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Sally Mackey

Researcher at Stanford University

Publications -  22
Citations -  2925

Sally Mackey is an academic researcher from Stanford University. The author has contributed to research in topics: Vaccination & T cell. The author has an hindex of 14, co-authored 20 publications receiving 2702 citations.

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Journal ArticleDOI

Effects of intensive multiple risk factor reduction on coronary atherosclerosis and clinical cardiac events in men and women with coronary artery disease. The Stanford Coronary Risk Intervention Project (SCRIP).

TL;DR: Intensive multifactor risk reduction conducted over 4 years favorably altered the rate of luminal narrowing in coronary arteries of men and women with coronary artery disease and decreased hospitalizations for clinical cardiac events.
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Effects of diet and exercise in men and postmenopausal women with low levels of HDL cholesterol and high levels of LDL cholesterol.

TL;DR: The NCEP Step 2 diet failed to lower cholesterol levels in men or women with high-risk lipoprotein levels who did not engage in aerobic exercise, highlighting the importance of physical activity in the treatment of elevated LDL cholesterol levels.
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Genetic and environmental determinants of human NK cell diversity revealed by mass cytometry

TL;DR: The data suggest that inhibitory receptors may contribute more to NK cell self-tolerance, whereas activating receptors may guide response to pathogens and tumors, and the possibility that discrete NK cell subpopulations could be harnessed for immunotherapeutic strategies in the settings of infection, reproduction, and transplantation.
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The effect of diet on plasma lipids, lipoproteins, and coronary heart disease.

TL;DR: A variety of alternative dietary strategies can be employed in conjunction with traditional dietary recommendations (i.e., reduce total fat, especially saturated fatty acids and dietary cholesterol) for the management of plasma lipid levels.
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Lineage tracing of human B cells reveals the in vivo landscape of human antibody class switching

TL;DR: It is discovered that closely related B cells often switch to the same class, but lose coherence as somatic mutations accumulate, suggesting that class switch recombination is directed toward specific isotypes by a cell-autonomous imprinted state.