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PubMed:19318519 JSONTXT 49 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-124 Sentence denotes Glycosylation profiles of epitope-specific anti-beta-amyloid antibodies revealed by liquid chromatography-mass spectrometry.
T1 0-124 Sentence denotes Glycosylation profiles of epitope-specific anti-beta-amyloid antibodies revealed by liquid chromatography-mass spectrometry.
T1 0-124 Sentence denotes Glycosylation profiles of epitope-specific anti-beta-amyloid antibodies revealed by liquid chromatography-mass spectrometry.
TextSentencer_T2 125-206 Sentence denotes Alzheimer's disease (AD) is the most prevalent form of age-related neurodementia.
T2 125-206 Sentence denotes Alzheimer's disease (AD) is the most prevalent form of age-related neurodementia.
T2 125-206 Sentence denotes Alzheimer's disease (AD) is the most prevalent form of age-related neurodementia.
TextSentencer_T3 207-315 Sentence denotes The accumulation of beta-amyloid polypeptide (Abeta) in brain is generally believed to be a key event in AD.
T3 207-315 Sentence denotes The accumulation of beta-amyloid polypeptide (Abeta) in brain is generally believed to be a key event in AD.
T3 207-315 Sentence denotes The accumulation of beta-amyloid polypeptide (Abeta) in brain is generally believed to be a key event in AD.
TextSentencer_T4 316-457 Sentence denotes The recent discovery of physiological beta-amyloid autoantibodies represents a promising perspective for treatment and early diagnosis of AD.
T4 316-457 Sentence denotes The recent discovery of physiological beta-amyloid autoantibodies represents a promising perspective for treatment and early diagnosis of AD.
T4 316-457 Sentence denotes The recent discovery of physiological beta-amyloid autoantibodies represents a promising perspective for treatment and early diagnosis of AD.
TextSentencer_T5 458-566 Sentence denotes The mechanisms by which natural beta-amyloid autoantibodies prevent neurodegeneration are currently unknown.
T5 458-566 Sentence denotes The mechanisms by which natural beta-amyloid autoantibodies prevent neurodegeneration are currently unknown.
T5 458-566 Sentence denotes The mechanisms by which natural beta-amyloid autoantibodies prevent neurodegeneration are currently unknown.
TextSentencer_T6 567-825 Sentence denotes The aim of the present study was to analyze the N-linked glycosylation of a plaque-specific, monoclonal antibody (clone 6E10) relevant for immunotherapy of AD, in comparison with the glycosylation pattern of an Abeta autoantibody isolated from an IgG source.
T6 567-825 Sentence denotes The aim of the present study was to analyze the N-linked glycosylation of a plaque-specific, monoclonal antibody (clone 6E10) relevant for immunotherapy of AD, in comparison with the glycosylation pattern of an Abeta autoantibody isolated from an IgG source.
T6 567-825 Sentence denotes The aim of the present study was to analyze the N-linked glycosylation of a plaque-specific, monoclonal antibody (clone 6E10) relevant for immunotherapy of AD, in comparison with the glycosylation pattern of an Abeta autoantibody isolated from an IgG source.
TextSentencer_T7 826-1019 Sentence denotes Liquid chromatography in combination with tandem mass spectrometry was used to analyze the glycopeptides generated by enzymatic degradation of the antibodies reduced and alkylated heavy chains.
T7 826-1019 Sentence denotes Liquid chromatography in combination with tandem mass spectrometry was used to analyze the glycopeptides generated by enzymatic degradation of the antibodies reduced and alkylated heavy chains.
T7 826-1019 Sentence denotes Liquid chromatography in combination with tandem mass spectrometry was used to analyze the glycopeptides generated by enzymatic degradation of the antibodies reduced and alkylated heavy chains.
TextSentencer_T8 1020-1230 Sentence denotes The oligosaccharide pattern of the 6E10 antibody shows primarily core-fucosylated biantennary complex structures and, to a low extent, tri- and tetragalactosyl glycoforms, with or without terminal sialic acids.
T8 1020-1230 Sentence denotes The oligosaccharide pattern of the 6E10 antibody shows primarily core-fucosylated biantennary complex structures and, to a low extent, tri- and tetragalactosyl glycoforms, with or without terminal sialic acids.
T8 1020-1230 Sentence denotes The oligosaccharide pattern of the 6E10 antibody shows primarily core-fucosylated biantennary complex structures and, to a low extent, tri- and tetragalactosyl glycoforms, with or without terminal sialic acids.
TextSentencer_T9 1231-1551 Sentence denotes The glycans associated with the serum anti-Abeta autoantibodies are of the complex, biantennary-type, fucosylated at the first N-acetyl glucosamine residue of the trimannosyl chitobiose core and contain zero to two galactose residues, and zero to one terminal sialic acid, with or without bisecting N-acetyl glucosamine.
T9 1231-1551 Sentence denotes The glycans associated with the serum anti-Abeta autoantibodies are of the complex, biantennary-type, fucosylated at the first N-acetyl glucosamine residue of the trimannosyl chitobiose core and contain zero to two galactose residues, and zero to one terminal sialic acid, with or without bisecting N-acetyl glucosamine.
T9 1231-1551 Sentence denotes The glycans associated with the serum anti-Abeta autoantibodies are of the complex, biantennary-type, fucosylated at the first N-acetyl glucosamine residue of the trimannosyl chitobiose core and contain zero to two galactose residues, and zero to one terminal sialic acid, with or without bisecting N-acetyl glucosamine.
TextSentencer_T10 1552-1722 Sentence denotes Glycosylation analysis of the Abeta-autoantibody performed at the peptide level revealed all four human IgG subclasses, with IgG(1) and IgG(2) as the dominant subclasses.
T10 1552-1722 Sentence denotes Glycosylation analysis of the Abeta-autoantibody performed at the peptide level revealed all four human IgG subclasses, with IgG(1) and IgG(2) as the dominant subclasses.
T10 1552-1722 Sentence denotes Glycosylation analysis of the Abeta-autoantibody performed at the peptide level revealed all four human IgG subclasses, with IgG(1) and IgG(2) as the dominant subclasses.