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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 9 (1993), S. 136-140 
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Psychological research 48 (1986), S. 251-257 
    ISSN: 1430-2772
    Source: Springer Online Journal Archives 1860-2000
    Topics: Psychology
    Notes: Summary Neurophysiological data from single cells in the monkey's visual association cortex as well as saccadic reaction time measurements in monkey and man are reported. When a monkey directs his attention to a peripheral light stimulus the visual activation of cortical cells responsive to that stimulus is increased. If visual attention is directed to a particular part of the visual field the saccadic reaction time is long (around 200 ms in monkey and above 200 ms in man). In contrast, if attention is disengaged from any location to which it might have been engaged before, monkeys and men can execute express saccades, that is, saccades after extremely short and stable reaction times (around 75 ms in monkey and 100 ms in man). The results are interpreted in the context of a hypothesis according to which the initiation of voluntary, visually guided saccades includes three premotor mechanisms: the computation of the target location, the decision to make a saccade, and the disengagement of attention.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Inflammation research 9 (1979), S. 58-60 
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Conclusions There are indications that actively sensitized cells differ in some morphological and functional respects from non-sensitized mast cells, e.g. they react to ionophore stimulation at lower concentrations than non-sensitized cells.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 53 (1997), S. 943-950 
    ISSN: 1420-9071
    Keywords: Key words. von Willebrand factor; recombinant protein; collagen binding; platelet aggregation; platelet binding; glycosylation; coagulation factor VIII.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. Recombinant von Willebrand factor (r-vWF) was produced in serum-free medium on a large scale in recombinant Chinese hamster ovary cells and was purified from fermentation supernatant by a combination of anion exchange chromatography and herapin affinity chromatography. Heparin affinity chromatography yielded r-vWF polymers of different degrees of multimerization. r-vWF was analysed by qualitative and quantitative functional analysis. We could show that while binding of r-vWF to platelets did not depend on multimerization of the molecule, ristocetin-induced platelet aggregation, binding to collagen and binding to heparin correlated directly with the extent of multimerization. Binding of recombinant coagulation factor VIII (r-FVIII) to r-vWF was studied by real-time biospecific interaction analysis and surface plasmon technology. The data indicated that binding of r-FVIII did not depend on r-vWF multimerization. Real-time biospecific interaction analysis suggested a potential stoichiometry of 2 to 2.5 r-vWF subunits per r-FVIII molecule. Kinetic analysis of the r-vWF-r-FVIII interaction gave a binding rate constant of 3 × 106 M−1 s−1 and an association constant of 2.5 × 109 M−1. Reaction of r-vWF with carbohydrate-specific lectins demonstrated that r-vWF contained a high proportion of N-glycans composed of mannose, galactose, glucose, N-acetylglucosamine and terminal sialic acid. Carbohydrate moities were covalently bound to the protein structure and were quantitatively removed from r-vWF only after protein denaturation. The results demonstrated that r-vWF produced on large scale under serum-free culture conditions exhibited qualitative and quantitative functional properties comparable to human plasma-derived vWF.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Inflammation research 12 (1982), S. 189-191 
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Elutriation is a cell separation method based on countercurrent centrifugation. For mast cell purificaiton it is superior to density gradient methods since no foreign protein or dense material has to be removed from the purified cells. The elutriation profiles of peritoneal rat mast cells differ considerably if the cells come from non-sensitized or actively sensitized donor animals and/or from different strains. This result is another indication of an altered morphological state of mast cells due to active immunization and is dependent on genetic factors. Cell aggregation proved to be the main obstacle to elutriation purification of guinea pig tissue mast cells. Human mast cells from adenoid tissues, however, could be brought to 70–90% purity, even if the elutriation profiles varied from donor to donor.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 183 (1991), S. 17-27 
    ISSN: 1432-0568
    Keywords: Blastocyst coverings ; Zona pellucida ; Neozona ; Preimplantation development ; Synchrony ; Rabbit
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Under physiological conditions the zona pellucida disappears in the rabbit between Day 3 and early Day 4 post coitum (p.c.) and is replaced by a new layer, the neozona. The dissolution of the zona pellucida and the formation of the neozona was investigated in three different experimental approaches, all of them characterized by non-physiological developmental conditions for the embryo: Prevention of embryo migration from the oviduct into the uterus by postcoital (48 h p.c.) tubal ligation, in vitro culture, and asynchronous embryo transfer into uteri of recipient rabbits. Embryos of age 21/2, 3, 4 and 41/2 days p.c. were cultured for 12 to 72 h. The media used for in vitro culture were supplemented with BSA, serum or with uterine secretions that were collected either synchronously or asynchronously to the developmental stage of the cultured embryos. Three-day-old embryos were transferred into uteri of pseudopregnant foster rabbits of either synchronous (Day 3) or asynchronous stages (Day 0, 2, 4, 5, 6) and were recovered 24 to 72 h after transfer. The transformation of the coverings was evaluated by light and transmission electron microscopy. The dissolution of the zona pellucida was greatly disturbed in tube-locked embryos, and in cultured embryos if standard protein supplements (BSA or serum) had been used for in vitro culture. In many cases the zona was still completely preserved after 2 or 3 days in culture, at a time when it normally would have already been replaced by the neozona in vivo. The dissolution in vitro, however, progressed incomparably better if the culture medium had been substituted with synchronous or asynchronous uterine secretions. The formation of the neozona could not be verified in cultured blastocysts. After embryo transfer, the dissolution of the zona pellucida was completed in most cases by 2 days after transfer, irrespective of the recipients' progestational stage. Present results indicate that uterine components are essential for the dissolution of the rabbit zona pellucida. These components appear to be present in the uterine cavity constitutively, i.e. independently of the uterine progestational transformation, and need not be in synchrony with the embryo's developmental stage for dissolution of the zona. Normal formation of the neozona does not take place under the non-physiological developmental conditions of in vitro culture.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 201 (2000), S. 349-355 
