one office, two young engineers enjoyed a beer and shot pool.

Google doesn't want its Googlers to have to worry about distractions in their life.

Concerned about the kids? Childcare is on campus. Need to shop and cook? Have the family dine at Google. Dirty laundry piling up? Bring it in to the office. Bring Fido too, so he doesn't get lonely. There's a climbing wall, nap pods (lay down in the capsule, set the alarm, zzzzz), a bowling alley, multiple gyms, a variety of healthy cafes, mini kitchens, and classes on anything from American Sign Language to Public Speaking. In a shared, community garden, Googlers plant seeds, knowing that if they get too busy, a landscaper will pull their weeds.

The company has no policy requiring people to be at work. But officials say Googlers want to come in.

"We work hard to create the healthiest, happiest and most productive work environments possible that inspire collaboration and innovation," said spokeswoman Katelin Todhunter-Gerberg.

Wheeler says the mega-complexes being built today will be hard to staff 10 years from now, and that the next era will see smaller workplaces where employers are responsible for meeting achievements and objectives, and have flexibility about when they come in to their office.

"When you look at how some of these companies operate, they're in effect, sweat shops. ... They want 80, 90, 100 hours of work. In order to even make that tolerable, of course you have to offer haircuts and food and places to sleep or else people would have to go home," he said.

? 2013 The Associated Press. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

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Judge: Jolie didn't plagiarize 'Blood and Honey'

(AP) ? A federal judge says actress Angelina Jolie didn't steal the story for her movie "In the Land of Blood and Honey" from a Croatian author.

City News Service reports Friday's tentative ruling in Los Angeles will throw out the suit accusing Jolie of copyright infringement.

In 2011, author James Braddock sued Jolie and the film company that made the film, saying it was partly based on his book "The Soul Shattering."

U.S. District Judge Dolly M. Gee wrote in a tentative ruling that the plots, characters and themes in the two works were not "substantially" similar, though both centered on war romances.

Jolie wrote, directed and co-produced the film.

Braddock has been ordered to tell the court why his complaint should not be dismissed with prejudice.

Associated Press

Source: http://hosted2.ap.org/APDEFAULT/4e67281c3f754d0696fbfdee0f3f1469/Article_2013-03-29-US-People-Jolie/id-cfd15534f0dd431782cae2ee557a682a

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Taking the US-bound Smart Electric Drive for a spin (video)

We take the USbound Smart Electric Drive for a test drive video

The eponymous "Smart car" has been buzzing around city streets in the US for over five years now. It's actually called the Fortwo, thanks to its limited seating capacity, and while it didn't prove to be an immediate hit, sales have been steadily increasing. An electric version of the car has been available in limited numbers overseas for years now, but finally this year it's coming to the US. And this is it. We got a chance to drive a green vinyl-wrapped Smart Electric Drive around some city streets ahead of the opening of the New York International Auto Show and came away reasonably impressed by this $25,000 EV -- the cheapest on the market. Join us after the break for our impressions.

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Source: http://www.engadget.com/2013/03/29/we-take-the-us-bound-smart-electric-drive-for-a-spin-video/

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Saturday, March 30, 2013

EPA further limits sulfur. Will higher gas prices follow?

The Environmental Protection Agency announced new standards on sulfur in gasoline Friday that many say will lead eventually to a hike in gas prices. The EPA expects a 1 cent per gallon increase; industry says it will be much more.

By David J. Unger,?Correspondent / March 29, 2013

Gasoline drips off a nozzle during refueling at a gas station in Altadena, Calif. A new rule from the EPA would reduce the amount of sulfur allowed in gasoline from 30 parts per million to 10 parts per million in 2017.

Mario Anzuoni/Reuters/File

Enlarge

The federal government proposed new standards Friday that further limit the amount of sulfur in gasoline. Compared with previous reductions, Friday's proposal is slight. But many say it's enough to increase the price Americans pay at the pump.

Skip to next paragraph

Why It Matters

Energy: New regulations translate to a gradual increase in gas prices.

Environment: Less sulfur means lower pollution and reduced health costs associated with poor air quality.

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"New requirements, new regulations are going to drive prices up," said Patrick DeHaan, senior petroleum analyst at GasBuddy.com, a gas price analysis website.?"This isn?t the biggest change but it will cost motorists."?

The jump could be as high as 9 cents in some places, according to the American Petroleum Institute (API), a trade association for the oil and gas industry.?

"Consumers care about the price of fuel, and our government should not be adding unnecessary regulations that raise manufacturing costs, especially when there are no proven environmental benefits," Bob Greco, director of?API's downstream group,?said in a statement Friday. "We should not pile on new regulations when existing regulations are working.? ?

Banks made?$32 billion on overdraft fees last year?

Bank customers may complain about hefty overdraft fees, but they?re using the service more and paying the price.

A new report from Moebs Services, a respected economic research firm, shows overdraft revenue at banks, credit unions and thrift institutions totaled $32 billion last year. That?s an increase of $400 million or 1.3 percent from 2011.

?Consumers use of overdrafts shows no indication of going away, and is actually increasing,? said Michael Moebs, who wrote the study.

At the current rate of growth, Moebs predicts revenue from overdraft fees will hit a new record by the end of 2016, topping the old record of $37 billion set in 2009.

The Moebs study found that about a quarter of the people with a consumer checking account ? that?s 38 million people ? frequently overdraft. The median overdraft is about $40.

More than half of the customers who frequently overdraft ? 57 percent or 20 million people ? go to payday lenders when they are short on funds.

Why? Because a payday loan is significantly cheaper.

?Payday lenders are the low-price source for short-term cash needs,? Moebs said. ?You can get a cash advance for $16 as opposed to $25 at a community bank, $27 a credit union and $30 at bank or thrift. Those are median prices.?

While the cost of an overdrawn account has been going up at many financial institutions, the price of borrowing from a payday lender has dropped. The median charge for a $100 cash advance dropped $1.50 from 2011 to 2012, from $17.50 to $16.

