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  • Nuclear Structure  (2)
  • Data analysis / ~ processing
  • Deep seismic sounding (espec. cont. crust)
  • Humans
  • Modelling
  • 2010-2014  (3)
  • 1
    Publication Date: 2013-09-07
    Description: Author(s): J. Snyder, T. Baumann, G. Christian, R. A. Haring-Kaye, P. A. DeYoung, Z. Kohley, B. Luther, M. Mosby, S. Mosby, A. Simon, J. K. Smith, A. Spyrou, S. Stephenson, and M. Thoennessen The neutron-unbound nucleus 15 Be was observed for the first time. It was populated using neutron transfer from a deuterated polyethylene target with a 59 MeV/u 14 Be beam. Neutrons were measured in coincidence with outgoing 14 Be particles and the reconstructed decay energy spectrum exhibits a resonan... [Phys. Rev. C 88, 031303] Published Fri Sep 06, 2013
    Keywords: Nuclear Structure
    Print ISSN: 0556-2813
    Electronic ISSN: 1089-490X
    Topics: Physics
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  • 2
    Publication Date: 2014-08-16
    Description: Author(s): J. K. Smith, T. Baumann, D. Bazin, J. Brown, S. Casarotto, P. A. DeYoung, N. Frank, J. Hinnefeld, M. Hoffman, M. D. Jones, Z. Kohley, B. Luther, B. Marks, N. Smith, J. Snyder, A. Spyrou, S. L. Stephenson, M. Thoennessen, N. Viscariello, and S. J. Williams The neutron decay of an unbound resonance in Be12 has been measured at 1243±21 keV decay energy with a width of 634±60 keV. This state was populated with a one-proton removal reaction from a 71 MeV/u B13 beam incident upon a beryllium target. The invariant mass reconstruction of the resonance was ac... [Phys. Rev. C 90, 024309] Published Fri Aug 15, 2014
    Keywords: Nuclear Structure
    Print ISSN: 0556-2813
    Electronic ISSN: 1089-490X
    Topics: Physics
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  • 3
    Publication Date: 2011-09-03
    Description: The efficacy and safety of biological molecules in cancer therapy, such as peptides and small interfering RNAs (siRNAs), could be markedly increased if high concentrations could be achieved and amplified selectively in tumour tissues versus normal tissues after intravenous administration. This has not been achievable so far in humans. We hypothesized that a poxvirus, which evolved for blood-borne systemic spread in mammals, could be engineered for cancer-selective replication and used as a vehicle for the intravenous delivery and expression of transgenes in tumours. JX-594 is an oncolytic poxvirus engineered for replication, transgene expression and amplification in cancer cells harbouring activation of the epidermal growth factor receptor (EGFR)/Ras pathway, followed by cell lysis and anticancer immunity. Here we show in a clinical trial that JX-594 selectively infects, replicates and expresses transgene products in cancer tissue after intravenous infusion, in a dose-related fashion. Normal tissues were not affected clinically. This platform technology opens up the possibility of multifunctional products that selectively express high concentrations of several complementary therapeutic and imaging molecules in metastatic solid tumours in humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Breitbach, Caroline J -- Burke, James -- Jonker, Derek -- Stephenson, Joe -- Haas, Andrew R -- Chow, Laura Q M -- Nieva, Jorge -- Hwang, Tae-Ho -- Moon, Anne -- Patt, Richard -- Pelusio, Adina -- Le Boeuf, Fabrice -- Burns, Joe -- Evgin, Laura -- De Silva, Naomi -- Cvancic, Sara -- Robertson, Terri -- Je, Ji-Eun -- Lee, Yeon-Sook -- Parato, Kelley -- Diallo, Jean-Simon -- Fenster, Aaron -- Daneshmand, Manijeh -- Bell, John C -- Kirn, David H -- Canadian Institutes of Health Research/Canada -- England -- Nature. 2011 Aug 31;477(7362):99-102. doi: 10.1038/nature10358.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Jennerex Inc., 450 Sansome Street, 16th floor, San Francisco, California 94111, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21886163" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Aged, 80 and over ; DNA, Viral/blood ; Female ; Gene Expression Regulation, Enzymologic ; Humans ; Infusions, Intravenous ; Male ; Middle Aged ; Neoplasms/pathology/surgery/*therapy/virology ; *Oncolytic Virotherapy ; Oncolytic Viruses/*physiology ; Organisms, Genetically Modified/physiology ; Poxviridae/*physiology ; Transgenes/genetics ; beta-Galactosidase/genetics/metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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