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  • 1995-1999  (48)
Collection
Year
  • 1
    Monograph available for loan
    Monograph available for loan
    New York [u.a.] : Oxford University Press
    Call number: M 08.0276
    Description / Table of Contents: This text describes the full range of charts, graphs, maps, diagrams and tables used daily to manage, analyze and communicate information. It features over 3000 illustrations, acting as a source on presenting information for anyone who writes or designs reports.
    Type of Medium: Monograph available for loan
    Pages: 448 S.
    ISBN: 9780195135329
    Location: Upper compact magazine
    Branch Library: GFZ Library
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  • 2
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A truncated soluble form of the murine class I major histocompatibility antigen complex H–2Dd was cloned using an Escherichia coli based system. It was expressed, refolded in vitro and crystallized in a complex with murine β2 microglobulin and the peptide RGPGRAFVTI from the V3-loop of the gp160 HIV-1 protein. Crystals belonging to the space group P212121 with cell dimensions a = 51.3, b = 92.5, c = 108.8 Å were obtained using two different crystallization conditions. The crystals contain one complex per asymmetric unit and diffract to at least 2.4 Å resolution.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 2724-2726 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 3713-3720 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In this paper, we consider how parity conservation limits the type of superpositions of chiral states that can be created and detected. We also show how spontaneous emission can cause the left and right hands of the superposition to become coupled to different states of the radiation field. This coupling, aside from being an interesting effect in its own right, helps to enforce the restrictions that parity conservation places upon superpositions of chiral states. Finally, we outline an analogy that exists between aspects of this work and the Einstein, Podolsky, Rosen paradox. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 2609-2613 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A density functional theory for the Kohn–Sham exchange energy of a bounded, closed shell system in a weak, uniform, magnetic field is presented. The form obtained vanishes when the electron density is radial and, unlike the unscreened exchange energy of a locally uniform electron gas, does not diverge due to the Coulomb interaction. The role of the exchange-correlation functional in the context of magnetic response theory is also examined. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature medicine 1 (1995), S. 2-4 
    ISSN: 1546-170X
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] To the editor — Nonsteroidal anti-inflammatory drugs (NSAIDs) are a widely used class of compounds that are prescribed as analgesic, antipyretic and anti-inflammatory agents1. NSAIDs can elicit potentially fatal hypersensitivity reactions (including anaphylaxis, bronchospasm and ...
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Perspectives in drug discovery and design 2 (1995), S. 353-361 
    ISSN: 1573-9023
    Keywords: Breast cancer cells ; Elastase ; Enzyme inhibitors ; Processing enzymes ; pro-TGF-α ; Serine proteinase ; TGF-α
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Transforming growth factor-α (TGF-α) is a mitogenic peptide hormone produced extracellularly, by tumor cells, and by virally and chemically transformed cells in culture. TGF-α is almost certainly derived from its precursor protein (pro-TGF-α) by limited endoproteolysis, but physiologically relevant processing enzyme(s) of the pro-TGF-α protein and the cellular or subcellular compartment in which processing takes place are not known with certainty. We previously detailed [Cappelluti, E. and Harris, R.B., Biochemistry, 32 (1993) 551] the discovery, characterization and purification of novel, elastase-like enzymes (molecular weight 38 000) from oncogenically transformed rat liver epithelial cells or cultural Schwann cells transfected with SV40-large T antigen. The elastase-like enzyme appeared to be specifically induced in the transformed epithelial cells compared with the level of enzyme in the nontransformed parental cells. In the intervening time, other elastase-like serine proteinases have been implicated in processing pro-TGF-α in other human carcinoma cell lines. We now report that the elastase-like enzymes, purified from transformed Schwann or liver epithelial cells, are inhibited in a time- and concentration-dependent fashion with three differently substituted monocyclic β-lactam-based compounds originally developed as specific inhibitors of polymorphonuclear leukocyte elastase, thus further supporting the elastase-like character of the putative pro-TGF-α processing enzymes. We also report the presence of the elastase-like enzyme in two different human malignant mammary cell lines, but even though MCF-7 cells receiving high doses of radiation in vitro show an increased level of expression of TGF-α, the elastase-like enzyme does not appear to be induced in these cells following irradiation.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Higher education 29 (1995), S. 77-92 
    ISSN: 1573-174X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Nature of Science, Research, Systems of Higher Education, Museum Science
    Notes: Abstract This paper is in two main sections. The first offers a brief historical account of the involvement of overseas students in the UK University system; the second reviews the literature on student attitudes to their stay, relating this to the contemporary experiences of a small cohort of students on a postgraduate professional training course in an older university. While overseas students have traditionally been perceived as somewhat problematic, more recently, driven by economic, political and intellectual considerations, the mode of analysis has moved away from situating the cause of any problems in the students themselves, and towards exploring the relations between the needs of overseas students and the resources dedicated by universities to meeting them. Unless universities take seriously the implications of having overseas students, which include organisational and staff development issues as well as the proper adaptation of teaching methods and techniques, there is serious potential for things to go wrong.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-4943
    Keywords: ANF ; atrial natriuretic factors ; atrial granule serine proteinase ; peptide inhibitors ; peptide aldehydes ; processing enzymes ; pseudo-bond inhibitors ; serine proteinase ; Swern oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Pseudo-peptide bond inhibitors (ψ-bond inhibitors) and peptide-aldehyde inhibitors of atrial granule serine proteinase, the candidate processing enzyme of pro-atrial natrieuretic factor, are prepared in high yield and purity by novel synthetic routes. The ψ-bond compounds retain essential residues for enzyme binding, but place the enzyme inhibition site in the midst of the peptide sequence. Thus, Bz-APR-ψ-LR and Bz-APR-ψ-SLRR can be considered “readthrough inhibitors” of atrial granule serine proteinase. The most potent ψ-peptide, Bz-APR-ψ-SLRR (IC50=250 ΜM), is about fivefold less potent than the best peptide-aldehyde inhibitor (EACA-APR-CHO), and both the ψ-bond and peptide-aldehyde compounds are competitive, reversible inhibitors of the enzyme. The ψ-bond peptides containing two C-terminal Arg residues are three-to tenfold more potent than the analogous compounds containing only one C-terminal Arg residue, confirming the importance of both Arg residues in the enzyme processing recognition site. As expected, because of their moderate potencies, the ψ-peptides are not useful affinity ligands for purification of atrial granule serine proteinase, but both peptide aldehydes are effective affinity ligands [Damodaran and Harris (1995),J. Protein Chem., this issue].
    Type of Medium: Electronic Resource
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