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  • Articles  (125)
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  • Articles  (125)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 115-131 
    ISSN: 0741-0581
    Keywords: Electron microscopy ; Fungal diagnosis ; Fungal therapy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Defects in cell-mediated immunity caused by infection with the human immunodeficiency virus (HIV) render AIDS patients particularly susceptible to fungal pathogens. Signs and symptoms of serious infection may be nonspecific, and early diagnosis and institution of antifungal therapy is essential to decrease morbidity and mortality in this patient population. In a symptomatic individual, invasive procedures are often required to establish a microbiologic diagnosis, and histopathologic examination of tissue by light and electron microscopy is often the first indication of a serious fungal infection in an AIDS patient.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 193-200 
    ISSN: 0741-0581
    Keywords: Thickness measurement ; Electron energy-loss spectroscopy (EELS) ; Inelastic mean free path ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: We discuss measurement of the local thickness t of a transmission microscope specimen from the log-ratio formula t = λ In (It/I0) where It and I0 are the total and zero-loss areas under the electron-energy loss spectrum. We have measured the total inelastic mean free path λ in 11 materials of varying atomic number Z and have parameterized the results in the form λ = 106F (E0/Em)/ln (2βE0/Em) where F = (1 + E0/1,022)/(1 + E0/511)2, the incident energy E0 is in keV, the spectrum collection semiangle β is in mrad, and Em = 7.6Z0.36. This formulation should allow absolute thickness to be determined to an accuracy of ±20% in most inorganic specimens.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 273-284 
    ISSN: 0741-0581
    Keywords: Superconductors ; Electron microscopy ; Perovskites ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: High-resolution transmission electron microscopes operating at 300 and 400 kV were used to investigate the crystallography and microstructure of the perovskitelike YBa2Cu3O7-x. In this paper, we evaluate the performance attainable with these microscopes both empirically and by computer modelling. Based upon the assumption that oxygen may be a key to superconductivity properties, we have also investigated the visibility of the oxygen sites as well as the heavier yttrium and barium ion positions and the lighter Cu atom positions. We propose a scheme for observing different twin orientations in these structures and hence the oxygen atom positions seen in projection for the [100] and [010].Our observations of both thick and thin regions of Y-Ba-Cu-O materials are reported as well as the problems of adjusting microscope parameters and specimen alignment to obtain interpretable images. We also give a preliminary report on the effects of heat treatment as seen in high-resolution micrographs to assess disorder of the heavy atoms and oxygen vacancies.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 9 (1988), S. 283-291 
    ISSN: 0741-0581
    Keywords: Ultrastructure ; Kidney ; Artifacts ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The aim of this presentation is to draw attention to the problems inherent in evaluating the ultrastructure of percutaneous renal biopsies and to discuss some of the special techniques which are useful in this area. It is important to realize that the ultrastructure as it appears in this kind of material does not necessarily reflect conditions in vivo. Comparison with suitable reference material may, however, permit reliable conclusions in terms of pathological diagnosis and pathogenesis. It is advocated that purely qualitative methods, which until now have predominated in ultrastructure work with renal biopsies, be replaced by morphometry and semiquantitative methods when it is possible and practical to do so in any research situation.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 1-1 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 105-113 
    ISSN: 0741-0581
    Keywords: Electron microscopy ; Histopathology ; Mycobacterium diagnosis ; Mycobacterium therapy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: This reviw examines an important bacterial infection in acquired immunodeficiency syndrome (AIDS). Despite occasional infections with bacteria such as Streptococcus pneumoniae, Haemophilus influenzae, Salmonella, and Nocardia in patients with AIDS, the primary problems of AIDS and invading bacterial infections center around mycobacteropsos. A unique feature of AIDS has been the common identification of disseminated infections with Mycobacterium avium-intracellulare. The following discussion examines our present understading of this group of organisms and how they interact with the compromised host.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 9 (1988), S. 293-298 
    ISSN: 0741-0581
    Keywords: Renal medulla ; Isolated perfusion ; Anoxic damage ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The tubular epithelial cells located in the renal medulla are normally working in a hypoxic milieu. In isolated rat kidneys perfused with a cell-free medium, the medullary thick ascending limbs of Henle's loop are selectively and reproducibly injured by the imbalance between oxygen demand and supply in this area. Hypoxic lesions rapidly progress from reversible to irreversible forms of cell damage. Reversible injury consists of chromatin margination and mitochondrial swelling, which can disappear upon restoration of an adequate balance of oxygenation. Irreversible injury consists of nuclear pyknosis and cytoplasmic fragmentation, lesions which persist after re-oxygenation or even progress to cell death. Reversible and irreversible phases of hypoxic injury in this distal tubule segment are comparable to, but different from, those previously defined for the proximal tubule.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 9 (1988), S. 395-411 
    ISSN: 0741-0581
    Keywords: Serial thick sections ; HVEM ; Stereoscopic viewing ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: A comprehensive computer-graphics-based system (STERECON) is described for tracing and digitizing contours from individual or stereopair electron micrographs. The contours are drawn in parallel planes within the micrographs. Provision is also made for tracing and digitizing in full three-dimensional (3-D) coordinates in any direction along linear structures such as cytoskeletal elements. The stereopair micrographs are viewed in combination with the contours being traced on a graphics terminal monitor. This is done either by projecting original electron micrograph (EM) negatives onto a screen and optically combining these images with contour lines being drawn on the monitor, or by first digitizing the images and displaying them directly on the monitor along with the contour lines. Prior image digitization allows computer enhancement of the structures to be contoured. Correction and alignment routines are included to deal with variable section thickness, section distortion and mass loss, variations in photography in the electron microscope, and terminal screen curvature when combining projected images with contour lines on the monitor. The STERECON system organizes and displays the digitized data from successive sections as a 3-D reconstruction. Reconstructions can be viewed in any orientation as contour stacks with hidden lines removed; as wire-frame models; or as shaded, solid models with variable lighting, transparency, and reflectivity. Volumes and surface areas of the reconstructed objects can be determined. Particular attention was paid to making the system convenient for the biological user. Users are given a choice of three different stereo-viewing methods.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988) 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 27-33 
    ISSN: 0741-0581
    Keywords: Electron microscopy ; Image processing ; Image registration ; Robustness ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The geometric registration of two electron microscopic images generally is performed by maximizing the cross-correlation coefficient between them. We show that a new similarity measure (the number of sign changes) is useful for performing simultaneously geometric and gray-level registration. This method is robust, which means that it provides a good estimation of the parameters even in the presence of outliers that cannot be described by the registration model.
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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 67-76 
    ISSN: 0741-0581
    Keywords: Synapse ; Taxi-bodies ; Horseradish peroxidase ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Thin sections of nervous tissue were viewed at different tilt angles using a transmission electron microscope equipped with a eucentric goniometer stage. In a comparison study of various degrees of tilt, one can observe additional morphological features within synaptic profiles, define subsynaptic structures such as Taxi-bodies, and clearly see the crystalline formation of cytochemical tracers. This study demonstrates the value of tilting thin-sections in the analysis of synapses and other biological material at the ultrastructural level.
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 53-65 
    ISSN: 0741-0581
    Keywords: Records ; Computer program ; Specimen block labels ; Specimen vial labels ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Conventionally, all specimen vial and block labels are handwritten or typed, a labor-intensive process open to human error, particularly in a lab that processes large numbers of samples. The computer program described in this report was developed to reduce or elimiate this problem. The program is menu-driven, asking specific information from the user, and runs on an IBM PC (or compatible). It is designed to accurately produce specimen collection vial labels, resin block labels, and data sheets for inclusion in a research notebook. A task that in the past may have required much time at the typewriter can now be accomplished without error in a few minutes. Although designed to fit the needs of a pathology laboratory, the program (written in BASIC) can be easily modified to fit other applications.
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 77-85 
    ISSN: 0741-0581
    Keywords: Fluorocarbons ; Cell culture ; Techniques ; Specimen preparation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Common methods for the preparation of cultured cells for concurrent light microscopy (LM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) are not completely satisfactory. This article describes how we grow mammalian cells on plastic disks made from Aclar film. Aclar is a transparent fluorinated-chlorinated thermoplastic that contains no volatile components and is, for all practical purposes, chemically inert. Cells adhere to it readily and remain attached after fixation, dehydration, and critical-point drying or embedding. The film also accepts heavy metal coating by ionic bombardment and is extremely stable in the vacuum of the SEM. LM observations are unhindered by Aclar, since the film is as transparent as glass. Fluorescence microscopy is possible with this film, since it exhibits no detectable autofluorescence. During SEM observation, the film has great dimensional stability, and the cells and heavy metal coating remain attached to the Aclar even under high-resolution operating conditions. TEM processing of specimens grown on Aclar is simplified by the fact that Aclar does not stick to the epoxy resins used in EM. Furthermore, Aclar is easily sectioned and does not damage knives used in ultramicrotomy. The use of Aclar film considerably simplifies the preparation of cultured cells for all types of microscopy. This method is particularly useful in correlating surface features between SEM and TEM observations.
