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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 96 (1974), S. 6994-7000 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 63 (1986), S. 650-654 
    ISSN: 1432-1106
    Keywords: Mouse somatosensory system ; Barrel ; Mystacial vibrissae ; Sensory innervation density ; Brain evolution ; Cortical magnification factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The whisker-to-barrel pathway of mice (an important component of the animal's somatosensory system) was studied in two experiments. In one, the cortical representation of a row of whiskers was caused to be larger by lesioning a neighbouring row of follicles, while the innervation density remained unchanged. In the second experiment mice, selectively bred for particular whisker and barrel patterns, showed for their supernumerary vibrissal follicles a relatively large cortical representation. On the basis of the second experiment we formulate a possible role of the sensory periphery in brain evolution.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 40 (1980), S. 419-431 
    ISSN: 1432-1106
    Keywords: Mouse barrelfield ; Somatosensory system ; Dendrite orientation ; Cortical plasticity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary There is a statistically significant order in the tangential orientation of stellate cell dendrites, both spiny and smooth, in layer IV of the barrelfield of the mouse parietal cortex. Neurones situated in a barrel side have most of their dendrites oriented towards the barrel hollow; those situated in the hollow preferentially orient their dendrites parallel to the long axis of the barrel. A quantitative measure of the orientation of individual dendrites in barrelfields of 60-day old mice was obtained using a semiautomatic computer-microscope and a minicomputer. In the same manner, the dendrite orientation of layer IV stellate cells was determined in barrelfields, whose (cytoarchitectonic) pattern had been experimentally altered through lesions of the middle row of the mystacial vibrissal follicles at birth. The dendrites of these cells are oriented in harmony with the novel parcellation of the cortex. Consequently, for cells in the altered areas of the barrelfields, the dendrite orientation is different from that of cells with identical positions in a normal field (see Fig. 8). We tentatively interpret these findings as an adaptation of dendrite orientation to an altered pattern of thalamic input to layer IV that, in turn, is a consequence of the peripheral manipulation.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1106
    Keywords: Auditory cortex ; Computer microscopy ; Dendrites ; Golgi ; Orientation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In the tangential plane (parallel to the pial surface) dendrites in the primary auditory cortex (A1) of cat were found to exhibit preferentially oriented growth. This was shown by means of a computer microscope study of Golgi-Cox stained neurons as seen in 100 μm and 300 μm thick tangential sections. Two techniques were used to represent the 3-dimensional structure of dendrites: the “dendritic stick” and the “dendritic trumpet”. The former dismembers a dendrite into its individual segments; the latter considers a dendrite as an entity and represents it by its centroid, its moments and the spatial dispersion of its branches. Both statistical and Fourier analyses of the data show that within the tangential plane there is a significant and consistent orientation of the dendritic sticks in a dorso-ventral direction which seems correlated with the cortical isofrequency contours observed in electrophysiological maps of the A1 region. The dendritic trumpet analyses also show a distinctly non-random vertical distribution of pyramidal cell basal dendrites but not of stellate cell dendrites.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 107 (1993), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Glucose-fructose oxidoreductase (GFOR) is a periplasmic enzyme of the ethanologenic, Gram-negative bacterium Zymomonas mobilis. It contains tightly bound NADP+ as cofactor. In Z. mobilis GFOR-recombinant strains, a precursor form of GFOR was accumulated. To assay the preGFOR for its NADP(H) content and enzymatic activity, it was purified from an overproducing strain. Using SDS-PAGE, the precursor subunit size was determined to approximately 45 kDa (compared with a 40 kDa subunit size for the mature GFOR subunit). The N-terminal amino acid sequence of the precursor was determined. The N-terminal residues of the GFOR matched with the signal sequence from the DNA sequence of the gene gfo. The precursor form of GFOR was enzymatically active and contained the cofactor NADP(H).
