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  • 1
    ISSN: 1432-0428
    Keywords: Keywords GLUT1, translocation, glucose, transport, hyperglycaemia, diabetes, trophoblast, placenta, pregnancy, electron microscopy.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Aims/hypothesis. We have recently shown that hyperglycaemia down-regulates the GLUT1 glucose transport system of term placental trophoblast. The reduction in GLUT1 protein alone was, however, not sufficient to explain the decrease in net glucose uptake, suggesting additional mechanisms. Therefore, we hypothesised that hyperglycaemia in vitro leads to a GLUT1 translocation from the trophoblast surface to intracellular sites.¶Methods. This was tested in our study by determining the subcellular distribution of GLUT1 in human term placental trophoblast (n = 5 placentas) cultured for 48 h with 5 compared with 25 mmol/l d-glucose in vitro using immunogold labelling.¶Results. Electron microscopic examination of cell profiles showed that 73 % of total GLUT1 molecules reside in the trophoblast plasma membrane under basal conditions. The reduced GLUT1 expression (–20 %; p 〈 0.05) after culture of the cells with 25 mmol/l glucose was accompanied by an internalisation of plasma membrane GLUT1, resulting in a loss of 40 % (p 〈 0.05) in cell surface transporter labelling. Western blotting identified a characteristically broad band between 55–65 kDa, confirming the specificity of the GLUT1 antiserum.¶Conclusion/interpretation. We postulate that in addition to down-regulating human GLUT1 protein concentrations, glucose exerts its autoregulatory effect on hexose transport in term placental trophoblast by altering GLUT1 partitioning between the plasma membrane and intracellular sites in favour of the latter. [Diabetologia (2000) 43: 173–180]
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 24 (1972), S. 269-273 
    ISSN: 1432-0584
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Plasma normaler und anämischer Ratten, markiert mit59FeCl3, wurde mit konzentrierten Retikulozyten inkubiert. Die Plasmaclearance von59Fe war signifikant rascher als jene des kalten Eisens. In weiteren Experimenten wurden unterschiedliche Mengen von markiertem und unmarkiertem Plasma derart gemischt, daß das Schlußvolumen, sowie die59Fe-, die56Fe- und die Transferrinkonzentration konstant blieben. Das Ausmaß der Radioeisenaufnahme durch Retikulozyten erwies sich als abhängig von der Zahl der voll-gesättigten Di-59Fe-Transferrinmoleküle. Beide Befunde belegen die Heterogenität des Plasmaeisenpools.
    Notes: Summary Plasma of normal and anaemic rats was labelled with59FeCl3 and incubated with packed reticulocytes. The rate of plasma clearance of59Fe was significantly accelerated compared to that of cold iron. In further experiments varying amounts of labelled and unlabelled plasma were mixed to give identical final volumes,59Fe-,56Fe- and transferrin-concentrations. The amount of radioactivity taken up by cells diminished with decreasing numbers of di-59Fe-transferrin molecules, present in the system. Both findings point to the functional heterogeneity of the plasma iron pool.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 66 (1988), S. 1084-1084 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-072X
    Keywords: Key words Freeze sectioning ; Fluorescent ¶oligonucleotide probes ; In situ hybridization ; Intestinal microorganisms ; Mastotermes darwiniensis ; Oxygen microsensors ; rRNA ; Termites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We examined the abundance and spatial distribution of major phylogenetic groups of the domain Bacteria in hindguts of the Australian lower termite Mastotermes darwiniensis by using in situ hybridization with group-specific, fluorescently labeled, rRNA-targeted oligonucleotide probes. Between 32.0 ± 7.2% and 52.3 ± 8.2% of the DAPI-stained cells in different hindgut fractions were detected with probe EUB338, specific for members of the domain Bacteria. About 85% of the prokaryotic cells were associated with the flagellates of the thin-walled anterior region (P3a) and the thick wall of the posterior region (P3b/P4) of the hindgut, as shown by DAPI staining. At most, half of the EUB338-detected cells hybridized with one of the other probes that targeted a smaller assemblage within the bacterial domain. In most fractions, cells were found in varying numbers with probe ALF1b, which targeted members of the α-Proteobacteria, whereas substantial amounts of sulfate-reducing bacteria, gram-positive bacteria with a high DNA G+C content and members of the Cytophaga-Flavobacterium cluster of the Cytophaga-Flavobacterium-Bacteroides (CFB) phylum could be detected only in the wall fraction of P3b/P4. This clearly indicates that the hindgut