| pubmed-article:1693434 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1693434 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:1693434 | lifeskim:mentions | umls-concept:C0034802 | lld:lifeskim |
| pubmed-article:1693434 | lifeskim:mentions | umls-concept:C0017636 | lld:lifeskim |
| pubmed-article:1693434 | lifeskim:mentions | umls-concept:C0003241 | lld:lifeskim |
| pubmed-article:1693434 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
| pubmed-article:1693434 | lifeskim:mentions | umls-concept:C0332466 | lld:lifeskim |
| pubmed-article:1693434 | lifeskim:mentions | umls-concept:C0205144 | lld:lifeskim |
| pubmed-article:1693434 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:1693434 | pubmed:dateCreated | 1990-7-12 | lld:pubmed |
| pubmed-article:1693434 | pubmed:abstractText | We have investigated human gliomas that amplify and rearrange the epidermal growth factor receptor gene, with generation of an in-frame deletion mutation of 802 nucleotides in the external domain. This in-frame deletion mutation generates a local amino acid sequence at the fusion junction of what normally were distant polypeptide sequences in the intact epidermal growth factor receptor. This 14-amino acid peptide was chemically synthesized, coupled to keyhole limpet hemocyanin, and used as an immunogen in rabbits. The elicited antibody reacted specifically with the fusion peptide in ELISA. The anti-fusion junction peptide antibody was purified by passage of the antiserum over a peptide affinity column with acidic elution. The purified antibody selectively bound the glioma deletion mutant as compared to the intact epidermal growth factor receptor as assessed by immunocytochemistry, immunofluorescence, immunoprecipitation with gel electrophoresis, and binding experiments using radioiodinated antibody. These data indicate that it is feasible to generate site-specific anti-peptide antibodies that are highly selective for mutant proteins in human tumors. The anti-peptide antibody described here, and other mutation site-specific antibodies, should be ideal candidates for tumor immunoimaging and immunotherapy. | lld:pubmed |
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| pubmed-article:1693434 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:1693434 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:1693434 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1693434 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:1693434 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:FriedmanH SHS | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:VogelsteinBB | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:BignerD DDD | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:ZalutskyM RMR | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:HumphreyP APA | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:FullerG NGN | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:KwatraM MMM | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:BignerS HSH | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:WongA JAJ | lld:pubmed |
| pubmed-article:1693434 | pubmed:author | pubmed-author:ArcherG EGE | lld:pubmed |
| pubmed-article:1693434 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1693434 | pubmed:volume | 87 | lld:pubmed |
| pubmed-article:1693434 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1693434 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1693434 | pubmed:pagination | 4207-11 | lld:pubmed |
| pubmed-article:1693434 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:1693434 | pubmed:year | 1990 | lld:pubmed |
| pubmed-article:1693434 | pubmed:articleTitle | Anti-synthetic peptide antibody reacting at the fusion junction of deletion-mutant epidermal growth factor receptors in human glioblastoma. | lld:pubmed |
| pubmed-article:1693434 | pubmed:affiliation | Department of Pathology, Duke University Medical Center, Durham, NC 27710. | lld:pubmed |
| pubmed-article:1693434 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1693434 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:1693434 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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