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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 13, 2004
Catecholamines potentiate LPS-induced expression of MMP-1 and MMP-9 in human monocytes and in the human monocytic cell line U937: possible implications for peri-operative plaque instabilityWalter S Speidl, Wolfgang G Toller, Christoph Kaun, et al.
Thrombosis and Haemostasis|November 16, 2004
Ultrasound affects distribution of plasminogen and tissue-type plasminogen activator in whole blood clots in vitroBranka Devcic-Kuhar, Stefan Pfaffenberger, Lisa Gherardini, et al.
Journal of Cellular and Molecular Medicine|March 21, 2009
The anti-angiogenic factor PEDF is present in the human heart and is regulated by anoxia in cardiac myocytes and fibroblastsKathrin Rychli, Christoph Kaun, Philipp J Hohensinner, et al.
Thrombosis and Haemostasis|March 8, 2003
2MHz ultrasound enhances t-PA-mediated thrombolysis: comparison of continuous versus pulsed ultrasound and standing versus travelling acoustic wavesStefan Pfaffenberger, Branka Devcic-Kuhar, Karem El-Rabadi, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|August 31, 2015
Pulmonary artery to aorta ratio for the detection of pulmonary hypertension: cardiovascular magnetic resonance and invasive hemodynamics in heart failure with preserved ejection fractionGültekin Karakus, Andreas A Kammerlander, Stefan Aschauer, et al.
JACC. Cardiovascular Imaging|December 20, 2015
T1 Mapping by CMR Imaging: From Histological Validation to Clinical ImplicationAndreas A Kammerlander, Beatrice A Marzluf, Caroline Zotter-Tufaro, et al.
Journal of Molecular and Cellular Cardiology|April 15, 2004
Prostaglandin E1 induces vascular endothelial growth factor-1 in human adult cardiac myocytes but not in human adult cardiac fibroblasts via a cAMP-dependent mechanismThomas Werner Weiss, Mohammad Reza Mehrabi, Christoph Kaun, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 5, 2013
Hereditary amyloidosis caused by R554L fibrinogen Aα-chain mutation in a Spanish family and review of the literatureMichael Haidinger, Johannes Werzowa, Renate Kain, et al.
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