Saturday, April 6, 2013

Antarctic blue whales pinpointed with sonar

Kylie Owen

The blow hole of an Antarctic blue whale.is easily seen as it breaks the ocean's surface.

By Becky Oskin
LiveScience

Whales may be the biggest animals on Earth, but finding them in the vast open ocean isn't easy.

Now, an Australia-led research team has demonstrated a novel idea for chasing down the massive marine mammals. To search for Antarctic blue whales, the group dropped sonar buoys in the Ross Sea west of Antarctica, and listened for whale calls. They triangulated the whale's location from their calls, and then sailed to the right spot.

During the research cruise, the scientists photographed 57 blue whales, collected 23 skin biopsy samples and stuck on two satellite-tracking tags. They also spotted 11 pygmy blue whales and eight humpback whales, among a total 720 cetacean species (the group that includes whales, dolphins and porpoises).

"In many respects our expectations of what we could achieve have been exceeded," the scientists wrote on the expedition's blog.

The deep, resonating song of Antarctic blue whales travels hundreds of kilometers across the Southern Ocean, Brian Miller, of the Australian Antarctic Division?and the lead marine mammal acoustician of the mission, said in a statement. The team returned with 626 hours of recordings, with 26,545 blue whale calls analyzed in real time. [See how they found the whales]

Virginia Andrews-Goff

The Amaltal Explorer is dwarfed by a tabular iceberg during the Antarctic voyage.

The whale's satellite tags will transmit never-before obtained data on how the whales feed near the edge of the Antarctic ice, marine biologist Virginia Andrews-Goff of the Australian Marine Mammals Center said in a statement.

The International Whaling Commission estimates the population of Antarctic blue whales is between 400 and 1,400 individuals. The leviathans were slaughtered to near extinction in the early 1900s by whalers, who took some 340,000 whales, according to a statement from the Australian government.

Researchers worldwide have used acoustic technology to track whale species for decades, including blue whales, humpback whales and right whales. This is the first time that scientists have located whales for tagging and identification by identifying their positions with sonar, the statement said.

Email Becky Oskin or follow her @beckyoskin. Follow us?@OAPlanet, Facebook?or Google+. Original article on LiveScience's OurAmazingPlanet.

Copyright 2013 LiveScience, a TechMediaNetwork company. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.

Source: http://feeds.nbcnews.com/c/35002/f/653377/s/2a61f26e/l/0Lscience0Bnbcnews0N0C0Inews0C20A130C0A40C0A50C176177620Eantarctic0Eblue0Ewhales0Epinpointed0Ewith0Esonar0Dlite/story01.htm

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Friday, April 5, 2013

Deadly new bird flu vindicates controversial research

By Kate Kelland, Health and Science Correspondent

LONDON (Reuters) - Scientists in the Dutch city of Rotterdam know precisely what it takes for a bird flu to mutate into a potential human pandemic strain - because they've created just such mutant viruses in the laboratory.

So as they watch with some trepidation the emergence in China of a strain of bird flu previously unknown in humans, they also argue it vindicates their controversial decision to conduct these risky experiments despite fierce opposition.

Above all else, what the world needs to know about this new strain of H7N9 bird flu is how likely it is to be able to spread efficiently among human populations.

And according to Ab Osterhaus, a world leading flu researcher who is head of viroscience of the Erasmus Medical Center in the Netherlands, studies his team and another in the United States have been doing are the best way to find out.

"At the moment we don't know whether we should go for a full-blown alert or whether we can sit back and say this is just a minor thing," Osterhaus told Reuters in a telephone interview.

"(To answer that) we need to know what this virus needs to become transmissible."

With 10 cases of the new H7N9 bird flu confirmed in people in China since Sunday, including four deaths, Beijing is mobilizing resources against the threat.

Japan and Hong Kong said they had also stepped up vigilance against the virus, and Vietnam banned imports of Chinese poultry.

MAKING A MONSTER?

The scientific work that can answer key risk questions is known as "gain of function" or GOF research. Its aim is to identify combinations of genetic changes, or mutations, that allow an animal virus to jump to humans.

By finding the mutations needed, researchers and ultimately health authorities are better prepared to assess how likely it is that a new virus could become dangerous and if so how soon they should begin developing drugs, vaccines and other scientific defenses.