microhabitats differ in the composition of their microbial community. In situ hybridization of cryosections through the hindgut showed only low numbers of bacteria attached to the P3a wall. In contrast, the wall of P3b was densely colonized by rod- and coccus-shaped bacteria, which could be assigned to the Cytophaga-Flavobacterium cluster of the CFB phylum and to the group of gram-positive bacteria with a high DNA G+C content, respectively. Oxygen concentration profiles determined with microelectrodes revealed steep oxygen gradients both in P3a and P3b. Oxygen was consumed within 100 μm below the gut surface, and anoxic conditions prevailed in the central portions of both gut regions, indicating that oxygen consumption in the hindgut does not depend on the presence of a biofilm on the hindgut wall.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-072X
    Keywords: Detection ; Extraction ; Frankia ; Oligonucleotides ; Probes ; Ribosomal RNA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Sequences of 16S rRNA of the nitrogen-fixing Frankia strain Ag45/Mut15 and the ineffective Frankia strain AgB1.9 were used to design a genus-specific oligonucleotide probe. Hybridization experiments of this Frankia probe and a second probe, specific for Nif+-Frankia strains only, were used to detect Frankia specific target sequences in RNA isolations from soil. A method is described for direct isolation of RNA from a loamy soil and a peat. Yields of about 10 ng RNA/g wet soil are obtained without detectable contamination with humic acids. Isolation of RNA after initial extraction of bacteria from soil resulted in significantly lower RNA yields, compared to the direct isolation procedure. Hybridization with both probes against rRNA isolations from Frankia-containing soil could detect target sequences within RNA isolations from 1 g wet soil with an estimated detection limit of 104 cells.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-072X
    Keywords: Key words Fluorescent oligonucleotide probes ; Planctomycetes ; rRNA ; Whole-cell hybridization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In situ hybridization with rRNA-targeted, fluorescent (Cy3-labeled) oligonucleotide probes was used to analyze bacterial community structure in ethanol- or paraformaldehyde-fixed bulk soil after homogenization of soil samples in 0.1% pyrophosphate by mild ultrasonic treatment. In ethanol-fixed samples 37 ± 7%, and in paraformaldehyde 41 ± 8% of the 4′, 6-diamidino-2-phenylindole(DAPI)-stained cells were detected with the bacterial probe Eub338. The yield could not be increased by enzymatic and/or chemical pretreatments known to enhance the permeability of bacterial cells for probes. However, during storage in ethanol for 7 months, the detectability of bacteria increased in both ethanol- and paraformaldehyde-fixed samples to up to 47 ± 8% due to an increase in the detection yield of members of the α-subdivision of Proteobacteria from 2 ± 1% to 10 ± 3%. Approximately half of the bacteria detected by probe Eub338 could be affiliated to major phylogenetic groups such as the α-, β-, γ-, and δ-subdivisions of Proteobacteria, gram-positive bacteria with a high G+C DNA content, bacteria of the Cytophaga-Flavobacterium cluster of the CFB phylum, and the planctomycetes. The analysis revealed that bacteria of the α- and δ-subdivision of Proteobacteria and the planctomycetes were predominant. Here, members of the α-subdivision of Proteobacteria accounted for approximately 10 ± 3% of DAPI-stained cells, which corresponded to 44 ± 16 × 108 cells (g soil, dry wt.)–1, while members of the δ-subdivision of Proteobacteria made up 4 ± 2% of DAPI-stained cells [17 ± 9 × 108 cells (g soil, dry wt.)–1]. A large population of bacteria in bulk soil was represented by the planctomycetes, which accounted for 7 ± 3% of DAPI-stained cells [32 ± 12 × 108 cells (g soil, dry wt.)–1]. The detection of planctomycetes in soil confirms previous reports on the occurrence of planctomycetes in soil and indicates a yet unknown ecological significance of this group, which to date has never been isolated from terrestrial environments.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 163 (1995), S. 235-241 
    ISSN: 1432-072X
