This is an application for continued support for the University of Chicago Cardiovascular Sciences Training Program (CTSP). This program is currently in its 29th year of support and provides training in basic and translational cardiovascular sciences to both predoctoral and postdoctoral trainees. This program began in 1970's with the application of molecular techniques to the heart to study ion channel function and mechanisms of cardiac arrhythmias. During the 1980's, molecular biology was introduced into the CSTP. In the 1990's, this program continued in its mission to bring scientific advances to cardiovascular research providing training in murine modeling, including targeted homologous recombination and transgenesis. Coupled with this, our program was one of the first to apply cardiac imaging and phenotyping to murine models of heart disease. In the last five years, we have used our combined expertise at the University of Chicago Biological Sciences Division to draw exceptional trainees to the field of cardiac devlopment and genetics, using the information from the human genome project to understand how individual genes contribute to the normal and abnormal function of the heart. In the next five years, we will build on the strengths of transdisciplinary training at the University of Chicago to investigate genome variation and its relevance to cardiovascular disease. In addition, we will use a systems approach to dissect the networks that are disrupted in heart failure and heart development. The University of Chicago has now created the Institute of Cardiovascular Research to promote interdepartmental efforts and to provide trainees within the CTSP an overarching structure in which they can develop into the next generation of cardiovascular scientists. We train a balance of clinically-skilled MD fellows who wish to pursue careers as physician-scientists, and we train PhD postdoctoral fellows who are directed towards careers in cardiovascular research. Complementing this, we train predoctoral students since this serves to attract young scientists to cardiovascular research early in their career. The mentors in this program derive from ten different departments, all housed on our unified campus and in close proximity. There are four major concentrations within the CSTP and these include: 1) Cardiomyocyte biology, 2) Genetics, Genomics and Systems, 3) Cardiac Development, and 4) Myocyte-vascular Interactions.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Institutional National Research Service Award (T32)
Project #
5T32HL007381-35
Application #
8494658
Study Section
NHLBI Institutional Training Mechanism Review Committee (NITM)
Program Officer
Carlson, Drew E
Project Start
1994-07-01
Project End
2014-06-30
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
35
Fiscal Year
2013
Total Cost
$314,853
Indirect Cost
$31,573
Name
University of Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Grinstein, Jonathan; Kruse, Eric; Sayer, Gabriel et al. (2018) Outflow Cannula Systolic Slope in Patients With Left Ventricular Assist Devices: A Novel Marker of Myocardial Contractility. ASAIO J :
Narang, Akhil; Mor-Avi, Victor; Prado, Aldo et al. (2018) Machine learning based automated dynamic quantification of left heart chamber volumes. Eur Heart J Cardiovasc Imaging :
Banovich, Nicholas E; Li, Yang I; Raj, Anil et al. (2018) Impact of regulatory variation across human iPSCs and differentiated cells. Genome Res 28:122-131
Grinstein, Jonathan; Imamura, Teruhiko; Kruse, Eric et al. (2018) Echocardiographic Predictors of Hemodynamics in Patients Supported With Left Ventricular Assist Devices. J Card Fail 24:561-567
Genovese, Davide; Singh, Amita; Volpato, Valentina et al. (2018) Load Dependency of Left Atrial Strain in Normal Subjects. J Am Soc Echocardiogr 31:1221-1228
Singh, Amita; Medvedofsky, Diego; Mediratta, Anuj et al. (2018) Peak left atrial strain as a single measure for the non-invasive assessment of left ventricular filling pressures. Int J Cardiovasc Imaging :
Bovo, Elisa; Mazurek, Stefan R; Zima, Aleksey V (2018) Oxidation of ryanodine receptor after ischemia-reperfusion increases propensity of Ca2+ waves during ?-adrenergic receptor stimulation. Am J Physiol Heart Circ Physiol 315:H1032-H1040
Imamura, Teruhiko; Juricek, Colleen; Nguyen, Ann et al. (2018) Predictors of Hemodynamic Improvement and Stabilization Following Intraaortic Balloon Pump Implantation in Patients With Advanced Heart Failure. J Invasive Cardiol 30:56-61
Dryer, Kathryn; Gajjar, Mark; Narang, Nikhil et al. (2018) Coronary microvascular dysfunction in patients with heart failure with preserved ejection fraction. Am J Physiol Heart Circ Physiol 314:H1033-H1042
Addetia, Karima; Maffessanti, Francesco; Muraru, Denisa et al. (2018) Morphologic Analysis of the Normal Right Ventricle Using Three-Dimensional Echocardiography-Derived Curvature Indices. J Am Soc Echocardiogr 31:614-623

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