A start-up is by definition lacking in experience. And though a few lucky ones have veteran leaders who’ve been through the process before, that’s the exception rather than the rule when it comes to university spinouts. It stands to reason, then, that start-up managers are in dire need of best practices, and that’s exactly what Georgia Tech’s Advanced Technology Development Center (ATDC) is delivering. The center has posted a series of best practice documents on its website in an attempt to reach out to more of the region’s start-ups than it can work with directly. “We’ve been trying to reach beyond the bricks and mortar of Georgia Tech, to figure out how to help accelerate companies that for some reason aren’t good candidates for our incubator,” says Stephen Fleming, vice provost of Tech’s Enterprise Innovation Institute and acting director of ATDC, a start-up accelerator. “How do we scale and reach people who we don’t share a water fountain with? One avenue is a better set of resources. These best practices are things we’ve been sharing with our existing clients for a long time,” Fleming comments. Several of those best practices – focusing on elevator pitches, business plan summaries, and investor communications – are detailed in an article in the December issue of Technology Transfer Tactics. For subscription information, CLICK HERE.
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GM Will Crank Cars 24-Hours A Day In Bid To Surpass Toyota In Efficiency
General Motors (GM) plans to experiment with running auto factories 24-hours a day.
It’s a bold move to become the most efficient auto producer in the world.
Even Toyota (TM) doesn’t run 24-hours, despite the fact that in many other industries 24-7 factories are common.
Given GM’s current overcapacity, this means that some factories will experiment with this new 24-hour operation, while others will be shuttered.
WSJ: The move comes as GM is closing other plants around the country. That means the 23-year-old Kansas City factory, which will add more than 900 jobs, as well as two other GM plants scheduled later for a third shift will become boom towns of sorts as other plants go dark.
What’s shocking is how, traditionally, only operating 69% of the days in a year used to be considered running at 100% capacity.
That’s no accident. The Obama administration auto task force that oversaw GM’s reorganization last spring was startled to learn that the industry standard for plants to be considered at 100% capacity was two shifts working about 250 days a year. In recommending that the government invest about $50 billion in GM, the task force urged the company to strive toward operating at 120% capacity by traditional standards.
Keep in mind that was just two shifts working 250 days a year, which is 500 shifts. Three shifts working 365 days could theoretically create output could be 1,085 shifts. That means that true output potential, from the same factories simply run more intensely could be 120% more than the industry currently imagines.
Yet some in the auto industry question whether 24-hour operation would ever be possible.
But industry manufacturing experts are skeptical, noting that the federal task force had limited automotive experience. “Do those guys understand the business?” asked Ron Harbour, whose Harbour Report is a widely followed analysis of auto-plant efficiency.
But come on, 24-hour operation has to be possible, even if difficult at first. The same goes for working more the 250 days a year.
In the long-run if done well, maximum intensity just makes sense from an efficiency stand point. In the future we’ll probably laugh about two shifts x 250 days a year. If we can fit entire libraries of data inside a mobile phone, or create biologically engineered drugs, running an auto factory 24 hours a day surely must be within reach as well.
Hopefully this GM gamble works out — and hopefully the auto union doesn’t prevent it from becoming the standard.
Join the conversation about this story »
See Also:
- Microsoft’s Departing CFO Joins GM As CFO And Vice-Chair
- GM CEO Fritz Henderson Stepping Down
- Fritz Henderson’s Daughter Calls GM Chairman "A SELFISH PIECE OF SH*T"
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CSU spinoff to commercialize “3D” Li-ion battery technology
Colorado State University’s clean energy commercialization arm, Cenergy, has co-founded Prieto Battery to manufacture charge insertion (Li-ion) batteries using a 3D structure to enable a larger functional surface area. The resulting batteries are cheaper, up to 1,000 times more powerful, and 10 times longer lasting than traditional batteries, according to CSU. Using an electrodeposition process, Amy Prieto, PhD, assistant professor of chemistry, grows nanowires that comprise the anode — the first key piece of the battery. She uses electrodeposition again to coat the tiny structures with a polymer electrolyte. Cathode material then is added around the coated nanowires, resulting in a three-dimensional battery. The nanowires that make up the anode cover a surface area that is 10,000 times greater than a traditional battery, Prieto says. The high number of three-dimensional wires creates a much larger functional surface area than other current batteries. According to Prieto, the electrodeposition manufacturing method is fast and inexpensive, allowing the technology to be scaled up to create batteries that can be used for everything from pacemakers to automobiles.
