The purpose of the Histology Core is to perform tissue processing and staining, immunohistochemistry, and in situ hybridization for Program investigators, this associates, and the Transgenic Core (Core B). Because each project and the Transgenic Core propose numerous experiments requiring histological processing of samples and microscopic detection techniques, the Histology Core will be staffed by a research technician and will occupy dedicated and equipped laboratory space. To expedite the processing of samples, the Core will be organized into functional sub- components, or laboratories, that are defined by the services provided. The Histology Laboratory will provide samples, cut sections, perform histological staining, and store tissue blocks. The Immunology laboratory will perform immunostaining, assist investigators in preparing immunoreagents, and maintain commonly used materials. The Molecular Biology Laboratory will be responsible for in situ hybridization procedures, including labeling probes and storing reagents. Most tissue and cells samples will be collected and submitted by personnel associated with the individual investigators and the Transgenic Core. Project and Core investigators or their associates will complete a Work Order form that will be used to catalogue the work requested and to record the date that each task is completed. The quality and results of analytical assays will be reviewed by Dr. Wilson with the Program Investigator or the co- investigator who is responsible for the experiment. Thus, the aim of this Core is to provide a center for correlative interactions among the Program investigators in histological studies of the skin and associated structures.

Project Start
2001-04-01
Project End
2002-03-31
Budget Start
Budget End
Support Year
4
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Klingelhofer, Jorg; Troyanovsky, Regina B; Laur, Oscar Y et al. (2003) Exchange of catenins in cadherin-catenin complex. Oncogene 22:1181-8
Lin, Meei-Hua; Kopan, Raphael (2003) Long-range, nonautonomous effects of activated Notch1 on tissue homeostasis in the nail. Dev Biol 263:343-59
Liu, Zhonghao; Xu, Jingsong; Colvin, Jennifer S et al. (2002) Coordination of chondrogenesis and osteogenesis by fibroblast growth factor 18. Genes Dev 16:859-69
Klingelhofer, Jorg; Laur, Oscar Y; Troyanovsky, Regina B et al. (2002) Dynamic interplay between adhesive and lateral E-cadherin dimers. Mol Cell Biol 22:7449-58
Neely, Melody N; Pfeifer, John D; Caparon, Michael (2002) Streptococcus-zebrafish model of bacterial pathogenesis. Infect Immun 70:3904-14
Kopan, Raphael; Lee, Jonghyeob; Lin, Meei-Hua et al. (2002) Genetic mosaic analysis indicates that the bulb region of coat hair follicles contains a resident population of several active multipotent epithelial lineage progenitors. Dev Biol 242:44-57
Dumin, J A; Dickeson, S K; Stricker, T P et al. (2001) Pro-collagenase-1 (matrix metalloproteinase-1) binds the alpha(2)beta(1) integrin upon release from keratinocytes migrating on type I collagen. J Biol Chem 276:29368-74
Lohi, J; Wilson, C L; Roby, J D et al. (2001) Epilysin, a novel human matrix metalloproteinase (MMP-28) expressed in testis and keratinocytes and in response to injury. J Biol Chem 276:10134-44
Lyon, W R; Madden, J C; Levin, J C et al. (2001) Mutation of luxS affects growth and virulence factor expression in Streptococcus pyogenes. Mol Microbiol 42:145-57
Madden, J C; Ruiz, N; Caparon, M (2001) Cytolysin-mediated translocation (CMT): a functional equivalent of type III secretion in gram-positive bacteria. Cell 104:143-52

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