Yet such work is highly controversial.

When two teams of scientists announced in late 2011 they had found out how to make a another strain of bird flu - H5N1 - into a form that could spread between people, alarm bells rang so loudly at the U.S. National Science Advisory Board for Biosecurity (NSABB) that it took the unprecedented step of seeking to censor publication of the studies.

In a series of GOF experiments, the scientists induced mutations into the H5N1 virus that made it transmissible among mammals through droplets in the air.

The NSABB said it feared details of the work, carried out by Ron Fouchier at the Rotterdam lab and by a second team led by Yoshihiro Kawaoka at the University of Wisconsin, could fall into the wrong hands and be used for bioterrorism.

"The fear was that they were making a monster," said Wendy Barclay, a flu virologist at Imperial College London.

An acrimonious debate ensued and flu researchers around the world agreed to a year-long moratorium on further experiments of this type until fears could be allayed.

Yet throughout the moratorium, some scientists argued the research was vital to preparing for the next flu pandemic, and that to abandon it would leave the world in the dark when new flu strains emerged.

VIRUSES JUMP FROM ANIMALS TO HUMANS

Barclay, who was a signatory on an open letter in January from 40 scientists calling for an end to the moratorium on bird flu transmissibility research, says current events in China underline why.

"What this H7N9 emergence does is show for sure that flu will emerge at regular intervals from animal sources," she said.

"And it underscores the fact that for each virus, we don't know whether it will be readily transmissible between humans when it emerges, or whether it will turn out to be a zoonotic dead end because when it reaches the human host there are barriers it can't overcome."

Some scientists, however, remain unconvinced of the value of deliberately manipulating viruses in laboratories - however secure they may be - to create and then analyze mutant flu strains that can spread between mammals.

Writing in the scientific journal Nature last week, Simon Wain-Hobson, chair of the Washington-based Foundation for Vaccine Research in the United States, accused flu researchers of going down a dangerous blind alley.

"The world has never been more densely populated," he wrote. "Is it appropriate for civilian scientists to make microbes more dangerous?"

Osterhaus, who has looked at genetic sequencing data from the new H7N9 bird flu strain samples in China and found some worrisome mutations have already occurred in the H7N9 strain, says such concerns are far outweighed by the fear of not knowing the potential risk of an emerging new virus.

"This virus might be on the brink of gaining function of transmissibility (in humans). I think it's crucial to know the rules of the game."

(Editing by Will Waterman)

Source: http://news.yahoo.com/deadly-bird-flu-vindicates-controversial-research-142717817.html

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5 Cooking Mistakes We All Make, and How to Fix Them

5 Cooking Mistakes We All Make, and How to Fix Them Cleaning your cast iron with soap and water? Squeezing every last bit of ground beef into that pan? Even if you know your way around the kitchen, there are a few mistakes nearly all of us make in the kitchen. Let's take a look at some common kitchen errors that may plague your cooking, and why they're bad for your food.

5 Cooking Mistakes We All Make, and How to Fix Them

You're Cleaning Cast Iron Pans with Soap and Water

The Problem: You've just finished dinner, and the cast iron pans you used to cook with are full of oil and stuck-on food. It's time to clean them, and you know cast iron pans require special treatment, but ain't nobody got time for that. You give them a quick scrub with a sponge and soapy water, rinse with hot water, and a dry them with a paper towel. You might think that a light scrub can't possibly hurt too much, but the moment that hot soapy water touched your pan, it started to destroy the "seasoning" on the pan, or the layer of fat and oil that's been cooked onto the iron itself over regular use. Photo by Ross Catrow.

It's that season that makes cooking with cast iron so great. Not only does it protect the iron of the pan from rust, it also provides a cooking surface that's non-stick, naturally oiling, and keeps your food from interacting with the oil of the pan. Some people even say the season imparts flavor. Here's the problem: since the season is all polymerized oil, hitting it with dish soap, and then scrubbing at it with a sponge and rinsing it with hot water causes those oils to break down and float away?taking that protective coating and washing it very literally down the drain. It may be easy, but it's destructive.