    Keywords: Key words In situ detection of mRNA ; Bacillus ; megaterium ; Extracellular neutral protease ; nprM ; In vitro transcripts ; Whole-cell hybridization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Transcripts of nprM, the gene encoding the major extracellular protease of Bacillus megaterium ATCC 14581, were detected by both Northern blot analysis and whole-cell hybridization with digoxigenin-labeled in vitro transcripts throughout the exponential growth phase and the early stationary phase. In cells of the late stationary phase, only low amounts of transcripts were observed with the two techniques. No transcripts could be detected in spores. In soil the presence of mRNA of nprM could be demonstrated by whole-cell hybridization in growing cells germinated from heat-activated spores until they reached the late transition state. No transcripts of nprM were detected in cells containing forespores. Both cells grown in pure culture and in soil had to be permeabilized with lysozyme to allow hybridization with digoxigenin-labeled probes. These results demonstrate the applicability of nucleic-acid probing techniques to localize microbial processes in soil. The approach described of detecting mRNA in fixed bacterial cells should facilitate in situ studies of gene transcription and specific activities in individual cells in heterogeneous environmental systems.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-0630
    Keywords: 42.10 ; 81.60 ; 82.50
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Experiments that demonstrate quantitatively the importance of laser absorption dynamics for ultraviolet laser ablation of organic materials are presented. Laser pulse transmission measurements have been performed on 0.1 μm spin-coated polyimide films at three ultraviolet wavelengths (193 nm, 248 nm, and 355 nm) over the fluence range 10−3 −10 J/cm2. Target transmission is observed to increase with increasing fluence by a factor of ∼5 at 193 nm, and a factor of ∼10 at 248 nm. In contrast, transmission decreases by approximately one half during 355 nm target irradiation. These results are analyzed theoretically with a two-level model of chromophore absorption. This theory is also applied to reported pulsed UV-laser polyimide ablation data. It is shown that an accurate description of the fluence-dependent film absorption leads to a prediction of the etch depth versus pulse fluence relationship in good agreement with experimental data.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    European radiology 6 (1996), S. 473-480 
    ISSN: 1432-1084
    Keywords: Color Doppler flow imaging ; Ultrasonography ; Lymphoma ; Lymph node ; Lymph node blood supply
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A total of 130 superficial lymph nodes were evaluated using color Doppler flow imaging (CDFI) in order to differentiate benign from malignant lympadenopathy. The patterns of intranodal flow signals detected at standardized conditions by CDFI were classified using eight self-defined criteria and were correlated with the histopathological or clinical diagnosis. Nonparametric discriminant analysis showed that four vascular patterns were suspicious of malignancy: (a) avascular areas, (b) displacement of intranodal vessels, (c) accessory peripheral vessels and (d) aberrant course of central vessels. Of the neoplastic lymph nodes (n = 73), 96 % showed at least one pathological vascular pattern. Malignancy could be excluded in 95 % of 57 reactive lymph nodes using these four criteria. Most reactive lymph nodes in contrast demonstrated a vascular hilus and/or vessels running at the long axis of the lymph node with branches to the cortex. There was a diagnostic accuracy of 41–82 % in the additionally evaluated sonomorphological (size, shape, echogenicity) and Doppler (increased Pourcelot's or pulsatility indices) criteria. The definitive interpretation of the promising results of this retrospective study requires confirmation of examiner independency as well as prospective evaluation.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-1084
    Keywords: Aneurysm, complications ; Aneurysm, therapy ; Catheterisation, complications ; Ultrasonography, therapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Sixty femoral pseudoaneurysms were identified by colour Doppler flow imaging over a period of 27 months. One group (n = 42) was treated immediately by ultrasound-guided compression repair (UGCR). In the remaining 18 pseduaneurysms a conservative theraphy attempt, which was successful in 9 patients within 1 week, preceded UGCR. Unsuccessful conservative theraphy did not prejudice the feasibility and outcome of UGCR. the success rate (50 of 51 UGCR) was higher than that reported in the literature, but was at the expense of a longer compression time.Multiple parameters were correlated with the compression time. A significant correlation was found with the size of the perfused lumen in the pseudoaneurysm and with the diameter, lenght and shape of the aneurysm neck. Follow-up at 24 h and 1 week after UGCR revealed 1 thrombotic complication and 4 partial recurrences. Within 1 week there was a significant decrease in the size of the (then thrombosed) pseudoaneurysms.
    Type of Medium: Electronic Resource
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