Over the past 10 years our center has been involved in multiple projects with collaborators interested in various aspects of neurobiology. Anatomical structures and pathological processes have been successfully investigated. Our improved technical skills have elicited our users who are now approaching us with more specific and demanding tasks; We are increasingly approached by neurogeneticists who wants us to characterize anatomy as well as pathology in various transgenic rodents with known genetic defects. We are being challenged by these projects not only because of the small-sized mouse brain but also because of the need to apply our MR proton stain knowledge base more efficiently and accurately. The biologist raises specific questions, i.e. is there atrophy? gliosis? neuronal degeneration? demyelination? and desires specific answers. The typical biologist is obviously incapable of translating this information into exact MR parameters. The MR physicist, on the other hand, often has insufficient knowledge of the biology involved to predict the outcome of a given MR proton stain. To improve efficiency and quality of future neuropathological projects we are proposing to take a more systematic approach by creating a neurohistological database which will make explicit connection between specific proton stains and well-characterized pathologies. Not only will we expand our general knowledge on contrast mechanisms we will also gain valuable """"""""diagnostic"""""""" information for future projects.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR005959-12
Application #
6493769
Study Section
Project Start
2001-09-01
Project End
2002-08-31
Budget Start
Budget End
Support Year
12
Fiscal Year
2001
Total Cost
$288,015
Indirect Cost
Name
Duke University
Department
Type
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Tang, Xinyan; Jing, Liufang; Richardson, William J et al. (2016) Identifying molecular phenotype of nucleus pulposus cells in human intervertebral disc with aging and degeneration. J Orthop Res 34:1316-26
Hodgkinson, Conrad P; Bareja, Akshay; Gomez, José A et al. (2016) Emerging Concepts in Paracrine Mechanisms in Regenerative Cardiovascular Medicine and Biology. Circ Res 118:95-107
Schmeckpeper, Jeffrey; Verma, Amanda; Yin, Lucy et al. (2015) Inhibition of Wnt6 by Sfrp2 regulates adult cardiac progenitor cell differentiation by differential modulation of Wnt pathways. J Mol Cell Cardiol 85:215-25
Roos, Justus E; McAdams, Holman P; Kaushik, S Sivaram et al. (2015) Hyperpolarized Gas MR Imaging: Technique and Applications. Magn Reson Imaging Clin N Am 23:217-29
He, Mu; Robertson, Scott H; Kaushik, S Sivaram et al. (2015) Dose and pulse sequence considerations for hyperpolarized (129)Xe ventilation MRI. Magn Reson Imaging 33:877-85
Huang, Lingling; Walter, Vonn; Hayes, D Neil et al. (2014) Hedgehog-GLI signaling inhibition suppresses tumor growth in squamous lung cancer. Clin Cancer Res 20:1566-75
Huang, Jing; Guo, Jian; Beigi, Farideh et al. (2014) HASF is a stem cell paracrine factor that activates PKC epsilon mediated cytoprotection. J Mol Cell Cardiol 66:157-64
Yuan, Ying; Gilmore, John H; Geng, Xiujuan et al. (2014) FMEM: functional mixed effects modeling for the analysis of longitudinal white matter Tract data. Neuroimage 84:753-64
He, Mu; Kaushik, S Sivaram; Robertson, Scott H et al. (2014) Extending semiautomatic ventilation defect analysis for hyperpolarized (129)Xe ventilation MRI. Acad Radiol 21:1530-41
Liu, Chunlei; Li, Wei (2013) Imaging neural architecture of the brain based on its multipole magnetic response. Neuroimage 67:193-202

Showing the most recent 10 out of 239 publications