Friday, December 30, 2011

Mayo Clinic to launch sequencing project for individual care

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December 30, 2011
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  Today's Top Story 
  • Mayo Clinic to launch sequencing project for individual care
    Mayo Clinic plans to initiate a pilot trial early next year to sequence the genomes of thousands of volunteers as part of a landmark project aimed at personalizing medical care. The genetic information will be stored and linked to the patients' medical records to help their doctors choose the most effective drugs for them while reducing side effects. "The advantage of whole genome sequencing is that you go after everything," said Dr. Gianrico Farrugia, director of Mayo Clinic's Center for Individualized Medicine in Minnesota. "... [I]t allows you to draw complex interaction pathways that you cannot draw by going after select genes." The Guardian (London) (12/27) LinkedInFacebookTwitterEmail this Story
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  Health Care & Policy 
 
  • NovaTarg to file IND for hepatitis C candidate in 2012
    NovaTarg is preparing to submit to the FDA next year an investigational new drug application for a hepatitis C drug, its first drug candidate. The firm received a $30,000 loan from the North Carolina Biotechnology Center to finance its research centered on AMPK, an enzyme that plays a role in how cells use energy. The research has applications in cancer, diabetes and liver disease treatments, NovaTarg said. MedCityNews.com (12/29) LinkedInFacebookTwitterEmail this Story
  • Researchers use stem cells to develop treatment for diseases
    Researchers at Stempeutics Research in Bangalore, India, are developing treatments for eight diseases, including heart problems and cerebral strokes, by growing mesenchymal stem cells from a donor's bone marrow in the lab. The cultured cells are intended to replace or regenerate diseased cells in a patient. The company plans to establish a facility that can produce large volumes of the cells. Business Standard (India) (12/28) LinkedInFacebookTwitterEmail this Story
  • Study links gene mutation to familial pancreatic cancer
    A study in Cancer Discovery found that people with mutations in the ATM gene are more prone to develop hereditary pancreatic cancer. Researchers sequenced 166 pancreatic cancer patients and found that four of them carried the ATM mutation while none of the 190 healthy individuals sequenced had the gene variant. The findings could result in the development of a new pancreatic cancer screening method for those who could be at hereditary risk, according to the researchers. HealthDay News (12/29) LinkedInFacebookTwitterEmail this Story
  • Research finds early warning sign for diabetes
    Mapping the variations in DNA methylation helped reveal a clear-cut, disease-predisposing DNA methylation "signature" in type 2 diabetes patients, Israeli researchers reported in Human Molecular Genetics. The technique may help provide an early warning for patients at risk of the disease and may also lead to the development of new treatment approaches in diabetes, researchers said. The Jerusalem Post (free registration) (12/29) LinkedInFacebookTwitterEmail this Story
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  Company & Financial News 
 
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  Featured Content 
 

  Food & Agriculture 
 
  • Hormone pathway could improve drought tolerance
    A team of plant cell biologists from the University of California, Riverside, have learned how to modify a plant's stress response pathway to increase its ability to respond to droughts. The discovery increases the ability of plant stress hormone receptors to turn on and continue working, and it could offer a new way of engineering crops suited to dry conditions. Minnesota Farm Guide (12/28) LinkedInFacebookTwitterEmail this Story
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  Industrial & Environmental 
  News from BIO 
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  Editor's Note 
  • SmartBrief will not publish Monday
    In observance of the New Year's holiday, SmartBrief will not publish Monday. Publication will resume Tuesday. Enjoy the holiday! LinkedInFacebookTwitterEmail this Story
  SmartQuote 
Anger makes dull men witty, but it keeps them poor."
--Francis Bacon,
British philosopher and statesman


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