The Administrative Core will provide logistic support for all program investigators. This core willimplement and oversee all the activities of the program, ensuring that collaboration and interactionsoccur whenever they would be beneficial to the program and that the scientific facilities functionwell. It will organize the internal and external review of the program. It will have responsibility fororganizing work in progress sessions and other interactive forums among program investigatorsand other investigators interested in tuberculosis vaccine development and biodefense. Thepersonnel of the core will also provide secretarial assistance to the principal investigators and theirresearch staffs, assisting with preparation and submission of manuscripts and other documentsrelated to the program project. Core A will maintain financial oversight and budget management forthe entire program. The core will also maintain and update the website that will be established forthis program, which forms a significant component of the program's data sharing plan.
The specificaims of the Administrative Core A will be:
Aim 1. Provide financial oversight of the grant, and coordinate the completion and submission of allnon-competitive reports and grant renewals.
Aim 2. Handle scheduling of all group meetings to ensure efficient communication among PO1investigators. This will include weekly data presentation meetings involving the participatinglaboratories, monthly meetings of the program principal investigators, quarterly internal reviewboard and yearly external review board meetings.
Aim 3. Assist the investigators of the program in identifying and recruiting new project personnel.
Aim 4. Assist in organizing the annual tuberculosis research symposia which will be coordinatedwith the external advisory board meeting.
Aim 5. Maintain and update the program's website to provide information about the program andthe resources it offers, and to assist in data sharing with investigators outside of the program.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI063537-04
Application #
7657134
Study Section
Special Emphasis Panel (ZAI1-VSG-M (S1))
Project Start
2008-04-01
Project End
2010-03-31
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
4
Fiscal Year
2008
Total Cost
$134,175
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Harbut, Michael B; Yang, Baiyuan; Liu, Renhe et al. (2018) Small Molecules Targeting Mycobacterium tuberculosis Type II NADH Dehydrogenase Exhibit Antimycobacterial Activity. Angew Chem Int Ed Engl 57:3478-3482
Kunnath-Velayudhan, Shajo; Goldberg, Michael F; Saini, Neeraj K et al. (2017) Transcriptome Analysis of Mycobacteria-Specific CD4+ T Cells Identified by Activation-Induced Expression of CD154. J Immunol 199:2596-2606
Glass, Lisa N; Swapna, Ganduri; Chavadi, Sivagami Sundaram et al. (2017) Mycobacterium tuberculosis universal stress protein Rv2623 interacts with the putative ATP binding cassette (ABC) transporter Rv1747 to regulate mycobacterial growth. PLoS Pathog 13:e1006515
Johnson, Alison J; Kennedy, Steven C; Lindestam Arlehamn, Cecilia S et al. (2017) Identification of Mycobacterial RplJ/L10 and RpsA/S1 Proteins as Novel Targets for CD4+ T Cells. Infect Immun 85:
Phuah, Jiayao; Wong, Eileen A; Gideon, Hannah P et al. (2016) Effects of B Cell Depletion on Early Mycobacterium tuberculosis Infection in Cynomolgus Macaques. Infect Immun 84:1301-1311
Carreño, Leandro J; Saavedra-Ávila, Noemí A; Porcelli, Steven A (2016) Synthetic glycolipid activators of natural killer T cells as immunotherapeutic agents. Clin Transl Immunology 5:e69
Foreman, Taylor W; Mehra, Smriti; LoBato, Denae N et al. (2016) CD4+ T-cell-independent mechanisms suppress reactivation of latent tuberculosis in a macaque model of HIV coinfection. Proc Natl Acad Sci U S A 113:E5636-44
Vergnolle, Olivia; Xu, Hua; Tufariello, JoAnn M et al. (2016) Post-translational Acetylation of MbtA Modulates Mycobacterial Siderophore Biosynthesis. J Biol Chem 291:22315-22326
Olsen, Aaron; Chen, Yong; Ji, Qingzhou et al. (2016) Targeting Mycobacterium tuberculosis Tumor Necrosis Factor Alpha-Downregulating Genes for the Development of Antituberculous Vaccines. MBio 7:
Prados-Rosales, Rafael; Carreño, Leandro J; Weinrick, Brian et al. (2016) The Type of Growth Medium Affects the Presence of a Mycobacterial Capsule and Is Associated With Differences in Protective Efficacy of BCG Vaccination Against Mycobacterium tuberculosis. J Infect Dis 214:426-37

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