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  • 1
    Online Resource
    Online Resource
    Wiley ; 2021
    In:  Nonprofit Management and Leadership Vol. 31, No. 4 ( 2021-06), p. 693-715
    In: Nonprofit Management and Leadership, Wiley, Vol. 31, No. 4 ( 2021-06), p. 693-715
    Abstract: Many nonprofit organizations rely on donations to fund their programs, and a robust literature predicts donations in large‐scale quantitative studies. The focus, however, is almost exclusively on the financial characteristics of the organizations, leaving the social context underexplored. In this article, we theorize how ecological context, organizational identity, and social network ties can shape donations. We use the new Internal Revenue Service (IRS) release of e‐filed nonprofit reporting forms to consider 95,518 501(c)3 nonprofits around 2015. Using lagged regression models, we find that organizations within a more favorable ecological context, those that use appeals to religion, and organizations with more volunteers report more donations. Furthermore, stressing affiliation with a geographic location is associated with more donations only under certain ecological conditions. The article concludes with a discussion of the implications of these results for nonprofit organizations and social theories regarding what influences donations to organizations.
    Type of Medium: Online Resource
    ISSN: 1048-6682 , 1542-7854
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2069718-1
    SSG: 3,2
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  • 2
    In: British Journal of Pharmacology, Wiley, Vol. 176, No. 13 ( 2019-07), p. 2238-2249
    Abstract: G protein‐gated inwardly rectifying K + (K ir 3) channels moderate the activity of excitable cells and have been implicated in neurological disorders and cardiac arrhythmias. Most neuronal K ir 3 channels consist of K ir 3.1 and K ir 3.2 subtypes, while cardiac K ir 3 channels consist of K ir 3.1 and K ir 3.4 subtypes. Previously, we identified a family of urea‐containing K ir 3 channel activators, but these molecules exhibit suboptimal pharmacokinetic properties and modest selectivity for K ir 3.1/3.2 relative to K ir 3.1/3.4 channels. Here, we characterize a non‐urea activator, VU0810464, which displays nanomolar potency as a K ir 3.1/3.2 activator, improved selectivity for neuronal K ir 3 channels, and improved brain penetration. Experimental Approach We used whole‐cell electrophysiology to measure the efficacy and potency of VU0810464 in neurons and the selectivity of VU0810464 for neuronal and cardiac K ir 3 channel subtypes. We tested VU0810464 in vivo in stress‐induced hyperthermia and elevated plus maze paradigms. Parallel studies with ML297, the prototypical activator of K ir 3.1‐containing K ir 3 channels, were performed to permit direct comparisons. Key Results VU0810464 and ML297 exhibited comparable efficacy and potency as neuronal K ir 3 channel activators, but VU0810464 was more selective for neuronal K ir 3 channels. VU0810464, like ML297, reduced stress‐induced hyperthermia in a K ir 3‐dependent manner in mice. ML297, but not VU0810464, decreased anxiety‐related behaviour as assessed with the elevated plus maze test. Conclusion and Implications VU0810464 represents a new class of K ir 3 channel activator with enhanced selectivity for K ir 3.1/3.2 channels. VU0810464 may be useful for examining K ir 3.1/3.2 channel contributions to complex behaviours and for probing the potential of K ir 3 channel‐dependent manipulations to treat neurological disorders.
    Type of Medium: Online Resource
    ISSN: 0007-1188 , 1476-5381
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2029728-2
    SSG: 15,3
    Location Call Number Limitation Availability
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