Moebs firmly believes many of the people who use a payday lender would rather not, if the cost of the overdraft penalty was more in line with what the payday stores charge. He puts that price point at $20.

What it really costs to cover an overdraft
Consumer groups have long asserted that overdraft fees are revenue generators, deliberately higher than the banks' cost of providing the service.

?It?s very clear that banks are gouging customers with incredibly high and outrageous overdraft fees that are not related to their cost,? said Ed Mierzwinski, consumer program director at U.S. PIRG.

A bill introduced in Congress last week (The Overdraft Protection Act of 2013) would require these fees to be ?reasonable and proportional.?

Moebs told me his costs studies, some of which were done for the Federal Reserve Bank, show the prices charged by the big financial institutions ?are legitimate? because their cost structures are so high.

He estimates that a megabank makes about $3 on each overdraft charge, the same profit the payday lender earns with a $100 loan. But because the overhead at the bank is so much higher, it has to charge $30 or $35 to make the same amount.

Smaller banks and credit unions have a smaller nut to crack, so they might be able to reduce the price on an overdraft. Moeb?s advice to these institutions: lower that price and you?ll get more customers.

Cheaper alternatives
Of course, the goal is to avoid overdraft charges. Check your account statement ? online, by phone or at an ATM ? to make sure you don?t try to spend money that?s not in your checking account.

?If you are likely to overdraft, the main street institutions are your best choice ? most credit unions and community banks and some of the thrifts ? because they have a lower overdraft fee,? Moebs said.

Debit-card transactions often cause an account to be overdrawn. Remember: Your bank or credit union will deny a point-of-purchase debit-card payment or cash withdrawal from an ATM if there is not enough money in the account to cover it, unless you ?opt in? to their overdraft protection plan. In that case, the transaction will go through and you?ll get hit with a fee.

A recent study by the Pew Charitable Trusts found that 54 percent of the customers who had overdrawn their accounts said they did not realize they had signed up for an overdraft service that cost money. Susan Weinstock, director of Pew?s Safe Checking in the Electronic Age Project, said this shows there is ?a very high level of confusion? about how this overdraft protection works.

Herb Weisbaum is The ConsumerMan. Follow him on Facebook and Twitter or visit The ConsumerMan website.


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FDA Approves 1st in New Class of Type 2 Diabetes Drugs - Health ...

glucose monitor FDA Approves 1st in New Class of Type 2 Diabetes Drugs

FRIDAY, March 29 (HealthDay News) ? The first in a new class of type 2 diabetes drugs was approved Friday by the U.S. Food and Drug Administration.

Invokana (canaglifozin) tablets are to be taken, in tandem with a healthy diet and exercise, to improve blood sugar control in adults with type 2 diabetes.

Invokana belongs to a class of drugs called sodium-glucose co-transporter 2 (SGLT2) inhibitors. It works by blocking the reabsorption of glucose (sugar) by the kidney and increasing glucose excretions in urine, the FDA said in a news release.

?We continue to advance innovation with the approval of new drug classes that provide additional treatment options for chronic conditions that impact public health,? Dr. Mary Parks, director of the division of metabolism and endocrinology products in the FDA?s Center for Drug Evaluation and Research, said in the news release.

About 24 million Americans have type 2 diabetes, and it accounts for more than 90 percent of diabetes cases diagnosed in the United States, the FDA said. If blood sugar levels are not carefully controlled, there is an increased risk for serious complications, including heart disease, blindness, and nerve and kidney damage, the agency added.

The FDA approval is based on the findings of nine clinical trials involving more than 10,000 patients. Patients who took the drug showed improvement in hemoglobin A1c levels (a measure of blood sugar control) and fasting blood sugar levels.

Invokana should not be used by people with type 1 diabetes or people with type 2 diabetes who have increased ketones in their blood or urine (diabetic ketoacidosis), severe kidney disease, kidney failure or who are on dialysis, the FDA said.

The agency told drug maker Janssen Pharmaceuticals that it must conduct five post-approval studies of the drug to determine the risk of problems such as heart disease, cancer, pancreatitis, liver abnormalities and pregnancy complications.

The most common side effects of Invokana are vaginal yeast infections and urinary tract infections. It may also cause dizziness and fainting.

More information

The U.S. National Institute of Diabetes and Digestive and Kidney Diseases has more about type 2 diabetes.

HEALTHDAY Web XSmall FDA Approves 1st in New Class of Type 2 Diabetes Drugs

Source: http://news.health.com/2013/03/29/fda-approves-1st-in-new-class-of-type-2-diabetes-drugs/

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Unlike AT&T, Verizon reportedly putting promotional muscle behind BlackBerry Z10 launch

By Jason Szep SIT KWIN, Myanmar (Reuters) - The Muslims of Sit Kwin were always a small group who numbered no more than 100 of the village's 2,000 people. But as sectarian violence led by Buddhist mobs spreads across central Myanmar, they and many other Muslims are disappearing. Their homes, shops and mosques destroyed, some end up in refugee camps or hide in the homes of friends or relatives. Dozens have been killed. ...

Source: http://news.yahoo.com/unlike-t-verizon-reportedly-putting-promotional-muscle-behind-142056565.html

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Imagine All the People Turning Blue And Green

Science Talk

Science writer Dennis Meredith talks about his new science fiction book The Rainbow Virus, in which a bioterror plot turns people all the colors of the rainbow.

More Science Talk

Science writer Dennis Meredith talks about his new science fiction book The Rainbow Virus, in which a bioterror plot turns people all the colors of the rainbow and more.