Prieto Battery is the first start-up produced by Cenergy. Prieto, who also serves as chief scientific officer for the new company, expects to demonstrate the first prototype of the battery by early next year. In February 2009, CSU’s TTO applied for a patent that encompasses all Prieto Battery technology. The patent has been exclusively licensed to the start-up. Bohemian Asset Management in Fort Collins, a privately held division of the Bohemian Cos., supplied the first round of funding for the company.
Source: Green Car Congress
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McChip introduces Ford Focus RS with 401 horses – Are you lovin’ it?
Filed under: Aftermarket, Performance, Hatchback, Ford, UK
401-hp Ford Focus tuned Mcchip-dkr – Click above for high-res image galleryThere are few things we love more than hooning around in a vigorous, purebred sports car – and that’s exactly how Mcchip-dkr describes its 401-horsepower Ford Focus RS. That’s the Stage 2 version delivering the “whole-blood athlete,” but if you want to work your way up to those heights, you can get the Stage 1 conversion for €799 ($1,142 USD). You’ll take your hatch from 301 stock horsepower to 345 and bump torque by about 50 lb-ft to 383 with an ECU upgrade.
But if 401 is your lucky horsepower number and you like the sound of 457 lb-ft. of torque, then you’ll need €4,499 ($6,421 U.S.). That pile of pounds will give you access to a new manifold, uprated intercooler, spark plugs, and a sports exhaust as well as the necessary ECU tweaks. Mcchip-dkr thankfully didn’t do anything regrettable to the Focus RS’ already terrific looks. What they’ve done with torque steer outside of the stock RS’ trick Revoknuckle and limited-slip setup is anyone’s guess.
Have a look at the press release after the jump, and there are more images of the car in the high-res gallery below.
Gallery: Mcchip-dkr Focus RS
[Source: Mcchip-dkr]
Continue reading McChip introduces Ford Focus RS with 401 horses – Are you lovin’ it?
McChip introduces Ford Focus RS with 401 horses – Are you lovin’ it? originally appeared on Autoblog on Tue, 22 Dec 2009 13:59:00 EST. Please see our terms for use of feeds.
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Attorneys to reveal strategies for slashing patent prosecution costs
Getting more out of your patent budget is more critical than ever in the current economic climate. And though these costs may seem largely outside your control, there are dozens of specific strategies you can adopt to significantly reduce your legal bills while improving overall patent quality. Technology Transfer Tactics’ Distance Learning Division has secured two top patent attorneys with numerous TTO clients to guide your efforts and stretch the dollars you spend on patent research, applications, filings and prosecution. On February 9, 2010, join Jean Baker, PhD, JD, head of the Intellectual Property Group at Quarles & Brady, and Jack Cook, JD, leader of the firm’s Research Institutions-Industry Team, for Patent Prosecution: Best Practices for Reducing Costs While Improving Patent Quality. They’ll provide cost-saving insights gained from years of working closely with and advising TTOs worldwide, with a singular focus on getting more out of your legal team, spending less, and enhancing patent quality even as billings decline. CLICK HERE for details and to register.
And don’t miss these outstanding audioprograms coming in January:
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Vytorin Update: Cancer Risk, Generic Challenge
A couple pieces of news today on Merck’s big cholesterol drug Vytorin, which has seen its share of trouble in the past couple years but remains widely prescribed:The FDA said it’s “unlikely” that Vytorin or Zetia, another Merck drug, increase the risk of cancer. But “an association cannot be definitively ruled out,” the agency said. Vytorin is a combination of two drugs — Zetia and a statin called simvastatin. It’s clear that simvastatin doesn’t raise cancer risk, the FDA said, but there’s not enough data to “definitively rule out” a cancer link for Zetia (known generically as ezetimibe).
The uncertainty comes from a study that found there were more cancers and cancer-related deaths in patients who took Vytorin, compared with those who received placebo. But other studies of the drug have not shown similar risk. Animal studies have not shown a cancer link. And the cancer risk found in the study came from combining several types of cancer together. “It is biologically less likely that a single drug increases the risk of a wide variety of cancer types,” the FDA said.
