Wednesday, May 2, 2012

Russian Classified Giant?s $75m From Accel Shows It?s 1999 In Emerging Economies

Screen Shot 2012-05-02 at 13.10.45Avito.ru, the biggest online classified ads site in Russia, has secured a fresh $75 million round of funding from Accel Partners' London office. Founded in 2008, Avito has so far landed $101 million from Accel, Baring Vostok Private Equity, Kinnevik, and Northzone. The capital will be used for expansion and hiring. Russia's classifieds ads business has plenty of room for growth becuase - guess what kids - it?s basically 1999 out there is Russia. And this large emerging market is playing through all those businesses models we know and love from back in the good 'ol days. Expect more of this.

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Plastic-powered plane aims to soar across England

10 hrs.

A globe-trotting, eco-minded adventurer aims to fly the length of England in a tiny plane powered by plastic rubbish ? if he can raise the funds needed to get the flight off the ground.

The adventure is the latest in a series of alternative-fuel journeys dreamed up by Andy Pag, a trained engineer who?s already driven a chocolate-powered truck across the Sahara Desert and a bus fueled with used cooking-oil around the world.?

For the microlight flight over England, Pag plans to use aviation fuel derived from waste plastics ? the stuff that?s unacceptable to recyclers and thus destined for the landfill.

Plastics, he explained, are chemically similar to hydrocarbon fuels ? both are made with long chains of hydrogen and carbon atoms, only their arrangements are different.?

The aviation fuel is created in a process that ?blows the chains apart and then reforms them in the size and shape of fuel molecules,? Pag said?in an email to msnbc.com Monday.

This is a Fischer Tropsch process, the same process used by the Germans in World War II to create diesel fuel from coal. "Using coal isn?t particularly environmentally friendly though, but obviously a waste product is,"?Pag added.

The use of plastics as a source of fuel is technically considered a synthesized fuel rather than a biofuel such as the chocolate and used cooking oil Pag used in his previous adventures.?

Similar to biofuels, though, the use of waste plastic is a way to cut down carbon dioxide emissions, he noted.?If the plastic bags were left in the landfill, they would, eventually, decompose to methane and carbon dioxide.

"By turning them into fuel, the CO2 still ends up in the atmosphere, but a load of ?purpose made? fuel is saved from being used, reducing total emissions," he said. "More simply, it puts a waste product to good use, reducing consumption and the associated emissions."

Of course, in world teeming with 7 billion people and at least 1 billion vehicles on the road, fuel from used plastic bags, chocolate?or even cooking oil is unlikely to curb our reliance on traditional fossil fuels.

"There is no cure-all solution," Pag said. "But if something helps, then I?m keen to take advantage of it."

And for now he wants to take advantage of all that plastic rubbish destined for the world?s landfills. To do so, he?s aiming to raise about $16,250 on Crowdfunder.?

To date, he has secured?only?about 1 percent of his target. Pag hopes a sponsor will back his cause and help cover the rest of the?trip's tab, which will include educational stops and will take about two?weeks to complete.?

--?Via Fast Company?

John Roach is a contributing writer for msnbc.com. To learn more about him, check out his website and follow him on Twitter. For more of our Future of Technology series, watch the featured video below.

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Australian Price Gouging Inquiry Targets Apple, Microsoft And Others

Apple Retail Store - SydneyGetting a new laptop or buying a new license for an operating system is often cheaper in the U.S. than in most other countries. Europeans, for example, are used to paying a hefty premium for Apple products and the situation is similar in Australia, where the cheapest MacBook Air currently costs about 15% more than in the United States. Now, however, the Australian government is starting a parliamentary inquiry into these pricing schemes. According to Australia's Sydney Morning Herald, the politicians behind this inquiry hope that calling these companies out publicly will result in prices dropping.

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Video: Rachel Maddow Destroys the Right Wing Myth That Women Don't Get Paid Less (Little green footballs)

Share With Friends: Share on FacebookTweet ThisPost to Google-BuzzSend on GmailPost to Linked-InSubscribe to This Feed | Rss To Twitter | Politics - Top Stories News, News Feeds and News via Feedzilla.

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Tuesday, May 1, 2012

Double-drug diabetes treatment disappoints in kids

NEW YORK (Reuters Health) - In a large new trial looking at ways to slow the progression of type 2 diabetes in children and teens, the addition of a second drug to the mainstay treatment metformin was only marginally more effective at controlling blood sugar than metformin alone.

Within a year, on average, half of kids on metformin and some 40 percent taking both metformin and rosiglitazone (Avandia) ended up having to resort to insulin injections to control their blood sugar, researchers reported Sunday at the annual meeting of the Pediatric Academic Societies in Boston and in the New England Journal of Medicine online.

