This competing continuation application seeks to extend the T32 DK07726 for an additional 5 years of funding and to increase the number of trainees from 4 to 5. This program, Research Training in Pediatric Nephrology, has provided the foundation for our training program for academic investigators in the area of 'pediatric nephrology. The goal of the Children's Hospital Boston Division of Nephrology's fellowship and research training programs is to develop academic physicians and scientists who will establish independent investigative careers in areas relevant to the understanding of childhood kidney diseases. Over the initial funding cycle from AY85-AY89, we firmly established our training program with both clinical and research faculty. Over the second funding cycle from AY90-AY94, we were able to accommodate a full complement of Pediatric Nephrology fellows at every level. During the third funding cycle from AY95-AY99 we expanded the program by adding biomedical scientists to our research faculty and we began to train postdoctoral research fellows. Over the most recent funding cycle from AY00-AY04, we have expanded beyond the level of a divisional training program for Pediatric Nephrologists and we are now training many postdoctoral research fellows interested in the basic science of renal disease. Thus, over the past 10 years, 70 trainees entered our program, 24 are still in training and 46 have completed training. Nearly all of these 46 currently hold full-time academic positions and 22 are currently funded investigators in diverse areas of research all relevant to pediatric nephrology. Furthermore, the trainees completing our program in the past 5 years received 72 awards, 29 grants and contributed to 286 publications. In addition, the research program of full-time division staff has also expanded significantly over the past 5 years, including an expansion of renal developmental biology, glomerular disease, vascular biology, transplantation, and immunology research efforts. Several of our trainees have joined the faculty and have developed complimentary research efforts in stem cell biology, receptor signaling pathways, and bioinformatics. Our research laboratories have undergone substantial expansion and will encompass over 7,000 square feet of space by 2004. We have established close research and training collaborations with laboratories at the Harvard Medical School, Brigham & Women's Hospital, Beth Israel Deaconess Medical Center, Harvard School of Public Health and the Massachusetts Institute of Technology. Thus, trainees who enter our program have exposure to a wide variety of individuals all dedicated to investigative nephrology and have opportunities for rigorous scientific training.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Institutional National Research Service Award (T32)
Project #
3T32DK007726-23S1
Application #
7243833
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Rankin, Tracy L
Project Start
1994-09-01
Project End
2009-06-30
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
23
Fiscal Year
2006
Total Cost
$54,240
Indirect Cost
Name
Children's Hospital Boston
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02115
Jobst-Schwan, Tilman; Schmidt, Johanna Magdalena; Schneider, Ronen et al. (2018) Acute multi-sgRNA knockdown of KEOPS complex genes reproduces the microcephaly phenotype of the stable knockout zebrafish model. PLoS One 13:e0191503
van der Ven, Amelie T; Connaughton, Dervla M; Ityel, Hadas et al. (2018) Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. J Am Soc Nephrol 29:2348-2361
Daga, Ankana; Majmundar, Amar J; Braun, Daniela A et al. (2018) Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. Kidney Int 93:204-213
Braun, Daniela A; Shril, Shirlee; Sinha, Aditi et al. (2018) Mutations in WDR4 as a new cause of Galloway-Mowat syndrome. Am J Med Genet A 176:2460-2465
van der Ven, Amelie T; Kobbe, Birgit; Kohl, Stefan et al. (2018) A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux. PLoS One 13:e0191224
Warejko, Jillian K; Schueler, Markus; Vivante, Asaf et al. (2018) Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ?43% of 35 Families With Midaortic Syndrome. Hypertension 71:691-699
Braun, Daniela A; Warejko, Jillian K; Ashraf, Shazia et al. (2018) Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome. Nephrol Dial Transplant :
Boneschansker, Leo; Jorgensen, Julianne; Ellett, Felix et al. (2018) Convergent and Divergent Migratory Patterns of Human Neutrophils inside Microfluidic Mazes. Sci Rep 8:1887
Warejko, Jillian K; Tan, Weizhen; Daga, Ankana et al. (2018) Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. Clin J Am Soc Nephrol 13:53-62
Tan, Weizhen; Lovric, Svjetlana; Ashraf, Shazia et al. (2018) Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center. Pediatr Nephrol 33:305-314

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