The Solution: Instead of using soap and water, try Alton Brown's method (seen in the video to the left). When you're finished cooking, pour a little oil into the pan (if there isn't any left from cooking), dump in a handful of kosher salt, and then just scrub the salt around the pan with an old rag or some wadded up paper towels. The salt will get dirty, and the pan will get clean. Dump out the salt, wipe the pan clean, and put it away. We've discussed this method before too, and it works brilliantly. This is the real beauty of cast iron: You don't actually have to wash it.

If your pan has started to lose its season, it's not too late: try re-seasoning your pan with flax seed oil (read here for more on why this method works), and toss it in the oven while you're baking to season and save time. Check our recent CrowdHacker guide for more tips.

You Thaw Meat at Room Temperature

5 Cooking Mistakes We All Make, and How to Fix ThemThe Problem: You need to figure out dinner tonight, but you forgot to pull something out of the freezer to thaw slowly in the fridge. You only have a few hours to thaw the steaks or chops you'll wind up cooking tonight, so you take them out of the fridge and put them right into the sink. Maybe you just leave them on the countertop?that'll thaw them out quickly, right? Perhaps, but you're risking your safety and the safety of your dinner guests in the process. Photo by Taryn.

Remember, the "danger zone" for bacterial growth in food is between 40?F and 140?F (5?C and 60?C), and sitting right in the middle of that is "room temperature," around 68?-70?F (20?-22?C). A couple of hours at room temperature will certainly make sure that the meat is thawed, but it's a field day for bacterial growth as well, especially as the deeper parts of your cut begin to come up to temp while the outsides have been room temperature for hours.

"But surely," you're asking, "It'll all come up to temp when I cook it, right?" Maybe, assuming you're sure to cook your meat until the core is minimum safe temperature for what you're making, but it's an incredible risk, and it doesn't take much E.Coli or Salmonella to make you really regret the way you thawed those porkchops or chicken thighs.

5 Cooking Mistakes We All Make, and How to Fix ThemThe Solution: Use a cold water bath to thaw your meats. It's fast, safe, and by far the easiest. It requires a little more attention than some other safe methods of quick-thawing, but it works the best. Just take your meat and put it in a sealed bag (if it's not already in one) and submerge it in a bowl of cold water. You'll need to change the water out every half-hour or so (so the water doesn't come to room temp and bacteria start growing) but I've found after a half-hour or so, the meat is thawed and ready to cook. Photo by Waifer X.

If you don't like that method, there are other ways to thaw meat quickly that are easy and safe. Both StillTasty and The USDA recommend one of three methods: In cold water like we described, in the fridge until the meat is properly thawed (since your fridge keeps food below the danger zone), and in the microwave (because some parts of the meat may be warmer than others or cook in the microwave when you do this, the USDA says you should cook the meat immediately after microwaving.) We've also mentioned a hot water method if you're in a hurry, but note: it only works with thin cuts of meat.

You're Overcrowding Your Pan, Baking Dish, Cookie Sheet, Etc.

5 Cooking Mistakes We All Make, and How to Fix ThemThe Problem: If you've ever baked cookies only to have them all stuck to one another, or sauteed meat or veggies in a pan only to have them take forever to cook through, the problem may be that you're overcrowding your pan. Perfect example: you're cooking up a batch of ground beef or turkey in the pan, and while everything seems great at first, over time the meat starts to get kind of gray and bubbly, releasing a ton of moisture that takes forever to cook away. Your meat isn't getting the delicious brown you'd hoped for. Sound familiar? You should have cooked it in batches. Photo by ilovebutter.

The same problem occurs in baking. If you've ever put meat in the oven only to take it out while it's swimming in its own bubbling juices, or baked french fries or veggies without making sure they're spread out evenly, you know what I'm talking about. Thankfully, it's an easy problem to fix.

The Solution: Separate your cooking into batches. It's simple, but that's all it takes. Resist the urge to try and get everything done in one go. Overcrowding your pan actually slows down the cooking process. If you're satueeing veggies, all of the moisture released as they cook stays in the pan and steams them, which gives you a mushy, wet mess, instead of the crisp, firm texture you're looking for.

