36 research outputs found

    Saint or Sinner?: A Reconsideration of the Career of Prince Alexandre de Merode, Chair of the International Olympic Committeeā€™s Medical Commission, 1967-2002

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    This article explores the role of Prince Alexandre de Merode in heading the IOCā€™s fight against drugs from the 1960s to 2002. History has not served de Merode very well. He has been presented in simplistic ways that emerge from context rather than evidence ā€“ as either a saint or a sinner. IOC-sanctioned accounts cast him in the mould of the saint: a moral and intelligent man who saved sports from doping. In contrast, sports academics have tended to portray him as a sinner: an ineffectual leader who did not develop either the testing systems or the punishments required to prevent doping and who deliberately concealed evidence of high-profile doping cases. This article assesses both representations before presenting information to support a richer and more complicated interpretation

    Genome sequences of four cluster P mycobacteriophages

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    Four bacteriophages infecting Mycobacterium smegmatis mc2155 (three belonging to subcluster P1 and one belonging to subcluster P2) were isolated from soil and sequenced. All four phages are similar in the left arm of their genomes, but the P2 phage differs in the right arm. All four genomes contain features of temperate phages

    Accumulation of intraneuronal AĪ² correlates with ApoE4 genotype

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    In contrast to extracellular plaque and intracellular tangle pathology, the presence and relevance of intraneuronal AĪ² in Alzheimerā€™s disease (AD) is still a matter of debate. Human brain tissue offers technical challenges such as post-mortem delay and uneven or prolonged tissue fixation that might affect immunohistochemical staining. In addition, previous studies on intracellular AĪ² accumulation in human brain often used antibodies targeting the C-terminus of AĪ² and differed strongly in the pretreatments used. To overcome these inconsistencies, we performed extensive parametrical testing using a highly specific N-terminal AĪ² antibody detecting the aspartate at position 1, before developing an optimal staining protocol for intraneuronal AĪ² detection in paraffin-embedded sections from AD patients. To rule out that this antibody also detects the Ī²-cleaved APP C-terminal fragment (Ī²-CTF, C99) bearing the same epitope, paraffin-sections of transgenic mice overexpressing the C99-fragment were stained without any evidence for cross-reactivity in our staining protocol. The staining intensity of intraneuronal AĪ² in cortex and hippocampal tissue of 10 controls and 20 sporadic AD cases was then correlated to patient data including sex, Braak stage, plaque load, and apolipoprotein E (ApoE) genotype. In particular, the presence of one or two ApoE4 alleles strongly correlated with an increased accumulation of intraneuronal AĪ² peptides. Given that ApoE4 is a major genetic risk factor for AD and is involved in neuronal cholesterol transport, it is tempting to speculate that perturbed intracellular trafficking is involved in the increased intraneuronal AĪ² aggregation in AD

    A factorial analysis of verbal learning tasks.

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