In the July 2018 issue of SLAS Discovery, a review article summarizes new methods of fragment-based lead discovery (FBLD) to
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Higher body fat linked to lower breast cancer risk in younger women
While obesity has been shown to increase breast cancer risk in postmenopausal women, a large-scale study co-led by a University
Majority of US adults prescribed epinephrine report not using it in an emergency: Study shows people said their epinephrine wasn’t available or thought it wasn’t necessary
The most effective, life-saving treatment for a severe allergic reaction (anaphylaxis) is epinephrine. Yet a new study shows in an
Flexible content delivery, student-faculty interaction frees time without hurting grades
Medical students face an intense schedule and workload and often struggle to juggle their priorities. Similarly, medical school faculty must
Combining different malaria vaccines could reduce cases by 91 percent
Using two experimental anti-malarial vaccines, which work in different ways, can greatly reduce the number of malaria infections in animal
How a single binge drinking episode affects gene that regulates sleep: Discovery explains alcohol’s link to brain activity, sleep disturbances
One in six U.S. adults binge drinks at least four times a month, according to the Centers for Disease Control
New subtype of prostate cancer: Tumors with alterations in the CDK12 gene were more responsive to immunotherapy, suggesting precision medicine approach
Researchers led by the University of Michigan Rogel Cancer Center have identified a new subtype of prostate cancer that occurs
Long periods of viral suppression shown to reduce cancer risk in aging HIV population
Early, sustained antiretroviral therapy (ART), which results in long-term viral suppression, helps to prevent AIDS-defining cancers and also non-AIDS-defining cancers,
1.35 million children’s lives saved by HiB and pneumococcal vaccines since 2000
Childhood deaths from two leading bacterial causes of pneumonia and meningitis, pneumococcus and Hib, declined sharply during the period 2000
Framework identifies genetic missense mutations linked to autism spectrum disorder
Missense mutations occur when there is a change in one gene’s DNA base pair, and the change results in the