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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 123-124 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 205-210 
    ISSN: 0741-0581
    Keywords: Review ; Chemical synapses ; Mammals ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: This paper provides a brief review of the historical development of our understanding of synaptic structure in the central nervous system. The basic structure of the synapse is reviewed as well as the development of ultrastructural techniques that have allowed the details of synaptic organization to be elucidated.
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 211-212 
    ISSN: 0741-0581
    Keywords: Transmission Electron Microscope ; Phosphors ; Viewing Screen ; Phosphor Viewing Screen ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: A simple procedure is described for the preparation of a totally inorganic, durable, strongly bonded, and non-shrinking phosphor viewing screen. The procedure requires no special apparatus or skills in order to prepare a fairly uniform high resolution screen in only about 0.5 hours plus drying time. The screens are suitable for use on an automatic exposure system where mechanical shock can destroy a screen.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 247-263 
    ISSN: 0741-0581
    Keywords: Ultrastructure ; Corpus striatum ; Pallidum ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The synaptic organization of the globus pallidus is reviewed with respect to present knowledge about neurons, fibers, axon terminals, and their intrinsic synaptic relationships. Information derived from studies employing Nissl stains, Golgi impregnations, lesion degeneration techniques, immunohistochemistry, and anterograde axonal labeling in various species are presented along with ultrastructural data. Studies indicate that the globus pallidus contains a principal efferent neuron with smooth or spiny dendrites and simple or complex terminal dendritic arborizations. This cell type receives convergent inputs from intrinsic and extrinsic sources and uses γ-aminobutyric acid as a transmitter. A smaller and separate population of pallidal projection neurons contains acetylcholine. Two other less frequent neuronal types, of small and medium size, have also been recognized. Three to six types of axonal boutons forming synaptic contacts with pallidal neurons have been recognized in various studies. Among these, three types (types I, II, and III) are the most prevalent. Studies indicate that the most frequent category (type I) originates from neostriatal neurons via radial fiber projections and contains immunoreactive GABA and enkephalins. The synaptic architecture of the globus pallidus is dominated by a mosaic-like arrangement of long dendrites that are ensheathed by longitudinally oriented axons making synapses en passant. Triadic synapses involving dendrites that are pre- and postsynaptic are encountered infrequently. Because both striatopallidal and pallidothalamic connections are inhibitory, pallidal target neurons in the thalamus may be “disinhibited” when the neostriatum is activated.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 283-292 
    ISSN: 0741-0581
    Keywords: Thalamus ; Presynaptic dendrite ; GABA ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: This study describes the synaptic organization of the thalamic reticular nucleus (TRN) in the rat, cat, and monkey using electron microscopy combined with immunocytochemistry, degeneration, or horseradish peroxidase (HRP) tracing methods. Three morphological types of terminals are described in the TRN of the rat: a small terminal with densely packed spherical vesicles (D-terminal), which originates from the cortex; a large terminal with loosely packed spherical vesicles (L-terminal), which originates in the dorsal thalamus; and a terminal containing flattened synaptic vesicles (F-terminal) that is probably a TRN recurrent collateral. The cortical input to the TRN has been shown by double-labeling studies to terminate directly upon TRN projection neurons. Similar classes of terminals are found in the TRN of cat and monkey, but there is in addition a large terminal with spherical synaptic vesicles that is invaginated by dendritic spines. Also present in the cat and monkey, but not in the rat, are vesicle-containing dendrites and dendritic appendages.In the rat, degeneration experiments indicate that the terminals of TRN projection neurons in the dorsal thalamus are F-terminals. These terminals contain flattened synaptic vesicles and exhibit GABA immunoreactivity.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 17-40 
    ISSN: 0741-0581
    Keywords: Electron microscopy ; Heteroduplex mapping ; Lentiviruses ; Retroviruses ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: A novel human lymphotropic virus capable of crippling the immune system by infecting and destroying T4 antigen-positive cells is now known to be the etiologic agent of the acquired immune deficiency syndrome (AIDS). The AIDS or human immunodeficiency virus (HIV) belongs to a family of RNA viruses called retroviruses. Several strains of HIV have been molecularly cloned, and DNA sequence comparisons have established that the proviral DNA genome is 9.7 kilobase pairs. The genome possesses characteristic retrovirus features including structural genes, flanked by long terminal repeats, in the order gag, pol, and env and, in addition, four unique nonstructural genes, several of which appear to be essential in regulating virus replication. Electron microscopy has played an important role in elucidating structural, genetic, and molecular properties of HIV and has aided in its classification as a member of the Lentivirnae retrovirus subfamily. Heteroduplex mapping methodologies pertinent to these findings are described. Although the relationships show considerable divergence, the similarities between HIV and lentiviruses are profound and encompass an indistinguishable morphology, genome sequence homology and topography, genomic diversity, and overlapping biology, including a preference for infecting cells of the immune system, a cytopathic effect in vitro, and the ability to produce a persistent, slowly progressing, degenerative disease in vivo. The newest HIV class (HIV-2) has recently been molecularly characterized. HIV-2 also bears all the hallmarks of a lentivirus but is more closely related to simian immunodeficiency viruses than the previously described HIV-1, despite a similar biology. The HIV-lentivirus phylogenetic relationship has broad implications for the AIDS disease process and has given new importance to the study of the natural history and pathogenesis of animal lentiviruses in searching for clues to prevent the spread of AIDS.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 133-135 
    ISSN: 0741-0581
    Keywords: Strongyloides stercoralis ; Strongyloidiasis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Strongyloides stercoralis, the only helminthic parasite that can complete its life cycle in the human host, is also the only helminthic parasite that has been reported with any frequency in AIDS patients. Symptoms include hives, skin eruptions, abdominal pain, perianal pruitis, diarrhea, and pneumonitis. Diagnosis is made by demonstrating rhabditiform larvae in the stool or female parasitic worms and eggs in the small intestinal mucosa; in disseminated cases, rhabditiform or filariform larvae can be found in liver, heart, lungs, thyroid, kidneys, adrenals, pancreas, lymph nodes, and central nervous system. Successful treatment has been achieved with thiabendazol. Strongyloidiasis is uncommon, but since cell-mediated immunity is important in combatting this organism, and since T-lymphocyte function is impaired in AIDS patients, strongyloidiasis should not be overlooked in the diagnosis of opportunistic illnesses in these individuals.
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  • 21
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 159-172 
    ISSN: 0741-0581
    Keywords: Gray scale enhancement ; Immotile cilia syndrome ; Electron microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Tracheal ciliary cross sections were examined with scanning transmission electron microscopy and the resultant images were digitized for image enhancement. A gray-scale histogram of each ciliary image was produced and manipulated to enhance the image for dynein arms. Tracheal epithelial tissue from the pig, rabbit, and dog, including dogs with immotile cilia syndrome, was examined by using this technique. Tissue from each animal was fixed with each of three different fixatives and sections were evaluated for preservation of dynein arms. The same fixative did not consistently provide optimal fixation for ciliary dynein arms in all three species examined. Each species, therefore, must be evaluated to determine the optimal fixative for preservation of normal ciliary ultrastructure. Digital image processing provides a mechanism for enhancing dynein arms in situ without the need for addition of special stains or the use of techniques such as image summation. With this technique it has been shown that about two-thirds of outer dynein arms are partially or completely missing on cilia from dogs with immotile cilia syndrome.
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  • 22
    Electronic Resource
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    Journal of Electron Microscopy Technique 8 (1988), S. 225-226 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 23
    Electronic Resource
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    Journal of Electron Microscopy Technique 8 (1988), S. 229-230 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: In problems of air or water pollution, or in evaluation of exposure to pathogenic dusts from biological specimens ( e.g., asbestos fibers) some typical particles can be used as tracers. As far as they have sufficiently typical properties (shape, color, anisotropy,…) particles are rapidly recognized and quantified by light microscopy (LM), even if they are very scarce or dispersed among large amounts of unsignificant ones. For accurate characterization, analytical electron microscopy (scanning or transmission) is required, but cannot be efficiently applied for low concentrations of particles. A technique using a high precision object-marker under LM has been developed in the past by Jedwab (1975) to be used with SEM, but there is actually no equivalent for TEM. Such a technique is proposed in this paper. Its major interest resides in the greater amount of analytical data available for one single particle (high magnification morphology, crystallographic structure, chemistry). Practical results were obtained with asbestos fibers and bodies recovered from biological specimens, but the technique can be extended to many other problems concerning micron-sized particles.
