TomTom Appoints Group Chief Technology Officer

AMSTERDAM–(Business Wire)–
TomTom today announces the appointment of Charles Davies as Group Chief
Technology Officer.

Charles will join the company from Nokia, where he was VP, Technology Adviser
and then interim Head of Technology and Architecture in Nokia Devices R&D. Prior
to the Nokia acquisition, Charles was Symbian’s CTO for six years. He joined
Symbian from Psion where he held a number of group board roles including
Software Director, Development Director, Managing Director, and CTO.

Commenting on the appointment, TomTom`s CEO Harold Goddijn said “I am delighted
that Charles will join TomTom as Group CTO. He brings with him more than twenty
years of experience and has been instrumental in shaping the technological
landscape as we know it. His pioneering view and insight into innovative
technological solutions will enable us to speed up both the pace of bringing new
solutions to market as well as to define our long term strategic positioning”.

Charles, who is a British national, holds a first class degree in Physics and a
PhD in Plasma Physics from Imperial College London, and is a Fellow of the Royal
Academy of Engineering.

As Group CTO, Charles will be responsible for the technology strategy across all
of the development communities within TomTom.

He will be a member of TomTom`s Executive Board.

About TomTom N.V.

TomTom N.V. (AEX: TOM2) is the world`s leading provider of location and
navigation solutions. Headquartered in the Netherlands it has over 3000
employees worldwide. More than 40 million people daily use its solutions, be it
in the form of dedicated portable navigation devices (PNDs), in-dash car systems
or tracking and tracing solutions for fleet management. In addition, hundreds of
millions of people use TomTom`s digital maps on the internet or mobile phone.

In 2009, TomTom reported €1.5 billion in revenues and a €340 million net cash
flow from operating activities. More information about TomTom can be found on
www.TomTom.com.

TomTom
Press contacts:
Kristina Nilsson
+31 20 757 5078
cc@tomtom.com
or
Investor Relations:
Richard Piekaar
+31 20 7 575 194
ir@tomtom.com

Copyright Business Wire 2010

How a pet pooch can help treat Parkinson”s

London, May 13 (ANI): A significant treatment for Parkinson”s disease has been revealed by doctors – a pet pooch.

Health of a 28-year-old woman with the brain disease improved thanks to her pooch.

The woman, who started taking large doses of four different drugs a day to control symptoms three years after being diagnosed, had a morphine pump for 14 hours a day and her health was deteriorating fast.

But after being given a highland terrier by a friend, docs reported improvements in symptoms and a drop in the drugs she needed, reports The Sun.

What’s more, she no longer needed her daily morphine.

Doctors at Imperial College London, who report her case in the Journal Of Neurology, said: “Remarkably sustained benefits occurred, with improvement in her walking and symptoms including appetite, sleep and bowel function, as well as socialisation.”

Docs are not able to zero in on the reason as to how the dog had such a dramatic effect, but they say that having to walk, feed and look after the pet encouraged her to exercise regularly. (ANI)

New finding may help in dengue fever fight

Washington, May 7 (ANI): A new study by scientists from Imperial College London has found that some of the human immune system”s defences against the virus that causes dengue fever actually help the virus to infect more cells.

According to the researchers, their new findings could help with the design of a vaccine against the dengue virus.

The study also brings scientists closer to understanding why people who contract dengue fever more than once usually experience more severe and dangerous symptoms the second time around.

Dengue fever is transmitted by a mosquito bite and is prevalent in sub-tropical and tropical regions including South East Asia and South America. Symptoms include high fever, severe aching in the joints and vomiting. The dengue virus can also cause hemorrhagic fever, which can be fatal.

Professor Gavin Screaton, the lead author of the study from Imperial College London, and his colleagues identified a set of antibodies, produced by the human immune system to fight off the dengue virus, that they believe scientists should avoid including in any new vaccine to prevent dengue fever.

The new research shows that these precursor membrane protein (prM) antibodies do not do a very effective job of neutralising the virus. Moreover, these antibodies actually help the virus to infect more cells.

The study suggests that when a person who has already been infected with one strain of dengue virus encounters a different strain of dengue virus, the prM antibodies awakened during the first infection spring into action again. However, rather than protecting the body from the second infection, these prM antibodies help the virus to establish itself.

This activity of the prM antibodies could explain why a second infection with a different strain of the virus can cause more harm than the first infection. The researchers believe that if a dengue virus vaccine contained prM antibodies, this could cause similar problems.

The researchers reached their conclusions after analysing individual antibodies to the dengue virus extracted from blood samples donated by infected volunteers.