    ISSN: 1432-0568
    Keywords: Key words Growth factor receptor ; ErbB receptors ; Signal transduction ; Trophoblast cells ; Endometrium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Proto-oncogenes are involved in the regulation of gene expression, for example after ligand binding to growth factor receptors. Expression of the proto-oncogenes c-fos, c-jun, c-ha-ras and c-myc was studied in in vivo grown and in vitro cultured bovine preimplantation blastocysts employing RT-PCR, ribonuclease protection assay and immunohistochemistry. Thirteen- and 14- day-old preimplantation blastocysts, i.e. stages before and during trophoblast elongation, were used. In in vivo-grown blastocysts c-fos, c-jun and c-ha-ras transcripts as well as c-Fos, c-Jun and c-Myc proteins were detected in all stages studied. Cultured blastocysts were treated with 10 nM epidermal growth factor and 10 nM transforming growth factor-alpha simultaneously. Epidermal growth factor and transforming growth factor-alpha treatment induced c-fos mRNA and c-Myc protein expression. The induction of downstream targets of the epidermal growth factor receptor by epidermal growth factor and transforming growth factor-alpha indicates a functional epidermal growth factor signal transduction pathway in elongating bovine blastocysts.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 73 (1995), S. 465-471 
    ISSN: 1432-1440
    Keywords: Complement ; mRNA ; Brain ; Aging ; Alzheimer's disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The levels and cellular localization of mRNA for complement C1q and C3 were examined by RNA gel blot and nonradioactive in situ hybridization in the frontal cortex of patients with Alzheimer's disease (AD) and age-matched controls. We found that the hybridization signal for C1q mRNA was markedly increased (approx. 3.5-fold) in the frontal cortex of AD patients compared to that in age-matched controls. In contrast to previous reports we also found that the levels of C3 mRNA, although well expressed, did not differ significantly between AD cases and age-matched controls. Nonradioactive in situ hybridization using digoxigenin-labeled riboprobes revealed that transcripts coding for both C1q and C3 were closely associated with neurons. These results support the hypothesis that complement could play a role in neuronal degeneration which has been observed in the brain of AD patients.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-0770
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Computer Science , Physics
    Notes: Abstract The dual center surround organization of retinal and geniculate neurons in two antagonistic subsystems B and D, having on-center or off-center receptive fields and signalling brightness or darkness respectively, has been studied by local light increments and decrements. Intensity response functions obtained by the introduction and withdrawal of small center spots either brighter or darker than a common homogeneous field are similar in a given neuron, but the phasic responses are stronger in on-center neurons than in off-center neurons. Center size increments and decrements, however, lead to equal excitations in the B- and D-system, respectively, provided that both luminance steps start from the same level and are of equal size on a linear scale. Decrementing and incrementing the surrounding luminance of the same optimal center spots lead to equal surround responses in the two subsystems if the two luminance steps terminate at the same level. This lateral activation is elicited by light decrement in the B-system and by light increment in the D-system. Center and surround responses within a given subsystem are of comparable amplitude, but generally slightly stronger responses are elicited by optimal center increments (decrements) than by the equivalent surround decrements (increments) which lead to the same spatial contrast for B-(D-) neurons. The symmetry relations between the B- and D-system and the equivalence relations between center and surround in each subsystem hold for retinal and geniculate neurons. The difference between center and surround response latencies is about 9 ms in both subsystems at the retinal and 14 ms at the geniculate level. Stimulus response functions of on- and off-center neurons are unified on the basis of linear relative luminance scales.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Biological cybernetics 55 (1986), S. 253-261 
    ISSN: 1432-0770
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Computer Science , Physics
    Notes: Abstract Reaction time measurements were used to test the possibility that an eye and a reach movement both aimed at the same visual target share a common final motor command. This hypothesis predicts highly correlated pairs of reaction times on a trial by trial basis. The experiments were based on the earlier observation that long saccadic reaction times (above 200 ms) with a large scatter (150–300 ms) are obtained if the central fixation point remained visible through out a trial (overlap paradigm), whereas extremely short saccadic reaction times (around 120 ms) with a small scatter (100–150 ms) occur if the fixation point was turned off some time (200 ms) before the target appeared (gap paradigm). In the overlap paradigm high correlations (coefficients up to 0.95) between saccadic and reach reaction times were obtained and the corresponding linear regression lines had a slope of almost one. In the gap paradigm, however, correlations were almost absent even though the mean reach reaction times were considerably decreased. These observations clearly contradict the “common command” hypothesis, but can be explained by the assumption that the execution of the reach movement depends on the completion of the preparation of the saccade but not vice versa (“one way synchronization” hypothesis).
    Type of Medium: Electronic Resource
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