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  • 24
    Electronic Resource
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    Journal of Electron Microscopy Technique 8 (1988), S. 233-235 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 25
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    Journal of Electron Microscopy Technique 8 (1988), S. 239-240 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 26
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 263-272 
    ISSN: 0741-0581
    Keywords: High Tc superconductors ; Electron microscopy ; HREM image stimulations ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Thin films of the superconductive oxide YBa2Cu3O7-x have been made by electron-beam coevaporation of the metals in an oxygen atmosphere onto single-crystal {001}-oriented SrTiO3 and yttria-stabilized zirconia (YSZ) substrates. The oxide films were superconducting in the as-deposited state (Tc = 81-83K, Jc = 106 A/cm2 at 4.2K). Bright-field imaging, selectedarea diffraction (SAD), and high-resolution imaging in the transmission electron microscope were used to characterize the microstructure of these films. All of the films were polycrystalline. On SrTiO3 the films were oriented, for the most part, with {110} parallel to the substrate surface. On YSZ, two microstructures were observed: one with smaller rectangular grains oriented with (100) or (010) parallel to the substrate surface and the other with (001) parallel to the surface (i.e., c-axis up).
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  • 27
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 8 (1988), S. 311-315 
    ISSN: 0741-0581
    Keywords: Hi-Tc superconductivity ; STEM ; Electronic structure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: We have obtained the electron-energy-loss spectra below 1,000 eV for YBa2Cu3O7-δ. The spectra show contributions from all elemental constituents, although the Y-signal is very weak owing to its small concentration. The low-loss region and the Ba-core losses are very similar to those obtained for BaO. The Cu absorption is similar to that seen in CuO with minor differences relating to Cu concentration and anisotropy. The oxygen 1s absorption has a shape that is quite different from that obtained in CuO and shows striking orientational anisotropy. Radiation damage in the microscope is a problem and leads to changes in the shape of the oxygen edge.
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  • 28
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    Journal of Electron Microscopy Technique 8 (1988), S. 307-309 
    ISSN: 0741-0581
    Keywords: Electron energy loss spectroscopy ; Varying O2 content ; Crystallographic orientation dependence of oxygen near edge features ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The high Tc superconducting material YBa2Cu3O7 shows a complex relationship between microstructure and oxygen content, which are controlled by length of heat treatment, atmosphere, and quench rate. An AEM investigation studying changes in the oxygen near edge features was undertaken. Electron energy loss spectroscopy (EELS) measurements have the important advantage that they can be made on single crystal grains, allowing orentation-dependent studies. Both ion-milled and crushed samples with varying O2 content were analyzed. The structure of YBaCu3O7 was determined by neutron diffraction to be orthorhombic with distinct Cu-O chains along the b-axis as well as Cu-O planes in the a - b plane. Therefore, by looking for a crystallographic dependence of the oxygen K-edge one might be able to distinguish inequivalent oxygen atoms by their core level binding energy and correlate site occupancy with varying O2 content. The EELS results on the oxygen K-edge are strongly dependent on oxygen content, most noticeably when the c-axis is parallel to the electron beam.
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    Journal of Electron Microscopy Technique 8 (1988), S. 325-337 
    ISSN: 0741-0581
    Keywords: YBa2Cu3O7 ; High Tc superconductor ; Martensitic transformation ; HRTEM ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Direct structure images of the YBa2Cu3O7-x high Tc superconducting ceramic (also called the 1-2-3 compound) at 1.7 Å resolution have been obtained for the [100] and [001] orientations. It was found that for the purposes of studying oxygen ordering in this compound it is better to use lattice images of lower resolution. The oxygen ordering was studied via the measurement of the bending of (100) and (110) lattice planes on crossing the (110) twin boundaries in crystals oriented in the [001] zone. Significant variations were found in the b/a ratios, owning to a variation in oxygen ordering, between different crystal grains, and between different regions in the same grain. For the three different 1-2-2 samples studied, the average b/a ration was 1.016, the same value as was found in neutron diffraction studies. The twin boundaries in the orthorhombic 1-2-3 phase are sharp and planar. It seems likely that the transformation from the high-temperature tetragonal phase to the lower-temperature orthorhombic phase is martensitic in nature. A new phase has been discovered on some of the twin boundaries. The new phase can be indexed as tetragonal with a = 7.5 ± 0.2 Å, and c = 6.8 ± 0.2 Å. It is possible that the new phase is stabilized by the stress which occurs at the twin boundaries.
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    Journal of Electron Microscopy Technique 8 (1988), S. 363-370 
    ISSN: 0741-0581
    Keywords: Three-dimensional organization ; Membrane glycoconjugates ; Gold labeling ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Recently, cytochemical techniques have been applied for localizing membrane components; however, transmission electron microscopy only provides two-dimensional information about their distribution. Scanning electron microscopy, on the other hand, offers the possibility of examining the three-dimensional architecture of biological samples. The fracture-label cytochemical technique was combined with the backscattered electron imaging (BEI) mode of the scanning electron microscope to visualize the in vivo distribution of lectin binding sites on freeze-fractured biological membranes in tissues and cells. Pancreatic and testicular tissues, fixed with glutaraldehyde, were freeze-fractured and labeled with Helix pomatialectin-gold or Ricinus communis I-gold complexes. The labeled specimens were then critical-point dried and replicated with platinum-carbon for routine transmission electron microscopy or with carbon alone for BEL. Lectin-gold labeling of fractured plasma and intracellular membranes observed with BEI showed a labeling pattern similar to that seen by the replica method. However, BEI-fracturelabel provided additional information about the distribution of the labeling with respect to three-dimensional organization of tissues and cells. Large sample areas could be examined, making this technique particularly useful as a survey method for specimens that are either differentially labeled or composed of heterogenous cell populations.
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    Journal of Electron Microscopy Technique 8 (1988), S. 401-432 
    ISSN: 0741-0581
    Keywords: Electron microscopy ; Immunoelectron microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The present review deals with the use of electron microscopy in the identification of pituitary cell types as well as the assessment of their functional state, in rat and man. Application of immunoelectron microscopy, especially immunogold techniques, utilizing multiple labeling in establishing differentiation and hormone content of cell types, is emphasized. Recent evidence of plurihormonality in various pituitary cell types indicates that the once axiomatic one cell-one hormone theory is untenable and that the present perception of pituitary cell types and their function requires modification. Detection of hormonal and nonhormonal substances in pituitary cell types, not associated with their known endocrine function, suggests that hypophysial cells may have yet unknown roles, possibly in the realm of paracrine and autocrine regulation.
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    Journal of Electron Microscopy Technique 8 (1988), S. 443-444 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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    Journal of Electron Microscopy Technique 9 (1988), S. 19-43 
    ISSN: 0741-0581
    Keywords: Continuum ; Thin sections ; Microdroplets ; Water content ; Bulk specimens ; Semithick specimens ; Mass loss ; Standards ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Qualitative X-ray microanalysis of biological specimens requires an approach that is somewhat different from that used in the materials sciences. The first step is deconvolution and background subtraction on the obtained spectrum. The further treatment depends on the type of specimen: thin, thick, or semithick. For thin sections, the continuum method of quantitation is most often used, but it should be combined with an accurate correction for extraneous background. However, alternative methods to determine local mass should also be considered. In the analysis of biological bulk specimens, the ZAF-correction method appears to be less useful, primarily because of the uneven surface of biological specimens. The peak-to-local background model may be a more adequate method for thick specimens that are not mounted on a thick substrate. Quantitative X-ray microanalysis of biological specimens generally requires the use of standards that preferably should resemble the specimen in chemical and physical properties. Special problems in biological microanalysis include low count rates, specimen instability and mass loss, extraneous contributions to the spectrum, and preparative artifacts affecting quantitation. A relatively recent development in X-ray microanalysis of biological specimens is the quantitative determination of local water content.
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    Journal of Electron Microscopy Technique 9 (1988), S. 83-98 
    ISSN: 0741-0581
    Keywords: X-ray microanalysis ; Pathology ; Diagnosis ; Cryo(ultra)-microtomy ; Cultured cells ; Freeze-drying ; Freeze-substitution ; Low-temperature embedding ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Many diseases are associated with a change in the distribution of diffusible ions at the cell or tissue level. These diseases can profitably be studied by X-ray microanalysis. This technique for the study of ion distribution requires the use of cryoprepared specimens. Analysis at low or medium resolution can be carried out on thick or semi-thick cryosections, or on frozenhydrated or freeze-dried embedded bulk samples. Such analyses are particularly useful in the initial stages of an investigation or when data from a large number of samples have to be acquired. Also X-ray microanalysis of cultured or single cells prepared by freeze-drying can be used to rapidly collect information on a large number of cells. Analysis at high resolution has to be carried out on thin sections: Cryosections or sections of freeze-substituted or freeze-dried embedded tissue. For the latter type of specimens, the use of low-temperature embedding methods may have important advantages.