The new research has been published in the journal Science. (ANI)

New rat study may help understand genetic basis of human hypertension

Washington, April 29 (ANI): Scientists have sequenced the genome of the spontaneously hypertensive rat, which could help understand causes of the disease in humans.

The spontaneously hypertensive rat (SHR) strain is the most widely studied animal model of human hypertension. Research on this strain has identified many genomic regions that likely harbour genetic variants that are responsible for the hypertension phenotype, however without a complete sequence of the hypertensive rat genome, it has been difficult to resolve many of these genomic changes and explore their molecular consequences.

Taking advantage of new technologies that are rapidly driving down the cost of DNA sequencing, an international team of researchers led by Timothy Aitman of the MRC Clinical Sciences Centre and Imperial College London have sequenced the first genome of a mammalian disease model with second-generation sequencing technology.

By comparing the SHR genome sequence with that of the rat reference genome sequence, Aitman and colleagues generated a nearly complete catalog of SHR genomic variants that could contribute to hypertension and other phenotypes.

They also found that genes known to be abnormally expressed in SHR are especially enriched for sequence variants.

The group expected that the genome sequence would reveal mutations disrupting a number of genes in the SHR strain, however the number of mutated genes they found was quite surprising – 788 genes are mutated in SHR compared to the reference genome, including 60 that are deleted altogether.

“So many major differences in protein sequence were unexpected because of the previous belief that differences in a small number of genes and proteins would be responsible for the phenotypic differences between such rat strains,” said Aitman.

Of the 788 mutated genes identified in the SHR genome, many are related to cellular functions such as ion transport and plasma membrane localization, as well as immunological and neurological processes.

The authors suggest that defects in these functional categories may be causally associated with the known phenotypes of this strain.

Aitman said that their characterization of genetic variation in the hypertensive rat would be invaluable for complete elucidation of the causes of hypertension and related traits at the molecular level in hypertensive rat.

“This in turn will pave the way for greater understanding of the genetic basis of hypertension in humans,” Aitman said.

The study has been published online in Genome Research. (ANI)

Five-minute screening test could cut risk of developing bowel cancer

London, Apr 28 (ANI): A five-minute screening test has been developed, which researchers say, could cut the risk of developing bowel cancer by a third.

The research led by Imperial College London has been published in the Lancet.

According to the 16-year study, funded by the Medical Research Council, the National Institute for Health Research, and Cancer Research UK, a single flexible sigmoidoscopy examination in men and women aged between 55 and 64 reduced the incidence of bowel cancer by a third, compared with a control group who had usual care.

Screening with flexible sigmoidoscopy (named the ”Flexi-Scope test” by the research team) was particularly effective in the lower bowel, where it halved incidence of the disease.

Over the course of the study, bowel cancer mortality was reduced by 43 percent in the group that had the Flexi-Scope test compared with the control group.

The randomised trial followed 170,432 people over an average period of 11 years, of whom 40,674 underwent a single Flexi-Scope exam.

Professor Wendy Atkin from the Department of Surgery and Cancer at Imperial College London, who led the research, said: “Our study shows for the first time that we could dramatically reduce the incidence of bowel cancer, and the number of people dying from the disease, by using this one-off test. No other bowel cancer screening technique has ever been shown to prevent the disease. Our results suggest that screening with Flexi-Scope could save thousands of lives.”

The Flexi-Scope test works by detecting and removing growths on the bowel wall, known as polyps, which can become cancerous if they are left untreated. Flexi-Scope is able to prevent cancer from developing by removing polyps before they become cancerous. (ANI)

Yeast cells decide whether to have sex with each other within 2mins of meeting

London, April 19 (ANI): Yeast cells can decide to mate within two minutes of meeting each other, a new research has found.

According to one of the authors of the study, from Imperial College London, the findings of the study could be helpful for researchers looking at how cancer cells and stem cells develop.

Yeasts are single-celled microbes that scientists often use as model organisms, to understand how cells work.

Yeasts usually reproduce asexually, by a process called budding, where a part of the cell is pinched off and becomes a new cell, identical to the original.

However, there are times when yeast cells reproduce sexually, by mating.

The mating process involves one cell of each sex joining together, then mixing their DNA and splitting apart again.

To do this, the cells each have to produce a nodule that they can join together, called a shmoo. The process of shmooing takes around two hours.

For the new study, researchers from Imperial College London, Université de Montréal, McGill University and the University of Edinburgh determined that a yeast cell”s decision to mate is controlled by a chemical change on a single protein.

This change takes place two minutes after the cell detects a pheromone produced by the opposite sex.

The study team also found that in order for the mating process to be switched on, the pheromone must reach a critical concentration in the environment around the yeast cell.

