The goal of the Phase III Microscopy Core is to provide COBRE investigators with imaging tools and training to make their cardiovascular research successful and sustainable. The Core will assist investigators with collect- ing microscopic images that will facilitate publication of their research, acquisition of further funding, and dis- covery of novel insights that push their research in new directions. The Core will provide state-of-the-art equipment and expertise in a variety of techniques, including histological and histochemical analyses, immu- nohistochemistry and immunocytochemistry, in-situ hybridization, photomicroscopy, computer-assisted image analysis and morphometry, live-cell imaging, intravital spinning-disk confocal and multiphoton microscopy, transmission electron microscopy, immunogold labeling, and advanced cryotechnologies such as freeze frac- ture and freeze etching. The Microscopy Core equipment and staff are centrally located in the OMRF Cardio- vascular Biology Research Program, in close proximity to the COBRE labs and the Cardiovascular Phenotyp- ing Core. This central location promotes a high level of interaction among Core users. The Core will be di- rected by two imaging experts, Drs. Florea Lupu and Courtney Griffin, with assistance from three experienced staff members. Building on its success during Phases I and II, the Microscopy Core will expand and accelerate research productivity and collaboration among COBRE investigators.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Center Core Grants (P30)
Project #
5P30GM114731-05
Application #
9924581
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2020-05-01
Budget End
2021-04-30
Support Year
5
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Oklahoma Medical Research Foundation
Department
Type
DUNS #
077333797
City
Oklahoma City
State
OK
Country
United States
Zip Code
73104
Donovan, Elise L; Lopes, Erika Barboza Prado; Batushansky, Albert et al. (2018) Independent effects of dietary fat and sucrose content on chondrocyte metabolism and osteoarthritis pathology in mice. Dis Model Mech 11:
Laurence, Jeffrey; Elhadad, Sonia; Ahamed, Jasimuddin (2018) HIV-associated cardiovascular disease: importance of platelet activation and cardiac fibrosis in the setting of specific antiretroviral therapies. Open Heart 5:e000823
Yago, Tadayuki; Liu, Zhenghui; Ahamed, Jasimuddin et al. (2018) Cooperative PSGL-1 and CXCR2 signaling in neutrophils promotes deep vein thrombosis in mice. Blood 132:1426-1437
Chugh, Seema; Barkeer, Srikanth; Rachagani, Satyanarayana et al. (2018) Disruption of C1galt1 Gene Promotes Development and Metastasis of Pancreatic Adenocarcinomas in Mice. Gastroenterology 155:1608-1624
Ghafoory, Shahrouz; Varshney, Rohan; Robison, Tyler et al. (2018) Platelet TGF-?1 deficiency decreases liver fibrosis in a mouse model of liver injury. Blood Adv 2:470-480
Gao, Siqi; Silasi-Mansat, Robert; Behar, Amanda R et al. (2018) Excessive Plasmin Compromises Hepatic Sinusoidal Vascular Integrity After Acetaminophen Overdose. Hepatology 68:1991-2003
Popescu, Narcis I; Silasi, Robert; Keshari, Ravi S et al. (2018) Peptidoglycan induces disseminated intravascular coagulation in baboons through activation of both coagulation pathways. Blood 132:849-860
Mancini, Donna; Monteagudo, Juan; Suárez-Fariñas, Mayte et al. (2018) New methodologies to accurately assess circulating active transforming growth factor-?1 levels: implications for evaluating heart failure and the impact of left ventricular assist devices. Transl Res 192:15-29
Liu, Zhenghui; Yago, Tadayuki; Zhang, Nan et al. (2017) L-selectin mechanochemistry restricts neutrophil priming in vivo. Nat Commun 8:15196
Laurence, Jeffrey; Elhadad, Sonia; Robison, Tyler et al. (2017) HIV protease inhibitor-induced cardiac dysfunction and fibrosis is mediated by platelet-derived TGF-?1 and can be suppressed by exogenous carbon monoxide. PLoS One 12:e0187185

Showing the most recent 10 out of 20 publications