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  • RAPD-PCR  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental and applied acarology 22 (1998), S. 649-666 
    ISSN: 1572-9702
    Keywords: T. urticae ; T. cinnabarinus ; specific status ; RAPD-PCR ; lobe morphology ; fecundity.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In Belgium, recently two new red carmine forms of Tetranychus sp. have appeared on tomato crops in glasshouses and in maize crops. These forms maintain their red colour even during summer and on other host plants such as French bean. Our aim was to establish their status and to compare them with strains of Tetranychus urticae and Tetranychus cinnabarinus. A strain of Tetranychus kanzawai, a distant relative of the same genus, was used as a control. The five strains tested were characterized by their own demographic parameters, probably because of a longseparated evolution on different host plants. The white eye strain of T. urticae was differentiated from the four other strains by scanning electron microscopy studies of the dorsal integument folds. An investigation using the random amplified polymorphic DNA-polymerase chain reaction (RAPD-PCR) showed T. cinnabarinus as a distinct group. However, the mixing of the individuals of the four other strains raises the question of the role of hybridization and host plant selection in the evolution of the Tetranychus complex. Exp Appl Acarol 22: 649–666 © 1998 Kluwer Academic Publishers
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-0646
    Keywords: Please supply keywords
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract The purpose of this study was to determine the efficacy and toxicity of amonafide in unresectable or recurrent head and neck cancer and to determine if the degree of toxicity with amonafide correlated with the acetylator phenotype of the patient. Thirty patients were registered on the study and received amonafide, 300 mg/m2, over two hours each day for five consecutive days every 21 days. There was one partial response [39] which lasted four months. The dose limiting toxicity was myelosuppression. Acetylator phenotype was determined prior to treatment using HPLC to quantitate caffeine metabolites in urine samples after administration of caffeine. This pharmacokinetic evaluation was performed in 21 patients and revealed that (17/21) 81% of the patients were slow acetylators and 19% of the patients were rapid acetylators. No association was found between acetylator phenotype and toxicity in our patient population. Based on this study, it appears that amonafide given at 300 mg/m2 for 5 consecutive days every 21 days is not active in squamous cell carcinoma of the head and neck, and that acetylator status does not correlate with toxicity.
    Type of Medium: Electronic Resource
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