Below this concentration, the yeast cell continues to reproduce asexually.

Dr Vahid Shahrezaei, one of the authors of the study from the Department of Mathematics at Imperial College London, said: “Shmooing is a very energy-intensive process for yeast cells. We think this switching process at a certain pheromone concentration may have evolved to make sure the cells only get prepared for sexual reproduction if a mate is sufficiently close enough and able to mate.”

The researchers used a highly complex mathematical model to find what switches the mating process on and off, factoring in experimental data about the concentration of pheromones around the cell, the concentrations of different proteins relevant to mating inside the cell and how strongly these proteins bind together.

Dr Shahrezaei said: “Yeast cells live in a very noisy environment – they are surrounded by different chemicals, including pheromones and food, and their own machinery inside the cell produces lots of biomolecules that interact with each other. We wanted to see how cells make sense of this noisy environment and work out what is happening, at a molecular level, to make a important decision like mating.

“By combining experiments and mathematical modelling that take lots of different factors into consideration, we have been able to show exactly what is happening inside a yeast cell to make it decide whether to mate with another cell. We also showed that the mechanism that leads the cells to make their decision is very robust, meaning it is not affected by molecular noise in the environment.”

Senior author Dr Stephen Michnick, a Université de Montréal biochemistry professor and Canada Research Chair in Integrative Genomics, said: “Although yeast is dramatically different from people, at a molecular and cellular level we have a lot in common.

“The same molecules that create the switching decision in yeast are found in very similar forms in human cells. Similar switching decisions to those made by yeast are made by stem cells during embryonic development and become dysfunctional in cancers.”

The study has appeared in the journal Nature. (ANI)

Yeast cells decide whether to have sex with each other within 2mins of meeting

London, April 19 (ANI): Yeast cells can decide to mate within two minutes of meeting each other, a new research has found.

According to one of the authors of the study, from Imperial College London, the findings of the study could be helpful for researchers looking at how cancer cells and stem cells develop.

Yeasts are single-celled microbes that scientists often use as model organisms, to understand how cells work.

Yeasts usually reproduce asexually, by a process called budding, where a part of the cell is pinched off and becomes a new cell, identical to the original.

However, there are times when yeast cells reproduce sexually, by mating.

The mating process involves one cell of each sex joining together, then mixing their DNA and splitting apart again.

To do this, the cells each have to produce a nodule that they can join together, called a shmoo. The process of shmooing takes around two hours.

For the new study, researchers from Imperial College London, Université de Montréal, McGill University and the University of Edinburgh determined that a yeast cell”s decision to mate is controlled by a chemical change on a single protein.

This change takes place two minutes after the cell detects a pheromone produced by the opposite sex.

The study team also found that in order for the mating process to be switched on, the pheromone must reach a critical concentration in the environment around the yeast cell.

Below this concentration, the yeast cell continues to reproduce asexually.

Dr Vahid Shahrezaei, one of the authors of the study from the Department of Mathematics at Imperial College London, said: “Shmooing is a very energy-intensive process for yeast cells. We think this switching process at a certain pheromone concentration may have evolved to make sure the cells only get prepared for sexual reproduction if a mate is sufficiently close enough and able to mate.”

The researchers used a highly complex mathematical model to find what switches the mating process on and off, factoring in experimental data about the concentration of pheromones around the cell, the concentrations of different proteins relevant to mating inside the cell and how strongly these proteins bind together.

Dr Shahrezaei said: “Yeast cells live in a very noisy environment – they are surrounded by different chemicals, including pheromones and food, and their own machinery inside the cell produces lots of biomolecules that interact with each other. We wanted to see how cells make sense of this noisy environment and work out what is happening, at a molecular level, to make a important decision like mating.

“By combining experiments and mathematical modelling that take lots of different factors into consideration, we have been able to show exactly what is happening inside a yeast cell to make it decide whether to mate with another cell. We also showed that the mechanism that leads the cells to make their decision is very robust, meaning it is not affected by molecular noise in the environment.”

Senior author Dr Stephen Michnick, a Université de Montréal biochemistry professor and Canada Research Chair in Integrative Genomics, said: “Although yeast is dramatically different from people, at a molecular and cellular level we have a lot in common.

“The same molecules that create the switching decision in yeast are found in very similar forms in human cells. Similar switching decisions to those made by yeast are made by stem cells during embryonic development and become dysfunctional in cancers.”

The study has appeared in the journal Nature. (ANI)

Dark chocolate good for liver disease patients

Doctors could soon be prescribing a dose of dark chocolate to help patients with liver disease, according to a new Spanish research.

The study suggests that dark chocolate can benefit patients suffering from liver cirrhosis and from dangerously high blood pressure in their abdomen.