"The results of the study were discouraging," said Dr. David Allen from the University of Wisconsin School of Medicine and Public Health in an NEJM editorial. "These data imply that most youth with type 2 diabetes will require multiple oral agents or insulin therapy within a very few years after diagnosis."

All 699 children included in the study had been diagnosed with type 2 diabetes two years or less before enrollment, so the rapid advance of about half to needing insulin marks an early start to a potential lifetime of complications and side effects -- from the diabetes itself and the medications used to treat the disease.

Type 2 diabetes, the form usually associated with obesity, was once considered an "adult" disease, but is showing up in more and more teenagers, paralleling a rise in childhood obesity. And the condition is harder to treat in kids, experts say.

Type 2 diabetes "progresses more rapidly" in youth, according to Dr. Phil Zeitler from the University of Colorado, Denver, who worked on the new study.

He and his colleagues were surprised at how quickly many of the youngsters needed to switch from oral medications to taking daily insulin shots, Zeitler told Reuters Health.

Also, Zeitler said, the teens in the study appeared to have complications, including infections and hospitalization, more often than adults do.

All the children in the study were overweight or obese, and ranged in age from 10 to 17 years old.

Youngsters with diabetes are a difficult population to work with, Zeitler noted. Many of them don't take their medications as instructed. And in the first place, to get type 2 diabetes before adulthood, "the toxicity of your lifestyle must be pretty severe," Zeitler said.

That's why all of the kids in the study got at least "basic lifestyle counseling," he emphasized -- for example, advice to stop drinking sugared sodas, eat less fast food, watch their diet in other healthy ways, take stairs instead of elevators and generally get more exercise.

Study enrollment began in July 2004 and follow-up continued through February 2011. All the kids in the study were taking metformin, a well-established diabetes drug, and a third were assigned to take the newer drug Avandia as well.

Another third of the kids were assigned a very intensive "lifestyle intervention," that involved more assignments for kids to complete, more interaction with counselors, and close involvement of at least one parent, in addition to taking metformin.

The kids' treatments were deemed failures if blood sugar and other signs pointed to their diabetes not being under control for a period of six months or more.

In the end, 52 percent of kids on metformin alone "failed" treatment, along with 39 percent of kids on metformin and Avandia and 47 percent of kids on metformin and lifestyle changes.

The median time it took for blood sugar control to be lost was just under a year.

The added benefit of Avandia was limited to girls, for reasons that are unclear, the researchers reported.

Also for unknown reasons, they noted, metformin alone was less effective for non-Hispanic black participants than other kids.

Surprisingly, kids on the combination of metformin and Avandia gained the most weight during the study, despite their slightly better rate of diabetes control. Kids in the lifestyle intervention group gained the least weight.

Zeitler pointed out, "You can see in the data a suggestion that there might be groups of children who respond to the very intensive intervention. Our challenge now is: Can we identify the kids who are going to respond to a lifestyle intervention and (just one oral diabetes medicine)?"

Conversely, he continued, the challenge is also to recognize from the start the kids for whom the intensive lifestyle intervention is "going to be ineffective and not worth the time and money."

Overall, 19 percent of the participants developed serious adverse effects such as severe hypoglycemia, diabetic ketoacidosis and lactic acidosis.

The rate in the treatment groups was 18 percent in the metformin-only group, 15 percent in the double-drug group and 25 percent in the group that received the very intensive lifestyle intervention, but the rate of specific problems, such as hyperglycemia, were not significantly higher between the groups.

Finding the reasons for the differences between these groups of children in their response to treatments will require further research, Zeitler and his colleagues conclude in their report.

In his editorial, Allen says it's critical to remember that the patients in this study are "youth immersed from a young age in a sedentary, calorie-laden environment that may well have induced and now aggravates their type 2 diabetes."

"Fifty years ago," the editorial continues, "children did not avoid obesity by making healthy choices; they simply lived in an environment that provided fewer calories and included more physical activity for all. Until a healthier 'eat less, move more' environment is created for today's children, lifestyle interventions like that in the ...study will fail."

SOURCE: http://bit.ly/InSsRZ New England Journal of Medicine, online April 29, 2012.

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'Don't Text Me' Is Every Lovelorn Gadget Geek's New Anthem [Video]

Biggie rapped about his Genesis. Jay-Z rapped about his pager. But DC rapper Boobe's new video covers the full spectrum of digital life: sometimes you just want everyone to fucking leave you alone online. More »


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Control of gene expression: Histone occupancy in your genome

ScienceDaily (Apr. 30, 2012) ? When stretched out, the genome of a single human cell can reach six feet. To package it all into a tiny nucleus, the DNA strand is tightly wrapped around a core of histone proteins in repeating units -- each unit known as a nucleosome. To allow access for the gene expression machinery the nucleosomes must open up and regroup when the process is complete.