Source: http://rss.sciam.com/click.phdo?i=8074f573ae8017fefdf86f9685de7f62

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Razer Edge Pro


Razer is a well-known name in the gaming community, with its green glowing snake logo stamped on all manner of mice, keyboards, and other specialized peripherals. But Razer's newest toy?the Razer Edge Pro gaming tablet?is way more than a mere plaything. First announced as "Project Fiona" back at CES 2012, this unique device has been designed to be the tablet for PC gamers. It has been tweaked and polished over months and months of refinement with feedback from pro gamers and enthusiasts alike. Boasting a dual-core Intel Core i7-3517U Ivy Bridge processor with 8GB of RAM and an Nvidia GeForce GT 640M LE graphics card with 2GB of dedicated memory, the result is a potent Windows laptop with more graphics and gaming chops than most laptops?and easily topping tablets like the Microsoft Surface Pro?and a playing experience that brings the game closer to you while letting you take the game wherever you want to go. The Edge Pro is the rare device that reimagines what the PC experience should be and delivers something that's not just different, but better, putting a full-fledged Windows experience into a more portable design, with the hardware to use it on the go, at your desk, or in the living room. That it's made to let you game anywhere just makes it a lot more fun.

Design
The Edge Pro is big for a tablet, but it's extremely slim and light for anything remotely capable of serious gaming. Measuring 7 by 11 by 0.8 inches (HWD) and weighing 2.14 pounds, the Edge Pro is significantly thicker than other Windows tablets, like the Microsoft Surface Pro, which is just 0.53 inch thick, and weighs slightly less at two pounds. But for all this heft, you get a lot more in terms of hardware?the Edge Pro and its less expensive standard variant, the Core i5-powered Razer Edge, are also the only Windows tablets on the market today to offer both Intel Core processing and discrete graphics. As tradeoffs go, this is pretty worthwhile.

And let's not forget that even the slimmest, lightest gaming laptops are considerably less portable. Our previous Editors' Choice for portable gaming laptops, the Maingear Pulse 11, is 1.5 inches thick and weighs 3.7 pounds. Razer's own made-for-portability Razer Blade laptop is still 0.88-inch thick, and 6.6 pounds. On top of that, you aren't likely to use the laptop for gaming without at least adding a gaming mouse to the mix, and you'll need to find a table or desk to sit at while you play?but the Edge Pro lets you play anywhere, without needing a mouse for all games.

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On any other system the 10.1-inch IPS display and its 1,366-by-768 resolution would be small and inadequate?though it's the same resolution of the screen on the Maingear Pulse 11?but because you'll be bringing the Edge Pro so much closer to your face, the smaller size and lower resolution aren't much of an issue. For a larger display and higher resolution, the HDMI port found on the accessory console dock does output at 1080p.

On the back of the tablet, which is made of the same cool black aluminum seen on the Razer Blade, you'll find Razer's distinctive logo, with three intertwined snakes that glow green when powered on. When we tested the speaker quality on the Edge Pro, I was surprised by the quality of the sound. While there's no bass to speak of, the sound itself is significantly better than most tablets?there's no buzzing at high volumes, and the sound is fuller than the thin, tinny sound heard on other tablets.

Features
On the tablet you'll find a docking port (which doubles as your power connector), a headphone jack, and a full-size USB 3.0 port. The USB port is easy to spot, because it's the same brilliant green we saw on the Razer Blade. The Razer Edge Pro is equipped with 802.11n Wi-Fi and Bluetooth 4.0 + HS, so it will pair up with any wireless peripherals you want.

Inside, the Razer Edge Pro is equipped with a 256GB solid-state drive, in addition to the aforementioned Intel processor and Nvidia graphics card. All of those heat generating components also require a cooling fan, and this one gets humming pretty early on?it's the only tablet we've reviewed where fan noise is a concern. But that fan is indispensable, as I measured surface temperatures between 114 and 130 degrees at various points during testing and use. It got particularly warm in the upper right-hand corner, but you won't likely be using the tablet alone during the most intense gaming. A lot of this heat buildup is dealt with by using the accessory gamepad dock, shielding the hot surfaces from your touch and giving you two external handles to hold. Handling the tablet won't be an issue while using the tablet on the desktop/console dock.

While the Edge Pro is free of any bloatware or spurious software trials, it does come with Razer's Launcher dashboard for browsing and launching games, and also comes preinstalled with Steam, saving you the step of downloading it yourself. Additionally, the Edge Pro is designed for compatibility with Steam Big Picture Mode when connected to an HDTV through the console dock.

Razer covers the Edge Pro with a one-year warranty, with an extended warranty available ($199.99 direct) to stretch it to two, and also adds a year of coverage for power cable, console dock, and gamepad dock (except battery). Docks and accessories are also covered by a one-year warranty.

While the tablet design doesn't really make for a system you can upgrade and maintain in the same way you can tweak and optimize a desktop PC, Razer tells us that the SSD inside can indeed be swapped out by the user. But tinkerer's beware?doing so will void the warranty.

Our review unit came with two docks, the Gamepad Dock ($249.99 direct), and a desktop cradle called the Console Dock ($99.99 direct). A third accessory?a keyboard for laptop-style functionality?is expected to be available in Q3 of this year, but specific details about features, availability, and pricing weren't available as of this writing.

Source: http://feedproxy.google.com/~r/ziffdavis/pcmag/~3/5-2kImcMQ9E/0,2817,2417136,00.asp

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Florida lottery winners to share $1 million prize with co-worker

MIAMI (Reuters) - A dozen Florida real estate agents who pooled their money and won $1 million in the Powerball lottery plan to share the earnings with a new co-worker who decided not to join the office pool.

"I don't think of any of us would be enjoying this one-tenth if we did it any other way," said Laurie Finkelstein Reader, who leads a team of realtors at Keller Williams Partner Realty in Plantation, Florida.

The 12 realtors each contributed $20 for the March 23 Powerball drawing.

But Jennifer Maldonado, who had only been in her job for two weeks, declined an offer to join them because she hadn't received her first paycheck.

"I was trying to be frugal," Maldonado said. "I had other things I needed to spend my $20 on. I said, you know what guys, I'll just skip this one."

The group ended up with a winning ticket and a prize of $83,300 each after taxes.

After celebrating the news, Finkelstein Reader sent a text message to the other 11 co-workers asking if they would be willing to share a part of their winnings with Maldonado, and they all agreed.

Maldonado said she didn't know how much money she'll get, but she plans to use it to take her 4-year-old son to Disney World.

"How can you win and just leave one of your co-workers out?" said Finkelstein Reader. "It seemed to us the natural thing to do."