It contains potent anti-oxidants, which reduce the post-prandial (after-meal) blood pressure in the liver (or portal hypertension) associated with damaged liver blood vessels (endothelial dysfunction).

“As well as advanced technologies and high science, it is important to explore the potential of alternative sources which can contribute to the overall wellbeing of a patient,” Professor Mark Thursz, MD FRCP, Vice Secretary of EASL and Professor of Hepatology, at Imperial College London said.

“This study shows a clear association between eating dark chocolate and portal hypertension and demonstrates the potential importance of improvements in the management of cirrhotic patients, to minimise the onset and impact of end stage liver disease and its associated mortality risks,” he added.

Cirrhosis is scarring of the liver as a result of long-term, continuous damage to the liver. In cirrhosis, circulation in the liver is damaged by oxidative stress and reduced antioxidant systems. After eating, blood pressure in the abdominal veins usually increases due to increased blood flow to the liver.

This is particularly dangerous and damaging to cirrhotic patients as they already have increased blood pressure in the liver (portal hypertension) and elsewhere, which, if severe, can cause blood vessel rupture.

Thus, eating dark chocolate may ultimately prevent this potential threat to cirrhotic patients.

In the study, 21 patients with end stage liver disease were randomised to receive a liquid meal containing white chocolate or one containing dark chocolate. Various measurements were taken before the meal and 30 minutes afterwards.

The dark chocolate meal caused a smaller rise in blood pressure in the liver than the white chocolate meal.

White chocolate does not contain any cocoa flavonoids, which have the anti-oxidant properties.

The study has been at the International Liver CongressTM 2010, the Annual Meeting of the European Association for the Study of Liver in Vienna, Austria.

Dark chocolate good for liver disease patients

Washington, April 16 (ANI): Doctors could soon be prescribing a dose of dark chocolate to help patients with liver disease, according to a new Spanish research.

The study suggests that dark chocolate can benefit patients suffering from liver cirrhosis and from dangerously high blood pressure in their abdomen.

It contains potent anti-oxidants, which reduce the post-prandial (after-meal) blood pressure in the liver (or portal hypertension) associated with damaged liver blood vessels (endothelial dysfunction).

“As well as advanced technologies and high science, it is important to explore the potential of alternative sources which can contribute to the overall wellbeing of a patient,” Professor Mark Thursz, MD FRCP, Vice Secretary of EASL and Professor of Hepatology, at Imperial College London said.

“This study shows a clear association between eating dark chocolate and portal hypertension and demonstrates the potential importance of improvements in the management of cirrhotic patients, to minimise the onset and impact of end stage liver disease and its associated mortality risks,” he added.

Cirrhosis is scarring of the liver as a result of long-term, continuous damage to the liver. In cirrhosis, circulation in the liver is damaged by oxidative stress and reduced antioxidant systems. After eating, blood pressure in the abdominal veins usually increases due to increased blood flow to the liver.

This is particularly dangerous and damaging to cirrhotic patients as they already have increased blood pressure in the liver (portal hypertension) and elsewhere, which, if severe, can cause blood vessel rupture.

Thus, eating dark chocolate may ultimately prevent this potential threat to cirrhotic patients.

In the study, 21 patients with end stage liver disease were randomised to receive a liquid meal containing white chocolate or one containing dark chocolate. Various measurements were taken before the meal and 30 minutes afterwards.

The dark chocolate meal caused a smaller rise in blood pressure in the liver than the white chocolate meal.

White chocolate does not contain any cocoa flavonoids, which have the anti-oxidant properties.

The study has been at the International Liver CongressTM 2010, the Annual Meeting of the European Association for the Study of Liver in Vienna, Austria. (ANI)

Now, play ‘Pong’ with the blink of an eye

Washington, Mar 27 (ANI): A computer game that is operated by eye movements has been developed by students at Imperial College London.

The revolutionary game could allow people with severe physical disabilities to become ”gamers” for the first time, scientists announced.

The students have adapted an open source game called ”Pong”, where a player moves a bat to hit a ball as it bounces around the screen. The adaptation enables the player to move the bat using their eye.

To play the game, the user wears special glasses containing an infrared light and a webcam that records the movement of one eye.

The webcam is linked to a laptop where a computer program syncs the player”s eye movements to the game.

The prototype game is very simple but the students believe that the technology behind it could be adapted to create more sophisticated games and applications such as wheelchairs and computer cursors controlled by eye movements.

One of the major benefits of the new technology is that it is inexpensive, using off-the-shelf hardware and costing approximately 25 pounds to make.