With meat, large, cold cuts rob the pan of heat every time you put one in, so overcrowding the pan actually lowers the temperature of the whole cooking surface. This increases the overall cooking time, and in the worst case brings the temperature of the pan down below the threshold required for the Maillard reaction to take place (approx 300?F/150?C). Even worse, the pan may linger above the boiling point of water (212?F/100?C), which means you're essentially steaming your meat, and that's no good. Give your food plenty of room to move around in the pan, and let them cook in a single layer.

You're Cooking at the Wrong Temperature

5 Cooking Mistakes We All Make, and How to Fix ThemThe Problem: Speaking of cooking temperatures, even the most seasoned home cook can catch themselves cooking either entirely too hot or too cold. Usually this applies to on-stove cooking, so sauteing, frying, and stir-frying are the big problems. Here are the symptoms:

  • When you're cooking too hot: You tossed those chicken breasts into a pan, and while the outside is cooked well, the inside is next to raw. Your scrambled eggs are brown and firm on the outside but still runny and liquidy on the inside. You can't seem to cook anything without setting off the smoke alarm? Sound familiar? Listen, every beginning cook has trouble controlling heat, but you don't need to fry everything to a crisp. The problem here is self-evident: Food isn't evenly cooked (which can lead to undercooked and dangerous-to-eat insides) at best, or completely burned and overdone at worst. Photo by normanack.
  • When you're cooking too cold: The opposite problem doesn't happen as often, but it's still an issue. Cooking with the heat down too low may get your dish done, but avoiding higher heat will keep liquids from simmering, herbs from wilting, flavors from developing, and aromas from opening up fully. It'll keep that delicious sear and browning action we just discussed from taking place on steaks and chops, and of course, you also run the risk of underdone food. Veggies and other foods where texture is important run the risk of being a bland mush that's been cooked down too far, too long.

5 Cooking Mistakes We All Make, and How to Fix ThemThe Solution: Get to know your stove or oven, and stop cooking everything on high heat. Here are a few quick ways:

  • Try all of your burners and watch them heat up. If you have an electric range, see how long each one takes to heat up. If you use gas, tweak the control knob to see the level of fine control you have over the flame intensity. With luck, you'll have great control over the level of heat your stove puts out. Sadly, not all stovetops really know the difference between "medium" and "medium high," and testing the burners is the only way to find out. Photo by Steven Depolo.
  • Use more than one burner. If your stovetop doesn't give you the control you need, don't just use a different burner?a smaller burner turned down may be the equivalent of "medium" of your large one. You'd be surprised how few home cooks really learn the difference between "medium high" and "high," or how many kitchens I've visited where the large front-corner burner is the only one anyone ever uses.
  • Make a heat map of your oven. Most commercial ovens have hot and cold spots. They can be hard to identify, but once you make a heat map with a cookie sheet and a few slices of bread, you'll see your oven's hot and cold spots.

You're Cooking with the Wrong Oils

5 Cooking Mistakes We All Make, and How to Fix ThemThe Problem: You probably already know that heating oil until it smokes is a very bad thing, and keeping multiple oils around for different purposes is a good idea. Still, frying everything with extra virgin olive oil is a surefire way to set off the smoke alarm every time you sautee, and baking with an extremely flavorful oil like sesame or coconut will certainly introduce flavors to your dish that you may not expect. Even though we talked about smoke points and which oils work best for which cooking methods, going just by smoke point (or by someone's diet book) isn't the best way to pick an oil. Photo by Arthur Caranta.

The Solution: Choose your oils not just for their smoke points, but for whether or not their flavor works with the type of food that you like to cook. If you like asian flavors, sesame oil is a great staple to keep around. If you prefer your oil also add its own savory, fatty flavor, consider cooking with more butter, lard, or ghee (clarified butter). Coconut oil is great for a number of reasons, but it can impart a nutty, rich flavor to lighter dishes you may not want.

Also, consider neutral oils that let the flavor of your dish shine through without adding their own. Safflower oil, for example, is completely neutral, and has a high smoke point. Grapeseed oil has a very light flavor that you may not even notice in your dishes, and is also well suited to high-temperature cooking. Don't just assume that you can do everything with olive oil or "vegetable oil," which is usually either a mix of oils or (more often) store-shelf code for "soybean oil."