Mylan, a big generics shop, said it had been sued by a Merck subsidiary for patent infringement because it applied to sell a generic version of Vytorin.
This is is the kind of lawsuit generic drug makers wear like a badge of honor these days. In its statement today, Mylan said it believes it is the first generic company to file this sort of application for Vytorin; if the company is correct, it will get a six-month window during which it’s the only generics company allowed to compete against Merck for sales of the drug.
An exclusivity period on a big drug like Vytorin — and it’s still a very big drug, despite the troubles it’s had — means a windfall for a company like Mylan.
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R&D Spending: Numbers for Pfizer, J&J, Merck, Lilly and Bristol
U.S. investment in R&D fell slightly this year, and is expected to start growing again next year, according to a new report out from the Battelle Memorial Institute, a nonprofit group that looks at that sort of thing.A story in this morning’s WSJ has more on the issue; Health Blog readers may be particularly interested in some numbers from the report on R&D spending at big U.S. drug companies.
Of course, company-by-company figures like these don’t tell the whole story, in part because of the effects of consolidation. For example, Pfizer’s R&D spending may climb next year because of the Wyeth acquisition, but continuing cuts could mean the company’s R&D spending is lower than this year’s combined R&D spending for Pfizer and Wyeth.
Nevertheless, a numbers dump can still be interesting. Here it is:
R&D Spending, in millions of dollars
Company Q1-Q3, ‘08 Q1-Q3, ‘09 Change Pfizer $5,642 $5,032 -10.8% J&J $5,469 $4,773 -12.7% Merck $3,419 $3,874 13.3% Eli Lilly $2,782 $3,110 11.8% Bristol-Myers Squibb $2,442 $2,590 6.1 Photo: Associated Press
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Cascade ProDrug, U-Oregon acquire Novacea technology
Cascade ProDrug, Inc., and the University of Oregon, both in Eugene, have completed an agreement that gives the company exclusive ownership of technology to create medicines that “turn on” in oxygen-starved tissues. The innovation could lead to improved treatments for cancer and other diseases marked by excessive cell growth. Under the terms of the deal, Cascade ProDrug becomes sole owner of a bundle of experimental compounds, technical data, and patent rights that previously belonged to Novacea, Inc. — a publicly traded corporation that merged with Transcept Pharmaceuticals, Inc., in February 2009. Novacea had generated the technology package focusing on a biochemical mechanism known as “hypoxia activation” during an R&D collaboration with the laboratory of John Keana, PhD, professor of synthetic organic chemistry, medicinal chemistry, and polymer surface functionalization at UO and the holder of more than 70 U.S. patents. When Novacea changed its R&D focus in 2008, UO acquired the technology to create the nucleus of a new spinout. The Cascade ProDrug deal provides UO with an equity stake in the company and royalties from any patented products that reach the marketplace. Cascade ProDrug also provided Transcept Pharmaceuticals a consideration package as part of the agreement.
Cascade ProDrug is developing targeted therapeutics against hyperproliferative diseases. The company’s initial focus is on anti-cancer medicines activated by tumor hypoxia. The platform technology acquired from UO enables the company to reformulate existing chemotherapy agents with the potential to make them safer and more effective in treating solid tumors. The body of work completed by Novacea and UO provides Cascade ProDrug a head start on a series of lead compounds, and Cascade ProDrug intends to contract research for final stages of preclinical trials and push toward the filing of an investigational new drug with the U.S. Food and Drug Administration.
Source: Newswise
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It’s Official: Wall Street Really Is Run By The Evil Empire
This is pretty much the perfect metaphor for 2009: Darth Vader ringing the opening bell at the New York Stock Exchange surrounded by a goon squad of Storm Troopers.