Eye movement systems that scientists currently use to study the brain and eye motion cost around 27,000 pounds, say the researchers.

Dr Aldo Faisal, the team”s supervisor from the Department of Computing and the Department of Bioengineering at Imperial College London, says: “Remarkably, our undergraduates have created this piece of neurotechnology using bits of kit that you can buy in a shop, such as webcams. The game that they”ve developed is quite simple, but we think it has enormous potential, particularly because it doesn”t need lots of expensive equipment. We hope to eventually make the technology available online so anyone can have a go at creating new applications and games with it and we”re optimistic about where this might lead. We hope it could ultimately provide entertainment options for people who have very little movement. In the future, people might be able to blink to turn pages in an electronic book, or switch on their favourite song, with the roll of an eye.” (ANI)

Harry Potter’s invisibility cloak created in 3D

Washington, Mar 19 (ANI): The magical cloak that featured in the Harry Potter series has become closer to reality, thanks to German scientists who’ve created a three-dimensional “invisibility cloak” that can hide objects by bending light waves.

Scientists from Karlsruhe Institute of Technology in Germany and Imperial College London reported their discovery in the journal Science.

The boffins used their cloak, made using photonic crystals with a structure resembling piles of wood, to conceal a small bump on a gold surface, reports Discovery News.

“It”s kind of like hiding a small object underneath a carpet — except this time the carpet also disappears,” they said.

“We put an object under a microscopic structure, a little like a reflective carpet,” said Nicholas Stenger, one of the researchers who worked on the project.

“When we looked at it through a lens and did spectroscopy, no matter what angle we looked at the object from, we saw nothing. The bump became invisible,” said Stenger.

The “cloak” hid an object from detection using light of wavelengths close to those that are visible to humans.

Now, the boffins are working to recreate the disappearing bump but on a larger scale.

Stenger said: “Theoretically, it would be possible to do this on a large scale but technically, it”s totally impossible with the knowledge we have now.” (ANI)

Scientists find meteorite that came from innermost asteroid belt between Mars and Jupiter

Washington, September 18 (ANI): In a very rare finding, scientists have discovered an unusual kind of meteorite in the Western Australian desert and have uncovered that it came from the innermost main asteroid belt between Mars and Jupiter.

Meteorites are the only surviving physical record of the formation of our Solar System.

However, information about where individual meteorites originated, and how they were moving around the Solar System prior to falling to Earth, is available for only a dozen of around 1100 documented meteorite falls over the past two hundred years.

According to Dr Phil Bland from the Department of Earth Science and Engineering at Imperial College London, the lead author of the study, “We are incredibly excited about our new finding. Meteorites are the most analysed rocks on Earth, but it’s really rare for us to be able to tell where they came from.”

The new meteorite, which is about the size of cricket ball, is the first to be retrieved since researchers from Imperial College London, Ondrejov Observatory in the Czech Republic, and the Western Australian Museum, set up a trial network of cameras in the Nullarbor Desert in Western Australia in 2006.

The researchers aim to use these cameras to find new meteorites, and work out where in the Solar System they came from, by tracking the fireballs that they form in the sky.

The new meteorite was found on the first day of searching using the new network, by the first search expedition, within 100m of the predicted site of the fall.

The meteorite appears to have been following an unusual orbit, or path around the Sun, prior to falling to Earth in July 2007, according to the researchers’ calculations.

The team believes that it started out as part of an asteroid in the innermost main asteroid belt between Mars and Jupiter.

It then gradually evolved into an orbit around the Sun that was very similar to Earth’s.

The new meteorite is also unusual because it is composed of a rare type of basaltic igneous rock.

According to the researchers, its composition, together with the data about where the meteorite comes from, fits with a recent theory about how the building blocks for the terrestrial planets were formed.

This theory suggests that the igneous parent asteroids for meteorites like today’s formed deep in the inner Solar System, before being scattered out into the main asteroid belt.

Asteroids are widely believed to be the building blocks for planets like the Earth, so the new finding provides another clue about the origins of the Solar System. (ANI)

Master gene that switches on disease-fighting cells identified

London, Sep 14 (ANI): British scientists have identified the master gene, called E4bp4, that causes blood stem cells to turn into disease-fighting ‘Natural Killer’ (NK) immune cells.

The discovery, by researchers at Imperial College London, UCL and the Medical Research Council’s National Institute for Medical Research, could one day help scientists boost the body’s production of these frontline tumour-killing cells, creating new ways to treat cancer.

By ‘knocking out’ E4bp4 in a mouse model, the researchers created the world’s first animal model entirely lacking NK cells, but with all other blood cells and immune cells intact.

