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  • 1
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 7 (1968), S. 1393-1399 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract TheLy-6 locus is now regarded as a gene complex consisting of at least five closely linked loci (Ly-6A-Ly-6E) whose polymorphic products are identified by monoclonal antibodies and distinguished by different tissue distributions.Ly-6 has been assigned by other investigators to chromosome (Chr) 9 (linked toThy-1 or to Chr 2. We report that theLy-6 gene complex, together with theXp-14 andGdc -1 loci, is situated on Chr 15 linked toGpt1. These new linkage data are derived from four sources: (1) three separate crosses that failed to demonstrate linkage ofLy-6 to eitherThy-4 on Chr 9 or to any of five genes present on Chr 2; (2) the NXSM recombinant inbred strains, which suggested the linkage ofLy-6 andXp-14 toGpt-1 on Chr 15; (3) severalGpt-1 andGdc-1 congenic strains that confirmed the assignment ofLy-6 andXp-14 to Chr 15; and (4) backcrosses that further confirmed the linkage ofLy-6, Gpt-1, Gdc-4, andXp-14, the probable gene order beingGpt-11/Ly-6 Xp-14-Gdc-1.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background We previously reported that ovalbumin–diphtheria toxin (OVA–DT) fusion protein eliminates mast cells bearing OVA-specific IgE and protects OVA-sensitized mice from fatal anaphylaxis induced by OVA challenge.Objective To prove the specificity of therapeutic effect of OVA–DT to allergy induced by OVA only and not by other allergens such as human serum albumin (HSA), and to examine the cytotoxic effect of OVA–DT on B cells bearing OVA-specific IgE.Methods Mice were sensitized with two different antigens, OVA and HSA, and then treated with OVA–DT. The therapeutic effect of OVA–DT on the allergy response to each of allergen was evaluated by anaphylactic test. The effect of OVA–DT on the production of allergen-specific Ig isotypes of the sensitized mice and the cytotoxic effect of OVA–DT on B cells expressing OVA-specific IgE were examined.Results OVA–DT suppressed only OVA-induced allergy but not HSA-induced allergy in mice sensitized with a mixture of OVA and HSA. The suppression was prolonged even to the mice boosted with the same allergen 14 days after last treatment of OVA–DT.In addition, when the sensitized mice were boosted with the same allergens 14 days after last treatment of OVA–DT, the mice showed to increase the production of OVA-specific IgG2a/IgG3 and decreased that of OVA-specific IgE. OVA–DT targeted B cells bearing OVA-specific IgE, and killed them by DT-mediated cytotoxicity.Conclusion The therapeutic effect of OVA–DT was specific to OVA-induced allergy and the suppression of OVA-induced allergy was continuously shown in the mice boosted with the same allergens. This is considered to be caused by the increase of OVA-specific IgG2a and IgG3, and because of the decrease of OVA-specific IgE by killing of B cells bearing OVA-specific IgE.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 76 (2000), S. 1525-1527 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Orange and yellow-colored light emission has been achieved at room temperature in the same elecroluminescent device (ELD) made on GaN thin films codoped with Er and Eu. The GaN film was grown by molecular-beam epitaxy on Si (111) substrates using solid sources for Ga, Er and Eu and a plasma source for N2. Simple Schottky devices were fabricated on the GaN films using indium–tin oxide (ITO) transparent electrodes. ELD spectra show that the yellow and orange colors result from the combination of green emission from Er (537, 558 nm) and red emission from Eu (621 nm). A color change was observed with applied bias, producing yellow at higher bias (−100 V) and orange at lower bias (−70 V). We have fabricated both relatively small (∼250 μm) and large (1.45 mm) ELDs. Parameters for the chromaticity diagram were calculated to be x=0.382, y=0.605 for the yellow emission and x=0.467, y=0.523 for the orange emission. This work shows the possibility of achieving any intermediate color in the spectrum from green to red by adjusting the concentration of Er and Eu in GaN. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 75 (1999), S. 1833-1835 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Upconversion luminescence has been obtained from Er-implanted GaN films by focused-ion-beam (FIB) direct write. FIB implantation was performed on GaN films grown by molecular beam epitaxy, hydride vapor phase epitaxy, and metalorganic chemical vapor deposition. After implantation, the GaN samples were annealed at 1100 °C for 1 h in various ambients (Ar, N2, and O2). Strong green upconversion was observed at 523 and 546 nm under red (840 nm) and infrared (1.0 μm) excitation. Upconversion intensity was measured for Er doses ranging from 4.3×1012 to 2.4×1016 atoms/cm2. Maximum upconversion intensity at 546 nm was observed at a dose of 1–2×1015 atoms/cm2, which corresponds to an atomic percentage of 0.3%–0.6%. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 73 (2000), S. 298-304 
