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A free floating commentary on culture, politics, economics, and religion based on a passionate commitment to the truth and a desire graciously to refute that which is contrary to it….
"He must hold firm to the sure word as taught, so that he may be able to give instruction in sound doctrine and also to confute those who contradict it."
--Titus 1:9, Revised Standard Version
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Heart disease patient Terence Gooding and breast cancer survivor Kathy Negro live 2,000 miles apart, but they stand shoulder-to-shoulder in the burgeoning field of personalized medicine.
They are among a small but growing number of American patients who have sought genetic testing to help guide their treatment. The genes in question, passed from parent to child, carry the blueprints for liver enzymes involved in processing many medications.
Scientists expect that in the not-too-distant future, patients will be tested routinely for a variety of genes that affect their response to drugs. The results should help doctors decide what and how much to prescribe, a major step forward in personalizing treatments for a range of ailments.
In the next three to five years, the cost of sequencing a person's genome will drop below $1,000 — less than the price of a colonoscopy, says National Institutes of Health director Francis Collins, who led the Human Genome Project to completion in 2003. Says Collins: "I think that will finally make pharmacogenomics" — the study of how variations in the human genome affect a person's responses to medications — "really practical."
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