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PubMed:12087473 JSONTXT 7 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-86 Sentence denotes Serological identification and expression analysis of gastric cancer-associated genes.
T1 0-86 Sentence denotes Serological identification and expression analysis of gastric cancer-associated genes.
TextSentencer_T2 87-381 Sentence denotes Serological identification of tumour antigens by recombinant expression cloning has proved to be an effective strategy for the identification of cancer-associated genes having a relevance to cancer aetiology and progression, and for defining possible targets for immunotherapeutic intervention.
T2 87-381 Sentence denotes Serological identification of tumour antigens by recombinant expression cloning has proved to be an effective strategy for the identification of cancer-associated genes having a relevance to cancer aetiology and progression, and for defining possible targets for immunotherapeutic intervention.
TextSentencer_T3 382-547 Sentence denotes In the present study we applied this technique to identify immunogenic proteins for gastric cancer that resulted in isolation of 14 distinct serum-reactive antigens.
T3 382-547 Sentence denotes In the present study we applied this technique to identify immunogenic proteins for gastric cancer that resulted in isolation of 14 distinct serum-reactive antigens.
TextSentencer_T4 548-894 Sentence denotes In order to evaluate their role in tumourigenesis and assess the immunogenicity of the identified antigens, we characterised each cDNA clone by DNA sequence analysis, mRNA tissue distribution, comparison of mRNA levels in cancerous and adjacent non-cancerous tissues and the frequency of antibody responses in allogeneic patient and control sera.
T4 548-894 Sentence denotes In order to evaluate their role in tumourigenesis and assess the immunogenicity of the identified antigens, we characterised each cDNA clone by DNA sequence analysis, mRNA tissue distribution, comparison of mRNA levels in cancerous and adjacent non-cancerous tissues and the frequency of antibody responses in allogeneic patient and control sera.
TextSentencer_T5 895-988 Sentence denotes Previously unknown splice variants of TACC1 and an uncharacterised gene Ga50 were identified.
T5 895-988 Sentence denotes Previously unknown splice variants of TACC1 and an uncharacterised gene Ga50 were identified.
TextSentencer_T6 989-1090 Sentence denotes The expression of a newly identified TACC1 isoform is restricted to brain and gastric cancer tissues.
T6 989-1090 Sentence denotes The expression of a newly identified TACC1 isoform is restricted to brain and gastric cancer tissues.
TextSentencer_T7 1091-1359 Sentence denotes Comparison of mRNA levels by semi-quantitative RT-PCR revealed a relative overexpression of three genes in cancer tissues, including growth factor granulin and Tbdn-1--an orthologue of the mouse acetyltransferase gene which is associated with blood vessel development.
T7 1091-1359 Sentence denotes Comparison of mRNA levels by semi-quantitative RT-PCR revealed a relative overexpression of three genes in cancer tissues, including growth factor granulin and Tbdn-1--an orthologue of the mouse acetyltransferase gene which is associated with blood vessel development.
TextSentencer_T8 1360-1563 Sentence denotes An unusual DNA polymorphism--a three-nucleotide deletion was found in NUCB2 cDNA but its mRNA level was consistently decreased in gastric tumours compared with that in the adjacent non-cancerous tissues.
T8 1360-1563 Sentence denotes An unusual DNA polymorphism--a three-nucleotide deletion was found in NUCB2 cDNA but its mRNA level was consistently decreased in gastric tumours compared with that in the adjacent non-cancerous tissues.
TextSentencer_T9 1564-1769 Sentence denotes This study has revealed several new gastric cancer candidate genes; additional studies are required to gain a deeper insight into their role in the tumorigenesis and their potential as therapeutic targets.
T9 1564-1769 Sentence denotes This study has revealed several new gastric cancer candidate genes; additional studies are required to gain a deeper insight into their role in the tumorigenesis and their potential as therapeutic targets.