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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 246 (1995), S. 387-396 
    ISSN: 1617-4623
    Keywords: Xenopus ovary ; cDNA expression library Yeast transformation ; Weel kinase ; Cell cycle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In fission yeast the Weel kinase and the functionally redundant Mikl kinase provide a regulatory mechanism to ensure that mitosis is initiated only after the completion of DNA synthesis. Yeast in which both Weel and Mik1 kinases are defective exhibit a mitotic catastrophe phenotype, presumably due to premature entry into mitosis. Because of the functional conservation of cell cycle control elements, the expression of a vertebrate weel or mikl homolog would be expected to rescue such lethal mutations in yeast. A Xenopus total ovary cDNA library was constructed in a fission yeast expression vector and used to transform a yeast temperature-dependent mitotic catastrophe mutant defective in both weel and mikl. Here we report the identification of a Xenopus cDNA clone that can rescue several different yeast mitotic catastrophe mutants defective in Weel kinase function. The expression of this clone in a weel/mikl-deficient mutant causes an elongated cell phenotype under non-permissive growth conditions. The 2.0 kb cDNA clone contains an open reading frame of 1263 nucleotides, encoding a predicted 47 kDa protein. Bacterially expressed recombinant protein was used to raise a polyclonal antibody, which specifically recognizes a 47 kDa protein from Xenopus oocyte nuclei, suggesting the gene encodes a nuclear protein in Xenopus. The ability of this cDNA to complement mitotic catastrophe mutations is independent of Weel kinase activity.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Bioelectromagnetics 13 (1992), S. 543-555 
    ISSN: 0197-8462
    Keywords: broadband irradiation ; short pulses ; tissue dispersion ; induced currents ; SARs ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: The finite-difference time-domain (FDTD) method has been used to calculate SARs and induced currents involving whole-body or partial-body exposures of models to spatially uniform or nonuniform (far-field or near-field), to sinusoidally varying EM fields, or to transient fields such as those associated with electromagnetic pulses. However, a weakness of the FDTD algorithm is that the dispersion of the tissue's dielectric properties is ignored and frequency-independent properties are assumed. Although this is permissible for continuous-wave or narrow-band irradiation, the results may be highly erroneous for short pulses, in which ultra-wide bandwidths are involved. In some recent publications, procedures are described for one- and two-dimensional problems for media in which the complex permittivity ∊ * (ω) may be described by a single-order Debye relaxation equation or a modified version thereof. These procedures based on a convolution integral describing D(t) in terms of E(t) cannot be extended to human tissues for which multiterm Debye relaxation equations must generally be used.We describe here a new differential-equation approach that can be used for general dispersive media. We illustrate the use of this approach by one- and three-dimensional examples of media for which ∊ * (ω) is given by a multiterm Debye equation, and for an approximate two-thirds muscle-equivalent model of the human body. Based on a single run involving a Gaussian pulse, the frequency-dependent FDTD [(FD)2TD] method allows calculations of SARs and induced currents at various frequencies by taking the Fourier components of the induced E fields. The (FD)2TD method can also be used to calculate coupling of the short (ultra-wideband) pulses to the human body. 1992 Wiley-Liss, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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