This Core provides for the production of transgenic animals for the programs in the POEMB. The use of conventional transgenic animals and gene targeting studies have become commonplace in the study of many biological systems. Study of the heart and lung is no exception, and our Component Leaders and new Investigators have depended on this Core during the pst granting period. The Core has established over 1200 conventional transgenic lines and 29 gene knockouts. Multiple projects continue to use transgenic mice in their studies. The Transgenic mouse Core has maintained a high rate of success; coupled with a large production, it has been able to keep its costs as one of the lowest in the U.S. The Core acts as a resource for the POEMB components ina the design and implementation of individual experiments. In addition to its production capabilities, the Transgenic mouse Core has utilized its products to search for new avenues of research. In collaboration with members of Dr. Jerry Lingrel's Lab, the Transgenic Mouse Cotre has screened for insertional mutants from the transgenic animals it has produced. One of these newly discovered mutants has now become a direct aim of Jerry Lingel's laboratory's research efforts. Other mutants are currently being assessed for inclusion to these studies.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL041496-10
Application #
6272854
Study Section
Project Start
1997-12-01
Project End
1998-11-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
10
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Cincinnati
Department
Type
DUNS #
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Sadayappan, Sakthivel; Finley, Natosha; Howarth, Jack W et al. (2008) Role of the acidic N'region of cardiac troponin I in regulating myocardial function. FASEB J 22:1246-57
Pattison, James Scott; Waggoner, Jason R; James, Jeanne et al. (2008) Phospholamban overexpression in transgenic rabbits. Transgenic Res 17:157-70
Kalinichenko, Vladimir V; Gusarova, Galina A; Kim, Il-Man et al. (2004) Foxf1 haploinsufficiency reduces Notch-2 signaling during mouse lung development. Am J Physiol Lung Cell Mol Physiol 286:L521-30
Small, Kersten M; McGraw, Dennis W; Liggett, Stephen B (2003) Pharmacology and physiology of human adrenergic receptor polymorphisms. Annu Rev Pharmacol Toxicol 43:381-411
Sanbe, Atsushi; Gulick, James; Hanks, Mark C et al. (2003) Reengineering inducible cardiac-specific transgenesis with an attenuated myosin heavy chain promoter. Circ Res 92:609-16
Liggett, Stephen B (2003) Polymorphisms of adrenergic receptors: variations on a theme. Assay Drug Dev Technol 1:317-26
Golovina, Vera A; Song, Hong; James, Paul F et al. (2003) Na+ pump alpha 2-subunit expression modulates Ca2+ signaling. Am J Physiol Cell Physiol 284:C475-86
Kalinichenko, Vladimir V; Zhou, Yan; Shin, Brian et al. (2002) Wild-type levels of the mouse Forkhead Box f1 gene are essential for lung repair. Am J Physiol Lung Cell Mol Physiol 282:L1253-65
Whitsett, Jeffrey A; Clark, Jean C; Picard, Lara et al. (2002) Fibroblast growth factor 18 influences proximal programming during lung morphogenesis. J Biol Chem 277:22743-9
Lim, Lorena; Kalinichenko, Vladimir V; Whitsett, Jeffrey A et al. (2002) Fusion of lung lobes and vessels in mouse embryos heterozygous for the forkhead box f1 targeted allele. Am J Physiol Lung Cell Mol Physiol 282:L1012-22

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