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    Journal of Electron Microscopy Technique 9 (1988), S. 65-82 
    ISSN: 0741-0581
    Keywords: Cryopreparation ; Cryosection ; Cryotransfer ; Microanalysis ; STEM ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The elemental composition and the ultrastructure of biological cells were studied by scanning transmission electron microscopy (STEM) combined with energy dispersive X-ray microanalysis. The preparation technique involves cryofixation, cryoultramicrotomy, cryotransfer, and freeze-drying of samples. Freeze-dried cryosections 100-nm thick appeared to be appropriate for measuring the distribution of diffusible elements and water in different compartments of the cells. The lateral analytical resolution was less than 50 nm, depending on ice crystal damage and section thickness. The detection limit was in the range of 10 mmol/kg dry weight for all elements with an atomic number higher than 12; for sodium and magnesium the detection limits were about 30 and 20 mmol/kg dry weight, respectively.The darkfield intensity in STEM is linearly related to the mass thickness. Thus, it becomes possible to measure the water content in intracellular compartments by using the darkfield signal of the dry mass remaining after freeze-drying. By combining the X-ray microanalytical data expressed as dry weight concentrations with the measurements of the water content, physiologically more meaningful wet weight concentrations of elements were determined.In comparison to freeze-dried cryosections frozen-hydrated sections showed poor contrast and were very sensitive against radiation damage, resulting in mass loss. The high electron exposure required for recording X-ray spectra made reproducible microanalysis of ultrathin (about 100-nm thick) frozen-hydrated sections impossible. The mass loss could be reduced by carbon coating; however, the improvement achieved thus far is still insufficient for applications in X-ray microanalysis. Therefore, at present only bulk specimens or at least 1-μm thick sections can be used for X-ray microanalysis of frozen-hydrated biological samples.
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    Journal of Electron Microscopy Technique 9 (1988), S. 115-144 
    ISSN: 0741-0581
    Keywords: Acute renal failure ; Glomerular filtration ; Kidney ; Nephrotic syndrome ; Podocytes ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The glomerular (visceral) layer of Bowman's capsule is comprised of a unique population of cells which have been termed “podocytes.:” Arising from these cells are large major processes and numerous smaller foot processes which completely surround underlying glomerular capillary loops. Podocyte foot processes interdigitate with each other and are separated by spaces (filtration slits) which are designed to facilitate flow of a large amount of filtrate across the glomerular wall. Podocytes exhibit dramatic morphological changes in response to the nephrotic syndrome and some forms of acute renal failure and may play an important role in the pathophysiology of these conditions. In vitro and in vivo studies have shown that a reduction in the sialic acid component of a thick anionic surface coat plays a major role in the morphological changes that these cells exhibit in the nephrotic syndrome. Also, it has been shown that filamentous actin concentrated mainly within podocyte foot processes are the contractile elements responsible for altering the shapes of these processes. There is evidence to suggest that by altering the shapes of their foot processes, podocytes in the normal kidney are able to alter the number of fully patent filtration slits and thereby actively regulate the rate of solute efflux across the glomerular wall. In vitro and in vivo studies have indicated that cytoplasmic microtubules are probably not involved in alterations of the podocyte foot processes but do appear important in maintaining the morphological integrity of podocyte cell bodies and their major processes. In the present paper, the morphological changes which glomerular podocytes exhibit in response to the nephrotic syndrome, various forms of acute renal failure, and during in vitro incubation are discussed along with studies of the possible roles of cytoplasmic microtubules, microtubules, and the glomerular anionic surface coat in these changes.
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    Journal of Electron Microscopy Technique 9 (1988), S. 265-281 
    ISSN: 0741-0581
    Keywords: Monoclonal antibodies ; Matrix proteins ; Na, K-ATPase ; Glomerular antigens ; Tubular antigens ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Immunocytochemistry of the kidney is a unique method to integrate physiology, biochemistry, and molecular biology with morphology. Both mono- and polyclonal antibody reagents are useful and each has advantages and disadvantages. Specificity with low background is of the greatest importance. Tissue preparation techniques depend on the antigen being studied as well as the methodology to be used. Pre- and postembedding techniques combined with visualization with peroxidase reaction products or with particulate markers such as ferritin and gold must be chosen for each individual circumstance to be studied. Important applications in the kidney have included studies of glomerular antigens, specific transport proteins, and segment-specific antigens of unknown specificity. Future utilization of this technique with new molecular probes will greatly enhance our knowledge of the biology of the kidney.
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    Journal of Electron Microscopy Technique 9 (1988) 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 9 (1988), S. 325-358 
    ISSN: 0741-0581
    Keywords: Filtering ; 3-D reconstruction ; Viruses ; Filaments ; Flagella ; Fourier transform ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Methods are described for the analysis of electron micrographs of biological objects with helical symmetry and for the production of three-dimensional models of these structures using computer image reconstruction methods. Fourier-based processing of one- and two-dimensionally ordered planar arrays is described by way of introduction, before analysing the special properties of helices and their transforms. Conceiving helical objects as a sum of helical waves (analogous to the sum of planar waves used to describe a planar crystal) is shown to facilitate analysis and enable three-dimensional models to be produced, often from a single view of the object. The corresponding Fourier transform of such a sum of helical waves consists of a sum of Bessel function terms along layer lines. Special problems deriving from the overlapping along layer lines of terms of different Bessel order are discussed, and methods to separate these terms, based on analysing a number of different azimuthal views of the object by least squares, are described. Corrections to alleviate many technical and specimen-related problems are discussed in conjunction with a consideration of the computer methods used to actually process an image. A range of examples of helical objects, including viruses, microtubules, flagella, actin, and myosin filaments, are discussed to illustrate the range of problems that can be addressed by computer reconstruction methods.
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    Journal of Electron Microscopy Technique 9 (1988), S. 413-419 
    ISSN: 0741-0581
    Keywords: Image processing ; Lattice defects ; Bacterial surface protein ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The surface protein of the archaebacterium Pyrodictium occultum forms two-dimensional periodic arrays of extremely poor order. Two variants of correlation averaging have been applied in order to retrieve the unit cell structure from electron micrographs of negatively stained samples: straightforward correlation averaging correcting for lateral displacements only and a more elaborate approach, including a partial compensation for rotational disorder. Surprisingly, both routes yield virtually identical structures. Inclusion of molecular motifs from highly disordered domains, which are rejected in the “straightforward” approach, appears not to improve resolution, possibly because the high local strain tends to distort the individual molecules.
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    Journal of Electron Microscopy Technique 10 (1988), S. 15-26 
    ISSN: 0741-0581
    Keywords: Scanning electron microscopy ; Ocular microvasculature ; Microcorrosion cast ; Injection replica ; Batson's ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: We have refined the technique of vascular corrosion casting with methacrylate to permit the reproduction of physiological states of vascular tone and to produce sturdy castings of ocular microvasculature. The method entails careful maintenance of homeostasis up to the moment of plastic perfusion, avoidance of vascular rinsing or fixation with the attendant anoxia, reduction of the viscosity of the casting resin without impairing the properties of the resultant polymer, addition of a cross-linking agent to increase the strength of the plastic, and injection at physiological temperature and pressure. This casting regimen reproduces the normal anatomical conditions of blood vessels and can be used to demonstrate altered conditions of vascular tone. In all instances, the second, untouched eye serves as a control for unilateral manipulations. Special problems of replicating the ocular vasculature are related to the intraocular pressure, which opposes the vascular perfusion pressure and constitutes an impediment to perfusion.
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    Journal of Electron Microscopy Technique 10 (1988), S. 119-121 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Topics: Natural Sciences in General
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    Journal of Electron Microscopy Technique 10 (1988), S. 127-127 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 10 (1988), S. 153-185 
    ISSN: 0741-0581
    Keywords: Acetylcholine receptor ; Active zones ; Endocytosis ; Exocytosis ; Freeze-fracture ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Because vertebrate neuromuscular junctions are readily accessible for experimental manipulation, they have provided a superb model in which to examine and test functional correlates of chemical synaptic transmission. In the neuromuscular synapse, acetylcholine receptors have been localized to the crests of the junctional folds and visualized by a variety of ultrastructural techniques. By using ultrarapid freezing techniques with a temporal resolution of less than 1 msec, quantal transmitter release has been correlated with synaptic vesicle exocytosis at discrete sites called “active zones.” Mechanisms for synaptic vesicle membrane retrieval and recycling have been identified by using immunological approaches and correlated with endocytosis via coated pits and coated vesicles. In this review, available ultrastructural, physiological, immunological, and biochemical data have been used to construct an ultrastructural model of neuromuscular synaptic transmission that correlates structure and function at the molecular level.
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    Journal of Electron Microscopy Technique 10 (1988), S. 129-151 
    ISSN: 0741-0581
    Keywords: Synapse ; Junction ; Spine ; Synapsin I ; Cerebellum ; Neurotransmission ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Application of rapid freezing, freeze substitution fixation, and freeze fracture techniques to the study of synaptic junctions in the mammalian central nervous system has revealed new aspects of synaptic structure that are consistent with and partially explicate advances in synaptic biochemistry and physiology. In the axoplasm adjacent to the presynaptic active zone, synaptic vesicles are linked to large spectrin-like filamentous proteins by shorter proteins that resemble synapsin I in morphology. This mesh of presynaptic filamentous proteins serves to concentrate synaptic vesicles in the vicinity of the active zone. The affinity with which the vesicles are bound by the mesh is probably modulated by the extent of phosphorylation at specific sites on the constituent filamentous proteins, and changes in the binding affinity result in changes in transmitter release.The structural organization of the postsynaptic density in Purkinje cell dendritic spines consists of very fine strands with adherent, heterogeneous globular proteins. Some of these globular proteins probably correspond to protein kinases and their substrates. The postsynaptic density, positioned at the site of the maximal depolarization caused by synaptic currents, apparently serves as a supporting framework for a variety of proteins, which respond to and transduce postsynaptic depolarization.At least two classes of filamentous protein fill the cytoplasm of spines with a complex mesh, which presumably contributes to maintenance of the spine shape. Membrane bound cisterns are a ubiquitous feature of Purkinje cell dendritic spines. Studies of rapidly frozen tissue with electron probe microanalysis and elemental imaging reveal that these cisterns take up and sequester calcium, which is derived from the extracellular space, and which probably enters the spine as part of the synaptic current.
