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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Solid state phenomena Vol. 141-143 (July 2008), p. 73-78 
    ISSN: 1662-9779
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Physics
    Notes: Thixo-forming is in the forefront of metal processing technology in the 21st century. Theresearch on thixo-co-extrusion of multi-layer tube as extension and development of the semi-solidforming technology is a completely new processing method for the composite material forming andis of great significance, in which different semi-solid billets (slurries) are extruded at the same timeto form multi-layer tubes. In this study, different sizes of column-shaped and ring-shaped billets ofAl/Mg alloys were firstly prepared by using specially designed molds. Then they were reheated byelectric-resistance furnace,microstructures from different heating laws were investigated. Lastly,FEM simulation on thixo-co-extrusion of double-layer tube with A356/AZ91 was conducted
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta mechanica solida Sinica 5 (1992), S. 125-133 
    ISSN: 0894-9166
    Keywords: effective stress ; elastoplasticity ; creep damage ; parametric variation principle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Based on the concept of the effective stress in continuum damage mechanics, this paper studies the damage-coupled problem in elastoplastic creep. By using the parametric variational principle developed from optimal control theory, a numerical principle for the problem discussed has been established, the proof for which is also given. It is found that the principle proposed has a normalized form and can easily be put into application by computer.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2017-09-06
    Description: pGlyco 2.0 enables precision N-glycoproteomics with comprehensive quality control and one-step mass spectrometry for intact glycopeptide identification Nature Communications, Published online: 5 September 2017; doi:10.1038/s41467-017-00535-2 Protein glycosylation is a heterogeneous post-translational modification that generates greater proteomic diversity that is difficult to analyze. Here the authors describe pGlyco 2.0, a workflow for the precise one step identification of intact N-glycopeptides at the proteome scale.
    Electronic ISSN: 2041-1723
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2014-09-21
    Description: Background: Oncolytic herpes simplex virus (HSV) can replicate in and kill cancer cells while sparing the adjacent normal tissue. Hepatocellular carcinoma (HCC) is amongst the most common and lethal cancers, especially in Third World countries. In this study, the cytotoxicity of a third-generation oncolytic HSV, G47?, was investigated in different human HCC cell lines and in an immortalized human hepatic cell line. Additionally, subcutaneous models of HCC were established to evaluate the in vivo anti-tumor efficacy of G47?. Methods: The HepG2, HepB, SMMC-7721, BEL-7404, and BEL-7405 human HCC cell lines and the HL-7702 human hepatic immortalized cell lines were infected with G47? at different multiplicities of infection (MOIs). The viability of infected cells was determined, and the G47? replication was identified by X-gal staining for LacZ expression. Two subcutaneous (s.c.) HCC tumor models of HCC were also established in Balb/c nude mice, which were intratumorally(i.t.) treated with either G47? or mock virus. Tumor volume and mouse survival times were documented. Results: More than 95% of the HepG2, Hep3B,and SMMC-7721 HCC cells were killed on by day 5 after infection with a MOI?s of 0.01. For the HL-7702 human hepatic immortalized cells, 100% of the cells were killed on by day 5 after infection with a MOI?s of 0.01. The BEL-7404 HCC cell line was less susceptible with about 70% cells were killed by day 5 after infection with a MOI?s of 0.01. Whereas the BEL-7405 HCC cells were the least susceptible, with only 30% of the cells were killed. Both the SMMC-7721 and BEL-7404 cells form aggressive sc tumor models. G47? replicates in the tumors, such that most of the tumors regressed after the G47?-treatment, and treated tumor-bearing mice survived much longer than the control animals. Conclusions: G47? effectively kills human HCC cells and an immortalized hepatic cell line at low MOI. Intra-tumor injection of G47? can induce a therapeutic effect and prolong the survival of treated mice bearing SMMC-7721 and BEL-7404 subcutaneously (s.c.) tumors. Thus, G47? may be useful as a novel therapeutic agent for HCC.
    Electronic ISSN: 1475-2867
    Topics: Medicine
    Published by BioMed Central
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