These five are just the tip of the iceberg. There are plenty of other common cooking mistakes many of us make all the time, and sometimes even knowing better doesn't stop us. The key is to remember why they're dangerous, cost us money, or make our food taste terrible: That's the key to putting an end to them for good.

Title photo made using Corey Seeman, Boring Soap, Consumatron, Biswarup Ganguly, and Juan de Vojn?kov.

Source: http://feeds.gawker.com/~r/lifehacker/full/~3/gAawRqXv1tM/5-cooking-mistakes-we-all-make-and-how-to-fix-them

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Thursday, April 4, 2013

China's homegrown GPS to open up for smartphones

Chinas homegrown GPS to open up for smartphone makers

Now that China is comfortable letting drivers access Beidou to get around the middle kingdom, it's decided that everyone else should get easy access as well. Talking to Xinhua News, state official Yang Qiangwen said that it won't be long before the nation's made-at-home GPS is adopted by local smartphone makers. The government is seeking to attract investment to promote the technology for public use, presumably lobbying domestic manufacturers to get on board -- before making similar overtures to the big boys elsewhere.

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Comments

Via: The Register

Source: Xinhua News

Source: http://www.engadget.com/2013/04/03/beidou-coming-to-phones/

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Why High Value Items Are Not Always The Best Target On Unique ...

You might just be after one product, but there are thousands of places that you could purchase from. A local store, high street store, commerce store, or one of the many bidding sites that are on the internet; they are all options. Here is the thing, more and more people are realising that the best option for them is to head for lowest unique bid websites. Why? Simply because the prices here can not be matched anywhere else in the world! In fact, even fake exports from various places end up being much more expensive.

Why are these items so cheap?
It is easy to explain; people do not generally understand how these sites work. Well, the minority do and they are taking advantage of everything they know. That being said, the majority of people are still focusing on commerce stores and what we know as the main stream auction sites. They continue to pay over the odds for MP4 players, scooters, GPS systems and more!

Why are high value items off the agenda?
When you first log onto one of the unique bidding sites, you might find that you are pushed towards the high value items. That is only natural as these items are more desirable. You will be seeing TV sets go for 0.5% of their retail price and MP4 players going for less than 1% of their retail price. The problem is that bidding on these websites is probably not as simple as you might imagine. The harsh reality is that these websites are full of people that actually know what they are doing. They have experience when it comes to bidding on these websites and therefore, they are much more likely to win these items than you are as a newbie.

So, should these websites be avoided?
No, of course not! Every single month, 100s of different items will be listed. Some items are extremely low in value, whereas others are extremely high in value. The good thing is that most of the experienced bidders will be aiming for the big prizes. This means that the lower value items are up for grabs, and a great chance for beginners to start. This is your chance to get a great deal on a huge range of products. Of course, you need to take your time and don't rush. If you rush, you could end up losing money and nobody wants to do that.

How can you lose money?
On unique bidding sites, you pay for each bid that you make. Essentially, if you want to be successful, it's best to devise a strategy. Of course, the only way you can make a proven strategy is by testing it out. This means that there is likelihood that you will lose some cash over a short space of time. Of course, this will be offset by the fact that eventually you will start winning items on a regular basis at a huge reduction in comparison to their actual retail prices. If you think you have come across a piece of information that can help your strategy, then write it down and make sure you use it in the future.

If you want more unique bid auction information take a look at the BidGrid website. Their how it works page does a great job of explaining everything in more detail. You can also bid for free in their practice auctions which is the best way to understand the lowest unique bid principles.

Source: http://articles.submityourarticle.com/why-high-value-items-are-not-always-the-best-target-on-unique-bid-sites-323156

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Phase 1 ALS trial is first to test antisense treatment of neurodegenerative disease: No serious adverse effects reported

Apr. 3, 2013 ? The initial clinical trial of a novel approach to treating amyotrophic lateral sclerosis (ALS) -- blocking production of a mutant protein that causes an inherited form of the progressive neurodegererative disease -- may be a first step towards a new era in the treatment of such disorders. Investigators from Massachusetts General Hospital (MGH) and Washington University School of Medicine report that infusion of an antisense oligonucleotide against SOD1, the first gene to be associated with familial ALS, had no serious adverse effects and the drug was successfully distributed thoughout the central nervous system.

