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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Gene Structure and Expression 1218 (1994), S. 366-374 
    ISSN: 0167-4781
    Keywords: (B. mori) ; (Silkworm) ; Diapause hormone ; Ovary ; Suboesophageal ganglion ; Transcription ; Trehalase ; cDNA
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0022-1910
    Keywords: Anti-diapause hormone serum ; Bombyx mori ; Diapause hormone ; Embryonic diapause ; Glycogen ; Ovaries ; Suboesophageal ganglion ; Trehalase
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0022-1910
    Keywords: Bombyx mori ; Diapause hormone ; Embryonic diapause ; Subesophageal ganglion ; Trehalase
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 39 (1977), S. 121-126 
    ISSN: 1432-1246
    Keywords: Blood lead ; Direct Chelation-extraction ; Flame atomic absorption spectrophotometry ; Flameless atomic absorption spectrophotometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Two series of lead-containing human blood samples, one series of 53 samples of blood impregnated with lead nitrate at various concentrations up to 100 µg/dl, and the other series of 50 samples obtained from lead-exposed workers and containing lead up to 70 µg/dl, were analyzed by the following three methods of different analytical principles; 1) the flame atomic absorption spectrophotometry after wet digestion, 2) the direct chelation-extraction (avoiding wet digestion; Hessel, 1968) followed by flame atomic absorption spectrophotometry, and 3) the flameless atomic absorption spectrophotometry. The results were compared mutually and also with those from 4) the automated analysis (Ikeda et al., 1977).It was proved that good agreements in measured values exist between any pair of the analytical methods out of the four, the correlation coefficients being higher than 0.8. The results by the second method agreed best with those by the first method (standard but time- and hand-consuming) with slope of the regression line next to 1 and a very small intercept. The advantages of the methods studied were compared.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 72 (1999), S. 516-520 
    ISSN: 1432-1246
    Keywords: Key words Biological monitoring ; Blood lead ; Urinary lead
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objectives: The aim of the present study is to investigate whether lead (Pb) in urine (Pb-U) can be a valid surrogate of lead in blood (Pb-B), the traditional biomarker of exposure to lead in occupational health. Methods: Blood and spot urine samples were collected from 258 workers of both sexes occupationally exposed to lead. The samples were analyzed for lead by graphite furnace atomic absorption spectrometry, and the correlation between Pb-B and Pb-U was examined by linear regression analysis before and after logarithmic conversion. Results: The correlation coefficient (0.824; P 〈 0.01) was largest when the relationship between Pb-B and Pb-U was examined with 214 cases of one sex (i.e., men) after Pb-U was corrected for a specific gravity (1.016) of urine (Pb-Usg) and both Pb-B and Pb-Usg were converted to logarithms. The geometric means (GMs) of Pb-B and Pb-Usg for the 214 men were 489 μg/l and 81 μg/l, respectively. When Pb-Usg was assumed to be 100 μg/l in this set of correlations, the 95% confidence range of Pb-B for the group mean was narrow, i.e., 543–575 μg/l (with GM of 559 μg/l), whereas that for individual Pb-B values was as wide as 355–881 μg/l. Conclusions: The correlation of Pb-U with Pb-B among workers occupationally exposed to Pb was close enough to suggest that Pb-U may be a good alternative to Pb-B on a group basis, but not close enough to allow Pb-U to predict Pb-B on an individual basis.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-136X
    Keywords: Trehalase ; Bean-shaped accessory gland ; Spermatophore ; Male mealworm beetle ; Tenebrio molitor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Trehalase from the bean-shaped accessory glands of the male mealworm beetle, Tenebrio molitor, was purified by acid treatment, with subsequent chromatography on columns of DEAE-cellulofine and Sephacryl S-300. The molecular masses of the native and the denatured forms were estimated to be 43 and 62 kDa by gel filtration and SDS-PAGE, respectively, an indication that the trehalase may be composed of a single polypeptide. The optimum pH of the reaction catalyzed by trehalase was 5.6–5.8. The K m for trehalose was 4.4 mmol·l−1. Immunohistochemical experiments with trehalase-specific antiserum showed that the enzyme was localized in one specific type of secretory cell in the bean-shaped accessory gland epithelium and within the semisolid secretory mass that was a precursor to the wall of spermatophore. SDS-PAGE and immunoblotting analysis revealed the presence of a polypeptide of about 62 kDa in the spermatophore, Immunohistochemical observations showed that the trehalase was located at the outgrowth in the anterior portion of the spermatophore. When a fresh spermatophore was immersed in phosphate-buffered saline it discharged sperm in the same manner as in the bursa copulatrix of the female. Before the rupture of the expanded bulb of the spermatophore, almost all of the trehalase had dissolved in the phosphate-buffered saline. The addition of validoxylamine A to the saline, a specific inhibitor of trehalase, did not affect the expansion and evacuation of the spermatophore. These results demonstrate that trehalase, synthesized by a specific type of secretory cell in the bean-shaped accessory gland epithelium, is actively passed into the lumen of the bean-shaped accessory gland and then incorporated into the spermatophore. Trehalase appears to be one of the structural proteins of the spermatophore, although the possibility can not yet be completely ruled out that the trehalase-trehalose system functions for the nourishment and/or activation of the sperm in the bursa copulatrix of the female.
    Type of Medium: Electronic Resource
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