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  • 2000-2004  (3)
  • 1975-1979
  • Lagrange interpolation polynomial  (1)
  • MAD 2  (1)
  • Macrobrachium nipponense  (1)
  • 1
    ISSN: 1573-0603
    Keywords: Macrobrachium nipponense ; Cell subculture ; pH ; Zn2+
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A cell culture system was devised for muscle cell of Macrobrachium nipponense in the study. The juvenile and adult shrimps were held in laboratory aquaria with penicillin 1000 IU/ml and streptomycin 1000 µg/ml for 12–24 hours. Cell cultures were established in medium 199 supplemented with 20% fetal bovine serum, 1 g/L glucose, 5.2 g/L NaCl, 1.43 g/L CaCl2, 0.05 g/L MgCl2, 100 IU/mL penicillin and 100 µg/ml streptomycin. Fibroblast-like cells were passaged up to three times and survived for 54 days. The results showed the optimum for subculture in vitro was in medium 199 with pH 7.6. Moreover, basal medium supplemented with Zn2+ 60 µg/L could enhance the growth of the muscle cells. It was found that better results for cell culture would be obtained more easily with juvenile shrimps caught in spring than adults in summer or autumn; and shrimps caught within 12 hours after ecdysis could grow much better than the intermoult shrimps.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Annals of the Institute of Statistical Mathematics 52 (2000), S. 557-573 
    ISSN: 1572-9052
    Keywords: Chebyshev polynomials ; convex combination ; extremal problems for polynomials ; Lagrange interpolation polynomial ; optimal discrimination designs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract The extrapolation design problem for polynomial regression model on the design space [−1,1] is considered when the degree of the underlying polynomial model is with uncertainty. We investigate compound optimal extrapolation designs with two specific polynomial models, that is those with degrees |m, 2m}. We prove that to extrapolate at a point z, |z| 〉 1, the optimal convex combination of the two optimal extrapolation designs |ξ m * (z), ξ2m * (z)} for each model separately is a compound optimal extrapolation design to extrapolate at z. The results are applied to find the compound optimal discriminating designs for the two polynomial models with degree |m, 2m}, i.e., discriminating models by estimating the highest coefficient in each model. Finally, the relations between the compound optimal extrapolation design problem and certain nonlinear extremal problems for polynomials are worked out. It is shown that the solution of the compound optimal extrapolation design problem can be obtained by maximizing a (weighted) sum of two squared polynomials with degree m and 2m evaluated at the point z, |z| 〉 1, subject to the restriction that the sup-norm of the sum of squared polynomials is bounded.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-675X
    Keywords: apoptosis ; cyclin B1/CDC 2 ; G2/M arrest ; MAD 2 ; paclitaxel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Paclitaxel (Taxol™) is a microtubule-interfering agent that induced persistent and transient G2/M arrest before apoptosis in human nasopharyngeal carcinoma (NPC) cells at high and low concentrations, respectively. In this study, we intended to explore the underlying molecular events and found that cellular cyclin B1/CDC 2 kinase activity was increased and persisted for 〉6 h upon paclitaxel treatment both at high and low concentrations. Furthermore, activation of MAD 2 checkprotein could account for the loss of cyclin B1 ubiquitination and the persistence of cyclin B1/CDC 2 activation in the cases. To investigate the involvement of cyclin B1 and MAD 2 activation in paclitaxel-induced apoptosis, we introduced affinity-purified anti-cyclin B1 and MAD 2 antibodies into NPC cells by electroporation before the further paclitaxel treatment. The antibodies against cyclin B1 and MAD 2 indeed attenuated paclitaxel-induced cytotoxicity and DNA fragmentation. Our study suggests that activation of cyclin B1/CDC 2 and MAD 2 were the M-phase events required for paclitaxel-induced apoptosis in NPC cells. The dys-regulated cyclin B1/CDC 2 activation could enhance the prometaphase progression, but activation of MAD 2 rendered cells inable to exit from the metaphase. Under this circumstance, cells were probably going to “mitotic catastrophe” and ultimately, destined to apoptosis.
    Type of Medium: Electronic Resource
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