| pubmed-article:9120011 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0002092 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0032385 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0330312 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0021083 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C1824952 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0205369 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0486805 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0376315 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0205164 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0439836 | lld:lifeskim |
| pubmed-article:9120011 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:9120011 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:9120011 | pubmed:dateCreated | 1997-4-24 | lld:pubmed |
| pubmed-article:9120011 | pubmed:abstractText | A novel approach to reduce the anaphylactic activity of allergens is suggested. The strategy makes use of the presence of conformational immunoglobulin E (IgE) epitopes on one of the most common allergens. The three dimensional structure of the major birch pollen allergen, Bet v 1, was disrupted by expressing two parts of the Bet v 1 cDNA representing amino acids 1-74 and 75-160 in Escherichia coli. In contrast to the complete recombinant Bet v 1, the fragments showed almost no allergenicity and exhibited random coil conformation as analyzed by circular dichroism. Both nonanaphylactic fragments induced proliferation of human Bet v 1-specific T cell clones, indicating that they harbored all dominant T cell epitopes and therefore may be considered as a basis for the development of a safe and specific T cell immunotherapy. | lld:pubmed |
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| pubmed-article:9120011 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9120011 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9120011 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:9120011 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:9120011 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9120011 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:9120011 | pubmed:issn | 0021-9738 | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:KraftDD | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:PastoreAA | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:ValentPP | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:EbnerCC | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:ValentaRR | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:SperrW RWR | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:EichlerH GHG | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:VrtalaSS | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:VangelistaLL | lld:pubmed |
| pubmed-article:9120011 | pubmed:author | pubmed-author:HirtenlehnerK... | lld:pubmed |
| pubmed-article:9120011 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9120011 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:9120011 | pubmed:volume | 99 | lld:pubmed |
| pubmed-article:9120011 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9120011 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9120011 | pubmed:pagination | 1673-81 | lld:pubmed |
| pubmed-article:9120011 | pubmed:dateRevised | 2011-6-21 | lld:pubmed |
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