The breakthrough model should help solve the mystery of the role that Natural Killer cells play in autoimmune diseases, such as diabetes and multiple sclerosis.

According to many scientists, these diseases are a result of malfunctioning NK cells that turn on the body and attack healthy cells, which cause disease instead of fighting it.

They believe that clarifying NK cells’ role could lead to new ways of treating these conditions.

Natural Killer cells – a type of white blood cell – are a major component of the human body’s innate, quick-response immune system, providing a fast frontline defence against tumours, viruses and bacterial infections.

The gene E4bp4 is the ‘master gene’ for NK cell production, which means it is the primary driver that causes blood stem cells in the bone marrow to differentiate into NK cells.

Led by Dr Hugh Brady, the researchers are hoping to progress with a drug treatment for cancer patients which reacts with the protein expressed by their E4bp4 gene, causing their bodies to produce a higher number of NK cells than normal, to increase the chances of successfully destroying tumours.

“If increased numbers of the patient’s own blood stem cells could be coerced into differentiating into NK cells, via drug treatment, we would be able to bolster the body’s cancer-fighting force, without having to deal with the problems of donor incompatibility,” Nature quoted Brady as saying.

The researchers proved the pivotal role E4bp4 plays in NK production when they knocked the gene out in a mouse model.

Without E4bp4 the mouse produced no NK cells whatsoever but other types of blood cell were unaffected.

“Now finally, with our discovery of the NK cell master gene and subsequent creation of our mouse model, we will be able to find out if the progression of these diseases is impeded or aided by the removal of NK cells from the equation. This will solve the often-debated question of whether NK cells are always the ‘good guys’, or if in certain circumstances they cause more harm than good,” said Brady.

The study has been published in Nature Immunology. (ANI)

Why pandemic swine flu causes more severe symptoms than seasonal flu

London, September 11 (ANI): Scientists at Imperial College London have warned that pandemic swine flu can infect cells deeper in the lungs than seasonal flu can.

They write in a research paper that this may help understand why people infected with the pandemic strain of swine-origin H1N1 influenza are more likely to suffer more severe symptoms than those infected with the seasonal strain of H1N1.

The researchers have also stressed the need for monitoring the current pandemic H1N1 influenza virus for any changes in the way it infects cells, which may make infections more serious.

Generally, influenza viruses infect cells by attaching to bead-like molecules on the outside of the cell, known as receptors. If a virus cannot find its specific receptors, it cannot get into the cell.

Seasonal influenza viruses attach to receptors found on cells in the nose, throat and upper airway, enabling them to infect a person’s respiratory tract.

In the current study, the researchers have found that pandemic H1N1 swine flu can also attach to a receptor found on cells deep inside the lungs, which can result in a more severe lung infection.

They say that the pandemic influenza virus’s ability to stick to the additional receptors may explain why the virus replicates, and spreads between cells more quickly.

“Most people infected with swine-origin flu in the current pandemic have experienced relatively mild symptoms. However, some people have had more severe lung infections, which can be worse than those caused by seasonal flu. Our new research shows how the virus does this – by attaching to receptors mostly found on cells deep in the lungs. This is something seasonal flu cannot do,” Nature Biotechnology quoted Professor Ten Feizi, from the Division of Medicine at Imperial College London, as having writte in the research paper.

The researchers found that pandemic H1N1 influenza bound more weakly to the receptors in the lungs than to those in the upper respiratory tract, which is why most people infected with the virus have experienced mild symptoms.

However, the researchers are concerned that the virus could mutate to bind more strongly to these receptors.

“If the flu virus mutates in the future, it may attach to the receptors deep inside the lungs more strongly, and this could mean that more people would experience serious symptoms. We think scientists should be on the lookout for these kinds of changes in the virus so we can try to find ways of minimising the impact of such changes,” said Prof. Feizi.

“Receptor binding determines how well a virus spreads between cells and causes an infection. Our new study adds to our understanding of how swine-origin influenza H1N1 virus is behaving in the current pandemic, and shows us changes we need to look out for,” added Prof. Feizi.

The financial assistance for the study came from the Wellcome Trust, the Medical Research Council and the Engineering and Physical Sciences Research Council. (ANI)

Why broccoli, cabbage, cauliflower are good for heart

Washington, Sept 5 (ANI): Here’s why broccoli, cabbage and cauliflower are good for the heart – a chemical found in these vegetables can boost a natural defence mechanism to protect arteries from disease.

The build up of fatty plaques in arteries called atherosclerosis leads to heart disease.

The Imperial College London team has shown that a protein that usually protects against plaque build up called Nrf2 is inactive in areas of arteries that are prone to disease.

Treatment with a chemical found in green “brassica” vegetables such as broccoli can activate Nrf2 in these disease-prone regions.

