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Genetic and Pharmacological Modifications of Thrombin Formation in Apolipoprotein E-deficient Mice Determine Atherosclerosis Severity and Atherothrombosis Onset in a Neutrophil-Dependent Manner

Overview of attention for article published in PLOS ONE, February 2013
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Title
Genetic and Pharmacological Modifications of Thrombin Formation in Apolipoprotein E-deficient Mice Determine Atherosclerosis Severity and Atherothrombosis Onset in a Neutrophil-Dependent Manner
Published in
PLOS ONE, February 2013
DOI 10.1371/journal.pone.0055784
Pubmed ID
Authors

Julian I. Borissoff, Jeroen J. T. Otten, Sylvia Heeneman, Peter Leenders, René van Oerle, Oliver Soehnlein, Sarah T. B. G. Loubele, Karly Hamulyák, Tilman M. Hackeng, Mat J. A. P. Daemen, Jay L. Degen, Hartmut Weiler, Charles T. Esmon, Joanne van Ryn, Erik A. L. Biessen, Henri M. H. Spronk, Hugo ten Cate

Abstract

Variations in the blood coagulation activity, determined genetically or by medication, may alter atherosclerotic plaque progression, by influencing pleiotropic effects of coagulation proteases. Published experimental studies have yielded contradictory findings on the role of hypercoagulability in atherogenesis. We therefore sought to address this matter by extensively investigating the in vivo significance of genetic alterations and pharmacologic inhibition of thrombin formation for the onset and progression of atherosclerosis, and plaque phenotype determination.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 57 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 2%
United States 1 2%
Netherlands 1 2%
Unknown 54 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 11 19%
Researcher 10 18%
Student > Master 8 14%
Student > Bachelor 7 12%
Professor > Associate Professor 5 9%
Other 8 14%
Unknown 8 14%
Readers by discipline Count As %
Agricultural and Biological Sciences 17 30%
Medicine and Dentistry 15 26%
Biochemistry, Genetics and Molecular Biology 9 16%
Pharmacology, Toxicology and Pharmaceutical Science 3 5%
Unspecified 1 2%
Other 3 5%
Unknown 9 16%