The P/F Program aims to support the development of new digestive diseases-related research initiatives. Limited funding will be provided for: 1) testing of novel hypotheses which may have impact on digestive diseases research, and 2) obtaining preliminary data to support future applications for extramural funding. Funds will be provided for up to four 1-2 year projects (with second year funding subject to competitive renewal), and three categories of investigators will be considered: 1) unfunded young investigators (or investigators holding career development awards) seeking to obtain independent grant support, 2) established investigators in other scientific fields who wish to enter the area of GI research, and 3) investigators currently involved in digestive diseases-related research who wish to pursue a new research direction not supported by their current grants. The budget is limited to $22,000 per year, per project, with a maximum total of $88,000. Applications will be solicited from every faculty member on an annual basis (in April, with a reminder sent via e-mail one month later as a means to increase the applicant pool), and additional announcements will be made in the DDRCC newsletter, the DDRCC Home Page, the Washington University Campus Newspaper, and the publication of the Washington University Academic Women's Network (AWNings). Promising postdoctoral fellows, instructors involved in GI research, and established investigators in other fields whose area of expertise could be applied to GI-related research, will be approached directly by the director of the program. Initial review of submitted projects will be carried out by members of the Executive Committee and the Internal Scientific Advisory Board. Outside reviewers will be sought if required expertise is missing. Following revision, selected projects will be evaluated and prioritized by an External Scientific Advisory Board consisting of six senior investigators from outside Washington University. The projects will be evaluated with respect to likelihood of developing into GI-related projects that will successfully compete for extramural (e.g., NIDDK) funding. An appropriate mechanism has also been developed for review of ongoing projects and allocation of second year funding. In preparation for this application, eight P/F projects were received and evaluated by at least six internal reviewers. The projects were ranked according to their averaged scores, and the top four (by Drs. Dieckgraefe, Simon, Wilson, and Heuckeroth) were included with the application. Also included were the critiques provided by the internal reviewers. The top two projects (Drs. Dieckgraefe and Simon) have been funded with seed money provided by the Dean of the Washington University School of Medicine (Dr. William Peck). Should this application for a DDRCC be funded, Drs. Dieckgraefe and Simon will be funded for a second year (subject to a satisfactory progress report) and Drs. Wilson and Heuckeroth will be funded for the first year.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
1P30DK052574-01A1
Application #
6346600
Study Section
Special Emphasis Panel (ZDK1-GRB-4 (J2))
Project Start
2000-03-01
Project End
2004-11-30
Budget Start
Budget End
Support Year
1
Fiscal Year
2000
Total Cost
$180,000
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Brenot, Audrey; Knolhoff, Brett L; DeNardo, David G et al. (2018) SNAIL1 action in tumor cells influences macrophage polarization and metastasis in breast cancer through altered GM-CSF secretion. Oncogenesis 7:32
Luo, Jialie; Feng, Jing; Yu, Guang et al. (2018) Transient receptor potential vanilloid 4-expressing macrophages and keratinocytes contribute differentially to allergic and nonallergic chronic itch. J Allergy Clin Immunol 141:608-619.e7
Tarr, Gillian A M; Oltean, Hanna N; Phipps, Amanda I et al. (2018) Strength of the association between antibiotic use and hemolytic uremic syndrome following Escherichia coli O157:H7 infection varies with case definition. Int J Med Microbiol 308:921-926
Baumann-Dudenhoeffer, Aimee M; D'Souza, Alaric W; Tarr, Phillip I et al. (2018) Infant diet and maternal gestational weight gain predict early metabolic maturation of gut microbiomes. Nat Med 24:1822-1829
Kumar, Pardeep; Kuhlmann, F Matthew; Chakraborty, Subhra et al. (2018) Enterotoxigenic Escherichia coli-blood group A interactions intensify diarrheal severity. J Clin Invest 128:3298-3311
Smith, Gordon I; Commean, Paul K; Reeds, Dominic N et al. (2018) Effect of Protein Supplementation During Diet-Induced Weight Loss on Muscle Mass and Strength: A Randomized Controlled Study. Obesity (Silver Spring) 26:854-861
Bockerstett, Kevin A; Wong, Chun Fung; Koehm, Sherri et al. (2018) Molecular Characterization of Gastric Epithelial Cells Using Flow Cytometry. Int J Mol Sci 19:
Porter, Lane C; Franczyk, Michael P; Pietka, Terri et al. (2018) NAD+-dependent deacetylase SIRT3 in adipocytes is dispensable for maintaining normal adipose tissue mitochondrial function and whole body metabolism. Am J Physiol Endocrinol Metab 315:E520-E530
Rubin, Deborah C (2018) CFTR and the Regulation of Crypt Cell Proliferation. Cell Mol Gastroenterol Hepatol 5:418-419
Hoshi, Masato; Reginensi, Antoine; Joens, Matthew S et al. (2018) Reciprocal Spatiotemporally Controlled Apoptosis Regulates Wolffian Duct Cloaca Fusion. J Am Soc Nephrol 29:775-783

Showing the most recent 10 out of 899 publications