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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 34 (1992), S. 219-230 
    ISSN: 1432-1432
    Keywords: CpG dinucleotides ; CpNpG trinucleotides ; Angiosperm gene sequences ; Arabidopsis thaliana gene sequences ; Methylation sites ; Deamination mutation ; DNA sequence analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The extent to which CpG dinucleotides were depleted in a large set of angiosperm genes was, on average, very similar to the extent of CpG depletion in total angiosperm genomic DNA and far less than the extent of CpG depletion in vertebrate genes. Gene sequences from Arabidopsis thaliana, a dicotyledonous species with relatively low levels of total 5-methylcytosine, were just as CpG depleted as the angiosperm genes in general. Furthermore, levels of TpG and CpA, the potential deamination mutation products of methylated CpG, were elevated in A. thaliana genes, supporting a high rate of deamination mutation as the cause of the CpG deficiency. Using a method that takes into account the dinucleotide frequencies within each sequence of interest, we calculated the expected frequencies of CpNpG trinucleotides, which are also highly methylated in angiosperm genomes. CpNpG trinucleotides were not extensively enriched or depleted in the angiosperm genes. Two hypotheses could account for our results. Differential depletion of CpG and CpNpG within angiosperm genes and differential depletion of CpG in angiosperm and vertebrate genes could arise from different efficiencies of mismatch repair or from different levels of cytosine methylation in the cell lineages that contribute to germ cells.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 34 (1992), S. 231-245 
    ISSN: 1432-1432
    Keywords: CpG islands ; CpG-rich DNA ; G+C content ; Angiosperm gene sequences ; Arabidopsis thaliana gene sequences ; DNA sequence analysis ; CpG methylation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary CpG islands, which are hypomethylated regions with clustered CpG dinucleotides resulting from a high G+C content and a lack of the normal CpG deficiency, are associated with a large number of vertebrate nuclear genes. There is some evidence that CpG islands may also be a feature of angiosperm genes. In mammalian and avian genes, candidate CpG islands can be readily identified by a simple set of sequence criteria. However, identification of candidate angiosperm CpG islands is more difficult due to the much higher ratio of observed/expected (O/E) CpG in the average angiosperm gene relative to the average vertebrate gene (see accompanying paper). We have developed sets of objective criteria that readily detect angiosperm DNA regions with a consistently high O/E CpG compared to the rest of the genome. These regions, which we call significant CpG-rich regions, always showed a CpG frequency equivalent to or greater than that expected from the base composition, suggesting that they may undergo positive selection for the presence of CpG dinucleotides. The significant CpG-rich regions were similar to vertebrate CpG islands in that they tended to be associated with the 5′ ends of genes, particularly of housekeeping genes, and in that they varied in location in tissue-specific genes. However, unlike the situation in mammalian and avian genes, DNA with a high O/E CpG did not surround the transcription start site of all angiosperm housekeeping genes. Significant CpG-rich regions in monocotyledonous species were G+C rich, like CpG islands. Significant CpG-rich regions in dicotyledonous species, on the other hand, differed from CpG islands but were similar to some CpG-rich regions in cold-blooded vertebrates (Xenopus and fish) in that they were A+T rich. We have argued that both the A+T-rich and the G+C-rich significant CpG-rich regions may fulfill the same function as the G+C-rich CpG islands of vertebrates.
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 72 (1968), S. 2862-2866 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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〉 72 (1968), S. 1834-1835 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The effects of substrate temperature and ion dose on silicon-on-insulator structures prepared by nitrogen implantation were characterized by transmission electron microscopy and Auger electron spectroscopy. Substrate temperatures below 200 °C during implantation result in amorphous surface layers that become polycrystalline after annealing. Implantation above 800 °C leaves the surface single crystalline containing a high density of defects. The majority of these defects are removed after annealing. High nitrogen doses (1.6×1018 cm−2 at 150 keV) resulted in two nitride layers separated by a porous region. This porous region may be attributed to the creation of N2 gas. A continuous nitride layer, without a porous region, was formed using a nitrogen dose of 9.4×1017 cm−2. When a nitrogen dose of 4×1017 cm−2 is used, however, it results in a two-phase layer containing amorphous nitride and Si crystallites.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 62 (1987), S. 657-661 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: X-ray photoemission from Ga 2p3/2 electrons was used to investigate the two polar {111} faces of a polished, single-crystal GaP wafer. It is shown directly by examining, for the first time, the contributions to the photoemission from electrons involved in Ga–Ga, Ga–P, and Ga–O bonds, that one of these faces consists solely of Ga atoms and the reverse face solely of P atoms. The same experiments on both faces of a similar {100} wafer showed that both {100} faces are the same.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1617-4623
    Keywords: Key wordsBactrocera tryoni  ;  Drosophila melanogaster  ; Lucilia cuprina  ;  Mariner  ;  Transposition assay
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Plasmid-based transposition assays were performed in developing embryos of the Australian sheep blowfly Lucilia cuprina and the Queensland fruit fly Bactrocera tryoni, using the mariner transposable element from Drosophila mauritiana. Transposition products were recovered that were identical in structure to those recovered from D. melanogaster. Only sequences delimited by the mariner terminal repeats were transposed and all insertions occurred at TA residues, and duplicated these. These are the hallmarks of mariner transpositions observed in the chromosomes of D. melanogaster and D. mauritiana, indicating that the plasmid-based assays are accurate indicators of mariner transposition activity. The recovery of precise transposition products from L. cuprina and B. tryoni demonstrates that mariner should be capable of producing germline transformants in these species. The results obtained from these assays suggests that they will be extremely useful in determining if mariner can transpose in other non-drosophilid insects and for investigating factors that might affect mariner transposition frequency.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Human highly repeated satellite sequences, cloned into M13, were used as templates to prepare single-stranded DNA probes containing bromodeoxyuridine (BrdUrd) in place of thymine. The probes were hybridised to human metaphase chromosomes and visualised using an indirect immunological detection procedure. The sensitivity and accuracy of the technique were tested using a BrdUrd-labelled probe of known copy number and location: a segment from the 2.5 kb Y chromosome repeat. The procedure proved to be reliable and fast, with a sensitivity similar to that of other in situ hybridisation techniques. The technique was then used to determine the chromosomal locations of a 100 bp repeat from human satellite 3. The satellite 3 probe hybridised to a large number of chromosomes and, surprisingly, the intensity of label at all locations remained unchanged when the slides were washed at a higher stringency. The resolution of the technique was very high and allowed accurate localisation of the satellite sequence. Hybridisation was observed in two regions of the subcentromeric heterochromatin of chromosome 9, in two locations at the centromere and short arm of all the acrocentric autosomes, and at the centromere and long arm of the Y chromosome. In addition the probe hybridised to centromeric heterochromatin in chromosomes 1, 16, 17 and 20. We believe that single-stranded BrdUrd-labelled probes should be very useful for detecting RNA transcripts in cells, and discuss ways by which the procedure could be modified to locate single copy DNA on chromosomes.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 255 (1977), S. 715-715 
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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