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Stories tagged: DNA sequencing

Vitamin D Regulates Genes Associated with Susceptibility to Autoimmune Diseases

by on Thursday, March 10, 2011

Vitamin D is, at this point, probably one of the trendiest vitamins around. Everyone suddenly seems to be getting their vitamin D level tested (specifically vitamin D3 or 25(OH)D, also called calcidiol) and, when levels are found to be deficient, taking supplements. In November 2010, the Institute of Medicine tripled its daily recommendations for vitamin D from 200 International Units to 600 [1]. Severe vitamin D deficiency causes rickets, which leads to a softening and weakening of the bones, so milk has been fortified with vitamin D to prevent rickets. Less dramatic vitamin D deficiency has been implicated in ailments ranging from cancer to heart disease to schizophrenia to autoimmune diseases to colds and the flu. But how does vitamin D act in the body — how can it contribute to so many different physiological processes?

Functions of vitamin D

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President Obama Resists Cuts to Biomedical Research Funding

by on Monday, February 28, 2011

In President Barack Obama’s State of the Union address last month, he argued that government support for research and development to fund innovation is a necessary and critical investment that must be made, even in the face of a rising national debt. A coalition of biomedical researchers support his vision on science. The 2012 budget President Obama sent to Congress earlier this month seeks an increase in funding for biomedical research at the National Institutes of Health (NIH) and in basic science at other agencies, while making cuts and freezes in many other areas of government.

Obama and biomedical research funding

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NHGRI Vision to Move Genomic Medicine from Base Pairs to Bedside

by on Friday, February 11, 2011

A new strategic plan from an arm of the National Institutes of Health envisions scientists being able to identify genetic bases of most single-gene disorders and gaining new insights into multi-gene disorders in the next decade. This should lead to more accurate diagnoses, new drug targets and the development of practical treatments for many who today lack therapeutic options, according to the plan from the National Human Genome Research Institute (NHGRI).

Base pairs to bedside

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1000 Genomes Project Publishes Analysis of Completed Pilot Phase

by on Wednesday, November 17, 2010

Small genetic differences between individuals help explain why some people have a higher risk than others for developing illnesses such as diabetes or cancer. Recently in the journal Nature, the 1000 Genomes Project, an international public-private consortium, published the most comprehensive map of these genetic differences, called variations, estimated to contain approximately 95 percent of the genetic variation of any person on Earth.

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NIH Expands Network Focused On How Genes Affect Drug Responses

by on Tuesday, September 7, 2010

NIH Research News

The National Institutes of Health plans to spend $161.3 million over the next five years to expand the Pharmacogenomics Research Network (PGRN), a nationwide collaborative of scientists focused on understanding how genes affect a person’s response to medicines.

“Thanks to breakthroughs in genome sequencing technologies and our growing understanding of genetic variation among individuals, there has never been a better time to propel the field of pharmacogenomics,” said NIH Director Francis S. Collins, M.D., Ph.D. “Through these studies, we are moving closer to the goal of using genetic information to help prescribe the safest, most effective medicine for each patient.”

Spearheaded by the NIH’s National Institute of General Medical Sciences (NIGMS) and launched in 2000, the PGRN has already identified gene variants linked to responses to medicines for different cancers, heart disease, asthma, nicotine addiction and other conditions.

The expanded network will continue research in these areas and move into new ones, including rheumatoid arthritis and bipolar disorder. Network scientists will also develop novel research methods and study the use of pharmacogenetics in rural and underserved populations.

The new awards include 14 scientific research projects and seven network resources. The resources will benefit PGRN scientists by:

  • offering deep DNA sequencing capacity by partnering with experts in this field
  • providing statistical analysis expertise
  • developing standardized terminology for pharmacogenomics research
  • piloting ways to learn about pharmacogenomics from de-identified medical records in health care systems
  • continuing and expanding a 2-year-old international collaboration with the Center for Genomic Medicine at the RIKEN Institute in Yokohama, Japan.

Read the full news release ...



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