    ISSN: 1432-1246
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objectives: To evaluate whether dimercaptosuccinic acid (DMSA) -chelatable lead, an estimate of current bioavailable lead stores, is a better predictor of lead-related symptoms than are other commonly used lead biomarkers. Methods: A total of 95 male lead workers from three lead industries (one secondary lead smelting facility, one polyvinyl chloride-stabilizer manufacturing plant, and one lead-acid storage battery factory), and 13 workers without occupational lead exposure recruited from an occupational health institute, were studied. Blood lead, blood zinc protoporphyrin (ZPP), 4 h DMSA-chelatable lead (after oral administration of 10 mg/kg DMSA), urine lead, and urinary δ-aminolevulinic acid levels were evaluated as predictors of 15 lead-related symptoms, assessed by self-administered questionnaire, with linear and logistic regression controlling for covariates. Total symptoms and symptoms in three categories (gastrointestinal, neuromuscular, and general) were evaluated. Results: The mean (SD) 4 h DMSA-chelatable lead level was 288.7 (167.7) μg, with a range from 32.4 to 789 μg in the 95 lead workers. The mean (SD) in the non-exposed subjects was 23.7 (11.5) μg with a range from 10.5 to 43.5 μg. Blood lead, blood ZPP, and spot urine lead levels ranged from 21.4 to 78.4 μg/dl, 40 to 331 μg/l, and 7.5 to 153.0 μg/l, respectively, in the lead workers, and from 4.0 to 7.2 μg/dl, 27 to 52 μg/l, and 2.9 to 15.5 μg/l in the non-exposed controls, respectively. The overall mean symptom score (SD), derived as the sum of 0 or 1 point for absence or presence of 15 symptoms, of the lead workers was 3.7 (2.0), compared to 1.2 (1.5) for the non-exposed workers. DMSA-chelatable lead was the best predictor of symptom scores in both crude and adjusted analyses, compared with the other biomarkers. Lead workers with DMSA-chelatable lead values greater than the median (260.5 μg) were 6.2 times more likely to have frequent tingling or numbness of the arms or legs and 3.3 times more likely to have muscle pain than subjects with lower chelatable lead values. Three symptoms (tingling or numbness of arm or leg, muscle pain, and feeling irritation at the slightest disturbance) evidenced a dose-dependent relationship with DMSA-chelatable lead levels. Conclusions: DMSA-chelatable lead was found to be the best predictor of lead-related symptoms, particularly of both total symptom scores and neuromuscular symptoms, than were the other other lead biomarkers.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 206 (1965), S. 90-92 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Table l. BIOLOGICAL ACTIVITY OF ACTIDIONE AND 3 OF ITS DERIVATIVES Strain* (6H〉 Degree of resistance in p.p.m. Genotype Anhydro- Dehydro- Dihydro-Actidione actidione actidione actidione + Of 0 10 10 40 + 0 0 10 10 22G14 AC* i 1 1 100 100 1450-16C V do* 6 6 600 600 ...
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of statistical physics 32 (1983), S. 203-204 
    ISSN: 1572-9613
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Genetica 36 (1965), S. 267-276 
    ISSN: 1573-6857
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A relatively high proportion of the cells of a particular strain ofSaccharomyces cerevisiae form slow-growing colonies when plated on .5p.p.m. actidione-agar. The production of this class of resistant mutant, which is not observed in unrelated strains, depends on the presence of a nuclear gene, designatedR. The slow-growing colony is comprised of both sensitive and resistant cells,i.e. resistant cells give rise to a varying proportion of daughter cells that are revertants to sensitivity during colony development. Resistance is generally stabilized and its transmission assured following a second exposure of resistant cells to the drug. Resistance of the stable mutant is inherited only by a small proportion of ascospores in crosses to sensitive strains but shows some features of mendelian transmission in crosses to a different resistant strain. The UV-induction of the slow-growing mutant shows a different pattern from that of gene mutation, although both categories have a nucleic acid action spectrum. Two alternative hypotheses are presented to explain the results, a) in which control of resistance is vested in a mutating cytoplasmic genetic unit and b) where resistance is dependent on the functional, state of a nuclear gene.
    Type of Medium: Electronic Resource
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