The analysis of gene expression patterns in normal and genetically altered mouse embryos is a major thrust in each individual project of this Program. To stream-line such analyses and to establish and provide state-of-the-art procedures of embryo analysis, the applicants propose to establish an EMBRYOLOGY CORE FACILITY. The duties of this core are: (1) to determine by in situ hybridization and immunohistochemistry the expression patterns of genes of interest in normal and genetically altered embryos; (2) to interpret these expression data in context of the experimental manipulation that was applied to the particular embryo; (3) to examine embryos with more conventional morphological and histological techniques; (4) to document and archive results of these studies either by conventional photography and/or video-based data processing. Importantly, participation of the researches who have brought in a particular project will be required at all levels. Such an interaction will enhance information transfer and educate members of the program about fundamental aspects of embryo analysis. The core consists of facilities (1) to section embryos, (2) to study sectioned and whole-mount embryos by conventional and confocal microscopy, and (3) to record video pictures that are then computer-processed and stored on disc to be accessible to all investigators of the program. These facilities will be operated by an experienced embryologist/histologist and histology technician, under the supervision of the core director.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL049953-03
Application #
3737123
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Liu, Yu; Kaneda, Ruri; Leja, Thomas W et al. (2014) Hhex and Cer1 mediate the Sox17 pathway for cardiac mesoderm formation in embryonic stem cells. Stem Cells 32:1515-26
Zeve, Daniel; Seo, Jin; Suh, Jae Myoung et al. (2012) Wnt signaling activation in adipose progenitors promotes insulin-independent muscle glucose uptake. Cell Metab 15:492-504
Verzi, Michael P; Stanfel, Monique N; Moses, Kelvin A et al. (2009) Role of the homeodomain transcription factor Bapx1 in mouse distal stomach development. Gastroenterology 136:1701-10
Shah, Viraj R; Koster, Maranke I; Roop, Dennis R et al. (2007) Double-inducible gene activation system for caspase 3 and 9 in epidermis. Genesis 45:194-9
Niu, Zhivy; Li, Ankang; Zhang, Shu X et al. (2007) Serum response factor micromanaging cardiogenesis. Curr Opin Cell Biol 19:618-27
Chang, Jiang; Xie, Min; Shah, Viraj R et al. (2006) Activation of Rho-associated coiled-coil protein kinase 1 (ROCK-1) by caspase-3 cleavage plays an essential role in cardiac myocyte apoptosis. Proc Natl Acad Sci U S A 103:14495-500
Zhang, Ying-Min; Bo, Jacqueline; Taffet, George E et al. (2006) Targeted deletion of ROCK1 protects the heart against pressure overload by inhibiting reactive fibrosis. FASEB J 20:916-25
Ilagan, Roger; Abu-Issa, Radwan; Brown, Doris et al. (2006) Fgf8 is required for anterior heart field development. Development 133:2435-45
Zhang, Shu Xing; Garcia-Gras, Eduardo; Wycuff, Diane R et al. (2005) Identification of direct serum-response factor gene targets during Me2SO-induced P19 cardiac cell differentiation. J Biol Chem 280:19115-26
Vlahopoulos, Spiros; Zimmer, Warren E; Jenster, Guido et al. (2005) Recruitment of the androgen receptor via serum response factor facilitates expression of a myogenic gene. J Biol Chem 280:7786-92

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