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  • 2015-2019  (82)
  • 2000-2004  (10)
  • 1990-1994  (17)
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  • 1
    Series available for loan
    Series available for loan
    Zurich : Cryospheric Commission of the Swiss Academy of Sciences (SCNAT)
    Associated volumes
    Call number: AWI G3-19-92381
    In: Permafrost in Switzerland, 2004/2005 and 2005/2006
    Type of Medium: Series available for loan
    Pages: XIV, 100 Seiten , Illustrationen
    Series Statement: Glaciological Report (Permafrost) / Permafrost Monitoring Switzerland 6/7
    Language: English
    Note: Contents: Imprint Published Reports Preface Summary Zusammenfassung Résumé Riassunto Resumaziun 1 Introduction 2 Weather and Climate 2.1 Weather and Climate in 2004/2005 2.2 Weather and Climate in 2005/2006 2.3 Climate Deviation from the Mean Value 1961–1990 2.4 Duration of the Snow Cover 3 Borehole Measurements 3.1 Active Layer Thickness 3.2 Permafrost Temperatures 3.2 ERT Monitoring Network 3.4 Conclusions Boreholes 4 Surface Temperatures 4.1 Surface Temperatures in Unconsolidated Sediments 4.2 Rock Surface Temperatures 4.3 Conclusions Surface Temperatures 5 Air Photos 5.1 Air Photos in 2004/2005 and 2005/2006 6 Conclusion 7 Selected Aspects of Permafrost Monitoring 7.1 Short-term Variations in Rock Glacier Kinematics 7.2 Destabilized Rock Glaciers 7.3 Conclusions Rock Glacier Dynamics Acknowledgements References Appendix
    Location: AWI Reading room
    Branch Library: AWI Library
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  • 2
    Publication Date: 2018-11-19
    Keywords: ddc:600
    Repository Name: Wuppertal Institut für Klima, Umwelt, Energie
    Language: English
    Type: report , doc-type:report
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  • 3
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 30 (1991), S. 4285-4286 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1211
    Keywords: Aotus nancymaae MHC class II DQ genes Allelic lineages Polymorphism Peptide binding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. The New World primate Aotus nancymaae has been recommended by the World Health Organization (WHO) as a model for evaluation of malaria vaccine candidates, given its susceptibility to experimental infection with the human malaria parasites Plasmodium falciparum and Plasmodium vivax. We present here the nucleotide sequences of the complete cDNA of MHC-DQA1 and of the polymorphic exon 2 segments of MHC-DQB1/DQB2. In a group of three nonrelated animals captured in the wild, five alleles of MHC-DQA1 could be identified. They all belong to one lineage, namely Aona-DQA1*27. This lineage has not been described in any other New World monkey species studied. In a group of 19 unrelated animals, 14 Aona-DQB1 alleles could be identified which are grouped into the two lineages Aona-DQB1*22 and Aona-DQB1*23. These lineages have been described previously in the common marmoset and cotton-top tamarin. In addition, two Aona-DQB2 sequences could be identified which are highly similar to HLA-DQB2 sequences. Essential amino acid residues contributing to MHC DQ peptide binding pockets number 1 and 4 are conserved or semi-conserved between HLA-DQ and Aona-DQ molecules, indicating a capacity to bind similar peptide repertoires. These results fully support the use of Aotus monkeys as an animal model for evaluation of future subunit vaccine candidates.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1211
    Keywords: Key words Aotus nancymaae ; Immunoglobulin kappa light chain (IGK) genes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract  Sequences of Aotus nancymaae immunoglobulin kappa light-chain rearrangements were analyzed after reverse transcription polymerase chain reaction. Among 22 in-frame rearrangements analyzed, 12 IGKV genes belonging to the families 1, 2, or 3 were identified. Aotus counterparts for all five human IGKJ genes were found. The identity of the deduced human and Aotus amino acid sequences was between 83% and 92% for junctional regions and 74% for the constant region. Sequence comparisons between rearrangements indicated that somatic mutations, the addition of nongermline-encoded nucleotides, and exonuclease trimming contribute to the generation of diversity of Aotus immunoglobulin kappa chains. The high identity of Aotus and human IGK genes is comparable to that of T-cell receptor genes and further supports the proposal to use the Aotus Plasmodium falciparum infection model for the evaluation of malaria vaccine candidates.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1420-9055
    Keywords: Neuston ; surface film ; surface-film enrichment ; phytoplankton succession ; Lake Zürich