Join the conversation about this story »
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Singapore-French nanotechnology laboratory opens
Two months after the Nanyang Technological University (NTU) signed a Memorandum of Understanding in Paris with the National Center for Scientific Research (CNRS) and the Thales Group of Companies to set up a joint research laboratory, the three parties are inaugurating the CNRS-International-NTU-Thales Research Alliance (CINTRA) Laboratory at NTU. The CINTRA Laboratory aims to develop nanotech innovations for computing, sensing, and communications applications. Over the next two years, about 50 Singapore and French researchers will work on critical challenges faced by existing technologies in the microelectronic and photonic industries to develop innovations that will meet future commercial, defense, and security needs. The application-driven challenges include the development of enabling technologies such as an imaging chip to process and display real-time multi-dimensional information and a low-power signal processing chip capable of super high-speed performance of a trillion bits (terabits) per second or more. The alliance brings together a research center, a university, and a private company to capitalize on fundamental research, applied research, and technology transfer, according to Olivier Caron, French Ambassador to Singapore. “This model should not only drive breakthroughs in innovation but should also result in bringing these innovations to the market,” Caron says.
Source: Nanowerk
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Beyonce to make appearance at Lady Gaga’s LA concert?
Lady Gaga may be surprising fans with appearances from Beyonce and Kanye West during her three concerts in LA. The 23-year-old recently kicked off three shows at Nokia Theatre LA Live and although her rep won’t confirm, E! online claims Beyonce, 28, and West, 32, will make appearances.
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Beyonce to perform at the 2010 Grammy Awards
Taylor Swift and Beyonce are among the artists set to perform next month at the 52nd annual Grammy Awards in Los Angeles, it was announced Tuesday. Other performers include the Black Eyed Peas, Maxwell and country trio Lady Antebellum. The Recording Academy said other performers will be announced later.
Beyonce, a 10-time Grammy winner, has 10 nominations, including record of the year for ‘Halo,’ album of the year for ‘I Am … Sasha Fierce’ and song of the year for ‘Single Ladies (Put a Ring on It).’ Country singer Swift has eight nominations, including record and song of the year for ‘You Belong With Me,’ and album of the year for ‘Fearless.’
The Grammy Awards will be presented at the Staples Center on January 31st. The show will air on CBS.
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Quick Holiday Appetizer: Beer Dip Recipe
During the Holidays the last thing anyone wants to think about (other then the big feast) is making appetizers. If anything we all want something that is fast, takes little effort to put together, and still tastes like a gourmet chef made it.
The best solution is to make a dip, nothing too fancy, but one that will probably last for a total of five minutes because it’s that good. Try making Beer Dip! Chances are you have beer in the fridge if you have guests coming over and the other ingredients you definitely have in the fridge.
Beer Dip Recipe
Ingredients:
2 packages (8 ounces each) cream cheese, softened
1/3 cup beer or nonalcoholic beer
1 envelope ranch salad dressing mix
2 cups (8 ounces) shredded cheddar cheese
Pretzels or Pita
Directions:
1. In a large mixing bowl, beat the cream cheese, beer and dressing mix until smooth. Stir in cheese. Serve with pretzels.
***
Beer is such an awesome thing to make food with. People underestimate it’s qualities and the different flavors and complexity beers have.
Happy Holidays!
Recipe Source: Beer Dip by Michelle Long in The Taste of Home Cookbook
Image Credit: iStockPhoto
Post from: Blisstree
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7 Reasons Why A Christmas Eve Vote On Health Care Would Be The Worst Gift Ever
(This guest post originally appeared at New Deal 2.0)
The Senate and the Obama Administration want to pass the Senate version of health care reform by Christmas Eve. In the end, the Senate probably will pass a bill. The nation, however, would be a lot better off if the Senate did not vote. Here’s why.
First, this legislation has become no more than a (bad) effort at insurance reform. It does not encompass any serious approach to reforming health care itself, which is by far the bigger problem.
Second, as health insurance itself it is a bad approach. As a small example, it does not even increase competition by allowing cross-state competition by insurers. So it guarantees 50 smaller state markets, each run by a somewhat different state insurance bureaucracy, most of the markets being too small to support real competition. Progressives wasted immense time touting a public option as a competitive measure — which it never could have been; but completely ignored dealing with markets directly so as to make them more competitive. The direction I have pointed to in previous blogs — making the exchanges the true center of reform — was never considered or never understood. (That’s another topic. It is scary how little is ever really understood about complicated legislation by the members of Congress who vote on it. In talking to several members a few months ago about health care, one told me that he estimated less than 10% of the members of the House could actually tell you the difference between Medicare and Medicaid.)