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    Journal of Electron Microscopy Technique 10 (1988), S. 213-227 
    ISSN: 0741-0581
    Keywords: Trigeminal nucleus oralis ; Small-diameter primary axons ; Synaptic glomeruli ; Horseradish peroxidase ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: This report examines the morphology and synaptic connections of small-diameter primary trigeminal axons that terminate in the border zone (BZ) and ventrolateral (VL) subdivisions of rat trigeminal nucleus oralis (Vo). Primary axons were made visible for light and electron microscopic analysis by utilizing the method of anterograde transport of horseradish peroxidase. BZ receives the terminal arborizations of two different populations of small-diameter primary axons. One of these arises from unmyelinated parent fibers and terminates in the dorsal one-half of BZ, while the other has small myelinated parent branches that arborize throughout the subdivision. Terminating within VL are the arbors of a second population of small myelinated primary axons. The endings of all three populations of primary axons lie in synaptic glomeruli. Endings in both subdivisions derived from small myelinated parent fibers lie centrally in glomeruli. Those in VL form axodendritic synapses on numerous dendritic shafts and spines, while endings in BZ glomeruli make at least one axodendritic synapse on one or two dendritic shafts. Endings of unmyelinated primary axons in BZ lie at the periphery of glomeruli where each forms a single axodendritic synapse on a central dendrite. It is at these asymmetrical axodendritic synapses that these three populations of primary axons are thought to transfer their inputs directly to the dendritic arbors of second-order BZ and VL neurons. Common to all three glomeruli is one or more small axonal endings filled with flattened synaptic vesicles that establish axoaxonic synapses on the primary ending as well as axodendritic synapses on the dendritic element(s) receiving primary input. In view of their symmetrical to intermediate synaptic contacts, these endings are thought to belong to axons derived from at least one source that can inhibit or diminish the firing rate of second-order BZ and VL neurons in response to primary input.
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    Journal of Electron Microscopy Technique 10 (1988), S. 315-316 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 10 (1988) 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 10 (1988), S. 373-374 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 10 (1988), S. 375-376 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 10 (1988), S. 115-116 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 10 (1988), S. 117-118 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 10 (1988), S. 125-126 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 10 (1988), S. 229-246 
    ISSN: 0741-0581
    Keywords: Cerebellum ; Cerebral cortex ; Dorsal column nuclei ; Cerebellar nuclei ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Ultrastructural studies are described that have identified in the basilar pontine nuclei (BPN), the synaptic boutons formed by the corticopontine, cerebellopontine, tectopontine, and dorsal column nucleipontine afferent projection systems. In addition, immunocytochemical studies visualized neuronal somata, dendrites, and synaptic boutons that contain immunoreactivity for GABA or the synthesizing enzyme glutamic acid decarboxylase (GAD).Based upon differences in the mode of degeneration and postsynaptic locus of degenerative synaptic boutons in the BPN, it is suggested that two types of cortical neurons and three classes of deep cerebellar nuclear cells project to the BPN. For similar reasons, it appears that two types of neurons in the dorsal column nuclei project to the BPN while only one type of afferent synaptic bouton takes origin from the superior colliculus. Furthermore it appears that the population of BPN neurons projecting to the paramedian lobule receives convergent inputs from the cutaneous periphery and the corresponding region of sensorimotor cortex. Studies employing GAD immunohistochemistry indicate that GABA-ergic neurons and axon terminals are present in the BPN and thus support the suggestion that a local inhibitory interneuron is present within the BPN. Taken together these observations suggest that basilar pontine neurons might play a more active role in the integration of various types of information destined for the cerebellar cortex than has previously been recognized.
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    Journal of Electron Microscopy Technique 8 (1988), S. 247-250 
    ISSN: 0741-0581
    Keywords: Crystallography ; Chemistry ; Stability ; Current density ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: This introductory article reviews the recent developments in high Tc superconducting ceramics. Particular emphasis is given to the structural and chemical aspects of these compounds that may be of interest to the electron microscopist. Included are some of the contributions made by electron microscopy techniques over the last 10 months. The applications of electron microscopy to solving practical problems associated with these exciting new materials are also discussed.
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    Journal of Electron Microscopy Technique 8 (1988), S. 285-295 
    ISSN: 0741-0581
    Keywords: Electron microscopy ; Vacancy ordering ; Phase transformation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The superconducting material Y1Ba2Cu3O7-δ has been investigated by electron microscopy. Special attention has been paid to the defects occurring in the material. Twinning on (110) or (110) planes is intrinsically related to the orthorhombicity, and when cooled slowly the twin bands are pseudoperiodic with an average width of ˜ 50 nm. The orthorhombic-tetragonal transition is reversible and diffusion controlled. Under particular conditions and in slightly reduced material a 2a0 X b0 superstructure resulting from vacancy ordering is formed. When kept in air under powder form the material seems to be unstable. Planar defects along (001) accompany the degeneration of the material.
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    Journal of Electron Microscopy Technique 8 (1988), S. 317-323 
    ISSN: 0741-0581
    Keywords: Superconductivity ; Perovskites ; Oxides ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Twins are ubiquitous in the perovskite superconductors. They form during cooling from high temperatures through the tetragonal-to-orthorhombic phase transformation. Their behavior has been studied by transmission electron microscopy using a liquid-nitrogen-cooled specimen holder. It is observed that extra twins sometimes form in coarse-twinned regions to give a “refined” twin structure; this is thought to be induced by thermal stresses from the electron beam. Prolonged electron irradiation (with little beam heating) results in transformation to tetragonal with a loss of the twin structure; this is probably due to disordering of the oxygen sublattice by knock-on displacement. The same transformations can be induced by deliberate electron beam heating. In both cases the twinned orthorhombic structure can be restored by re-ordering of the oxygen ions, in the first case by removing the beam and in the second case by allowing the specimen to cool.
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    Journal of Electron Microscopy Technique 8 (1988), S. 343-348 
    ISSN: 0741-0581
    Keywords: Cryo-microscopy ; Quick freeze ; La Crosse virus ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: A guillotine-type quick freezing device and a bio-hazard containment box have been designed, constructed, and used to prepare vitrifiedhydrated specimens of viruses in their native environment. Special design considerations include the preservation of the specimen in its natural state in vitrified ice, prevention of virus aerosols escape, and control of the potentially explosive air-coolant vapor mixtures.
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    Journal of Electron Microscopy Technique 8 (1988), S. 371-379 
    ISSN: 0741-0581
    Keywords: Casuarina ; Cellulase ; Cell walls ; Codium ; Colloidal gold ; Dictyostelium ; Udotea ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The enzyme-linked colloidal gold affinity labelling technique was tested as a method to localize cellulose on thin sections of plant cell walls and slime mold spores. Commercially available cellulase from cultures of Trichoderma reesei, the main components being cellobiohydrolase I and II (CBH I, CBH II) and endoglucanase (EG), was linked to colloidal gold by using standard techniques and applied as a dilute, buffered suspension to thin sections. After brief exposure, e.g., 15-30 minutes, cellulose exposed on the surface of sections was labelled with the enzyme-gold complex. Poststaining did not appear to have a deleterious effect on the labelled sections. The specificity of labelling was demonstrated by its complete inhibition when carboxymethylcellulose was incorporated in the labelling mixture, by lack of labelling of 1,4-β-mannans or 1,3-β-xylans in noncellulosic walls of marine algae, by lack of labelling of 1,4-β-glucans in chitin, by much lower labelling density when done at 4°C, and by lack of labelling when sections were predigested with cellulase. Labelling with the crude commercial cellulase was compared to labelling with purified CBH I-, CBH II-, and EG-linked colloidal gold, and the labelling pattern was similar. This method was found useful on conventionally fixed material and required no special preparation other than the use of inert (Ni or Au) grids and 0.5% gelatin to reduce nonspecific binding of the gold complex. Labelling was similar in the several embedding resins tested: LR White, Lowicryl K4M, Epon 812, and Spurr's. The cellulase-gold probe remained active for at least 4 weeks at 4°C and much longer when frozen at -80°C in 20% glycerol. This technique should prove useful in studies of cellulose degradation and cellulose deposition and of the interaction of cellulose with other wall components.
