The Aim of the Imaging Core is to provide enabling technology in histology and microscopy for all five participants in this Developmental Biology COBRE. The Core will be housed in a 5000 square foot suite in OMRF's new Research Tower. Major pieces of equipment include standard upright and inverted microscopes, a Zeiss LSM-510 META laser scanning confocal microscope, a Hitachi H-7600 transmission electron microscope fitted with an AMT 2Kx2K ES 4.0 digital camera, a Zeiss TIRF microscope, a structured illumination microscope with Colibri LED illumination, and a newly acquired Zeiss LSM-710 multiphoton microscope with a Becker and Hickl FLIM system and full physiological capabilities. Sample preparation equipment includes two automatic tissue processors, a paraffin embedder, four microtomes, cryostats, a tissue trimmer and an automatic coverslipper. Dr. Paul Kincade, an expert in the use of fluorescence microscopy, will be the Director of the Imaging Core and technical assistance and day-to-day management will be provided by Mr. Ben Fowler who has managed the facility for more than a decade. Access to the Imaging Core will be free of charge for all COBRE participants. The research projects of all five Junior Investigators depend on histology and various types of microscopy (fluorescence, confocal, electron, and multiphoton), so this Core will be heavily used and is essential for the success of this COBRE.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM103636-02
Application #
8625780
Study Section
Special Emphasis Panel (ZGM1-TWD-B)
Project Start
Project End
Budget Start
2014-03-01
Budget End
2015-02-28
Support Year
2
Fiscal Year
2014
Total Cost
$94,080
Indirect Cost
$38,080
Name
Oklahoma Medical Research Foundation
Department
Type
DUNS #
077333797
City
Oklahoma City
State
OK
Country
United States
Zip Code
73104
Bhaskaran, Shylesh; Pharaoh, Gavin; Ranjit, Rojina et al. (2018) Loss of mitochondrial protease ClpP protects mice from diet-induced obesity and insulin resistance. EMBO Rep 19:
Siefert, Joseph C; Clowdus, Emily A; Goins, Duane et al. (2018) Profiling DNA Replication Timing Using Zebrafish as an In Vivo Model System. J Vis Exp :
Borga, Chiara; Park, Gilseung; Foster, Clay et al. (2018) Simultaneous B and T cell acute lymphoblastic leukemias in zebrafish driven by transgenic MYC: implications for oncogenesis and lymphopoiesis. Leukemia :
Wren, Jonathan D (2018) Algorithmically outsourcing the detection of statistical errors and other problems. EMBO J 37:
Georgescu, Constantin; Wren, Jonathan D (2018) Algorithmic identification of discrepancies between published ratios and their reported confidence intervals and P-values. Bioinformatics 34:1758-1766
Snider, Timothy A; Richardson, Arlan; Stoner, Julie A et al. (2018) The Geropathology Grading Platform demonstrates that mice null for Cu/Zn-superoxide dismutase show accelerated biological aging. Geroscience 40:97-103
Sansam, Courtney G; Pietrzak, Katarzyna; Majchrzycka, Blanka et al. (2018) A mechanism for epigenetic control of DNA replication. Genes Dev 32:224-229
Arriens, Cristina; Wren, Jonathan D; Munroe, Melissa E et al. (2017) Systemic lupus erythematosus biomarkers: the challenging quest. Rheumatology (Oxford) 56:i32-i45
Duan, Hongliang; Li, Yu; Arora, Daleep et al. (2017) Discovery of a Benzamide Derivative That Protects Pancreatic ?-Cells against Endoplasmic Reticulum Stress. J Med Chem 60:6191-6204
de Castro, Rodrigo O; Previato, Luciana; Goitea, Victor et al. (2017) The chromatin-remodeling subunit Baf200 promotes homology-directed DNA repair and regulates distinct chromatin-remodeling complexes. J Biol Chem 292:8459-8471

Showing the most recent 10 out of 57 publications