(Reporting by Kevin Gray; Editing by Leslie Gevirtz)

Source: http://news.yahoo.com/florida-lottery-winners-share-1-million-prize-co-233910699.html

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Thursday, March 28, 2013

Ex-CIA chief aided WWII hero's Arlington burial

ALBANY, N.Y. (AP) ? When Dr. Rene Joyeuse's request for burial at Arlington National Cemetery was rejected, the family of the decorated Swiss-born World War II spy launched a campaign to get the decision reversed. Months later, Joyeuse is getting his wish, thanks in part to the involvement of the nation's top covert operators, including CIA Director David Petraeus.

Before resigning amid a sex scandal last November, Petraeus played a key role in convincing Pentagon officials that Joyeuse, a retired doctor from upstate New York, deserved to lie in rest among some of America's greatest military heroes, people familiar with the situation told The Associated Press.

"It got attention at the highest levels, very high up. That's how important he (Joyeuse) was," said Charles Pinck, president of the OSS Society, whose membership includes a dwindling number of veterans of the Office of Strategic Services, the nation's World War II intelligence agency and forerunner of the CIA.

Petraeus, Pinck added, "took a lead role to get this approved."

A memorial service and inurnment of Joyeuse's cremated remains will be held Friday afternoon at Arlington. It will be a final tribute for a warrior spy-turned-surgeon who spent his post-war years pioneering heart research and emergency trauma care from New York to Hawaii.

"We're finally putting him somewhere he belongs," said Marc Joyeuse, the veteran's oldest of two sons. "Being a soldier, that's where he wanted to be."

It almost didn't happen. After Joyeuse died in June at 92 in Saranac Lake, N.Y., his family's request for his inurnment at Arlington was rejected because he hadn't served in the U.S. military. According to military records, Joyeuse worked for the OSS but was officially a member of the Free French Forces, enlisting after France's surrender to Germany in 1940.

Marc, his brother, Remi, and their mother, Suzanne, started an effort to have the decision reversed by the Department of the Army, which runs Arlington. They contacted Patrick K. O'Donnell, a military historian who had interviewed Joyeuse a decade earlier for a book on World War II espionage.

O'Donnell had met Petraeus several years earlier at a Wounded Warriors event when the four-star Army general was commanding American troops in Iraq and Afghanistan. Two weeks after Joyeuse's death, O'Donnell emailed Petraeus, describing the family's quest and the veteran's wartime heroics.

The exploits are straight out of a Hollywood movie: nighttime parachute drops behind enemy lines before the D-Day invasion in France, shootouts with SS troops, dodging Nazi collaborators, helping hundreds of downed American airmen elude capture. His actions earned him the Distinguished Service Cross, the nation's second-highest military honor, pinned on him by Gen. Dwight D. Eisenhower, supreme command of Allied forces in Europe.

"Someone once said the ideal OSS candidate was a Ph.D. who could handle himself in a bar fight," said Pinck, a private-sector security consultant whose father was an OSS agent. "I think Rene Joyeuse typified that."

Petraeus' emailed responses to O'Donnell in late June, copies of which the author shared with the AP, show the CIA director was "checking into it." On July 20, Petraeus wrote a letter to Secretary of the Army John McHugh, highlighting Joyeuse's accomplishments and supporting his family's request for a review of Arlington's decision.

At the bottom of the letter, a copy of which was also provided to the AP, Petraeus wrote: "The situation seems very unique and the rationale quite exceptional. It would mean a great deal to the agency family and its forerunner, the OSS. Many thanks ? Dave."

Other military members and intelligence operatives wrote letters in support of Joyeuse, including Adm. William McRaven, commander of the U.S. Special Operations Command. McRaven's letter referred to Joyeuse, who became a U.S. citizen in 1975, as "a true American patriot."

Asked whether the Petraeus and McRaven letters helped the family's cause, Maj. Chris Kasker, a spokesman for McHugh, responded in an email: "The letters were certainly appreciated and a testimony to the extraordinary contributions of Dr. Joyeuse to the United States military. But exceptions to policy are based on a variety of factors that look at the totality of one's service. Because of this, they are extremely rare."

On Nov. 9, a letter from the executive director of the Army National Military Cemeteries to Suzanne Joyeuse notified her that the family's request for burial at Arlington had been approved. It was the same day Petraeus resigned as director of CIA, acknowledging an extramarital affair with his biographer.

Messages left with Robert B. Barnett, Petraeus' lawyer, weren't returned.

While it might seem unusual for a CIA director to take interest in a veteran's burial dispute, in Joyeuse's case, Petraeus was paying homage to a fellow soldier-spy, said O'Donnell, whose latest book, "Dog Company," tells the story of U.S. Army Rangers in World War II.

"He is a soldier's soldier," O'Donnell said. "That was his motivation."

Source: http://news.yahoo.com/ex-cia-chief-aided-wwii-heros-arlington-burial-063033814.html

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LG Optimus G now shipping to the UK from Expansys

LG Optimus G

After a somewhat ridiculously long wait, the LG Optimus G is finally available in the U.K. from at least one retailer. Expansys, which put the phone up for pre-order just shy of a couple weeks ago, now has the device in stock and ready to ship. This is the same Optimus G we know and love, and its coming out of the box with Jelly Bean on board (rightfully so) compared to the ICS we saw at the initial release. The price has dropped just slightly from the pre-order, now £469.99 (incl. VAT) for the SIM-free version.

It may seem like old news if you've seen the Optimus G available for several months here in the states, but those of you in the U.K. still interested in picking one up can head to the source link below.

Source: Expansys



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Falcons agree to 2-year deal with Osi Umenyiora

ATLANTA (AP) ? The Atlanta Falcons found a replacement for John Abraham on Wednesday by reaching an agreement with free-agent defensive end Osi Umenyiora on a two-year, $8.5 million contract.

The Falcons released the 34-year-old Abraham, the team leader with 10 sacks in 2012, on March 1, the same day they also released running back Michael Turner and cornerback Dunta Robinson.

