This is the renewal application for Years 21-25 of a training program designed to produce investigators at the cutting edge of research in the area of pediatric gastroenterology (GI). Trainees will be at the postdoctoral level and a mixture of MDs supported for 3 years and PhDs supported for 2 years for a total request of 5 stipends/yr. to accomplish these goals. The program traditionally has placed strong emphasis on molecular biology, the rationale being that molecular approaches are of central importance in both study and treatment of diseases associated with pediatric GI. In the current proposal there is also emphasis on bringing the results of molecular research to the bedside with opportunities for intense training in clinical research. The mentors (7 MDs, 2 MD/PhDs and 10 PhDs) represent a multidisciplinary group of experienced investigators from various departments at Baylor College of Medicine (BCM), the University of Texas Health Science Center, and the MD Anderson Cancer Center. Their research covers four broad areas that are important to pediatric GI, namely: mucosal biology, molecular hepatology, immunology and inflammation, and translational biology. All mentor laboratories are well funded and well equipped. Existing faculty members (17 of 19) have excellent track records of interaction and participation in our training program activities. The two new faculty members have outstanding mentoring histories. The Program Director, Robert J. Shulman, MD maintains ultimate authority for the program and manages day-to-day operations. He is assisted by an Associate Program Director (Douglas G. Burrin, PhD for additional expertise in basic science research). Major administrative decisions (e.g., selection of trainees) are handled by an Executive Committee, which includes the Program Director, Associate Director, three other program faculty, and a senior faculty member not associated with this grant. The training program for MD fellows includes research rotations to facilitate selection of a mentor. Both MD and PhD trainees have individual research committees, must prepare a written research proposal to be defended to the research committee, and have periodic reviews that include academic and career assessment. Both MD and PhD fellows are required to attend a biweekly research seminar series, a monthly journal club, and a thrice yearly scientific social. All trainees (MD and PhD) must present at these meetings. Trainees are selected from a highly competitive applicant pool that already exists at BCM. Over the past 10 years trainees have performed well with 80% of MDs and 100% of PhDs remaining in academia. The majority of these have been successful in securing either internal or external funding for their research including R01, K08, K01, and R21 grants, as well as from other competitive sources. The current proposal includes several new features designed to enrich and enhance the existing program including: 3 years of research training for all MDs, a Clinical Scientist Training Program for MD trainees intent on a clinical research career, and for PhDs trainees, interactions with the interdepartmental Graduate Program in Translational Biology &Molecular Medicine.
The education and training of young MD and PhD researchers is the lifeblood of continued progress in medical care. This training grant fills a critical need by preparing these individuals to work at the cutting edge of biomedical research in gastrointestinal, liver, as well as their related nutritional diseases. By training young MD and PhD researchers side by side, this program also reinforces the importance of intellectual cross fertilization. NOTE: The criteria scores and the critiques given below were provided by the reviewers assigned to this application. These do not necessarily reflect the positions of the reviewers at the close of the group discussion or the final majority opinion of the group, although the reviewers were asked to amend their criteria scores and critiques if their positions changed during the discussion. Please note that the criteria scores are not averaged in arriving at the final overall impact scores. If the reviewers have not changed their criteria scores after the discussion, those shown in the critiques may reflect the opinion of the reviewers before the meeting. The Resume and other initial sections of the summary statement are the authoritative representations of the final outcome of the group discussion. If there is any discrepancy between the reviewers'commentaries and the priority/impact score on the face page of this summary statement, the priority/impact score should be considered the most accurate representation of the final outcome of the group discussion.
|Guthrie, Gregory; Kulkarni, Madhulika; Vlaardingerbroek, Hester et al. (2016) Multi-omic profiles of hepatic metabolism in TPN-fed preterm pigs administered new generation lipid emulsions. J Lipid Res 57:1696-711|
|Hiremath, Girish; Byramji, Darius; Pacheco, Ann et al. (2016) Eosinophilic Esophagitis in Children and Its Relationship with Parental Allergies: Texas Children's Hospital Experience. Dig Dis Sci 61:501-6|
|Ihekweazu, Faith D; Nagy-Szakal, Dorottya; Fishman, Douglas S et al. (2016) Hyperlipasemia in Pediatric Inflammatory Bowel Diseases. Pancreas 45:e2-3|
|Preidis, Geoffrey A; Luna, Ruth Ann; Hollister, Emily B et al. (2016) The mucosal microbiota in a young child with severe non-Helicobacter gastritis. Therap Adv Gastroenterol 9:749-51|
|Ng, Kenneth; Stoll, Barbara; Chacko, Shaji et al. (2016) Vitamin E in New-Generation Lipid Emulsions Protects Against Parenteral Nutrition-Associated Liver Disease in Parenteral Nutrition-Fed Preterm Pigs. JPEN J Parenter Enteral Nutr 40:656-71|
|Leung, Daniel H; Narang, Amrita; Minard, Charles G et al. (2016) A 10-Year united network for organ sharing review of mortality and risk factors in young children awaiting liver transplantation. Liver Transpl 22:1584-1592|
|Ross, CanÃ¡ L; Spinler, Jennifer K; Savidge, Tor C (2016) Structural and functional changes within the gut microbiota and susceptibility to Clostridium difficile infection. Anaerobe 41:37-43|
|Spinler, Jennifer K; Ross, CanÃ¡ L; Savidge, Tor C (2016) Probiotics as adjunctive therapy for preventing Clostridium difficile infection - What are we waiting for? Anaerobe 41:51-57|
|Qu, Lin; Murakami, Kosuke; Broughman, James R et al. (2016) Replication of Human Norovirus RNA in Mammalian Cells Reveals Lack of Interferon Response. J Virol 90:8906-23|
|Hollier, John M; Czyzewski, Danita I; Self, Mariella M et al. (2016) Pediatric Irritable Bowel Syndrome Patient and Parental Characteristics Differ By Care Management Type. J Pediatr Gastroenterol Nutr :|
Showing the most recent 10 out of 82 publications