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Samples of surface films and of the underlying bulk water at 0.2 m depth were taken in Lake Zürich on 48 occasions in 1986, 1988 and 1989, with the aim of assessing the appropriateness of applying existing neuston nomenclature to the organisms found in these films, of determining which organisms accumulate there during which periods of time, and of assessing the importance of the phytoplankton community in the development of neustonic biocoenoses. Lake Zürich surface films were found to support a community of high population density, consisting of organisms which had migrated from the benthal or pelagial, or which had entered the film via the atmosphere or inflowing rivers. In all samples, species originating from within the phytoplankton community accounted for the greatest proportion of the total abundance. Several of these species were found to exhibit a special preference for the surface biotope, viz. those with a relative frequency (rF) exceeding 10%, a mean enrichment factor (Ef) exceeding 100, and, in the majority of cases, with a greater concentration of individuals in the surface film than in the underlying bulk water layer. We suggest that only those organisms occurring in the surface films of large water bodies which fulfil the above criteria should be considered as belonging to the planktoneuston, in order to distinguish them from other species, the occurrence of which in surface films is merely coincidental. The fact that planktoneustonic algae are dominant in the surface films of Lake Zürich means that changes in the species composition of the planktonic algal biocoenosis directly affect the species composition of the neustonic algal biocoenosis. Thus, just as in the underlying bulk water, a succession can be observed in the algal biocoenosis of the surface films. However, because of the higher abundance of planktoneustonic algae there, this succession is distinct from that occurring in the pelagial. Factors bringing about these differences which are discussed for the case of the dominant planktoneustonic algae are: alterations in specific gravity; positive phototaxis; and enhancement of growth rates in surface films as compared with the underlying bulk water.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-4919
    Keywords: poly(ADP-ribose)polymerase ; poly(ADP-ribose) glycohydrolase ; DNA repair ; chromatin ; nucleosomal unfolding ; NAD+
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The enzymes poly(ADP-ribose)polymerase and poly(ADP-ribose) glycohydrolase may cooperate to drive a histone shuttle mechanism in chromatin. The mechanism is triggered by binding of the N-terminal zinc-finger domain of the polymerase to DNA strand breaks, which activates the catalytic activities residing in the C-terminal domain. The polymerase converts into a protein carrying multiple ADP-ribose polymers which displace histones from DNA by specifically targeting the histone tails responsible for DNA condensation. As a result, the domains surrounding DNA strand breaks become accessible to other proteins. Poly(ADP0ribose) glycohydrolase attacks ADP-ribose polymers in a specific order and thereby releases histones for reassociation with DNA. Increasing evidence from different model systems suggests that histone shuttling participates in DNA repairin vivo as a catalyst for nucleosomal unfolding.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    BioEssays 16 (1994), S. 557-564 
    ISSN: 0265-9247
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Mutations in specific genes result in birth defects, cancer, inherited diseases or lethality. The frequency with which DNA damage is converted to mutations increases dramatically when the cellular genome is replicated. Although DNA damage poses special problems to the fidelity of DNA replication, efficient mechanisms exist in mammalian cells which function to replicate their genome despite the presence of many damaged sites. These mechanisms operate in either error-prone or error-free modes of DNA synthesis, and frequently involve DNA strand-pairing reactions. Genetic studies in yeast and other eukaryotes suggest that replication through DNA damage is highly regulated and catalysed by complex biochemical machineries composed of many specialised gene products. Knowledge of the molecular details by which such factors facilitate the replication of damaged DNA in mammalian cells should reveal basic rules about how DNA damage induces mutagenesis and carcinogenesis.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 2017-07-31
    Description: Xeroderma pigmentosum C (XPC) protein initiates the global genomic subpathway of nucleotide excision repair (GG-NER) for removal of UV-induced direct photolesions from genomic DNA. The XPC has an inherent capacity to identify and stabilize at the DNA lesion sites, and this function is facilitated in the genomic context by UV-damaged DNA-binding protein 2 (DDB2), which is part of a multiprotein UV–DDB ubiquitin ligase complex. The nuclear enzyme poly(ADP-ribose) polymerase 1 (PARP1) has been shown to facilitate the lesion recognition step of GG-NER via its interaction with DDB2 at the lesion site. Here, we show that PARP1 plays an additional DDB2-independent direct role in recruitment and stabilization of XPC at the UV-induced DNA lesions to promote GG-NER. It forms a stable complex with XPC in the nucleoplasm under steady-state conditions before irradiation and rapidly escorts it to the damaged DNA after UV irradiation in a DDB2-independent manner. The catalytic activity of PARP1 is not required for the initial complex formation with XPC in the nucleoplasm but it enhances the recruitment of XPC to the DNA lesion site after irradiation. Using purified proteins, we also show that the PARP1–XPC complex facilitates the handover of XPC to the UV-lesion site in the presence of the UV–DDB ligase complex. Thus, the lesion search function of XPC in the genomic context is controlled by XPC itself, DDB2, and PARP1. Our results reveal a paradigm that the known interaction of many proteins with PARP1 under steady-state conditions could have functional significance for these proteins.
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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