6,767 research outputs found

    Collective treatment of the giant resonances in spherical nuclei

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    In a collective treatment the energies of the giant resonances are given by the boundary conditions at the nuclear surface, which is subject to vibration in spherical nuclei. The general form of the coupling between these two collective motions is given by angular-momentum and parity conservation. The coupling constants are completely determined within the hydrodynamical model. In the present treatment the influence of the surface vibrations on the total photon-absorption cross section is calculated. It turns out that in most of the spherical nuclei this interaction leads to a pronounced structure in the cross section. The agreement with the experiments in medium-heavy nuclei is striking; many of the experimental characteristics are reproduced by the present calculations. In some nuclei, however, there seem to be indications of single-particle excitations which are not yet contained in this work

    Diffuse and weak Bragg scattering from quasicrystals: pitfalls and opportunities

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    The influence of limited experimental reciprocal space resolution on the appearance of diffraction patterns from quasicrystals is discussed. Using simulated data from a perfectly ordered one-dimensional Fibonacci chain it is shown that realistic experimental resolution effects may lead to artificial ‘diffuse scattering' of significant intensity. Two different diffuse features are identified in simulations of macroscopically sized crystals. A broad and almost smooth diffuse background is found, which strongly inceases with decreasing reciprocal space resolution. In addition, a set of of narrow diffuse peaks having profiles similar to thermal and phasonic diffuse scattering is present, which is only seen in high resolution patterns. The former diffuse scattering represents unresolved Bragg reflections, while the latter is due to truncation effects coming from the finite crystal size. The relevance of the findings for the understanding of real experimental diffraction patterns is discussed on the examples of diffuse scattering from d-Al70Co12Ni18 and i-Al64Cu23Fe13. Finally, some criteria for distinguishing disorder diffuse scattering from artificial diffuse scattering are give

    Volumetric measurement of tank volume

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    A method is disclosed for determining the volume of compressible gas in a system including incompressible substances in a zero-gravity environment consisting of measuring the change in pressure (delta P) for a known volume change rate (delta V/delta t) in the polytrophic region between isothermal and adiabatic conditions. The measurements are utilized in an idealized formula for determining the change in isothermal pressure (delta P sub iso) for the gas. From the isothermal pressure change (delta iso) the gas volume is obtained. The method is also applicable to determination of gas volume by utilizing work (W) in the compression process. In a passive system, the relationship of specific densities can be obtained

    A Very Strong Enhancer Is Located Upstream of an Immediate Early Gene of Human Cytomegalovirus

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    A strong transcription enhancer was identified in the genomic DNA (235 kb) of human cytomegalovirus (HCMV), a ubiquitous and severe pathogen of the herpesvirus group. Cotransfection of enhancerless SV40 DNA with randomly fragmented HCMV DNA yielded two SV40-HCMV recombinant viruses that had incorporated overlapping segments of HCMV DNA to substitute for the missing SV40 enhancer. Within HCMV, these enhancer sequences are located upstream of the transcription initiation site of the major immediate-early gene, between nucleotides -118 and −524. Deletion studies with the HCMV enhancer, which harbors a variety of repeated sequence motifs, show that different subsets of this enhancer can substitute for the SV40 enhancer. The HCMV enhancer, which seems to have little cell type or species preference, is severalfold more active than the SV40 enhancer. It is the strongest enhancer we have analyzed so far, a property that makes it a useful component of eukaryotic expression vectors

    The SV40 "enhancer trap"

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    Case Report: Familial Gastric Cancer and Chordoma in the Same Family

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    Gastric cancers are the second most common malignancy in the world and represent a major burden to all societies even though the incidence of disease is decreasing in the industrialized world. The aetiology of the disease is complex and is believed to be primarily due to environmental factors but a small proportion of cases are recognised as being associated with genetic factors. Two inherited forms of stomach cancer have been identified, one which is associated with familial clusterings of stomach cancer and the other being a subgroup of families that belong to hereditary non polyposis colorectal cancer (or Lynch syndrome). In this report we present a small nuclear family which is unusual in that there is a clustering of malignancy which includes stomach cancer, colorectal cancer and chordoma. Genetic analysis failed to reveal any causative mutation in genes associated with HNPCC or in E-cadherin. Together, the clinical picture in this family may indicate that other genetic factors are behind this family's clustering of malignancy

    A long and complex enhancer activates transcription of the gene coding for the highly abundant immediate early mRNA in murine cytomegalovirus

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    Using the simian virus 40 "enhancer trap" approach, we have identified a transcription enhancer located just upstream of the major immediate early gene of murine cytomegalovirus. This enhancer has several striking properties. (.) Together with the enhancer ofhuman cytomegalovirus, it is the strongest transcription enhancer found to date. (ö) It is an extremely long enhancer, spanning >700 base pairs. (ÜI) It consists of a rather complex pattern of sequence repeats, the longest of which is 181 base pairs. Also, several types of short sequence motifs are scattered throughout the enhancer in monomeric, heterodimeric, or homodimeric (palindromic) form. These motifs have been identified to be components of other enhancers and promoters, and they are presumably binding sites for specific nuclear factors. Our analysis suggests that enhancers are composed of a modular arrangement of short conserved sequence motifs and that enhancer strength is correlated with the redundancy of these motifs
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