Third, the myriad of small projects and experiments included in the bill and intended to try out various approaches to health care reform all add up to nothing. There will be a few earnest efforts, but they will point to difficult health care choices which the House and the Senate have indicated they do not want to make. I do not have anything against most of these efforts, I just think that like the poem, “they don’t do any good, and they don’t do any harm.” They certainly are not a reason to pass legislation this important.
Fourth, as this bill, if it were to pass, heads toward conference with the House bill — which is worse — none of us know what will emerge, but we know one thing with great certainty. The result will be worse than the Senate bill. The conference is part of the process to produce anything, but no one has ever thought it made anything any better. The process is dedicated to testing the lowest limits of the barely acceptable.
Fifth, this bill will not slow down health care cost growth. There is absolutely no one in the known universe whether for or against this bill who in private would not agree with that statement. It is possible for the CBO, working on a very carefully phrased question and doing a static analysis, to conclude that the revenue raised by the bill will very slightly exceed the costs imposed. But even that is probably not the case. So the bill will increase the deficit; therefore cut into every other public program you might care about — kiss goodbye to any real infrastructure investment; and make even worse our long run debt problem without improving anything. One or two people commenting on my blogs have called me a “deficit terrorist,” a phrase I love and am having tee shirts made for; but the long run deficit and debt problems we face really do impose a different kind of discipline on us.
Sixth, all of the political dynamics I have ever seen work against any future effort — after this bill passes — to improve its direction. Senator Rockefeller has said that he expects annual efforts to improve legislation after it passes. That is a complete fantasy. This bill gives everything away up front, and does not face up to any of the really difficult questions of cost and reform. There is no theory anyone can state with a straight face that gets you to a reasonable expectation that if we let this one go by, it will become steadily better.
Finally, we have begun to hear the dreaded song. When a supporter of something says with a sense of irritation and superior practicality that we “can’t let the best be the enemy of the good,” you know that he or she has run out of arguments and is reverting to shouting. If you play poker — I have played fairly seriously for 45 years — you learn to read the “tells.” This song is a completely dependable “tell.”
The best process going forward would start with the Senate not voting. Then the Obama Administration, which now has a more fully matured policy process with much firmer grounding then it did when this health issue began — prematurely in my view — last spring, could put forward a clear set of views regarding what it wanted and did not want in terms of policy. Ideally, we could then start with a sense of how to alter the fundamental incentives of the system; and we could make the changes step by step. An early step, for example, could be to insure all minors below the age of 18. In any case, I do not think it is wise to try to change in a fundamental way 17% of the largest economy in the world all at one jump.
Roosevelt Institute Braintruster Bo Cutter is formerly a managing partner of Warburg Pincus, a major global private equity firm. Recently, he served as the leader of President Obama’s Office of Management and Budget (OMB) transition team.
Join the conversation about this story »
See Also:
- DEJA VU: Alabama Congressman Switches Parties To GOP On Eve Of Healthcare Vote
- 10 New Taxes Americans Will Get Slapped With To Pay For Healthcare
- Inches Away From Finish Line, Abortion Divide May Still Torpedo Healthcare Bill
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Isabeli Fontana

Victoria’s Secret supermodel Isabeli Fontana goes topless for Homem Vogue. The 26-year-old Brazilian enchanter struts her flawless figure in this photo spread shot by Jacques Dequeker.
Continue reading for more images.
Source: Egotastic
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FDA Finds It Unlikely That Vytorin Or Zetia Increases Risk Of Cancer, But Such A Link Is Possible
December 2009 Update From FDA For Its August 2008 Early Communication About Safety Review of Ezetimibe / Simvastatin (Vytorin) And Ezetimibe (Zetia)
(Posted by Tom Lamb at DrugInjuryWatch.com)
On December 22, 2009 the FDA issued an update about its August 2008 Early Communication which described a possible association between the use of Vytorin – a combination of simvastatin (Zocor) and ezetimibe (Zetia) – and an increased risk of cancer and cancer-related death compared to placebo.
As you may recall, that August 2008 Early Communication was based on preliminary results from the Simvastatin and Ezetimibe in Aortic Stenosis (SEAS) trial.