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 84 (1991), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract The enzyme glucose-fructose oxidoreductase (GFOR) from the Gram-negative ethanologenic bacterium Zymomonas mobilis was purified to homogeneity and was shown to be a tetrameric protein with a subunit size of Mr 42 500. Using immunogold-labelling in combination with electron microscopy, ultrathin sections of Z. mobilis wild type cells showed that the enzyme GFOR is located in the periplasm off the bacterial cells. Z. mobilis strains which carried the cloned gfo gene on plasmid pSUP104, had 5–6-fold increased GFOR enzyme activities. Moreover, these cells accumulated large amounts of a presumable unprocessed pre-GFOR protein (Mr 48 000).
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1460-9568
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Response properties of single units in the mouse barrel cortex were studied to determine the sequence in which the neurons that form a cortical column become activated by a single‘natural’stimulus. Mice (n= 11) were anaesthetized with urethane. For a total of 153 cells, grouped by cortical layer, responses to a standardized deflection of a single whisker were characterized using poststimulus time and latency histograms. Usually, for each unit, data were collected for stimulation of its principal whisker (PW; the whiskers corresponding to the barrel column in which the cell was located) and of the four whiskers surrounding the PW. In all layers, PW stimulation evoked responses at shorter latency than surround whisker stimulation. In layers II – III and IV a bimodal distribution of cells according to latency to PW stimulation was found. Statistical analysis indicated the presence of two classes of cells in each of these layers:‘fast’units (latency 〈 15 ms) and 'slow’units (latency 〉15 ms). The great majority of cells in layers I, V and VI fired at latencies of 〉20 ms to PW stimulation. In general, stimulation of surround whiskers evoked a smaller response than PW stimulation. The fast cells of layer IV showed the greatest response to PW stimulation (mean = 1.78 spikes/100 ms poststimulus). Their firing was maximal during the 10–20 ms poststimulus epoch, while the slow layer IV cells fired maximally during the 20 – 30 ms poststimulus epoch. Surround inhibition occurred in all layers within the first 10 ms after stimulus onset, during which period the fast cells are the most active ones, and are thus likely to be responsible for the surround inhibition. This notion is supported by an analysis of spike duration that showed that eight of the ten cells with a thin spike (supposed to be GABAergic; McCormick et al., J. Neurophysiol., 54, 782 – 806, 1985), had PW latencies of 〈15 ms. We conclude that the activation of a barrel column is initially inhibitory in nature.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0168-1656
    Keywords: FIA ; Fiber-optic biosensor ; Glucose-fructose-oxidoreductase ; NADPH-dependent fluorescence
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    European archives of oto-rhino-laryngology and head & neck 138 (1934), S. 122-130 
    ISSN: 1434-4726
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zusammenfassung Das Krankheitsbild der “Glossitis rhombica mediana” war, obwohl keineswegs selten, hinsichtlichUrsache und Wesen bis heute ungeklärt; sie wurde als chronische Entzündung aufgefaßt und vielfach ohne sichere Anhaltspunkte mit Lues, Tuberkulose und verschiedenen anderen Erkrankungen in Zusammenhang gebracht. Eine Reihe eigener Beobachtungen weisen nach, daß dieser Erkrankungfehlerhafte, überschüssige Gefäßbildungen nach Art der Angiome bzw. Gefäßnävi zugrunde liegen. DieLokalisation der Erkrankung im Bereiche derembryonalen Anlage des Tuberculum impar an der Zunge läßt sie in die Gruppe derfissuralen Angiome einreihen. Befunde chronischer Entzündung sowie Veränderungen im Epithel werden sekundär durch chronische Reize fehlerhaften und funktionell minderwertigen Gewebes erklärt.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 295 (1982), S. 691-693 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Experiments in rats show that the foot and toe representation is present in the medial two-thirds of the dorsal horn of segments L4 and L5 of the spinal cord. If this region is searched to a depth of 1 mm with fluid-filled microelectrodes in intact adult rats anaesthetized with Nembutal, an average ...
    Type of Medium: Electronic Resource
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