Program Project CORE (Jacquin, Rhoades) - Seven facilities/functions will be made available: 1) A single """"""""morphometry"""""""" facility in St. Louis for staining and analyzing the long-range projections and dendrites of single trigeminal neurons, and for analyzing spatial distribution patterns of populations of trigeminal neurons, during normal development and after various experimental perturbations. Drs. Jacquin, Arends and Woolsey will oversee its use by all of the Program Project participants. 2) A single electron microscopy facility in St. Louis for tissue processing and documentation of ultrastructural reorganization during normal development and after experimental manipulations. Dr. Zahm will oversee its use. 3) A single tissue culture facility in Toledo for assessing the role of afferent-and target-related factors in axon target selection and the development of axon arborization patterns. Dr. Hankin will oversee its use. 4) A single facility in Toledo for the housing and preparation of experimental animals. Dr Rhoades will oversee its use. 5) Timely transmission of baseline data, experimental materials and ideas between the different laboratories. 6) External review by an External Advisory Committee and invited seminar speakers. 7) Administration. By instituting these CORE facilities and functions we: 1) Make technical upgrades developed in one laboratory available to all of the component projects. 2) Make optimum use of individual experimental animals to increase the power of conclusions drawn. 3) Ensure that the data obtained from the different laboratoaries are comparable and analysed in a like manner so as to circumvent common pitfalls associated with the correlation of findings obtained by independent observers and different analytic techniques. 4) Provide means for experimental and conceptual integration and facilitation. 5) Provide frequent and regularly scheduled meetings for internal and external reviews of our progress. 6) Administer the various projects. All requisite equipment and personnel are currently funcitoning within our Program Project.

Project Start
1997-02-15
Project End
1998-02-14
Budget Start
Budget End
Support Year
12
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Jacquin, Mark F; Arends, Joop J A; Renehan, William E et al. (2015) Whisker-related circuitry in the trigeminal nucleus principalis: Topographic precision. Somatosens Mot Res 32:8-20
Xiang, Chuanxi; Arends, Joop J A; Jacquin, Mark F (2014) Whisker-related circuitry in the trigeminal nucleus principalis: ultrastructure. Somatosens Mot Res 31:141-51
Pluto, Charles P; Chiaia, Nicolas L; Rhoades, Robert W et al. (2005) Reducing contralateral SI activity reveals hindlimb receptive fields in the SI forelimb-stump representation of neonatally amputated rats. J Neurophysiol 94:1727-32
Genc, Baris; Ulupinar, Emel; Erzurumlu, Reha S (2005) Differential Trk expression in explant and dissociated trigeminal ganglion cell cultures. J Neurobiol 64:145-56
Vadivelu, Sudhakar; Platik, Marina M; Choi, Luke et al. (2005) Multi-germ layer lineage central nervous system repair: nerve and vascular cell generation by embryonic stem cells transplanted in the injured brain. J Neurosurg 103:124-35
Gandhi, Rohan; Ryals, Janelle M; Wright, Douglas E (2004) Neurotrophin-3 reverses chronic mechanical hyperalgesia induced by intramuscular acid injection. J Neurosci 24:9405-13
McDonald, John W; Becker, Daniel; Holekamp, Terrence F et al. (2004) Repair of the injured spinal cord and the potential of embryonic stem cell transplantation. J Neurotrauma 21:383-93
Genc, Baris; Ozdinler, P Hande; Mendoza, April E et al. (2004) A chemoattractant role for NT-3 in proprioceptive axon guidance. PLoS Biol 2:e403
Ulupinar, Emel; Unal, Nedim; Erzurumlu, Reha S (2004) Morphometric analysis of embryonic rat trigeminal neurons treated with different neurotrophins. Anat Rec A Discov Mol Cell Evol Biol 277:396-407
Wright, Douglas E; Ryals, Janelle M; McCarson, Kenneth E et al. (2004) Diabetes-induced expression of activating transcription factor 3 in mouse primary sensory neurons. J Peripher Nerv Syst 9:242-54

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