The objective of the Morphology Core is to enhance the ability of the Center Investigators to perform digestive and liver research. The Morphology Core strives to provide high quality service and support to scientists with a commitment to teaching the techniques and providing the reagents necessary to perform morphologic analysis of gastrointestinal tract and liver tissues. This Core has grown substantially and has been extremely successful since July 1997, when it initiated services and provided reagents to Investigators of the Center for Molecular Studies in Digestive and Liver Disease. Dr. Silberg became the Director of the Morphology Core in 1998. The growth of the Core resulted in the hiring of Gary Swain, Ph.D. as the Technical Director. Drs. Silberg and Swain have been essential in expanding the scientific aspects of the Core by teaching techniques to Center Investigators and assisting in the development of protocols for new antibodies for immunohistochemistry. With the addition of two full time technicians, the Core has been able to provide quality services in a timely manner to the Center Investigators. The following description will outline the services provided by the Morphology Core. Morphologic data generated by some of the principle investigators will be presented as examples of the type and quality of work that can be expected. An important aspect of this core has been the collaboration and interactions that have occurred among its investigators. The Morphology Core is located on the 6th floor of the Clinical Research Building, in rooms adjacent to the scientific investigators in the Division of Gastroenterology, and easily accessible to all Center Investigators. Due to the close proximity of the Morphology Core to the user laboratories, it has become an important vehicle for Center Investigators, fellows, and technicians to collaborate and consult while performing immunohistochemistry or using the imaging equipment. Collaborations have been built through these interactions and we anticipate fostering future collaborations in this fashion. Importantly, the Molecular Biology Core is located across the hall from the Morphology Core, allowing for cohesive interactions in tissue procurement and analysis (e.g., Tissue bank, H&E sections and RNA extractions).

Project Start
2002-07-15
Project End
2007-06-30
Budget Start
Budget End
Support Year
6
Fiscal Year
2002
Total Cost
$161,817
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Karakasheva, Tatiana A; Dominguez, George A; Hashimoto, Ayumi et al. (2018) CD38+ M-MDSC expansion characterizes a subset of advanced colorectal cancer patients. JCI Insight 3:
Uribe-Herranz, Mireia; Bittinger, Kyle; Rafail, Stavros et al. (2018) Gut microbiota modulates adoptive cell therapy via CD8? dendritic cells and IL-12. JCI Insight 3:
Facompre, Nicole D; Harmeyer, Kayla M; Sahu, Varun et al. (2018) Targeting JARID1B's demethylase activity blocks a subset of its functions in oral cancer. Oncotarget 9:8985-8998
Estrada, Michelle A; Zhao, Xiao; Lorent, Kristin et al. (2018) Synthesis and Structure-Activity Relationship Study of Biliatresone, a Plant Isoflavonoid That Causes Biliary Atresia. ACS Med Chem Lett 9:61-64
DeLong, Jonathan H; Hall, Aisling O'Hara; Konradt, Christoph et al. (2018) Cytokine- and TCR-Mediated Regulation of T Cell Expression of Ly6C and Sca-1. J Immunol 200:1761-1770
Williams, Bianca; Correnti, Jason; Oranu, Amanke et al. (2018) A novel role for ceramide synthase 6 in mouse and human alcoholic steatosis. FASEB J 32:130-142
Karakasheva, Tatiana A; Lin, Eric W; Tang, Qiaosi et al. (2018) IL-6 Mediates Cross-Talk between Tumor Cells and Activated Fibroblasts in the Tumor Microenvironment. Cancer Res 78:4957-4970
Bengsch, Bertram; Ohtani, Takuya; Herati, Ramin Sedaghat et al. (2018) Deep immune profiling by mass cytometry links human T and NK cell differentiation and cytotoxic molecule expression patterns. J Immunol Methods 453:3-10
Moreira, Leticia; Bakir, Basil; Chatterji, Priya et al. (2018) Pancreas 3D Organoids: Current and Future Aspects as a Research Platform for Personalized Medicine in Pancreatic Cancer. Cell Mol Gastroenterol Hepatol 5:289-298
Das, Koushik K; Heeg, Steffen; Pitarresi, Jason R et al. (2018) ETV5 regulates ductal morphogenesis with Sox9 and is critical for regeneration from pancreatitis. Dev Dyn 247:854-866

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