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    Journal of Electron Microscopy Technique 8 (1988), S. 441-442 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 9 (1988) 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 64
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    Journal of Electron Microscopy Technique 9 (1988), S. 45-56 
    ISSN: 0741-0581
    Keywords: Electron probe analysis ; Ultramicrovolumes ; Subnanoliter ; Micropipettes ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: X-ray microanalysis can be used to quantitatively determine the elemental composition of microvolumes of biological fluids. This article describes the various steps in preparation of microdroplets for analysis: The manufacturing of micropipettes, the preparation of the specimen support, the deposition of droplets on the support, shock-freezing, and lyophilization. Examples of common artifacts (incomplete rehydration prior to freezing or partial rehydration after lyophilization) are demonstrated. Analysis can be carried out either by wavelength-dispersive analysis, which is the most sensitive method, or by energy-dispersive analysis, which is more commonly available. The mininum detectable concentration is 0.05 mmol · liter-1 for 0.1-nl samples analyzed by wavelength-dispersive spectrometry and 0.5-1 mmol · liter-1 for samples analyzed by energy-dispersive spectrometry. A major problem, especially in wavelength-dispersive analysis, where high beam currents are used, is radiation damage to the specimen; in particular chloride (but also other elements) can be lost. Quantitative analysis requires the use of standard solutions with elemental concentration in the same range as those present in the specimen.
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    Journal of Electron Microscopy Technique 9 (1988), S. 145-170 
    ISSN: 0741-0581
    Keywords: Freeze-fracture ; Immunocytochemistry ; Cell membrane structure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: In this review, we demonstrate how differentiated membrane domains can be detected in epithelial cells using conventional light and electron microscopy, freeze-fracture electron microscopy and the immunoand cytochemical detection of membrane components. Using specific examples from the kidney, we show how the polarized insertion of these components into either apical or basolateral plasma membrane regions on either side of the tight junction barrier is related to specific functions of principal and intercalated cells in the collecting duct. In addition, distinct basal and lateral membrane domains have been revealed in some cells that are maintained in the absence of a tight junctional barrier in the plane of the membrane. This suggests that other factors, possibly related to cytoskeletal elements, may be involved in the functional segregation of these membrane areas. We propose that epithelial cell plasma membranes should be subdivided into apical, lateral and basal regions, and that the term “basolateral” may be an oversimplification.
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 9 (1988), S. 209-210 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 9 (1988), S. 235-263 
    ISSN: 0741-0581
    Keywords: Kidney tubules ; Mesangial cells ; Cell growth ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Methods for the establishment and growth of renal cell types in culture are reviewed, with emphasis on current trends. General techniques available for the isolation and culture of glomerular cells have progressed from explant to enzyme dissociation and cloning techniques. The growth characteristics and properties of cultured glomerular endothelial, epithelial, mesangial, and bone-marrow-derived cells are discussed. Studies are described in which cultures of contractile mesangial cells have led to an elucidation of their role both in normally functioning glomeruli and in disease states. Renal tubule culture techniques also have progressed from mixed tissue explants and cell isolates to fractionation of enriched tubule populations and growth of specific, individually microdissected proximal convoluted, proximal straight, thick ascending limb of Henle's loop, and collecting tubules. The differentiated tubule epithelial-specific properties of such primary cultures are discussed in relation to those of permanently growing cell lines such as MDCK and LLC-PK1. Renal tubule cultures will be invaluable for the study of the role of hormones and extracellular matrix in epithelial growth and polarity of normal structure and function. In addition, in vitro models of cultured renal tubules have been established to study the effects of age, nephrotoxins, and anoxic injury.
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    Journal of Electron Microscopy Technique 8 (1988), S. 3-15 
    ISSN: 0741-0581
    Keywords: Human T-cell leukemia virus type I (HTLV-I) ; Human T-cell leukemia virus type II (HTLV-II) ; Human immunodeficiency virus (HIV) ; Lymphadenopathy-associated virus type II (LAV-II) ; Acquired immunodeficiency syndrome (AIDS) ; Human T lymphotropic virus type III; IV (HTLV-III; HTLV-IV) ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: We compared the ultrastructure of the human retroviruses by thin-section electron microscopy of infected lymphocytes. Virus particles form at the plasma membrane without involvement of a cytoplasmic precursor. Budding forms of human T-cell leukemia virus types I and II (HTLV-I and -II) consist of a crescent-shaped nulceoid separated from the envelope by an intermediate layer. Mature forms of these viruses are about 100 nm in diameter. The nucleoid is electron lucent and almost completely fills the virion. There is about a 10-nm space between the envelope and nucleoid. The envelope has fuzzy surface projections. HTLV-I and -II resemble other type C retroviruses in morphology. Budding forms of human immunodeficiency virus (HIV, LAV, HTLV-III) also have a crescent-shaped nucleoid but not an intermediate layer between the core and envelope. The envelope has rod-shaped surface projections. Mature forms of HIV have an electron-dense nucleoid that is eccentric and bar- or cone-shaped. Particles have the same ultrastructure as retroviruses of the Lentivirus genus. HIV is readily distinguishable from HTLV-I and -II by thin-section electron microscopy. HIV is usually found in extracellular spaces by transmission electron microscopy of thin sections, and scanning electron microscopy of HIV-infected T4 lymphocytes also shows many particles on the surface of these cells. Lymphadenopathy-associated virus type II (LAV-II) has the same internal ultrastructure as HIV, but its surface projections are more prominent, being about three times the length of those of HIV. Human T lymphotropic virus type IV (HTLV-IV) has the same morphology as LAV-II.
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    Journal of Electron Microscopy Technique 8 (1988), S. 137-158 
    ISSN: 0741-0581
    Keywords: Kaposi's sarcoma ; Lymphoma ; Histology ; Ultrastructure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Malignancies frequently arise in patients infected with human immunodeficiency virus (HIV), including those patients classified as having the acquired immunodeficiency syndrome (AIDS). Currently, Kaposi's sarcoma and certain types of lymphoma are considered to develop as a result of HIV infection, and other cancers have also been reported in these patients. For the most part, ultrastructural study of HIV-associated malignancies has been limited to Kaposi's sarcoma; the ultrastructural features of the epidemic form of this disease are generally the same as those of the classical form. The occurrence of these cancers in HIV-infected individuals appears to be related to the immunodeficiency caused by this virus, but the basic etiologic mechanisms remain unknown. In general, only palliative treatments are presently available for HIV-associated malignancies.
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    Journal of Electron Microscopy Technique 8 (1988), S. 179-183 
    ISSN: 0741-0581
    Keywords: Axonal degeneration ; Electron microscopy ; Human ; Visual pathways ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: It is a widely held belief that the products of axonal degeneration in the CNS are transitory and are caused by metabolic and phagocytic processes. However, recent light microscopic examinations of human and primate brains using the paraphenylene diamine staining method (PPD), which stains degenerating axons, have confirmed that the products of degeneration persist for years in visual pathways. The routine utilization of the PPD method for delineating human visual pathways requires further confirmation of axonal degeneration. Optic nerves, optic tracts, and lateral geniculate nuclei were collected from human brains that had clinical documentation of optic nerve damage prior to death. Optic nerves, optic tracts, and lateral geniculate nuclei taken from the brains of cynomolgus monkeys that had undergone enucleation 3 months to 1 year prior to sacrifice were also examined. All tissue was processed for electron microscopy; ultrathin sections were cut for electron microscopy, and consecutive sections were cut for light microscopy.In all cases, the homology of the degenerated processes was confirmed between the light microscopic (PPD) and the electron microscopic sections. Such ultrastructural examination demonstrates that the products of axonal degeneration remain in the primate visual system longer than previously supposed.
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 8 (1988), S. 251-262 
    ISSN: 0741-0581
    Keywords: Superconductivity ; Long-range order ; Microstructure ; Convergent beam electron diffraction ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: We show that high-resolution transmission electron microscopy can be used directly to reveal the structure of the metal framework and its defects in Ba2YCu3O7. The use of dynamical effects under carefully selected and controlled conditions allows the detection of long-range order in the disposition of the oxygen vacancies, but inevitable misalignments make the quantification of the order parameter difficult. Specimen preparation methods are compared, and a wide-angle convergent-beam pattern is demonstrated.
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    Journal of Electron Microscopy Technique 8 (1988), S. 297-306 
    ISSN: 0741-0581
    Keywords: Defects ; Polymorphs ; Structure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: We review recent results obtained at Northwestern using high-resolution electron microscopy to study high-temperature superconductors. While in general these materials form large, very perfect single crystal grains which display very few imperfections, there is also evidence of slip defects, amorphous regions, and order-disorder transformations. We also report that the gadolinium-based superconductors and in one case yttrium-based superconductors show evidence for some copper solid solubility in the form of copperrich planar defects. The structure of a metastable trigonal polytype is also reported, as are the effects of electron beam and water vapor damage to the materials.
