application): The proposed training program will provide predoctoral trainees with a solid academic background in molecular pathogenesis, with a particular emphasis on host-pathogen interactions. Training will include relevant course work, regularly scheduled seminars and journal clubs, and rigorous laboratory training with the goal of preparing students for careers in research related to the goals of this program. Recent recruitment efforts have resulted in the formation of a critical mass of established investigators in the broad area of microbial pathogenesis, and accordingly this application proposes to establish an integrated training program for predoctoral students in host-pathogen interactions. In addition to their common research interests, many of these faculty already have substantial evidence for collaborative interactions. Faculty research interests encompass areas including regulation of virulence gene expression, host-pathogen interactions, molecular immunology and immune defense, molecular virology and bioinformatics. The program consists of 13 faculty, all of whom are current NIH grant holders and who, as a group, have had a substantial training history. As a whole, this group enjoys national and international recognition in their respective fields. The training faculty represents a broad range of departmental affiliations, including the Departments of Microbiology and Medicine at Boston University School of Medicine, the Division of Biomedical Engineering at Boston University, and the Department of Molecular and Cell Biology in the Goldman School of Dental Medicine. The major goal of the program will be to 1) recruit and enroll students of the highest quality, including underrepresented minorities; 2) provide these trainees with a multidisciplinary background in molecular pathogenesis coupled with intensive laboratory training in a particular research topic; 3) teach the trainees critical thinking skills and how to ask relevant and feasible research questions; 4) instill these trainees with a sense of ethical behavior; 5) t help develop effective written and oral communication skills among the trainees; and 6) to facilitate collaborative interactions among both students and faculty of the host-pathogen interaction training program.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
1T32AI007642-01
Application #
6152667
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Quackenbush, Robert L
Project Start
2000-09-30
Project End
2005-06-30
Budget Start
2000-09-30
Budget End
2001-06-30
Support Year
1
Fiscal Year
2000
Total Cost
$72,190
Indirect Cost
Name
Boston University
Department
Type
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Bailey, Allen J; Gerst, Kyle; Finn, Peter R (2018) Delay discounting of losses and rewards in alcohol use disorder: The effect of working memory load. Psychol Addict Behav 32:197-204
Gunn, Rachel L; Gerst, Kyle R; Lake, Allison J et al. (2018) The effects of working memory load and attention refocusing on delay discounting rates in alcohol use disorder with comorbid antisocial personality disorder. Alcohol 66:9-14
Finn, Peter R; Gerst, Kyle; Lake, Allison et al. (2017) Decisions to Attend and Drink at Party Events: The Effects of Incentives and Disincentives and Lifetime Alcohol and Antisocial Problems. Alcohol Clin Exp Res 41:1622-1629
Gerst, Kyle R; Gunn, Rachel L; Finn, Peter R (2017) Delay Discounting of Losses in Alcohol Use Disorders and Antisocial Psychopathology: Effects of a Working Memory Load. Alcohol Clin Exp Res 41:1768-1774
Dai, Junyi; Gunn, Rachel L; Gerst, Kyle R et al. (2016) A random utility model of delay discounting and its application to people with externalizing psychopathology. Psychol Assess 28:1198-1206
Finn, Peter R; Gunn, Rachel L; Gerst, Kyle R (2015) The Effects of a Working Memory Load on Delay Discounting in Those with Externalizing Psychopathology. Clin Psychol Sci 3:202-214
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Tremaglio, Chadene Z; Noton, Sarah L; Deflube, Laure R et al. (2013) Respiratory syncytial virus polymerase can initiate transcription from position 3 of the leader promoter. J Virol 87:3196-207
Samuelson, John; Bushkin, G Guy; Chatterjee, Aparajita et al. (2013) Strategies to discover the structural components of cyst and oocyst walls. Eukaryot Cell 12:1578-87
Noton, Sarah L; Deflube, Laure R; Tremaglio, Chadene Z et al. (2012) The respiratory syncytial virus polymerase has multiple RNA synthesis activities at the promoter. PLoS Pathog 8:e1002980

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