This application proposes continued funding for an interdisciplinary Iowa Training Program in Kidney and Hypertension research. The program provides research training for adult and pediatric nephrology fellows as well as PhD scientists interested in kidney and hypertension research in the University of Iowa, Carver College of Medicine. The primary purpose of the program is to provide intensive rigorous training for clinicians and scientists in broad ranges of areas related to kidney biology and disease and hypertension to transform this knowledge into improvements in patient care. The training program has been continuously funded for the past 25 years. The applicant pool is robust, and the program has filled consistently. The graduates from the program have published important contributions to biomedical research, and many have obtained faculty positions and received external funding for their research. The program faculty comprises 41 physician- scientists and basic scientists from 11 Departments with expertise in a broad range of scientific disciplines that are relevant to the kidney and hypertension. The training program research portfolio is organized into five themes based on and integrated with the existing strengths of research on campus: ion transport physiology and cell biology, renal genetics, hypertension, diabetes and renal metabolic diseases, and clinical and translation research in kidney diseases. The training curriculum includes mentored research training, didactic courses that include optional elective graduate-level courses, grant-writing workshop, and required courses in ethics and the responsible conduct of research, and attendance to journal clubs, works-in-progress and research seminar series. Specific training opportunities for patient-oriented research consist of a certification program in patient-oriented research and a Master or PhD degree in Translational Medicine.

Public Health Relevance

There remain significant gaps in our understanding of the pathogenesis and optimal treatment of kidney disease and hypertension. The Training Program proposes to train clinicians and scientists to better understand kidney physiology and disease and the pathophysiology of hypertension disorders. A better understanding of kidney disease and hypertension will lead to better prevention and treatments of the disorders.

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 #
2T32DK007690-26
Application #
9489417
Study Section
Special Emphasis Panel (ZDK1)
Program Officer
Rys-Sikora, Krystyna E
Project Start
1992-07-15
Project End
2023-06-30
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
26
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Stilley, Julie A W; Segaloff, Deborah L (2018) Deletion of fetoplacental Fshr inhibits fetal vessel angiogenesis in the mouse placenta. Mol Cell Endocrinol 476:79-83
Zahr, Roula S; Peterson, Ryan A; Polgreen, Linnea A et al. (2016) Diabetes as an increasingly common comorbidity among patient hospitalizations for tuberculosis in the USA. BMJ Open Diabetes Res Care 4:e000268
Stilley, Julie A W; Guan, Rongbin; Santillan, Donna A et al. (2016) Differential Regulation of Human and Mouse Myometrial Contractile Activity by FSH as a Function of FSH Receptor Density. Biol Reprod 95:36
Picconi, Jason L; Muff-Luett, Melissa A; Wu, Di et al. (2014) Kidney-specific expression of GFP by in-utero delivery of pseudotyped adeno-associated virus 9. Mol Ther Methods Clin Dev 1:14014
Stilley, Julie A W; Christensen, Debora E; Dahlem, Kristin B et al. (2014) FSH receptor (FSHR) expression in human extragonadal reproductive tissues and the developing placenta, and the impact of its deletion on pregnancy in mice. Biol Reprod 91:74
Stilley, Julie A; Guan, Rongbin; Duffy, Diane M et al. (2014) Signaling through FSH receptors on human umbilical vein endothelial cells promotes angiogenesis. J Clin Endocrinol Metab 99:E813-20
Goddeeris, Matthew M; Wu, Biming; Venzke, David et al. (2013) LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy. Nature 503:136-40
Birt, Julie A; Nabli, Henda; Stilley, Julie A et al. (2013) Elevated peritoneal fluid TNF-? incites ovarian early growth response factor 1 expression and downstream protease mediators: a correlation with ovulatory dysfunction in endometriosis. Reprod Sci 20:514-23
Sinah, Namita; Williams, Charlotte A; Piper, Robert C et al. (2012) A set of dual promoter vectors for high throughput cloning, screening, and protein expression in eukaryotic and prokaryotic systems from a single plasmid. BMC Biotechnol 12:54
Stilley, Julie A W; Birt, Julie A; Sharpe-Timms, Kathy L (2012) Cellular and molecular basis for endometriosis-associated infertility. Cell Tissue Res 349:849-62

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