The team replaced Turner by signing Steven Jackson to a three-year, $12 million deal March 14. Now Umenyiora joins Jackson as Atlanta's second major free-agent addition.

The Falcons scheduled a news conference with Umenyiora for Thursday.

The 31-year-old Umenyiora gives the Falcons a slightly younger replacement at defensive end, but his production has declined in recent years. He had only six sacks for the Giants in 2012, when he started only four of 16 games. He had 55 tackles, five for losses, and one forced fumble.

He had a career-high 14? sacks in 2005, when he was a first-team All-Pro selection. He has reached double figures in sacks only one of the last four years ? 11? in 2010.

Umenyiora, 6-foot 3 and 255 pounds, was a second-round pick from Troy State by New York in 2003. He has 75 sacks, 31 forced fumbles and 13 fumble recoveries in his career and helped the Giants win two Super Bowl championships.

He set an NFL record with 10 forced fumbles in 2010 and a Giants record with six sacks in a 2007 win over Philadelphia.

The presence of defensive ends Jason Pierre-Paul and Justin Tuck made Umenyiora a part-time starter last season, but he'll be expected to replace Abraham as the Falcons' top pass-rusher. Defensive end Kroy Biermann was second on the Falcons with only 4 sacks last season.

Umenyiora's agent, Tom Condon, couldn't be immediately reached for comment.

Umenyiora made a brief reference to his new NFL home on his Twitter feed when he tweeted "(hash)RISE UP" ? the Falcons' slogan.

Source: http://news.yahoo.com/falcons-agree-2-deal-osi-umenyiora-015236611--nfl.html

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Mapping The Microbes That Flourish On Fruits And Veggies

You call it salad. The bacteria call it home.

iStockphoto.com

You call it salad. The bacteria call it home.

iStockphoto.com

Deadly microbes like salmonella and E. coli can lurk on the surface of spinach, lettuce and other fresh foods. But many more benign microbes also flourish there, living lives of quiet obscurity, much like the tiny Whos in Dr. Seuss' Whoville. Until now.

Scientists at the University of Colorado have taken what may be the first broad inventory of the microbes that live on strawberries, lettuce, tomatoes and eight other popular fresh foods.

It turns out the invisible communities living on our food vary greatly, depending on the type and whether it's conventional or organic.

Mung bean sprouts, for one, harbor very different bacteria than alfalfa sprouts. Grapes, apples and peaches house a greater variety of bacteria than veggies. And mushrooms are living in a microbial room of their own, sharing very few bacteria with the other foods tested.

That's quite different from strawberries, tomatoes and spinach. They had similar surface bacteria, with most coming from one family, the Enterobacteriaceae. That family includes E. coli but many, many other harmless and perhaps beneficial bacteria, too. Enterobacteriaceae was also the most common family, accounting for about one-third of all the microbes overall.

The good news: Most of the bacterial horde is benign.

Still, the sprouts "had a pretty high number of different types of bacteria associated with them, especially alfalfa sprouts," according to Jonathan Leff, an associate scientist at the Cooperative Institute for Research in Environmental Sciences at the University of Colorado, who led the study.

Dangerous bacteria on sprouts have caused numerous outbreaks, including one in Germany that killed at least 31 people.

Organic-labeled produce had different microbial communities than the conventionally grown food, with the organic microbes generally more diverse and the conventionally grown having more Enterobacteriaceae.

Is that good? We don't know. And we also don't know why they're different. "We can't say that this is attributable to the farming practice itself," Leff told The Salt. "It could be transport and storage."

Also on the don't-know list is how the differences in fruit and vegetable microbiomes affect human health. "We can't say how we should act in terms of our daily purchases or how we eat," Leff says.

But understanding the microbiomes of fruits and vegetables, he says, may ultimately make it possible to figure out ways to delay spoilage in fresh produce, or to learn how the food bacteria interact with each other and with the millions of bacteria in the human gut.

The researchers published their results in the online journal PLoS One.

Source: http://www.npr.org/blogs/thesalt/2013/03/27/175478950/mapping-the-microbes-that-flourish-on-fruits-and-veggies?ft=1&f=1007

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Justices Show Reluctance for Broad Marriage Ruling (WSJ)

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Source: http://news.feedzilla.com/en_us/stories/politics/top-stories/295093770?client_source=feed&format=rss

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Wednesday, March 27, 2013

Kerry in Paris to talk Syria with French

Secretary of State John Kerry arrives in Paris, Tuesday, March 26, 2013. Kerry went to Paris for talks with French officials about aid to the Syrian opposition and the situation in Mali. (AP Photo/Jason Reed, Pool)

Secretary of State John Kerry arrives in Paris, Tuesday, March 26, 2013. Kerry went to Paris for talks with French officials about aid to the Syrian opposition and the situation in Mali. (AP Photo/Jason Reed, Pool)

Secretary of State John Kerry presents a birthday cake to traveling CBS correspondent Margaret Brennan, right, during a flight from Kabul to Paris, Tuesday, March 26, 2013. Kerry went to Paris for talks with French officials about aid to the Syrian opposition and the situation in Mali. (AP Photo/Jason Reed, Pool)

Secretary of State John Kerry presents a birthday cake to traveling CBS correspondent Margaret Brennan, right, on a from Kabul to Paris, Tuesday, March 26, 2013. Kerry went to Paris for talks with French officials about aid to the Syrian opposition and the situation in Mali. (AP Photo/Jason Reed, Pool)

PARIS (AP) ? U.S. Secretary of State John Kerry is in Paris for talks with French officials about aid to the Syrian opposition and the situation in Mali.

Kerry arrived in the French capital Tuesday on the last leg of a five-nation trip that also took him to Israel, the Palestinian Authority and Jordan with President Barack Obama and then on his own to Iraq and Afghanistan.

He will see the French foreign minister on Wednesday. France is one of several European nations that would like to send military aid to the Syrian rebels. It also has been urging the U.S. to boost its assistance.

Kerry will also meet with French business leaders and entrepreneurs to discuss how to promote economic growth and create jobs on both sides of the Atlantic, said State Department spokeswoman Jennifer Psaki.

