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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 68 (1985), S. 311-318 
    ISSN: 1432-0533
    Keywords: Cytoplasmic filaments ; Neurons ; Progressive supranuclear palsy ; Neurofibrillary tangles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In contrast to the ultrastructure of Alzheimer's neurofibrillary tangles (NFT), which has been well characterized as accumulations of paired helical 10-nm filaments (PHF) with 80-nm regular constrictions, the morphology of the neurofibrillary changes of PSP remains ill-defined. Until recently, the fine structure of PSP tangles was generally accepted as 15-nm straight filaments or tubules, although many reports describing different electron-microscopic findings have appeared in the literature. In this report, we present morphological data indicating a protofilamentous substructure present in straight filaments of PSP which has some points of similarity with the protofilamentous architectures which have been reported for paired helical filaments of Alzheimer's disease. The straight filaments were found to be composed of six or more helically symmetric 2–5-nm protofilaments. We conclude that despite the varied morphology of filaments in neurofibrillary tangles observed in PSP there may be some underlying identity at the molecular level with the PHF of neurofibrillary tangles of Alzheimer's disease.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 26 (1973), S. 237-246 
    ISSN: 1432-0533
    Keywords: Familial Amyotrophic Lateral Sclerosis ; Neurofibrillary Degeneration ; Cytoplasmie Inclusions ; Cerebral Cortex ; Amygdala
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In familial amyotrophic lateral sclerosis associated with dementia there was symmetrical involvement of the amygdala, insula, and fronto-temporal cortex. The cortical lesions were most severe in the superior frontal gyri and the infero-lateral temporal lobes, while the adjacent cingulate gyri and hippocampi were spared. One patient with dementia and another with slight mental abnormality had cerebral lesions which varied in extent, but were of the same type and pattern. Although the clinical and histological findings are variable, the disease seems to be a distinct entity, closely allied to amyotrophic lateral sclerosis, but also having features in common with Guamanian amyotrophic lateral sclerosis, and amyotrophic lateral sclerosis-dementia complex of sporadic occurrence.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics, Section A 322 (1979), S. 445-460 
    ISSN: 0375-9474
    Keywords: Pionic atoms
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Brain and Cognition 8 (1988), S. 348-378 
    ISSN: 0278-2626
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine , Psychology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Applied microbiology and biotechnology 54 (2000), S. 390-396 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract We have described a procedure for the isolation of mutants of Tetrahymena thermophila with hyperscretion of phospholipase A1 (PLA1). Using random chemical mutagenesis, uniparental cytogamy, genetic crossing and a new, fast and effective screening procedure, four PLA1-hypersecretory mutants were isolated. The screening procedure is based on the formation of a halo appearing around cylindrical holes in a lecithin-containing agar plate filled with cell-free supernatants. About 3,940 clones were tested with this procedure in primary screening for hypersecretory features, of which 60 putative hypersecretory mutants were isolated, subcloned and tested in a secondary screening. Of these, four selected mutants showed 1.8–2.2 more PLA1 activity in the cell-free supernatants compared to the wild-type strain CU 438.1. Hypersecretion was only observable for PLA1; no increased activity for two other lysosomal enzymes could be detected. These hypersecretory mutants of T. thermophila can be very useful for increasing the yield of PLA1 in fermentation processes. This is particularly relevant because, in contrast to other phospholipases, PLA1 is not available on the commercial market for fine chemicals and little is known about the role of PLA1 in cell signaling and metabolism.
    Type of Medium: Electronic Resource
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