Protesters are accusing Enrique Pena Nieto, Mexico's newly elected president, of giving gifts to voters before the election.
By Galia Garcia Palafox,?Associated Press / July 8, 2012
A masked indigenous woman from Oaxaca protests outside Mexico's Federal Electoral Institute (IFE) in Mexico City July 5. Mexico's Enrique Pena Nieto was a clear victor in the presidential election, according to a second tally of votes made after the runner-up refused to accept defeat.
Edgard Garrido/REUTERS
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Tens of thousands of people marched in?Mexico's?capital on Saturday to protest Enrique Pena Nieto's apparent win in the country's presidential election, accusing his long ruling party of?buying?votes.
The protesters were angered by allegations that Pena Nieto's Institutional Revolutionary Party gave out bags of groceries, pre-paid gift cards and other goods to voters ahead of July 1 national elections.
The students, unionists and leftists in the march carried signs reading, "Pena, how much did it cost to become president?" and "Mexico, you pawned your future for 500 pesos."?Mexico?City officials put the size of the crowd that reached its central Zocalo plaza at 50,000.
"The fraud was carried out before (the election),?buying?votes, tricking the people," said Gabriel Petatan Garcia, a geography student who carried a sign in Finnish.
Protesters also carried signs in English, Japanese, French, German and other languages to call the attention of the international press.
Pena Nieto, a youthful, 45-year-old married to a soap opera star, won last Sunday's election by 6.6 percentage points, according to the official count, bringing the PRI back to power after 12 years in opposition. The party had ruled?Mexico?for 71 consecutive years, with what critics say was the help of corruption, patronage and?vote?fraud.
PRI officials deny the vote-buying charge and say the?vote?was free and fair.
The final?vote?count had Pena Nieto getting 38.21 percent support, leftist Andres Manuel Lopez Obrador of the Democratic Revolution Party with 31.59 percent, and Josefina Vazquez Mota of the conservative National Action Party with 25.41. The small New Alliance Party got 2.29 percent.
The final?vote?count must be certified in September by the Federal Electoral Tribunal. The tribunal has declined to overturn previously contested elections, including a 2006 presidential?vote?that was far closer than last Sunday's.
Accusations of vote-buying began surfacing in June, but sharpened later when people rushed to grocery stores on the outskirts of?MexicoCity to redeem pre-paid gift cards worth about 100 pesos ($7.50). Many said they got the cards from PRI supporters before the elections.
Lopez Obrador said millions of voters had received either pre-paid cards, cash, groceries, construction materials or appliances.
Some marchers covered the heads of statues with plastic shopping bags from Soriana ? the supermarket chain where the gift cards were redeemable ? to underline their protest.
"We have to come out in the streets to denounce that the PRI bought?votes, and there were people who sold them," said 32-year-old psychologist Raquel Ruiz.
Some protesters felt that overturning the election result would be difficult at this point, while others thought there were judicial means to still prevent Pena Nieto from assuming the presidency.
Lopez Obrador said he will file a formal legal challenge to the?vote?count in electoral courts in the coming days based on the allegation that PRI vote-buying illegally tilted millions of?votes.
Simply giving away such gifts is not illegal under Mexican electoral law, as long as the expense is reported to electoral authorities. Giving gifts to influence?votes?is a crime, though is not generally viewed as grounds for overturning an election.
Leonardo Valdes, the president of the Federal Electoral Institute, has said he doesn't see any grounds for overturning the results but that an investigation into the gift cards had been launched.
PRI spokesman Eduardo Sanchez said earlier this week that the gift-card event had been "a theatrical representation" mounted by the left. Sanchez claimed supporters of Lopez Obrador took hundreds of people to the stores, dressed them in PRI T-shirts, gave them gift cards, emptied store shelves to create an appearance of panic?buying, and brought TV cameras in to create the false impression that the PRI had given out the cards.
Cesar Yanez, the spokesman for Lopez Obrador's campaign, denied the PRI accusation.
Cloud video services company QuickPlay Media is announcing today that Chicago-based private equity firm Madison Dearborn Partners will be paying about $100 million to take a majority stake in the company. With the deal, Madison Dearborn has essentially bought out QuickPlay Media's previous investors, which include General Catalyst, Ventures West, J.L Albright, and Up Capital. With the close of the deal, Madison Dearborn and QuickPlay employees will own pretty much the entire company, with a small number of minority shareholders retaining a stake, including Toronto-based Difference Capital. Prior to the sale, QuickPlay Media had raised a total of $43 million, CEO Wayne Purboo told me.
Contact: David Orenstein david_orenstein@brown.edu 401-863-1862 Brown University
Methylation provides signal of unique mix of leukocytes
PROVIDENCE, R.I. [Brown University] When a person is sick, there is a tell-tale sign in their blood: a different mix of the various types of immune cells called leukocytes. A group of scientists at several institutions including Brown University has discovered a way to determine that mix from the DNA in archival or fresh blood samples, potentially providing a practical new technology not only for medical research but also for clinical diagnosis and treatment monitoring of ailments including some cancers.