Associated Press

Source: http://hosted2.ap.org/apdefault/cae69a7523db45408eeb2b3a98c0c9c5/Article_2013-03-26-Kerry/id-68f1e45309074c0e8bea9a2b9291d0ca

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Scientists discover that DNA damage occurs as part of normal brain activity

Monday, March 25, 2013

Scientists at the Gladstone Institutes have discovered that a certain type of DNA damage long thought to be particularly detrimental to brain cells can actually be part of a regular, non-harmful process. The team further found that disruptions to this process occur in mouse models of Alzheimer's disease?and identified two therapeutic strategies that reduce these disruptions.

Scientists have long known that DNA damage occurs in every cell, accumulating as we age. But a particular type of DNA damage, known as a double-strand break, or DSB, has long been considered a major force behind age-related illnesses such as Alzheimer's. Today, researchers in the laboratory of Gladstone Senior Investigator Lennart Mucke, MD, report in Nature Neuroscience that DSBs in neuronal cells in the brain can also be part of normal brain functions such as learning?as long as the DSBs are tightly controlled and repaired in good time. Further, the accumulation of the amyloid-beta protein in the brain?widely thought to be a major cause of Alzheimer's disease?increases the number of neurons with DSBs and delays their repair.

"It is both novel and intriguing team's finding that the accumulation and repair of DSBs may be part of normal learning," said Fred H. Gage, PhD, of the Salk Institute who was not involved in this study. "Their discovery that the Alzheimer's-like mice exhibited higher baseline DSBs, which weren't repaired, increases these findings' relevance and provides new understanding of this deadly disease's underlying mechanisms."

In laboratory experiments, two groups of mice explored a new environment filled with unfamiliar sights, smells and textures. One group was genetically modified to simulate key aspects of Alzheimer's, and the other was a healthy, control group. As the mice explored, their neurons became stimulated as they processed new information. After two hours, the mice were returned to their familiar, home environment.

The investigators then examined the neurons of the mice for markers of DSBs. The control group showed an increase in DSBs right after they explored the new environment?but after being returned to their home environment, DSB levels dropped.

"We were initially surprised to find neuronal DSBs in the brains of healthy mice," said Elsa Suberbielle, DVM, PhD, Gladstone postdoctoral fellow and the paper's lead author. "But the close link between neuronal stimulation and DSBs, and the finding that these DSBs were repaired after the mice returned to their home environment, suggest that DSBs are an integral part of normal brain activity. We think that this damage-and-repair pattern might help the animals learn by facilitating rapid changes in the conversion of neuronal DNA into proteins that are involved in forming memories."

The group of mice modified to simulate Alzheimer's had higher DSB levels at the start?levels that rose even higher during neuronal stimulation. In addition, the team noticed a substantial delay in the DNA-repair process.

To counteract the accumulation of DSBs, the team first used a therapeutic approach built on two recent studies?one of which was led by Dr. Mucke and his team?that showed the widely used anti-epileptic drug levetiracetam could improve neuronal communication and memory in both mouse models of Alzheimer's and in humans in the disease's earliest stages. The mice they treated with the FDA-approved drug had fewer DSBs. In their second strategy, they genetically modified mice to lack the brain protein called tau?another protein implicated in Alzheimer's. This manipulation, which they had previously found to prevent abnormal brain activity, also prevented the excessive accumulation of DSBs.

The team's findings suggest that restoring proper neuronal communication is important for staving off the effects of Alzheimer's?perhaps by maintaining the delicate balance between DNA damage and repair.

"Currently, we have no effective treatments to slow, prevent or halt Alzheimer's, from which more than 5 million people suffer in the United States alone," said Dr. Mucke, who directs neurological research at Gladstone and is a professor of neuroscience and neurology at the University of California, San Francisco, with which Gladstone is affiliated. "The need to decipher the causes of Alzheimer's and to find better therapeutic solutions has never been more important?or urgent. Our results suggest that readily available drugs could help protect neurons against some of the damages inflicted by this illness. In the future, we will further explore these therapeutic strategies. We also hope to gain a deeper understanding of the role that DSBs play in learning and memory?and in the disruption of these important brain functions by Alzheimer's disease."

###

Gladstone Institutes: http://www.gladstone.ucsf.edu

Thanks to Gladstone Institutes for this article.

This press release was posted to serve as a topic for discussion. Please comment below. We try our best to only post press releases that are associated with peer reviewed scientific literature. Critical discussions of the research are appreciated. If you need help finding a link to the original article, please contact us on twitter or via e-mail.

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Source: http://www.labspaces.net/127429/Scientists_discover_that_DNA_damage_occurs_as_part_of_normal_brain_activity

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NASA to restore Apollo engines found on ocean floor

The recovery of the Apollo 11 rocket engines by Amazon CEO Jeff Bezos is a historic find, say NASA officials, who say the agency plans to restore the engines.

By Nancy Atkinson,?Universe Today / March 22, 2013

The thrust chamber of one of five first stage F-1 rocket engines used to launch one of NASA's mighty Saturn V rocket on a historic Apollo moon mission is seen on the floor of the Atlantic Ocean in this Bezos Expeditions image.

Bezos Expeditions

Enlarge

Last year, Amazon.com founder Jeff Bezos announced that he had located some of the Apollo F-1 rocket engines and planned to recover them. He and his Bezos Expedition team were successful in recovering engines that helped power Apollo astronauts to the Moon and have now brought ?a couple of your F-1s home,? Bezos said in a message to NASA. On the Bezos Expedition website, Bezos called the recovery ?an incredible adventure.?

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NASA was happy about the recovery as well.

?This is a historic find and I congratulate the team for its determination and perseverance in the recovery of these important artifacts of our first efforts to send humans beyond Earth orbit,? said NASA Administrator Charlie Bolden in a statement. ?We look forward to the restoration of these engines by the Bezos team and applaud Jeff?s desire to make these historic artifacts available for public display.?

