? CORE A The Administrative Core (Core A) provides administrative, fiscal, biorepository, database and analystic oversight for the entire Program, including the three Projects and Scientific Cores B and C. The Administrative Core promotes interactions among individual research projects and Cores to enhance the effectiveness of the Program. The Core securely maintains the program clinical database and centralized biorepository for human clinical samples from clinical studies of the program and those samples and data received from partnerships with NIH networks and industry. Core A provides the necessary biostatistical support for each individual project/core and, very importantly serves for analyses of data from model systems and human clinical studies across projects, so that integration and synergistic concepts can rapidly advance goals of the program. Thus, the biostatistics portion of Core A performs statistical analyses, including standard comparison methods, modeling support of biomarker studies, transcriptomic and mitochondrial haplogroup anaylses, and aids Project Leaders in interpreting, integrating, and sharing data and results from the analyses.The Core coordinates Program-wide meetings and exchange of information as well as manages reviews of the Program by Internal and External Advisory Boards and coordinates and promotes the interactions between the Program and Industry, Biotech and Pharma partners.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL103453-10
Application #
9986003
Study Section
Special Emphasis Panel (ZHL1)
Program Officer
Noel, Patricia
Project Start
Project End
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
10
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Cleveland Clinic Lerner
Department
Type
DUNS #
135781701
City
Cleveland
State
OH
Country
United States
Zip Code
44195
Herjan, Tomasz; Hong, Lingzi; Bubenik, Jodi et al. (2018) IL-17-receptor-associated adaptor Act1 directly stabilizes mRNAs to mediate IL-17 inflammatory signaling. Nat Immunol 19:354-365
Sweeny, Elizabeth A; Singh, Anuradha Bharara; Chakravarti, Ritu et al. (2018) Glyceraldehyde-3-phosphate dehydrogenase is a chaperone that allocates labile heme in cells. J Biol Chem 293:14557-14568
Reichard, Andrew; Wanner, Nicholas; Stuehr, Eric et al. (2018) Quantification of airway fibrosis in asthma by flow cytometry. Cytometry A 93:952-958
Asosingh, Kewal; Weiss, Kelly; Queisser, Kimberly et al. (2018) Endothelial cells in the innate response to allergens and initiation of atopic asthma. J Clin Invest 128:3116-3128
Reichard, Andrew; Asosingh, Kewal (2018) The role of mitochondria in angiogenesis. Mol Biol Rep :
Yang, Hui; Zhu, Yun; Chen, Xing et al. (2018) Structure of a prokaryotic SEFIR domain reveals two novel SEFIR-SEFIR interaction modes. J Struct Biol 203:81-89
Cai, Gang; Zhu, Liang; Chen, Xing et al. (2018) TRAF4 binds to the juxtamembrane region of EGFR directly and promotes kinase activation. Proc Natl Acad Sci U S A 115:11531-11536
Stober, Vandy P; Johnson, Collin G; Majors, Alana et al. (2017) TNF-stimulated gene 6 promotes formation of hyaluronan-inter-?-inhibitor heavy chain complexes necessary for ozone-induced airway hyperresponsiveness. J Biol Chem 292:20845-20858
Husta, Bryan C; Raoof, Suhail; Erzurum, Serpil et al. (2017) Tracheobronchopathy From Inhaled Corticosteroids. Chest 152:1296-1305
Chen, Jiwang; Sysol, Justin R; Singla, Sunit et al. (2017) Nicotinamide Phosphoribosyltransferase Promotes Pulmonary Vascular Remodeling and Is a Therapeutic Target in Pulmonary Arterial Hypertension. Circulation 135:1532-1546

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