The key to the new technique, described in two recent papers, is that scientists have identified in each kind of leukocyte a unique chemical alteration to its DNA, called methylation. By detecting these methylation signatures in a patient's blood sample and applying a mathematical analysis, the researchers are able to determine the relative levels of different leukocytes and correlate those with specific diseases.
"You can simply look at the DNA and discern from the methylation marks the relative abundance of different type of leukocytes," said Karl Kelsey, professor of pathology and laboratory medicine in the Warren Alpert Medical School of Brown University and a senior author on both papers. "It's a way to more easily interrogate the immune system of a lot of people."
Other tests, using flow cytometry, can already sort through the abundance of different leukocytes in a blood sample, but they require the blood to be fresh and leukocyte cell membranes to be intact. Because the DNA in a blood sample remains even after cells have died and degraded, tests based on detecting methylation could help doctors or researchers analyze a patient's blood sample that has either aged or has simply not been kept fresh.
In a paper published in advance online June 19 in Cancer Epidemiology, Biomarkers, and Prevention, the researchers describe using their technique to distinguish accurately which blood samples came from patients with head and neck squamous cell carcinoma, ovarian cancer, or bladder cancer. By using methylation to determine the leukocyte populations in each sample, they could predict that the same samples were as much as 10 times more likely to have come from a patient with ovarian cancer than a healthy control patient, six times more likely to be from a head and neck cancer patient than a healthy control, or twice as likely to be from a bladder cancer patient than a control.
"Our approach represents a simple, yet powerful and important new tool for medical research and may serve as a catalyst for future blood-based disease diagnostics," wrote the authors, who hail from Dartmouth, Oregon State University, the University of Minnesota, and the University of CaliforniaSan Francisco, as well as Brown. Several authors worked with Kelsey at Brown during the research.
They describe the technique and its analytical methods in deep mathematical detail in another paper published in May in BMC Bioinformatics. They also report experiments that included analyses of the leukocyte mix of noncancer conditions such as Down syndrome and obesity.
The paper found many examples of differences between the immune cell mix of healthy controls and people with specific illnesses. For example, obese African Americans had an estimated increase in granulocyte leukocytes of about 12 percentage points. People with Down syndrome, had 4.8 percentage points fewer B cells. For head and neck cancer, they noted a 10.4 percentage point drop in CD4+ T-lymphocytes.
"Any disease that has an immune-cell mediated component to it would have applicability," Kelsey said.
In both papers, the authors said they expect that the technique will be applied in clinical and research efforts.
"Our approach provides a completely novel tool for the study of the immune profiles of diseases where only DNA can be accessed," the authors wrote in Cancer Epidemiology Biomarkers and Prevention. "That is, we believe this approach has utility not only in cancer diagnostics and risk-prediction, but can also be applied to future research (including stored specimens) for any disease where the immune profile holds medical information."
###
In addition to Kelsey, other authors on both papers are Devin Koestler, Carmen Marsit, and Brock Christensen of Dartmouth; E. Andres Houseman of Oregon State; Heather Nelson of Minnesota; William Accomando of Brown; and John Wiencke of UCSF. On the Cancer Epidemiology Biomarkers and Prevention paper, Scott Langevin of Brown and Margaret Karagas of Dartmouth are co-authors.
The National Institutes of Health funded the research in both papers. Support for the Cancer Epidemiology Biomarkers and Prevention paper also came from the Flight Attendant Medical Research Institute.
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AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.
Contact: David Orenstein david_orenstein@brown.edu 401-863-1862 Brown University
Methylation provides signal of unique mix of leukocytes
PROVIDENCE, R.I. [Brown University] When a person is sick, there is a tell-tale sign in their blood: a different mix of the various types of immune cells called leukocytes. A group of scientists at several institutions including Brown University has discovered a way to determine that mix from the DNA in archival or fresh blood samples, potentially providing a practical new technology not only for medical research but also for clinical diagnosis and treatment monitoring of ailments including some cancers.
The key to the new technique, described in two recent papers, is that scientists have identified in each kind of leukocyte a unique chemical alteration to its DNA, called methylation. By detecting these methylation signatures in a patient's blood sample and applying a mathematical analysis, the researchers are able to determine the relative levels of different leukocytes and correlate those with specific diseases.
"You can simply look at the DNA and discern from the methylation marks the relative abundance of different type of leukocytes," said Karl Kelsey, professor of pathology and laboratory medicine in the Warren Alpert Medical School of Brown University and a senior author on both papers. "It's a way to more easily interrogate the immune system of a lot of people."
