The Genomics/Proteomics Core is designed to support all the Projects in the Program Project for the Specific Aims that address the regulation of gene and protein expression. The Genomics/ Proteomics Core is also designed to interact with all the other Cores, especially Core-D (Biostatistics/Bioinformatics). Genomics and Proteomics are combined to offer a link, both logical and biological, between gene expression, transcript stability, protein translation and post-translational modifications. The Core will combine focused techniques (to investigate one specific product of interest) and large-scale profiling at both the gene and protein levels. The Genomics/ Proteomics Core will provide technical assistance to the different Projects for the processing of samples, whereas the preparation of the samples themselves will be the responsibility of the investigators from the different Projects and from Core B (Physiology). Once the samples are processed, the raw data will be transmitted to these investigators and to Core D (Biostatistics) who will be in charge of the data analysis and extraction of results. Additional techniques related to gene and protein expression that would require fixed samples will be done in collaboration with Core E (Pathology).

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL069020-10
Application #
8133518
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
2013-06-30
Budget Start
2010-09-01
Budget End
2013-08-31
Support Year
10
Fiscal Year
2010
Total Cost
$307,870
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Type
DUNS #
623946217
City
Newark
State
NJ
Country
United States
Zip Code
07107
Vatner, Dorothy E; Zhang, Jie; Oydanich, Marko et al. (2018) Enhanced longevity and metabolism by brown adipose tissue with disruption of the regulator of G protein signaling 14. Aging Cell :e12751
Guers, John J; Zhang, Jie; Campbell, Sara C et al. (2017) Disruption of adenylyl cyclase type 5 mimics exercise training. Basic Res Cardiol 112:59
Zhang, Jie; Zhao, Xin; Vatner, Dorothy E et al. (2016) Extracellular Matrix Disarray as a Mechanism for Greater Abdominal Versus Thoracic Aortic Stiffness With Aging in Primates. Arterioscler Thromb Vasc Biol 36:700-6
Vatner, Stephen F (2016) Why So Few New Cardiovascular Drugs Translate to the Clinics. Circ Res 119:714-7
Jose Corbalan, J; Vatner, Dorothy E; Vatner, Stephen F (2016) Myocardial apoptosis in heart disease: does the emperor have clothes? Basic Res Cardiol 111:31
Bravo, Claudio A; Vatner, Dorothy E; Pachon, Ronald et al. (2016) A Food and Drug Administration-Approved Antiviral Agent that Inhibits Adenylyl Cyclase Type 5 Protects the Ischemic Heart Even When Administered after Reperfusion. J Pharmacol Exp Ther 357:331-6
Zhao, Xin; Balaji, Poornima; Pachon, Ronald et al. (2015) Overexpression of Cardiomyocyte ?1A-Adrenergic Receptors Attenuates Postinfarct Remodeling by Inducing Angiogenesis Through Heterocellular Signaling. Arterioscler Thromb Vasc Biol 35:2451-9
Pachon, Ronald E; Scharf, Bruce A; Vatner, Dorothy E et al. (2015) Best anesthetics for assessing left ventricular systolic function by echocardiography in mice. Am J Physiol Heart Circ Physiol 308:H1525-9
Vatner, Dorothy E; Yan, Lin; Lai, Lo et al. (2015) Type 5 adenylyl cyclase disruption leads to enhanced exercise performance. Aging Cell 14:1075-84
Sehgel, Nancy L; Sun, Zhe; Hong, Zhongkui et al. (2015) Augmented vascular smooth muscle cell stiffness and adhesion when hypertension is superimposed on aging. Hypertension 65:370-7

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