Titlebook: Biological Markers of Alzheimer’s Disease; François Boller,Robert Katzman,Yves Christen Conference proceedings 1989 Springer-Verlag Berlin

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Tau 64 and Tau 69: Two Early Biochemical Markers of Neurofibrillary Degeneration,, called tau 64 and tau 69, were also found in a biopsy, suggesting that they may be early markers of neurofibrillary degeneration. Tau 64 and tau 69 have a high MW due to their abnormal phosphorylation, as shown by the alkaline phosphatase treatment which provoked a decrease in their MW..A parallel

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A cDNA Encodes Epitopes Shared Between Microtubule-Associated Protein MAP2 and Alzheimer Neurofibrin of MAP2 immunoreactivity in neurofibrillary tangles is not directly related to an overex-pression of this protein. This also strengthens the hypothesis implicating post-translational modifications of cytoskeletal proteins as mechanisms of neurofibrillary tangles formation.

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Relationship Between Tau, Paired Helical Filaments, Amyloid and the Intellectual Deterioration in t. The three methods revealed a systematically different number of changes. The pathological changes best linked to dementia were those in NFT revealed by tau antiserum. A higher proportion of amyloid-rich plaques was noted in the least affected cases, suggesting that tau and PHF epitopes appeared se

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,Molecular Insights into Alzheimer’s Disease, micellar phases. Similar transformations in vivo could induce the formation of vesicles (micellar) and the fusion of membranes (hexagonal II) with important biological consequences. Computer modeling studies demonstrate the PME to have striking conformational similarities with the neurotransmitters

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,Altered Protein Kinase and Amyloid ß-Protein Precursor in Alzheimer’s Disease: Which Comes First?,important for growth factor-mediated cell maintenance is the battery of protein kinases, in particular, PKC. PKC mediates many functions of nerve growth factor, the best-characterized neurotrophic factor. Both the kinases, including PKC, and the phosphorylation levels are altered in AD brains, where

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,Cerebrospinal Fluid-Based Laboratory Test for Alzheimer’s Disease,ntigens in cerebrospinal fluid (CSF) of patients with Alzheimer’s disease (AD) and non-AD controls. Our results showed higher levels of PHF antigens in CSF of AD patients than in CSF of non-AD controls. Although the range of values overlaps with those of non-AD controls, the higher values of PHF ant

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