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    Journal of Electron Microscopy Technique 8 (1988), S. 339-341 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 76
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    Journal of Electron Microscopy Technique 8 (1988), S. 355-361 
    ISSN: 0741-0581
    Keywords: Electropolishing ; TEM ; δ′ ; T1 and θ′ precipitates ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Ion milling is commonly used to prepare specimens for observation under transmission electron microscope (TEM). This technique sometimes introduces artifacts in specimens contributing to misleading interpretation of TEM results as observed in the present investigation of Al-Li-Cu alloys. This type of alloy, in general, contains several kinds of precipitates, namely δ′ T1, and θ′. It is found that ion milling even for a short time produces drastic changes in the precipitate characterics as compared to standard electropolishing methods of specimen preparation for TEM. Careful analysis of selected area diffraction patterns and micrographs shows that after ion milling δ′ precipitates are very irregular, whereas other precipitates coarsen and they are surrounded by misfit dislocations. In situ hot-stage TEM experiments were performed to relate the microstructure to that observed in the ion-milled specimen. Results and causes of ion milling effects on the microstructure are discussed in relation to standard electropolishing techniques and in situ hot-stage experiment.
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    Journal of Electron Microscopy Technique 8 (1988), S. 389-390 
    ISSN: 0741-0581
    Keywords: Preparation ; High-voltage electron microscope ; Settling ; Phosphor ; Viewing screen ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: A technique is described for preparing uniform, durable phosphor layers for viewing screens suitable for the transmission electron microscope; a settling procedure is used. The example described here is for a high-voltage instrument, but with adjustment of the coating density, the technique should be equally suitable for screen preparation for transmission electron microscopes that operate at lower acceleration voltages.
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    Journal of Electron Microscopy Technique 8 (1988), S. 381-388 
    ISSN: 0741-0581
    Keywords: Image processing ; Molecular structure ; Resolution assessment ; Optical density response ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Some aspects of digitization of electron micrographs have been investigated. The performances of a flat-bed, a rotating drum, and a diode array scanner have been evaluated. Estimates have been achieved for resolution, mechanical and optical stability, and optical density response. It is concluded that for routine transmission electron microscopy of, for example, negatively stained biologic specimens, a diode array scanner produces data good enough to obtain resolutions at a level normally expected. High speed is the major advantage with this type of equipment. However, for high-resolution work it is necessary to use a conventional scanner with a relatively slow scan speed.
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    Journal of Electron Microscopy Technique 8 (1988), S. 433-439 
    ISSN: 0741-0581
    Keywords: Modulation transfer function ; Phase contrast ; Amplitude contrast ; Emulsion ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Focus in transmission electron microscopy, especially at low-to-moderate powers, is usually achieved by an empirical, though largely haphazard, process of defocusing the objective below what is known to be perfect focus as defined by the absence of Fresnel diffraction fringes at the edges of holes. In this article we provide a precise, empirical method of focus, whose rationale resides in the less-than-perfect image transfer from the image space of the objective to the negative, i.e., the modulation transfer function. In practice, “perfect focus,” as defined above, is established with a beam deflector (“wobbler”), to which underfocus is then applied routinely by reference to a table. Such “critical underfocus” values have to be calibrated, as described here, for each microscope and depend on all factors that influence contrast, that is, accelerating voltage, condenser defocus and coherence of illumination, focal length of the objective, aperture sizes, combination of intermediate and projection lenses, and the properties of the photographic emulsion.
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    Journal of Electron Microscopy Technique 9 (1988), S. 3-17 
    ISSN: 0741-0581
    Keywords: X-ray microanalysis ; Biology ; Specimen preparation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: This paper gives an introduction to X-ray microanalysis for biologists. The physical principles of X-ray microanalysis and the instrumentation used in wavelength-dispersive and energy-dispersive analysis are reviewed. A special problem in biological microanalysis is the adequate preparation of the specimen: The preparative method must retain the localization of the element(s) of interest and allow identification of morphological features at the level of analytical resolution. Conventional preparation methods for electron microscopy have only a limited applicability in biological X-ray microanalysis, and often cryomethods have to be used. Methods for qualitative analysis and some common pitfalls and artefacts are discussed. The possibilities and limitations of electron-probe X-ray microanalysis with regard to biological specimens are compared to those of other microanalytical techniques.
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 9 (1988), S. 99-112 
    ISSN: 0741-0581
    Keywords: Elemental analysis ; Ultrastructural cytochemistry ; Enzyme histochemistry ; Biogenic amines ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: X-ray microanalysis (XRMA) has been applied to a wide variety of cytochemical problems, but the most valuable applications have been to the validation of cytochemical methods (by the qualitative or quantitative analysis of reaction products), and to the simultaneous localization of more than one substance, which cannot easily be achieved by using alternative methods. The latter applications involve stoichiometric studies (the quantitative relationships between reaction products and substrates), and distribution studies. Ultrastructural cytochemistry with XRMA is limited by the need to use high-brightness electron sources. Apart from the limited availability of such sources, they may cause unacceptable damage to the specimen.Preparation methods for cytochemistry using XRMA are reviewed; in principle these do not differ from those used for other cytochemical applications, but it is important not to introduce extraneous elements (from fixative, buffer, or embedding medium) into the specimen, where the additional X-ray peaks may interfere with the analysis.Quantification in XRMA of cytochemical preparations poses special problems, because the addition of the reaction product to the specimen alters the yield of continuum X rays, used for assessing the mass of the specimen, and also dilutes endogenous elements. However, measurement of ratios between characteristic elemental peaks is a useful method in X-ray microanalytical cytochemistry, and it is concluded that one of the most important attributes of XRMA for cytochemical purposes is the ease with which the substances of interest can be measured.
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    Journal of Electron Microscopy Technique 9 (1988), S. 211-212 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Journal of Electron Microscopy Technique 9 (1988), S. 213-234 
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    Keywords: Electron microscopy ; Nephron ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The minipig has a multilobar kidney with a wide cortex and short papilla. The vascular bundles are of a simple type. Although short and long looped nephrons are both present, the short looped kind predominates. The minipig has many morphological similarities to dog and human kidneys. One particularly unique feature of the minipig papillary collecting duct cells, however, is the presence of electron-dense granules in the basal cytoplasm which appear to be secreted into the lateral intercellular spaces, perhaps forming a water-tight seal in a manner analogous to membrane-coating granules found in the epidermis of skin.
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  • 85
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    Journal of Electron Microscopy Technique 9 (1988), S. 299-299 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 86
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    Journal of Electron Microscopy Technique 9 (1988), S. 301-324 
    ISSN: 0741-0581
    Keywords: Fourier ; Filtering ; Moiré pattern ; Lattice ; Disorder ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Methods are described for the analysis of electron micrographs of regular biological objects. Fourier-based processing of one-dimensionally ordered arrays is described by way of introduction, before analysing two-dimensional crystals in projection with the aim of enhancing signal:noise ratio and thus of feint features that were initially obscured. This form of analysis is then extended to decomposing the moiré patterns formed when sheets overlap, thereby enabling the separation of interfering image patterns. Analogous forms of an analysis can also be applied to objects with rotational symmetry. Methods for treating the effect of the microscope imaging system and compensating for lattice disorder in crystalline specimens are also discussed.
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  • 87
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    Journal of Electron Microscopy Technique 9 (1988), S. 421-424 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 88
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    Journal of Electron Microscopy Technique 9 (1988), S. 425-425 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 89
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    Journal of Electron Microscopy Technique 10 (1988), S. 7-14 
    ISSN: 0741-0581
    Keywords: HREM ; Supported particle ; SMSI ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: High-resolution electron microscopy has been used to characterize the platinum particles supported on TiO2 or ZnO. After reduction at elevated temperatures, the metallic particles display a regular, faceted shape, and several superstructures, Pt3 Ti(C), Pt3 Ti(H), PtTi, and PtZn, have been found. These results, which may involve strong metal-support interaction, have been confirmed by optical diffraction and image simulation.
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  • 90
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    Journal of Electron Microscopy Technique 10 (1988), S. 45-51 
    ISSN: 0741-0581
    Keywords: Freeze fracture ; Thermocouple ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: In the Balzers rotary cold table, the recording thermocouple is located 45 mm below the specimen stage. As a result, there is inconsistency between the temperature indicated by the thermocouple gauge and the actual temperature of the specimen carrier. This inconsistency is most notable and can lead to problems when the cold table temperature is changed, such as during the procedure when fracturing at one temperature is followed by etching at a higher temperature.In this article, we describe modifications to the Balzers rotary cold table that permit the constant measurement of actual specimen temperature in the stationary, off, and rotating positions. The changes involve the use of a miniature temperature-sensing diode (TFD-Omega), mounted on the cradle that accepts standard counterflow, rapid-loading specimen stages.
