Core C will support the establishment and maintenance of the COBRE Gene Array Core facility. The Core will provide the interface, expertise, training and mentoring in gene array analysis necessary for the advancement of COBRE projects on different epithelia including Project 1: """"""""Transepithelial ion transport and its regulation"""""""" (renal collecting ducts and vas deference), Project 2: """"""""Intestinal epithelial migration: NSAID, polyamine-depletion, and depolarized membrane potential"""""""" (equine intestinal epithelia), and Project 3: """"""""Molecular basis of protein and vesicle traffic in epithelia"""""""" (pancreatic acinar cells and renal proximal tubules). These projects depend critically on comparisons in gene expression between different experimental conditions. The Core will provide gene array processing by outsourcing to other facilities in conjunction with a local analysis facilities to process the data. This analysis facility in conjunction with the provided expertise, training and mentoring will enable COBRE investigators to establish themselves through advancing their research on epithelia in health and disease.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
1P20RR017686-01
Application #
6691449
Study Section
Special Emphasis Panel (ZRR1)
Project Start
2002-09-30
Project End
2007-08-31
Budget Start
Budget End
Support Year
1
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Kansas State University
Department
Type
DUNS #
City
Manhattan
State
KS
Country
United States
Zip Code
66506
Ishiguro, Susumu; Kawabata, Atsushi; Zulbaran-Rojas, Alejandro et al. (2018) Co-treatment with a C1B5 peptide of protein kinase C? and a low dose of gemcitabine strongly attenuated pancreatic cancer growth in mice through T cell activation. Biochem Biophys Res Commun 495:962-968
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Ohta, Naomi; Ishiguro, Susumu; Kawabata, Atsushi et al. (2015) Human umbilical cord matrix mesenchymal stem cells suppress the growth of breast cancer by expression of tumor suppressor genes. PLoS One 10:e0123756

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