The administrative core will function as a resource to assist project and core leaders, and all personnel for administrafive tasks associated with this program project. It serves a vital function to facilitate and allow investigators to focus as much attenfion on scientific and research acfivifies. The core will ensure efficient and fimely execufion of scientific, budgetary and administrative requirements and deadlines associated with the program project. The communicafion and coordination of these administrative acfivities by the core will be paramount in reaching the objectives and goals of the program project. Goal and Objectives: The goal of Administrafive Core A is to provide administrative support for all investigators participafing in this translafional Program Project grant. This goal will be achieved by addressing the following objectives: Objective 1: To provide administrative support for budgetary and personnel resource management Objecfive 2: To provide administrafive support for the coordinafion of scientific and review meefings Objecfive: To provide administrafive support for regulatory and scientific reporting of research activities

Public Health Relevance

The administrative core will provide administrafive support for all investigators participafing in this translational Program Project grant. It serves a vital function to facilitate and allow investigators to focus as much attention on scientific and research activifies. The core will ensure efficient and fimely execufion of scientific, budgetary and administrafive requirements and deadlines associated with the program project.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL108801-02
Application #
8380532
Study Section
Special Emphasis Panel (ZHL1-PPG-A)
Project Start
Project End
Budget Start
2012-07-01
Budget End
2013-06-30
Support Year
2
Fiscal Year
2012
Total Cost
$173,821
Indirect Cost
$76,442
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
Ryter, Stefan W; Choi, Augustine M K (2016) Targeting heme oxygenase-1 and carbon monoxide for therapeutic modulation of inflammation. Transl Res 167:7-34
Lee, Seonmin; Suh, Gee-Young; Ryter, Stefan W et al. (2016) Regulation and Function of the Nucleotide Binding Domain Leucine-Rich Repeat-Containing Receptor, Pyrin Domain-Containing-3 Inflammasome in Lung Disease. Am J Respir Cell Mol Biol 54:151-60
Piantadosi, Claude A (2016) Cardioprotective role of S-nitrosylated hemoglobin from rbc. J Clin Invest 126:4402-4403
Liu, Fei; Haeger, Christina Mallarino; Dieffenbach, Paul B et al. (2016) Distal vessel stiffening is an early and pivotal mechanobiological regulator of vascular remodeling and pulmonary hypertension. JCI Insight 1:
Tsoyi, Konstantin; Hall, Sean R R; Dalli, Jesmond et al. (2016) Carbon Monoxide Improves Efficacy of Mesenchymal Stromal Cells During Sepsis by Production of Specialized Proresolving Lipid Mediators. Crit Care Med 44:e1236-e1245
Suliman, Hagir B; Zobi, Fabio; Piantadosi, Claude A (2016) Heme Oxygenase-1/Carbon Monoxide System and Embryonic Stem Cell Differentiation and Maturation into Cardiomyocytes. Antioxid Redox Signal 24:345-60
Ghanta, Sailaja; Tsoyi, Konstantin; Liu, Xiaoli et al. (2016) Mesenchymal Stromal Cells Deficient in Autophagy Proteins are Susceptible to Oxidative Injury and Mitochondrial Dysfunction. Am J Respir Cell Mol Biol :
Nakahira, Kiichi; Pabon Porras, Maria Angelica; Choi, Augustine M K (2016) Autophagy in Pulmonary Diseases. Am J Respir Crit Care Med 194:1196-1207
Moon, Jong-Seok; Nakahira, Kiichi; Chung, Kuei-Pin et al. (2016) NOX4-dependent fatty acid oxidation promotes NLRP3 inflammasome activation in macrophages. Nat Med 22:1002-12
Zhang, Ruoyu; Nakahira, Kiichi; Guo, Xiaoxian et al. (2016) Very Short Mitochondrial DNA Fragments and Heteroplasmy in Human Plasma. Sci Rep 6:36097

Showing the most recent 10 out of 66 publications