Genetics
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Making medicine out of RNA
Ribonucleic acid, a key player in cellular protein production, is used, with increasing success, by biotechnologists bent on preventing and curing diseases.
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Genome sequencing at Stanford Health Care
Stanford Medicine now provides a service that harnesses the power of genome sequencing to identify the source of diseases and help target treatments.
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Human biology registers two seasons
A Stanford Medicine study finds that changes in molecular patterns in Californians correspond with two nontraditional “seasons.”…
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Race, ethnicity, ancestry in science
Alice Popejoy, a postdoctoral scholar who studies biomedical data sciences, speaks to the role — and pitfalls — of race, ethnicity and ancestry in research.
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Early Polynesian, Native American contact
Deep-genome analyses conducted by Stanford Medicine researchers and their collaborators have settled a long-brewing controversy about whether ancient Polynesians and Native Americans had contact.
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$1.49 million for inflammation research
The Chan Zuckerberg Initiative has awarded $1.49 million to research projects involving Stanford Medicine scientists who will investigate emerging ideas about the role of inflammation in disease.
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Study reveals molecular effects of exercise
Researchers at the School of Medicine have shown how exercise changes the body at a molecular level and have identified blood markers of fitness.
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Twin registry gets new home at Stanford
Studies of identical versus fraternal twins reveal the relative contributions of heredity and the environment to numerous human traits. Now, Stanford has its own twin registry.
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New members of the National Academy of Sciences
Howard Chang of dermatology and of genetics, Richard Lewis of molecular and cellular physiology, and Peter Sarnow of microbiology and immunology were elected to the National Academy of Sciences.
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Reprogramming cells to build tiny structures
Researchers have developed a method for building nanoscale structures with genetically reprogrammed cells.
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Stanford center helps patients with rare genetic disease
From migraines to strokes to brain bleeds, the symptoms of HHT are varied. Diagnosis is often delayed, yet early care can prevent both bothersome and deadly side effects.
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