"This therapy directly targets the cause of this form of ALS -- a mutation in SOD1, which was originally discovered here at the MGH by my mentor Robert Brown," says Merit Cudkowicz, MD, chief of Neurology at MGH and senior author of the report in Lancet Neurology, which has been released online. "It's very exciting that we have reached a stage when we can start clinical trials against this type of ALS."

ALS causes the death of motor neurons in the brain and spinal cord, stopping transmission of neural signals to nerve fibers and leading to weakness, paralysis and usually death from respiratory failure. Only 10 percent of ALS cases are inherited, and mutations in SOD1 -- which produce an aberrant, toxic form of the protein -- account for about 20 percent of familial cases. Although that first SOD1 mutation was identified 20 years ago by the team lead by Brown -- who is now professor and chief of Neurology at the University of Massachusetts Medical School -- a technology that directly addresses such mutations became available only recently.

The current study, the first author of which is Timothy Miller, MD, PhD, of Washington University, used what are called antisense oligonucleotides -- small, single-stranded DNA or RNA molecules that prevent production of a protein by binding to its messenger RNA. While antisense medications have been tested against several types of disease, this was the first trial in a neurological disorder, making the assurance of safety -- a primary goal of a phase 1 study -- particular important. Studies in animal models led by Miller and others found that the experimental antisense drug used in this trial reduced expression of mutated and nonmutated SOD1 and slowed the progression of ALS.

Conducted at the MGH, Washington University, Johns Hopkins University and the Methodist Neurological Institute in Houston, the trial enrolled a total of 21 patients with SOD1 familial ALS. Four sequential groups of participants received spinal infusions over an 11-hour period of the antisense drug or a placebo, with the active drug being administered at one of four dosage levels. Since participants in one group were free to join a subsequent group more than 60 days later, seven received two infusions and two received a total of three.

Some of the participants reported the type of adverse effects typically associated with spinal infusions -- headache and back pain -- with no difference between the active drug and placebo groups. Participants who receive subsequent infusions reported fewer adverse effects. Cerebrospinal fluid samples taken immediately after infusion revealed the presence of the antisense oligonucleotidein all participants receiving the drug at levels close to what was predicted based on animal studies. Analysis of spinal cord samples from one participant who had later died from ALS found drug levels highest at the site of the infusion and lowest at the furthest point and suggested that prior estimates of how long the drug would persist in the spinal cord were accurate.

Cudkowicz notes that the next step will be a larger study to address long-term safety and take a first look at the effectiveness of antisense treatment against ALS "This is a very important step forward for neurodegenerative disorders in general," she explains. "There are other ALS gene mutations that antisense technology may be useful against. There also is an ongoing study of a different oligonucleotide against spinal muscular atrophy, and ongoing preclinical studies in Huntington's disease, myotonic dystrophy and other neurological disorders are in development.

"The first person with ALS that I cared for had SOD1 ALS," she adds, "and I promised her a commitment to finding a treatment for this form of the disease. It's so gratifying to finally be at the stage of knowledge where we can start testing this treatment in patients with SOD1 ALS. We also hope that this treatment may apply to the broader population of patient with sporadic ALS." Cudkowicz is the Julieanne Dorn Professor of Neurology at Harvard Medical School.

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The above story is reprinted from materials provided by Massachusetts General Hospital.

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


Journal Reference:

  1. Timothy M Miller, Alan Pestronk, William David, Jeffrey Rothstein, Ericka Simpson, Stanley H Appel, Patricia L Andres, Katy Mahoney, Peggy Allred, Katie Alexander, Lyle W Ostrow, David Schoenfeld, Eric A Macklin, Daniel A Norris, Georgios Manousakis, Matthew Crisp, Richard Smith, C Frank Bennett, Kathie M Bishop, Merit E Cudkowicz. An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study. The Lancet Neurology, 2013; DOI: 10.1016/S1474-4422(13)70061-9

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/health_medicine/genes/~3/pNA1_xAHlrM/130403141451.htm

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Tell me what you want me to say and I will say it (Unqualified Offerings)

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

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