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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 348 (1994), S. 317-325 
    ISSN: 1434-601X
    Keywords: 12.38.Lg ; 13.60.Fz ; 14.20.Dh
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We consider the spin-averaged nucleon forward Compton scattering amplitude in heavy baryon chiral perturbation theory including all terms to order $$\mathcal{O}(q^4 )$$ . The chiral prediction for the spin-averaged forward Compton scattering amplitude is in good agreement with the data for photon energiesω≦110 MeV. We also evaluate the nucleon electric and magnetic Compton polarizabilities to this order and discuss the uncertainties of the various counter terms entering the chiral expansion of these quantities.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1463
    Keywords: GDNF ; in situ hybridization ; cell death ; Parkinson's disease ; adult ; newborn infant
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Glial cell line-derived neurotrophic factor (GDNF) is a potent neurotrophic factor for dopaminergic neurons. Since dopaminergic neurons degenerate in Parkinson's disease, this factor is a potential therapeutical tool that may save dopaminergic neurons during the pathological process. Moreover, a reduced GDNF expression may be involved in the pathophysiology of the disease. In this study, we tested whether altered GDNF production may participate in the mechanism of cell death in this disease. GDNF gene expression was analyzed by in situ hybridization using riboprobes corresponding to a sequence of the exon 2 human GDNF gene. Experiments were performed on tissue sections of the mesencephalon and the striatum from 8 patients with Parkinson's disease and 6 control subjects matched for age at death and for post mortem delay. No labelling was observed in either group of patients. This absence of detectable expression could not be attributed to methodological problems as a positive staining was observed using the same probes for sections of astroglioma biopsies from human adults and for sections of a newborn infant brain obtained at post-mortem. These data suggest that GDNF is probably expressed at a very low level in the adult human brain and its involvement in the pathophysiology of Parkinson's disease remains to be demonstrated. GDNF may represent a powerful new therapeutic agent for Parkinson's disease, however.
    Type of Medium: Electronic Resource
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