There is no indication so far from Bezos of which flight these engines were from. Last year when Bezos made his announcement, he said they had found the engines from Apollo 11, but it may be been difficult to determine exactly which flight the ones found were from. In total, NASA launched 65 F-1 engines, five per flight, on 13 Saturn V boosters between 1967 and 1973. Supposedly there would be serial numbers to make the identification of which flight these engines were from. Bezos indicated on his blog they were still on the ship, so perhaps the identification will come later.

Five F-1 engines were used in the 138-foot-tall S-IC, or first stage, of each Saturn V, which depended on the five-engine cluster for the 7.5 million pounds of thrust needed to lift it from the launch pad. Each of the engines stands 19 feet tall by 12 feet wide and weigh over 18,000 pounds.

Bezos and his team spent three weeks at sea, working almost 3 miles below the surface. ?We found so much,? Bezos wrote. ?We?ve seen an underwater wonderland ? an incredible sculpture garden of twisted F-1 engines that tells the story of a fiery and violent end, one that serves testament to the Apollo program. We photographed many beautiful objects in situ and have now recovered many prime pieces. Each piece we bring on deck conjures for me the thousands of engineers who worked together back then to do what for all time had been thought surely impossible.?
See more images and descriptions at the Bezos Expeditions website.

Source: http://rss.csmonitor.com/~r/feeds/science/~3/bouK2n0cLKk/NASA-to-restore-Apollo-engines-found-on-ocean-floor

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Meeting broad, varied, competing priorities in conservation

Mar. 25, 2013 ? Solutions that meet the broad, varied, and often competing priorities of conservation are difficult to come by. Research published in the March 28 edition of the Proceedings of the National Academy of Sciences takes a hard look at why, in an effort to find ways to resolve the issue.

"People often think of conservation solutions that are effective, cost-efficient, and equitable -- the so-called triple bottom line solutions -- as the holy grail, the best possible outcome," said Ben Halpern, researcher at UC Santa Barbara's National Center for Ecological Analysis and Synthesis (NCEAS), and the lead author of the paper titled, "Achieving the triple bottom line in the face of inherent trade-offs among social equity, economic return and conservation."

As stakeholders, conservationists, and governments work diligently to achieve cost-efficient and effective conservation solutions that are also fair, it becomes obvious that reaching one goal often comes at the expense of another.

"We developed and tested methods for discovering these ideal solutions and found a surprising result," said Halpern. "As you increase the equity of how conservation benefits are distributed to people, you compromise your ability to maximize conservation outcomes."

To examine the relationship of equity, which relates to how a person or group perceives the relative availability (or deprivation) of resources, to the other conservation goals in the triple bottom line, the researchers used three very different case studies dealing with marine conservation to test their ideas: the process to create marine protected areas (MPAs) off the central coast of California; the southeast Misool MPA in Raja Ampat in eastern Indonesia; and the Coral Triangle in southeast Asia. In each case, as conservation scores and outcomes were increased (usually the result of limiting access to certain areas or the amount and/or species that can be taken from those areas), equity declined.

Meanwhile, the study also showed that both equity and conservation could be achieved, but by raising total budgets, sacrificing the goal of cost-efficiency.

Although triple bottom line outcomes are touted as ideal, said Halpern, the reality is that few people probably actually want such outcomes.

"Different people have more or less invested in managed systems and so don't necessarily expect to receive equal benefits," he said. "For example, if I've fished a place for 40 years and based my entire livelihood on that, whereas my neighbor just moved to town and fishes once a month recreationally, why should we be treated equally when it comes to making decisions about managing fisheries?"

Carissa Klein, a co-author from The University of Queensland, pointed out that "although equity can compromise conservation outcomes, it plays a significant role in conservation." Highly inequitable solutions, according to the study, decrease the likelihood of success because those disenfranchised have little motivation to adhere to conservation programs. But, while increased equity increases the likelihood of self-enforcement, it is also likely that ignoring a vocal and powerful minority will lower the chances of success.

So are there any decisions that can guarantee achieving the triple bottom line of effectiveness, cost-efficiency, and equitable conservation outcomes? Yes and no, said Klein. "It depends some on how one defines equity, and people have different types of equity that they care about. It may be easy to have equity in stakeholder engagement, i.e. all affected parties engaged in the process of making a decision, even if the outcome is inequitable. This may ultimately satisfy all the stakeholder groups."

"There's no single way to achieve triple bottom line outcomes," said Halpern. "Instead, we provide a tool for transparently and quantitatively understanding where, why, and how one can increase the chances of achieving these outcomes, and in which cases it is not likely possible," he said.

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The above story is reprinted from materials provided by University of California - Santa Barbara.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. Benjamin S. Halpern, Carissa J. Klein, Christopher J. Brown, Maria Beger, Hedley S. Grantham, Sangeeta Mangubhai, Mary Ruckelshaus, Vivitskaia J. Tulloch, Matt Watts, Crow White, and Hugh P. Possingham. Achieving the triple bottom line in the face of inherent trade-offs among social equity, economic return, and conservation. PNAS, March 25, 2013 DOI: 10.1073/pnas.1217689110

Note: If no author is given, the source is cited instead.

Disclaimer: Views expressed in this article do not necessarily reflect those of ScienceDaily or its staff.

Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_environment/~3/-OljYiPYlow/130325160630.htm

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Tuesday, March 26, 2013

You don't 'own' your own genes: Researchers raise alarm about loss of individual 'genomic liberty' due to gene patents

Mar. 25, 2013 ? Humans don't "own" their own genes, the cellular chemicals that define who they are and what diseases they might be at risk for. Through more than 40,000 patents on DNA molecules, companies have essentially claimed the entire human genome for profit, report two researchers who analyzed the patents on human DNA.

Their study, published March 25 in the journal Genome Medicine, raises an alarm about the loss of individual "genomic liberty."

In their new analysis, the research team examined two types of patented DNA sequences: long and short fragments. They discovered that 41 percent of the human genome is covered by longer DNA patents that often cover whole genes. They also found that, because many genes share similar sequences within their genetic structure, if all of the "short sequence" patents were allowed in aggregate, they could account for 100 percent of the genome.