“We found that the innermost layer of cells at branches and bends of arteries lack the active form of Nrf2, which may explain why they are prone to inflammation and disease,” BBC News quoted lead researcher Dr Paul Evans as saying.

“Treatment with the natural compound sulforaphane reduced inflammation at the high-risk areas by ‘switching on’ Nrf2.

“Sulforaphane is found naturally in broccoli, so our next steps include testing whether simply eating broccoli, or other vegetables in their ‘family’, has the same protective effect.

“We also need to see if the compound can reduce the progression of disease in affected arteries,” he added.

Professor Peter Weissberg, medical director of the British Heart Foundation, which funded the research said that the new findings provide a possible mechanism by which eating vegetables protects against heart disease.

During the study, the researchers genetically engineered mice to lack the Nrf2 protein.

The research found that in straight sections of arteries Nrf2 was present in the endothelial ‘lining’ cells. Through its action on other proteins, it prevented the cells from becoming inflamed, an early stage in the development of atherosclerosis.

The study appears in Arteriosclerosis Thrombosis and Vascular Biology. (ANI)

Healthy lifestyle simplest, best way to cut breast cancer risk

London, Sept 1 (ANI): A healthy lifestyle, including keeping weight down, exercising for 30 minutes a day and limiting alcohol to a single drink a day, is the simplest and best way for women to cut the risk of breast cancer, says a new study.

The study by the World Cancer Research Fund (WCRF ) has found the strongest evidence yet that lifestyle is linked to the risk of developing breast cancer, reports The Times.

The research came to the conclusion after showing that more than four out of ten cases could be prevented if women exercised, limited their alcohol intake and maintained a healthy weight.

Breastfeeding also helps to reduce the risk of developing the disease, the scientists at Imperial College London said.

Arlene Wilkie, director of research and policy at Breast Cancer Campaign, said: “This review provides further evidence that maintaining a healthy weight throughout life along with regular exercise will reduce the risk of health problems such as breast cancer, heart disease, high blood pressure, diabetes and arthritis.” (ANI)

Costs of adapting to climate change could be much greater than expected

London, August 28 (ANI): A new study has determined that the global cost of adapting to climate change has been grossly underestimated, and it could be much greater than expected.

According to a report in Nature News, although it doesn’t provide concrete new estimates, the report suggests that the total cost of adapting to climate change could be at least 2-3 times more than the previous estimate from the United Nations Framework Convention on Climate Change (UNFCCC).

That figure, published in 2007, suggested that the annual cost from 2030 would be between 49 billion dollars and 171 billion dollars.

The main difference, according to the study, is that the UN number did not account for climate change’s effects on key sectors such as energy, manufacturing, tourism and natural ecosystems.

“The UNFCCC’s estimations were made in a few weeks and weren’t independently reviewed,” said the study’s lead author, Martin Parry, a visiting research fellow at the Grantham Institute for Climate Change at Imperial College London and a former co-chair of a working group of the Intergovernmental Panel on Climate Change (IPCC).

The UNFCCC numbers were initially intended to come from a literature review of other economic studies, according to Sudhir Sharma, manager of financial cooperation and capacity building at the UNFCCC secretariat in Bonn, Germany.

But the team working on the estimates soon realized that there were massive gaps in the information needed.

The cost of adapting to climate change requires knowledge about what effects climate change will have, what the options are for responding to those changes, and how much those options will cost, according to Sharma.

Sharma argues his group’s estimates weren’t intended to be the final word, but rather a ball-park figure to get the negotiations rolling.

“We clearly indicated that this was not an exhaustive study,” he said. “Our objective was to kick-start the process of putting numbers on the cost of adaptation so that other groups could pick up the baton and refine them,” he added.

The latest study, published by the IIED and the Grantham Institute, has picked up that baton.

It suggests that the UNFCCC estimate of 11 billion dollars per year for adapting to changes in water supply overlooks the expenses of floods and of transporting water from areas of plenty to areas to that need it.

But although the report says previous estimates for adaptation are too low, it doesn’t provide numbers, he admits.

“We didn’t try to come up with new numbers – we pointed out the gaps,” said Sharma. (ANI)

Costs of adapting to climate change could be much greater than expected

London, August 28 (ANI): A new study has determined that the global cost of adapting to climate change has been grossly underestimated, and it could be much greater than expected.

According to a report in Nature News, although it doesn’t provide concrete new estimates, the report suggests that the total cost of adapting to climate change could be at least 2-3 times more than the previous estimate from the United Nations Framework Convention on Climate Change (UNFCCC).

