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Robert D. Rosenberg

Researcher at Technische Universität München

Publications -  471
Citations -  44373

Robert D. Rosenberg is an academic researcher from Technische Universität München. The author has contributed to research in topics: Mammography & Heparan sulfate. The author has an hindex of 113, co-authored 459 publications receiving 42876 citations. Previous affiliations of Robert D. Rosenberg include Dana Corporation & University of Pennsylvania.

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The Purification and Mechanism of Action of Human Antithrombin-Heparin Cofactor

TL;DR: It is suggested that heparin binds to the inhibitor and causes a conformational change which results in a more favorable exposure of the arginine reactive site, allowing a rapid interaction with thrombin.
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Plasma fibrinogen level and the risk of major cardiovascular diseases and nonvascular mortality: an individual participant meta-analysis.

TL;DR: In this article, a large-scale individual participant meta-analysis was conducted to assess the relationship of fibrinogen levels with risk of major vascular and non-vascular outcomes based on individual participant data.
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Individual and combined effects of age, breast density, and hormone replacement therapy use on the accuracy of screening mammography.

TL;DR: The accuracy of screening mammography is best in older women and in women with fatty breasts, and the individual and combined effects of age, breast density, and HRT use on mammographic accuracy are examined.
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A novel role for 3-O-sulfated heparan sulfate in herpes simplex virus 1 entry

TL;DR: It is shown that heparan sulfate modified by a subset of the multiple D-glucosaminyl 3-O-sulfotransferase isoforms provides sites for the binding of a third viral glycoprotein, gD, and for initiation of HSV-1 entry.
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Antisense c- myb oligonucleotides inhibit intimal arterial smooth muscle cell accumulation in vivo

TL;DR: The use of local delivery of antisense c-myb oligonu-cleotide to suppress intimal accumulation of rat carotid arterial smooth muscle cells is reported to suggest that antisense oligonucleotides can be used to define the in vivo biological role of specific macromolecules in the blood vessel wall.