Furthermore, the study's lead author, Dr. Christopher E. Mason of Weill Cornell Medical College, and the study's co-author, Dr. Jeffrey Rosenfeld, an assistant professor of medicine at the University of Medicine & Dentistry of New Jersey and a member of the High Performance and Research Computing Group, found that short sequences from patents also cover virtually the entire genome -- even outside of genes.

"If these patents are enforced, our genomic liberty is lost," says Dr. Mason, an assistant professor of physiology and biophysics and computational genomics in computational biomedicine at the Institute for Computational Biomedicine at Weill Cornell. "Just as we enter the era of personalized medicine, we are ironically living in the most restrictive age of genomics. You have to ask, how is it possible that my doctor cannot look at my DNA without being concerned about patent infringement?"

The U.S. Supreme Court will review genomic patent rights in an upcoming hearing on April 15. At issue is the right of a molecular diagnostic company to claim patents not only on two key breast and ovarian cancer genes -- BRCA1 and BRCA2 -- but also on any small sequence of code within BRCA1, including a striking patent for only 15 nucleotides.

In its study, the research team matched small sequences within BRCA1 to other genes and found that just this one molecular diagnostic company's patents also covered at least 689 other human genes -- most of which have nothing to do with breast or ovarian cancer; rather, its patents cover 19 other cancers as well as genes involved in brain development and heart functioning.

"This means if the Supreme Court upholds the current scope of the patents, no physician or researcher can study the DNA of these genes from their patients, and no diagnostic test or drug can be developed based on any of these genes without infringing a patent," says Dr. Mason.

One Patented Sequence Matched More Than 91 Percent of Human Genes

Dr. Mason undertook the study because he realized that his research into brain and cancer disorders inevitably involved studying genes that were protected by patents.

Under U.S. patent law, genes can be patented by those researchers, either at companies or institutions, who are first to find a gene that promises a useful application, such as for a diagnostic test. For example, the patents received by a company in the 1990s on BRCA1 and BRCA2 enables it to offer a diagnostic test to women who may have, or may be at risk for, breast or ovarian cancer due to mutations in one or both of these genes. Women and their doctors have no choice but to use the services of the patents' owner, which costs $3,000 per test, "whereas any of the hundreds of clinical laboratories around the country could perform such a test for possibly much less," says Dr. Mason.

The impact on these patents is equally onerous on research, Dr. Mason adds.

"Almost every day, I come across a gene that is patented -- a situation that is common for every geneticist in every lab," says Dr. Mason.

Dr. Mason and his research partner sought to determine how many other genes may be impacted by gene patents, as well as the overall landscape of intellectual property on the human genome.

To conduct the study, Dr. Mason and Dr. Rosenfeld examined the structure of the human genome in the context of two types of patented sequences: short and long fragments of DNA. They used matches to known genes that were confirmed to be present in patent claims, ranging from as few as 15 nucleotides (the building blocks of DNA) to the full length of all patented DNA fragments.

Before examining the patented sequences, the researchers first calculated how many genes had common segments of 15 nucleotide (15mer), and found that every gene in the human genome matched at least one other gene in this respect, ranging from as few as five matches 15mer to as many as 7,688 gene matches. They also discovered that 99.999 percent of 15mers in the human genome are repeated at least twice.

"This demonstrates that short patent sequences are extremely non-specific and that a 15mer claim from one gene will always cross-match and patent a portion of another gene as well," says Dr. Mason. "This means it is actually impossible to have a 15mer patent for just one gene."

Next, researchers examined the total sequence space in human genes covered by 15mers in current patent claims. They found 58 patents whose claims covered at least 10 percent of all bases of all human genes. The broadest patent claimed sequences that matched 91.5 percent of human genes. Then, when they took existing gene patents and matched patented 15mers to known genes, they discovered that 100 percent of known genes are patented.

"There is a real controversy regarding gene ownership due to the overlap of many competing patent claims. It is unclear who really owns the rights to any gene," says Dr. Rosenfeld. "While the Supreme Court is hearing one case concerning just the BRCA1 patent, there are also many other patents whose claims would cover those same genes. Do we need to go through every gene to look at who made the first claim to that gene, even if only one small part? If we resort to this rule, then the first patents to be granted for any DNA will have a vast claim over portions of the human genome."

A further issue of concern is that patents on DNA can readily cross species boundaries. A company can have a patent that they received for cow breeding and have that patent cover a large percentage of human genes. Indeed, the researchers found that one company owns the rights to 84 percent of all human genes for a patent they received for cow breeding. "It seems silly that a patent designed to study cow genetics also claims the majority of human genes," says Dr. Rosenfeld.

Finally, they also examined the impact of longer claimed DNA sequences from existing gene patents, which ranged from a few dozen bases up to thousands of bases of DNA, and found that these long, claimed sequences matched 41 percent (9,361) of human genes. Their analysis concluded that almost all clinically relevant genes have already been patented, especially for short sequence patents, showing all human genes are patented many times over.

"This is, so to speak, patently ridiculous," adds Dr. Mason. "If patent claims that use these small DNA sequences are upheld, it could potentially create a situation where a piece of every gene in the human genome is patented by a phalanx of competing patents."

In their discussion, the researchers argue that the U.S. Supreme Court now has a chance to shape the balance between the medical good versus inventor protection, adding that, in their opinion, the court should limit the patenting of existing nucleotide sequences, due to their broad scope and non-specificity in the human genome.

"I am extremely pro-patent, but I simply believe that people should not be able to patent a product of nature," Dr. Mason says. "Moreover, I believe that individuals have an innate right to their own genome, or to allow their doctor to look at that genome, just like the lungs or kidneys. Failure to resolve these ambiguities perpetuates a direct threat to genomic liberty, or the right to one's own DNA."

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Story Source:

The above story is reprinted from materials provided by Weill Cornell Medical College.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. Jeffrey Rosenfeld, and Christopher E Mason. Pervasive sequence patents cover the entire human genome. Genome Medicine, 2013 (in press) DOI: 10.1186/gm431

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/~3/jAfUr59mL1E/130326101614.htm

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