Other tests, using flow cytometry, can already sort through the abundance of different leukocytes in a blood sample, but they require the blood to be fresh and leukocyte cell membranes to be intact. Because the DNA in a blood sample remains even after cells have died and degraded, tests based on detecting methylation could help doctors or researchers analyze a patient's blood sample that has either aged or has simply not been kept fresh.
In a paper published in advance online June 19 in Cancer Epidemiology, Biomarkers, and Prevention, the researchers describe using their technique to distinguish accurately which blood samples came from patients with head and neck squamous cell carcinoma, ovarian cancer, or bladder cancer. By using methylation to determine the leukocyte populations in each sample, they could predict that the same samples were as much as 10 times more likely to have come from a patient with ovarian cancer than a healthy control patient, six times more likely to be from a head and neck cancer patient than a healthy control, or twice as likely to be from a bladder cancer patient than a control.
"Our approach represents a simple, yet powerful and important new tool for medical research and may serve as a catalyst for future blood-based disease diagnostics," wrote the authors, who hail from Dartmouth, Oregon State University, the University of Minnesota, and the University of CaliforniaSan Francisco, as well as Brown. Several authors worked with Kelsey at Brown during the research.
They describe the technique and its analytical methods in deep mathematical detail in another paper published in May in BMC Bioinformatics. They also report experiments that included analyses of the leukocyte mix of noncancer conditions such as Down syndrome and obesity.
The paper found many examples of differences between the immune cell mix of healthy controls and people with specific illnesses. For example, obese African Americans had an estimated increase in granulocyte leukocytes of about 12 percentage points. People with Down syndrome, had 4.8 percentage points fewer B cells. For head and neck cancer, they noted a 10.4 percentage point drop in CD4+ T-lymphocytes.
"Any disease that has an immune-cell mediated component to it would have applicability," Kelsey said.
In both papers, the authors said they expect that the technique will be applied in clinical and research efforts.
"Our approach provides a completely novel tool for the study of the immune profiles of diseases where only DNA can be accessed," the authors wrote in Cancer Epidemiology Biomarkers and Prevention. "That is, we believe this approach has utility not only in cancer diagnostics and risk-prediction, but can also be applied to future research (including stored specimens) for any disease where the immune profile holds medical information."
###
In addition to Kelsey, other authors on both papers are Devin Koestler, Carmen Marsit, and Brock Christensen of Dartmouth; E. Andres Houseman of Oregon State; Heather Nelson of Minnesota; William Accomando of Brown; and John Wiencke of UCSF. On the Cancer Epidemiology Biomarkers and Prevention paper, Scott Langevin of Brown and Margaret Karagas of Dartmouth are co-authors.
The National Institutes of Health funded the research in both papers. Support for the Cancer Epidemiology Biomarkers and Prevention paper also came from the Flight Attendant Medical Research Institute.
[ | E-mail | Share ]
?
AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.
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Apple has removed the EPA (Environmental Protection Agency) EPEAT (Electronic Product Environmental Assessment Tool) certification from 39 of their product lines, including displays and computers. The Wall Street Journal quotes Robert Frisbee, CEO of EPEAT:
?[Apple] said their design direction was no longer consistent with the EPEAT requirements,? Frisbee said. The company did not elaborate, Frisbee said. ?They were important supporters and we are disappointed that they don?t want their products measured by this standard anymore.?
The general assumption seems to be that with products like the new iPad and the Retina MacBook Air, Apple's design and manufacturing process is emphasizing thinness and lightness over recyclability and repairability. This may or may not matter to consumers, who are increasingly faced with disposable, appliance-like consumer electronics. However, some private and public organizations require EPEAT certification for bulk purposes. Would they bend or break their own rules just to get Apple products on the floor?
There's no EPEAT certification for tablets or smartphones, and the iPad and iPhone comprise the vast majority of Apple's earnings. Even for Macs, consumer purchases likely dwarf organizational buying.
EPEAT is also only part of the typical environmental checklist Apple presents during new product announcements. Whether Apple decides they're important enough to go with a different certification, to create their own, or ultimately to blaze ahead with no particular environmental certification remains to be seen.
iMore's Ally Kazmucha, who also operates iOS device repair shop, PXLFIX, has previously taken issue with Apple's increasing divergence from repairable technology, as has iFixit's Kyle Wiens writing for Wired, and Richard Gaywood at TUAW.
Would lack of EPEAT certification stop you from buying any other Apple products?
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The Future of Health Now has assembled a group of doctors, speakers, dreamers and innovators who are all uniquely-focused on niche areas in the rapidly-intersecting worlds of western and natural medicine. Right now FOHN has made available over 20 Interviews in their official web site here ? http://www.healthpotent.com/go-get/fohn/ featuring a number of household names like Tim Ferriss of the 4 Four Body, Dr. Mark Hyman, Dr. Daniel Amen, Bill Phillips, Daphne Oz and John Mackie the Co-CEO of Whole Foods.
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Public release date: 9-Jul-2012
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