From the December 2009 safety update about Vytorin and Zetia, which is titled “Follow-Up to the August 2008 Early Communication About an Ongoing Safety Review of Ezetimibe/Simvastatin (marketed as Vytorin), Simvastatin (marketed as Zocor) and Ezetimibe (marketed as Zetia) – FDA Investigates a Report from the SEAS Trial”:
FDA has now completed its review of the data from the SEAS trial as well as a review of interim data from two large-scale ongoing cardiovascular trials with Vytorin – the SHARP and IMPROVE-IT trials. Based on the currently available information, FDA believes it is unlikely that Vytorin or Zetia increase the risk of cancer or cancer-related death, but at this time an association cannot be definitively ruled out…. [footnotes omitted]
The SHARP trial is placebo-controlled, but uses a lower dose of Vytorin (10/20 mg) than was used in the SEAS trial. The IMPROVE-IT trial compares Vytorin 10/40 mg to simvastatin 40 mg. An interim analysis of the cancer data from these two trials, which includes a total of 20,617 patients, did not show an increased risk of cancer with Vytorin. There was an increase in the number of cancer-related deaths, with 97 deaths in the Vytorin groups compared to 72 deaths in the control groups, but this finding was not statistically significant.
When completed, the SHARP and IMPROVE-IT trials will provide additional data to further assess cancer risk with simvastatin and ezetimibe. The SHARP trial is expected to be completed in 2010 and IMPROVE-IT in 2012.
As for other serious side effects which have been associated with Vytorin and Zetia, back in September 2008 we reported about two medical journal articles which described a case of liver disease involving Zeita and a case of liver failure possibly linked to Vytorin.
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DrugInjuryLaw.com: Legal Information And News About Prescription Drug Side Effects
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Major Brands Dominate The Most-Visited Mobile Web Sites
There’s really no major surprises when it comes to the big players on the mobile web, according to two reports released today. In fact, all of the top destinations are already major internet brands, unlike the mobile applications in which some small companies have made a name for themselves.
Nielsen said the top websites visited on a mobile phone from January to September, include Google (NSDQ: GOOG) search, Yahoo (NSDQ: YHOO) Mail, Gmail, The Weather Channel and Facebook. In a second list, Nielsen detailed the top brands accessed on the mobile phone. Those include: Yahoo, Google, MSN/WindowsLive/Bing, AOL (NYSE: AOL) Media Network and The Weather Channel. In a separate report released today by Opera, which details monthly usage based on what people are visiting via their mobile browser, the results were very similar. The top five were: Google, Facebook, Yahoo, MySpace and Wikipedia. The only new company to the list was Amazon.com (NSDQ: AMZN), which came in at 10th.
Both companies also released a list of the top handsets. Opera’s list does not include the iPhone because its browser is not available in iTunes, however, Nielsen ranked the iPhone in first place with 4 percent of all U.S. subscribers. That figure is a bit deceiving because other handset-makers like RIM (NSDQ: RIMM) and LG (SEO: 066570) dominate the rankings with various handset models. RIM’s various models actually translates to a 8 percent penetration rate. Overall, smartphones are owned by 15 percent of all households. Surprisingly, the popular, but low-end and aging Motorola (NYSE: MOT) Razr continues to rank third with 2.3 percent of the install base.
In Opera’s rankings, the BlackBerry comes in third, but also dominates the rankings, spanning from sixth place to 10th place. LG comes in second with the Lotus.
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Opening Ceremony – Spring/Summer 2010 Footwear Preview

The footwear offered by Opening Ceremony continually fuses the trends of today with tricked-out details that become must-haves for tomorrow. Their Spring/Summer 2010 collection steps out with lean, low oxfords rendered in pine and navy suede planted on thin white soles after which things get especially edgy: chunked-up Tricker’s style saddle brogues with jagged-toothed Goth-kid soles, and boldly bizarre lace-up/zip-up oxfords signaling the 90s desperate attempt for resurrected fashion relevance.
Continue reading for more images.
Source: Selectism
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Confused…New DX…or are we yet?