In the May 1, 2012, issue of Genes & Development, researchers at the Stowers Institute for Medical Research demonstrate how failure to restore order has lasting consequences. During the process of gene expression, a factor known as Chd1 promotes nucleosome reassembly on the DNA strand. Without it, yeast cells are unable to attach a chemical mark called ubiquitin to one of the four types of histone proteins, which in turn hampers nucleosome re-establishment throughout the entire yeast genome. In mammalian cells, this important step could be perturbed in disease states such as cancer.

"We have used the yeast Saccharomyces cerevisiae as a model system to study histone mono-ubiquitination and found that the mechanism is conserved in human cells," says Stowers Investigator Ali Shilatifard, Ph.D., who led the study. Why that's important dates back to studies initiated a decade ago on a gene called MLL, which is involved in the development of an aggressive type of leukemia in infants.

Previously, when Shilatifard's group analyzed the yeast version of MLL, they found that it enzymatically modified a histone called H3 by decorating it with a biochemical flag. In this case, that flag was not an ubiquitin, but rather a methyl group. Genes occupied by nucleosomes containing methylated H3 are generally switched on. Later, the lab confirmed that the same histone methylase activity was evolutionarily conserved from yeast to human cells, setting the stage for the molecular analysis of MLL activity in yeast.

The current study is based on a concept known as "histone crosstalk." It posits that rather than acting individually, histones within a nucleosome, particularly H3 and H2B, carry on a complex biochemical conversation among themselves based on how they are chemically modified. For example, previous studies had hinted that mono-ubiquitination at one histone (H2B) precedes methylation of another (H3), suggesting that the primary role of the former was to stimulate the latter. Thus, in this paper, Shilatifard and his team asked whether the sole function of H2B mono-ubiquitination was to regulate H3 methylation.

What Jung Shin Lee, Ph.D., a postdoctoral researcher and the study's first author, and Alexander Garrett, a bioinformatics specialist in the Shilatifard lab and co-author, found was unexpected: although yeast carrying mutant Chd1 showed a loss of H2B ubiquitination, H3 methylation was fairly unaffected. "Surprisingly, when we looked genome-wide, we observed that methylation patterns of other histones within nucleosomal complexes were fairly normal in Chd1 mutants," says Lee. "That told us that there are other functions associated with ubiquitination of H2B besides methylation of H3."

To reveal what those functions were, the investigators applied a technique that has been mastered by Penn State biochemist Frank Pugh, Ph.D. The methodology, known as nucleosomal occupancy mapping, can nail down to a single DNA base the very spot on a DNA strand where a complex of histone proteins is sitting -- not in just one gene, but in all 5,700 or so yeast genes simultaneously.

Collaborating with Pugh's lab, Shilatifard's group used the technique to map loci where nucleosomes formed in the genome of normal versus Chd1-mutant yeast. Mutants showed decreased occupancy of nucleosomes compared to non-mutant cells, particularly in longer genes, suggesting that mutants have difficulty recreating the proper nucleosome array after gene expression.

"To synthesize RNA from DNA, the normal chromosome structure must be loosened to make way for RNA polymerases, enzymes that transcribe DNA," explains Garrett. "After that, the DNA must be re-condensed through the reassembly of nucleosomes." That, rather than H3 methylation, is the primary activity impaired when the protein Chd1 is nonfunctional. Finally, the investigators experimentally manipulated cultured human cells to eliminate expression of the human counterpart of Chd1 -- a molecular trick equivalent to analyzing Chd1-mutant yeast -- and observed impaired mono-ubiquitination of human H2B, just like in yeast.

"These experiments show that the function of Chd1 that we see in single-celled yeast is conserved in humans," says Shilatifard, praising what he calls the awesome power of yeast biochemistry and genetics. "Basically, we are able to use yeast as a test tube to discover what the function of these proteins is in you and me. Given the fact that histone mono-ubiquitination is associated with processes that can lead to the development of human cancer, the molecular information obtained in yeast are indispensable for better understanding the role these factors play during human development and disease pathogenesis," says Shilatifard.

Additional co-authors of the study from the Stowers Institute include Yoh-Hei Takahashi, Ph.D., Deqing Hu, Ph.D., and Chris Seidel, Ph.D. Also contributing were Kuangyu Yen, Ph.D. of the Pennsylvania State University, and Jessica Jackson of St. Louis University School of Medicine.

Funding for the study came from the National Institute of General Medicine, the Alex's Lemonade Stand Foundation for Childhood Cancer, and the Stowers Institute for Medical Research.

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