That figure, published in 2007, suggested that the annual cost from 2030 would be between 49 billion dollars and 171 billion dollars.

The main difference, according to the study, is that the UN number did not account for climate change’s effects on key sectors such as energy, manufacturing, tourism and natural ecosystems.

“The UNFCCC’s estimations were made in a few weeks and weren’t independently reviewed,” said the study’s lead author, Martin Parry, a visiting research fellow at the Grantham Institute for Climate Change at Imperial College London and a former co-chair of a working group of the Intergovernmental Panel on Climate Change (IPCC).

The UNFCCC numbers were initially intended to come from a literature review of other economic studies, according to Sudhir Sharma, manager of financial cooperation and capacity building at the UNFCCC secretariat in Bonn, Germany.

But the team working on the estimates soon realized that there were massive gaps in the information needed.

The cost of adapting to climate change requires knowledge about what effects climate change will have, what the options are for responding to those changes, and how much those options will cost, according to Sharma.

Sharma argues his group’s estimates weren’t intended to be the final word, but rather a ball-park figure to get the negotiations rolling.

“We clearly indicated that this was not an exhaustive study,” he said. “Our objective was to kick-start the process of putting numbers on the cost of adaptation so that other groups could pick up the baton and refine them,” he added.

The latest study, published by the IIED and the Grantham Institute, has picked up that baton.

It suggests that the UNFCCC estimate of 11 billion dollars per year for adapting to changes in water supply overlooks the expenses of floods and of transporting water from areas of plenty to areas to that need it.

But although the report says previous estimates for adaptation are too low, it doesn’t provide numbers, he admits.

“We didn’t try to come up with new numbers – we pointed out the gaps,” said Sharma. (ANI)

Scientists find ‘stopwatch for the solar system’

London, August 26 (ANI): In a new study, a team of scientists has described how aluminium radioisotopes can now offer precise timing of events 4.5 billion years ago, and thus have been dubbed as the ‘stopwatch for the solar system’.

According to a report by BBC News, the study shows that the rate of decay of isotopes can now be relied upon to give accurate measures of time for that period.

It is hoped that this will give new insights into how the Solar System formed in its first five million years.

The scientists showed how aluminium radioisotopes were uniformly distributed in the region where the Solar System was formed.

As the isotopes decayed steadily across the early Solar System, this allows their use as a type of clock for that period.

“We can now use the isotopes to measure the age of different chondrules, parts of meteorites, and understand far more about the early part of our Solar System,” one of the scientists, Johan Villeneuve, told BBC News.

The findings could also shed light on the origins of the planets.

Philip Bland, from Imperial College London, described the research as “a really nice study”.

“With their high precision measurements, they are able to date formation times for chondrules very precisely,” he said.

“And what is interesting is that they’ve shown that these building blocks for asteroids, and possibly for planets as well, formed over an extended period of two to three million years,” he added. (ANI)

Parasites’ quirky trick to persuade immune cells to invite them in for dinner

Washington, Aug 21 (ANI): Scientists from Imperial College London have found that parasite leishmania tricks immune system to let it enter the body and cause skin infection.

Leishmaniasis is an infection caused by Leishmania parasites that cause disfiguring and painful skin ulcers, and in severe cases the infection can also spread to the internal organs.

Patients with the infection often suffer from social exclusion because of their disfigurement.

Leishmania parasites are transmitted by sand flies. After the parasites infect a sand fly, they make a sticky gel so that when the fly bites a human, it regurgitates this gel into the body.

The new study conducted over mice showed that the gel persuades immune cells known as macrophages to feed the parasites, rather than killing them.

The gel helps the parasites to establish an infection by enticing macrophages to the bite site. Macrophages usually kill invading pathogens by eating and digesting them.

However, the gel persuades macrophages to engulf the parasites and feed them rather than digest them.

This happens within the first few days following infection, enabling the parasites to establish themselves and infect the skin.

“Leishmaniasis is a very debilitating disease, yet we know comparatively little about the way the parasites are transmitted by sand flies,” said Dr Matthew Rogers, lead author of the study from the Division of Investigative Science at Imperial College London.

“This is because when scientists study the disease they usually inject the parasite into tissues without including the gel or the sand fly’s saliva. Our new research shows that we must consider the way the parasites enter the body – along with the gel and saliva – if we are to recreate infection and get an accurate picture of what is going on.

“Our new research shows that Leishmania parasites are very cunning – they make their own gel to control the human immune system so they can establish a skin infection.

“There is more work to be done here – our previous work in mice has suggested that injecting a synthetic version of the gel into people might provide them with some protection against infection and we would like to explore this further,” he added.

The study is published in PLoS Pathogens. (ANI)