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  • Abnormal mitochondria  (1)
  • Alzheimer's disease  (1)
  • Amphipathic α-helical peptide  (1)
  • 1
    ISSN: 0005-2736
    Keywords: Amphipathic α-helical peptide ; Circular dichroism ; Lipid-peptide interaction ; Liposome ; Tryptophan fluorescence ; α-Aminomyristic acid
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neurology 247 (2000), S. 633-635 
    ISSN: 1432-1459
    Keywords: Key words Amyloid β protein ; Amyotrophic lateral sclerosis ; Skin ; Alzheimer's disease ; Enzyme-linked immunosorbet assay
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Distinct vascular and periadnexal immunoreactivity have been observed for amyloid b protein (Aβ) in skin from patients with amyotrophic lateral sclerosis (ALS). We used an enzyme-linked immunosorbent assay to make a more quantitative comparison of Aβ concentrations between ALS patients and controls. The insoluble fractions of skin samples from ALS patients contained significantly higher Aβ concentrations per milligram protein than those from controls. Various alterations in extracellular matrix components have been reported to occur in the skin of patients with ALS, and several matrix constituents have been shown to affect processing and aggregation of Aβ in human brain. Taking these previous findings together with those of the present study, our observations suggest that changes in extracellular matrix in skin of ALS patients may facilitate aggregation and deposition of Aβ.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1459
    Keywords: Continuous muscle fibre activity ; Myokymia ; Axonal degeneration ; Abnormal mitochondria ; Filamentous body
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Histological and ultrastructural studies were performed on nerve and muscle biopsy specimens from two patients with the syndrome of continuous muscle fibre activity. The characteristics of muscle biopsies were as follows. By light microscopy, internal nuclei were present in many of the fibres. By electron microscopy many fibres contained filamentous bodies and subsarcolemmal aggregates of mitochondria embedded in the peripheral zone of cytoplasm, and occasional mitochondria with disorganized or branched cristae were larger than normal. Biopsies of sural nerves revealed a decreased number of myelinated fibres, clusters of small myelinated fibres, and evidence of active axonal degeneration such as disintegrated myelin segments and degenerated axon components, as well as loss of axonal contents. With the present biopsy findings, it is suggested that the pathological process of this syndrome affects peripheral nerves as well as muscles.
    Type of Medium: Electronic Resource
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