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  • 91
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    Journal of Electron Microscopy Technique 10 (1988), S. 113-114 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 92
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    Journal of Electron Microscopy Technique 10 (1988), S. 87-111 
    ISSN: 0741-0581
    Keywords: Cryo-electron microscopy ; Cryofixation ; Vitreous ice ; Plunge-cooling ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The controlled environment vitrification system (CEVS) permits cryofixation of hydrated biological and colloidal dispersions and aggregates from a temperature- and saturation-controlled environment. Otherwise, specimens prepared in an uncontrolled laboratory atmosphere are subject to evaporation and heat transfer, which may introduce artifacts caused by concentration, pH, ionic strength, and temperature changes. Moreover, it is difficult to fix and examine the microstructure of systems at temperatures other than ambient (e.g., biological systems at in vivo conditions and colloidal systems above room temperature). A system has been developed that ensures that a liquid or partially liquid specimen is maintained in its original state while it is being prepared before vitrification and, once prepared, is vitrified with little alteration of its microstructure. A controlled environment is provided within a chamber where temperature and chemical activity of volatile components can be controlled while the specimen is being prepared. The specimen grid is mounted on a plunger, and a synchronous shutter is opened almost simultaneously with the release of the plunger, so that the specimen is propelled abruptly through the shutter opening into a cryogenic bath. We describe the system and its use and illustrate the value of the technique with TEM micrographs of surfactant microstructures in which specimen preparation artifacts were avoided. We also discuss applications to other instruments like SEM, to other techniques like freeze-fracture, and to novel “on the grid” experiments that make it possible to freeze successive instants of dynamic processes such as membrane fusion, chemical reactions, and phase transitions.
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  • 93
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    Journal of Electron Microscopy Technique 10 (1988), S. 187-204 
    ISSN: 0741-0581
    Keywords: Sympathetic nervous system ; Parasympathetic nervous system ; Enteric nervous system ; Ultrastructure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The ultrastructure of synapses in the autonomic nervous system is reviewed. The synaptic organization of the parasympathetic ganglia is relatively simple. Preganglionic axons form synapses either on the soma or on short perikaryal processes of the ganglionic neurons. The presynaptic terminals have a cholinergic morphology and contain mainly small clear vesicles with a few large dense cored vesicles. A few neuropeptides have been localized to the large dense cored vesicles of these terminals. The postganglionic parasympathetic axons ramify within their target tissues where they form close associations, but not true synaptic contacts. Sites of release of transmitter are recognized morphologically as varicosities along the length of the axon that contain clusters of small clear vesicles with a few large dense cored vesicles. The organization of the sympathetic nervous system is somewhat more complex. In addition to acetylcholine, enkephalin also exists in these terminals, probably in the large dense cored vesicles. There are at least three types of ganglion cell neurons in the paravertebral portion of the sympathetic nervous system: those that contain norepinephrine alone, those that contain norepinephrine along with neuropeptide Y, and those that contain acetylcholine and vasoactive intestinal polypeptide. The first type provides innervation to the parenchyma of the target tissues, while the second mainly innervates blood vessels. The third type innervates the sweat glands. In the prevertebral ganglia, a fourth type of neuron exists that contains norepinephrine and somatostatin. This neuron probably innervates the gut. Preganglionic terminals of the cholinergic type form synaptic connections mainly with the dendrites of the sympathetic ganglion neurons. In addition to the types of synapses described for the paravertebral ganglia, neurons in the prevertebral ganglia receive synaptic connections from dorsal root ganglia and from the enteric nervous system. The sympathetic ganglia also contain interneurons that receive preganglionic synapses and form efferent synapses with some of the principal ganglion cells. The interneurons have been shown to contain a variety of transmitters, including norepinephrine, epinephrine, dopamine, serotonin, and a number of neuropeptides. The postganglionic sympathetic axons have a similar morphology to the parasympathetic axons. They form networks in their targets, and the axons display varicosities with concentrations of both small and large vesicles. After appropriate fixation, these vesicles are seen to possess dense cores. The morphology of the enteric nervous system has the greatest complexity. There are sensory neurons, interneurons and motor neurons of various types. In addition, it receives extrinsic connections from both the sympathetic and parasympathetic nervous system. The synaptic ultrastructure is correspondingly complex, with a large number of different, morphologically disticnt types of synaptic terminals. The function and transmitter content of these terminals is beginning to be elucidated.
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  • 94
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    Journal of Electron Microscopy Technique 10 (1988), S. 265-281 
    ISSN: 0741-0581
    Keywords: Basal ganglia ; Corticostriatal ; Striatonigral ; Nigrostriatal ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The striatum, the main component of the basal ganglia, is composed of mainly one type of neuron, the so-called medium spiny neuron. This neuron cell type, which constitutes over 90% of striatal neurons, is the major output neuron of the striatum. Combined ultrastructural neuroanatomical methods have elucidated the organization of afferent connectivity to these neurons. The major physiologic function of striatal efferent activity appears to be inhibition of tonically active GABAergic neurons in the globus pallidus and substantia nigra pars reticulata. Thus, the excitatory input from the cerebral cortex, whose afferents make asymmetric synapses with the spines of medium spiny neurons, appears to drive the efferent activity of the striatum. Other extrinsic and intrinsic afferent synapses are situated in a position to regulate the effect of the corticostriatal excitatory input to the medium spiny neurons. For example, dopaminergic afferents from the midbrain make mainly symmetric synapses with the spine necks and dendritic shafts of the medium spiny neurons. Medium spiny neurons themselves have local axon collaterals, in addition to their efferent axon that exits the striatum, which serve to link together local clusters of medium spiny neurons. These local axon collaterals, which contain either GABA, substance P, or enkephalin, also make mainly symmetric synapses with the necks of spines or dendritic shafts of medium spiny neurons. Other afferents with similar synaptic connections to these neurons arise from cholinergic or somatostatinergic striatal intrisinic neurons. Additionally, the patterns of extrinsic and intrinsic afferents to medium spiny neurons and their extrinsic projections are related to the organization of medium spiny neurons into two mosaically organized macroscopic compartments, the striatal patches and matrix.
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  • 95
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    Journal of Electron Microscopy Technique 10 (1988), S. 293-313 
    ISSN: 0741-0581
    Keywords: Neurotransmitter release ; Synaptic receptors ; Dendrites ; Axons ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The mechanisms suspected as contributors to the regulation of synaptic strength act at a variety of sites along the causal chain that links activity in a presynaptic neuron to activity in a postsynaptic one. At several places in this chain, morphological factors are expected to have a powerful influence, and at several others, key insights into the mechanisms controlling synaptic action have been achieved using morphological techniques. A variety of presynaptic mechanisms controlling the release of neurotransmitter have been most directly shown to regulate the potency of synaptic connections. Traditional interpretations of the effect of postsynaptic geometry on synaptic strength need to be reevaluated in light of new views of the functional properties of dendritic membrane, and the new neurophysiological data must be incorporated into a more comprehensive view of the behavior of spatially distributed excitable membrane with specific patterns of distributed synaptic inputs.
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  • 96
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    Journal of Electron Microscopy Technique 8 (1988) 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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  • 97
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    Journal of Electron Microscopy Technique 8 (1988), S. 41-78 
    ISSN: 0741-0581
    Keywords: Viral diagnosis/detection ; Electron microscopy/light microscopy ; Antiviral therapy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The following communication is a tripartite synopsis of the role of viral infection in the acquired immunodeficiency syndrome (AIDS). The first section describes the impact of viral opportunistic infection in AIDS; for each virus, clinical presentation and diagnosis, laboratory diagnostic approaches (with emphasis on electron microscopy), and therapeutic interventions attempted to date are discussed. The second segment explores current theories on the pathogenesis of AIDS, and describes diagnostic and therapeutic approaches to the syndrome itself. The final section catalogues ultrastructural anomalies in the cells of AIDS patients, many of which have been mistakenly identified as etiologic agents.
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  • 98
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    Journal of Electron Microscopy Technique 8 (1988), S. 201-210 
    ISSN: 0741-0581
    Keywords: Modulation ; Interfaces ; Order ; Analytical electron microscopy ; Atom probe field-ion microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: A comparison of transmission electron microscopy (TEM) and atom probe field-ion microscopy (APFIM) is presented with respect to the interpretation of complex microstructures, phase identification, determination of crystallographic order, and analysis of interfaces. The capabilities, spatial resolutions, and limitations of each technique are discussed with examples taken from combined analytical electron microscopy (AEM) and APFIM studies. Both techniques are extremely powerful for routine characterization of a wide range of materials, although care must be exercised in experimentation and interpretation. The combined use of TEM and APFIM is synergistic and extends their individual capabilities from the macro scale to the atomic level.
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  • 99
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    Journal of Electron Microscopy Technique 8 (1988), S. 223-224 
    ISSN: 0741-0581
    Keywords: Simultaneous tissue processing ; Multi-unit container ; Labor-saving device ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: A simple device is described that aids the processing of large numbers of tissue blocks for light or electron microscopy. The device has a number of compartments into which different tissue blocks can be placed. Each compartment has a fine mesh floor, allowing the free exchange of the reagents used in tissue processing, and a gentle flow of the reagents is promoted by a magnetic stirring bar, or a rotary mixer. All the materials used are resistant to solvents such as propylene oxide. The device is labor-saving in that many blocks can be processed as easily as a single block. The device may also be of value in quantitative microscopy, since it ensures that all tissue blocks examined experience an identical processing history.
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    Journal of Electron Microscopy Technique 8 (1988), S. 227-228 
    ISSN: 0741-0581
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
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