Our Center continues to be composed of four Research Projects, two Cores (one Animal Genotyping and Phenotyping Core focused on support for the intensive and advanced in vivo animal studies proposed, and one Administrative Core), all led by the same investigators as for the last submission, and three Pilot and Feasibility Projects. Dr. Agnes Fogo continues as the Principal Investigator of the Center. She also continues as Project Leader of Project 1, which maintains focus on mechanisms of tubulointerstitial fibrosis. Her exciting recent data has identified thymosin (34 as a key molecule linked to glomerulosclerosis. Additional new data now point to increased thymosin |34 in the fibrotic interstitium, with regulation of its activity and metabolism linked to the renin angiotensin system and possibly TGF-p. In Project 2, Dr. lekuni Ichikawa will continue to function as Project Leader. His state-of-the-art approaches to gene manipulation at a cell-specific level have led to a novel and exciting project that will focus on mechanisms of podocyte proliferation and differentiation after injury. Project 3 will continue to be led by Dr. Valentina Kon. She will continue study of the role of infiltrating and resident vascular cells in atherosclerosis, now focusing on the mechanisms of renal injuryinduced acceleration in atherosclerosis. Dr. Allison Eddy will still lead project 4. Her previous work on macrophage scavenger receptors and renal fibrosis has been extended to the current exciting projects, which will focus on how upregulation of scavenger receptors in the renal tubules per se contributes to tubulointerstitial inflammation and fibrosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center (P50)
Project #
5P50GM081883-02
Application #
7642550
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
2
Fiscal Year
2008
Total Cost
$676,728
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Mayhew, Michael B; Iversen, Edwin S; Hartemink, Alexander J (2017) Characterization of dependencies between growth and division in budding yeast. J R Soc Interface 14:
Maxwell, Colin S; Magwene, Paul M (2017) When sensing is gambling: An experimental system reveals how plasticity can generate tunable bet-hedging strategies. Evolution 71:859-871
Gibson, Tyler M; Gersbach, Charles A (2015) Single-molecule analysis of myocyte differentiation reveals bimodal lineage commitment. Integr Biol (Camb) 7:663-71
Magwene, Paul M (2014) Revisiting Mortimer's Genome Renewal Hypothesis: heterozygosity, homothallism, and the potential for adaptation in yeast. Adv Exp Med Biol 781:37-48
Sankararaman, Swaminathan; Efrat, Alon; Ramasubramanian, Srinivasan et al. (2014) On Channel-Discontinuity-Constraint Routing in Wireless Networks. Ad Hoc Netw 13:153-169
Bristow, Sara L; Leman, Adam R; Simmons Kovacs, Laura A et al. (2014) Checkpoints couple transcription network oscillator dynamics to cell-cycle progression. Genome Biol 15:446
Saunders, Lindsay R; McClay, David R (2014) Sub-circuits of a gene regulatory network control a developmental epithelial-mesenchymal transition. Development 141:1503-13
Warner, Jacob F; McClay, David R (2014) Perturbations to the hedgehog pathway in sea urchin embryos. Methods Mol Biol 1128:211-21
Liu, Shiping; Lorenzen, Eline D; Fumagalli, Matteo et al. (2014) Population genomics reveal recent speciation and rapid evolutionary adaptation in polar bears. Cell 157:785-94
Haase, Steven B; Wittenberg, Curt (2014) Topology and control of the cell-cycle-regulated transcriptional circuitry. Genetics 196:65-90

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