1,118 research outputs found

    The impact of financing constraints on investment.

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    This thesis is an empirical and theoretical analysis of the impact of financing constraints on firm-level investment behaviour. Its primary objectives are to model this impact, and to test the restrictions these models place on the data. Chapter 1 contains a discussion of these themes, and provides an overview of the thesis. Chapter 2 addresses the empirical question of whether innovative firms are financially constrained. To answer this question, several structural investment equations are tested, and the sensitivity of physical investment expenditures to internal finance is compared across innovative and non-innovative firms. The investment expenditures of innovative firms are found to be more sensitive to cash flow than those of non-innovative firms. These results support the hypothesis that innovative firms are financially constrained. The third chapter builds a theoretical model to explain a widely reported fact in the inventory literature, which is that the variance of production exceeds the variance of sales. This fact contradicts a prediction of the standard Linear-Quadratic model of inventory investment, and for this reason is often referred to as the "excess variance of production" puzzle. In this chapter, a model of inventory investment is built. It is shown that when financing constraints are imposed on the model, it can explain the excess variance of production puzzle. In the absence of these constraints, the model does not deliver this result. The fourth chapter returns to the theme of identifying financially constrained firms. A weakness of existing tests of financing constraints is that they are not both direct and structural. This chapter addresses that criticism by constructing a model of investment from which is derived a simple and direct, structural test of the null hypothesis that a group of firms is financially constrained. The test is implemented on a panel of U.S. manufacturing firms. The results support the findings of existing tests

    The State-of-the-Art Questionnaire on Applied Systems Analysis: A Report on the Responses

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    This publication is the second report by the Survey Project on the structure and content of a proposed Series of monographs and a Handbook to survey the state-of-the-art of applied systems analysis. In the first report (RR-76-16, Systems Analysis: An Outline for the State-of-the-Art Survey Publications, July 1976), we presented a revised outline and current guidelines for the Survey Project publication program; in the present document, the sequel. we discuss the response to a questionnaire -- distributed widely throughout the systems analyst community -- upon which our revised outline is based. This report should be of interest to the questionnaire respondents, and to a wider audience as well. in that it reflects what some 160 analysts and others associated with systems analysis think about systems analysis, what they consider to be vital and important in this area, and what they think to be peripheral or of minor relevance

    Systems Analysis: An Outline for the State-of-the-Art Survey Publications

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    IIASA plans to organize, commission, and publish a Series of volumes and a Handbook to survey the international state-of-the-art of applied systems analysis. This report provides the Survey Project's explication of the concept of applied systems analysis; it describes in detail the proposed Series and Handbook, including purpose, audience, international character, level of presentation, authors, reviewers, and remuneration policies. An outline spanning the field of interest of applied systems analysis is designed to help prospective authors with the choice of topics. Guidelines are provided for the acceptability of volumes for the Series, and suggestions for prospective authors on the preparation of prospectuses (outlines) for Series monographs are included. These prospectuses are submitted to the Editorial Board and special liaison committees established in each of IIASA's National Member Organizations. A summary checklist of procedures for development of Series volumes is provided in the Appendix

    Non trivial generalizations of the Schwinger pair production result

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    We present new, non trivial generalizations of the recent Tomaras, Tsamis and Woodard extension of the original Schwinger formula for charged pair production in a constant field.Comment: 11 page

    A conditional Smg6 mutant mouse model reveals circadian clock regulation through the nonsense-mediated mRNA decay pathway.

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    Nonsense-mediated messenger RNA (mRNA) decay (NMD) has been intensively studied as a surveillance pathway that degrades erroneous transcripts arising from mutations or RNA processing errors. While additional roles in physiological control of mRNA stability have emerged, possible functions in mammalian physiology in vivo remain unclear. Here, we created a conditional mouse allele that allows converting the NMD effector nuclease SMG6 from wild-type to nuclease domain-mutant protein. We find that NMD down-regulation affects the function of the circadian clock, a system known to require rapid mRNA turnover. Specifically, we uncover strong lengthening of free-running circadian periods for liver and fibroblast clocks and direct NMD regulation of Cry2 mRNA, encoding a key transcriptional repressor within the rhythm-generating feedback loop. Transcriptome-wide changes in daily mRNA accumulation patterns in the entrained liver, as well as an altered response to food entrainment, expand the known scope of NMD regulation in mammalian gene expression and physiology

    A novel Smg6 mouse model reveals regulation of circadian period and daily CRY2 accumulation through the nonsense-mediated mRNA decay pathway

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    Nonsense-mediated mRNA decay (NMD) has been intensively studied as a surveillance pathway that degrades erroneous transcripts arising from mutations or RNA processing errors. While additional roles in controlling regular mRNA stability have emerged, possible functions in mammalian physiology in vivo have remained unclear. Here, we report a novel conditional mouse allele that allows converting the NMD effector nuclease SMG6 from wild-type to nuclease domain-mutant protein. We analyzed how NMD downregulation affects the function of the circadian clock, a system known to require rapid mRNA turnover. We uncover strong lengthening of free-running circadian periods for liver and fibroblast clocks, and direct NMD regulation of Cry2 mRNA, encoding a key transcriptional repressor within the rhythm-generating feedback loop. In the entrained livers of Smg6 mutant animals we reveal transcriptome-wide alterations in daily mRNA accumulation patterns, altogether expanding the known scope of NMD regulation in mammalian gene expression and physiology

    Effective action for scalar fields and generalised zeta-function regularisation

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    Motivated by the study of quantum fields in a Friedman-Robertson-Walker (FRW) spacetime, the one-loop effective action for a scalar field defined in the ultrastatic manifold R×H3/ΓR\times H^3/\Gamma, H3/ΓH^3/\Gamma being the finite volume, non-compact, hyperbolic spatial section, is investigated by a generalisation of zeta-function regularisation. It is shown that additional divergences may appear at one-loop level. The one-loop renormalisability of the model is discussed and making use of a generalisation of zeta-function regularisation, the one-loop renormalisation group equations are derived.Comment: Latex, 16 pages, no figures; Latex mistakes corrected; accepted for publication in Physical Review
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