Hi everyone. My name is Elizabeth, my daughter Sam just turned 5 years old. In November she had a bad asthma attack and was prescribed prednisone. While on it, I noticed she was drinking a ton and peeing a lot. I was curious if it was a side effect of the medication and so, of course, I googled it. Everything I found said that if you notice increased drinking and urination while on prednisone to talk to your doctor because it could be a sign of diabetes. Apparently prednisone is a glucocortosteroid…or something like that. We went for a follow up asthma appointment and I mentioned the frequent drinking to my daughters doctor. She started to just brush it off as no big deal, but I reminded her that one other time my daughter was hospitalized for her asthma she had a high blood sugar reading and also that my dad was type 1. With that she said we should do a urine test. Sure enough she was spilling glucose in her urine. We were to follow up with a fasting glucose test. That came back borderline. So she wasn’t diabetic, but something was going on. We were told to wait three weeks to be sure the steroids were out of her system. We went yesterday for the tests, a fasting and a glucose tolerance test. Her fasting number was 87 which I am told is normal, but her glucose tolerance test came back at 497 and it’s supposed to be under 120. There are more test results we are waiting for-all things I can’t recall. Unfortunately the doctor sent us for the test and is gone on vacation this week, so we were only able to talk to her NP. She seemed confused by the whole thing and basically said that if she is not a diabetic right now, her body is certainly headed that way and is unable to process sugars properly. The NP is calling the children’s hospital and getting them in on it.I have no idea what is really happening and waiting is killing me…
Thank you for listening and letting me get this out. I think having a dad with type 1 really makes it hard for me. I remember growing up I always swore I would never get married if I got t1…I didn’t want to put my kids through the highs and lows of D. The doctors called my dad a brittle diabetic, his sugars were really hard to control. I certainly didn’t want to pass it on to my kids. My dad was 14 when he was DX. When I was a kid he was on dialysis, until I was 9 and he was given a kidney transplant. When I was 17 he had a heart attack and last November When he was 62 and I was 32, my dad passed away. When we first started talking D with our 5 year old she cried saying she didn’t want to die like Papa. How sad for a 5 year old! We told her medicine is so much better now then when Papa was younger.
So much to comprehend and process. Forgive my rambling, but I am an inner jumbled mess and trying to keep it together on the outside for my daughter.
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Tōdaiji Daibutsuden: The Great Buddha Hall
Japan, Asia | Unusual Monuments
There are many amazing things about Tōdai-ji and the Daibutsuden or ‘Great Buddha Hall’ in Nara, Japan: the gigantic bronze Buddha, which nearly bankrupted Japan to build in 751, or the fact that this massive Buddha sits in the worlds largest wooden building, (once even larger as the current incarnation is only 70% of what the original was), or the ancient treasures such as a octagonal lamp from the 700s, or the healing pillars, which if one can squeeze through, they are said to be guaranteed a place in heaven, but the most surprising sight at the temple, is the deer.
Known as Sika Deer, they wander through the temples, sleep in corners, and generally stand around as tourists take their pictures. Once considered sacred messengers of the Shinto gods, and protected, they were later hunted to near extinction. Though they have been variously protected and hunted throughout their history in Japan, their population is strong today, and many have become tame and established themselves in cities and touristy areas, feeding from the hands of delighted visitors. They are even known to come up and bite visitors gently on the buttocks signaling that they desire crackers.
Despite having been damaged and destroyed multiple times, due to fire, earthquakes and accident (in 855 the head of the giant Buddha suddenly fell off) both the buildings and the statues have been continually repaired and today Tōdai-ji, or the Great Eastern Temple complex, and the Daibutsuden or ‘Great Buddha Hall’ it contains are in excellent shape.
The entryway to the temple is behemoth, with two towering guardians on each side, protecting the great Buddha. The Buddha itself, the world’s largest statue of the Buddha Vairocana (or Birushana in Japananese) is seen as the universal aspect of the Buddha, a sort of all in one Buddha. The statue weighs some 500 tonnes and is a towering 14.98 meters (49.1 ft) tall, with a 5.33 meter (17.5 ft) long face. His hair is made of 966 individual bronze balls, and creating this massive bronze Buddha in the 700s occupied much of
Japan’s bronze production for many years.Inside the massive temple, there were numerous artifacts to observe beyond the Great Buddha. One can learn the history of the building and area surrounding. As Nara was once the capital of Japan, there was much intriguing history to digest. Among the many things to see are miniature replicas of the temple and the grounds, various Buddhist statues, and the (somewhat unfair to the overweight) healing pillars, wooden columns with a hole in the bottom that brings good luck, and some even say entrance to heaven, if you can squeeze through it.



































