| pubmed-article:15136641 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15136641 | lifeskim:mentions | umls-concept:C0025664 | lld:lifeskim |
| pubmed-article:15136641 | lifeskim:mentions | umls-concept:C0028833 | lld:lifeskim |
| pubmed-article:15136641 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
| pubmed-article:15136641 | lifeskim:mentions | umls-concept:C0052350 | lld:lifeskim |
| pubmed-article:15136641 | lifeskim:mentions | umls-concept:C0243071 | lld:lifeskim |
| pubmed-article:15136641 | lifeskim:mentions | umls-concept:C2699006 | lld:lifeskim |
| pubmed-article:15136641 | lifeskim:mentions | umls-concept:C0205547 | lld:lifeskim |
| pubmed-article:15136641 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:15136641 | pubmed:dateCreated | 2004-5-11 | lld:pubmed |
| pubmed-article:15136641 | pubmed:abstractText | Routine application of (18)F-labeled peptides for quantitative in vivo receptor imaging of receptor-expressing tissues and quantification of receptor status using PET is limited by the lack of appropriate radiofluorination methods for routine large-scale synthesis of (18)F-labeled peptides. To satisfy this demand, a new (18)F-labeling methodology based on the chemoselective oxime formation between an unprotected aminooxy-functionalized peptide and an (18)F-labeled aldehyde or ketone was investigated and optimized with respect to peptide conjugation. | lld:pubmed |
| pubmed-article:15136641 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15136641 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15136641 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15136641 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:15136641 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15136641 | pubmed:month | May | lld:pubmed |
| pubmed-article:15136641 | pubmed:issn | 0161-5505 | lld:pubmed |
| pubmed-article:15136641 | pubmed:author | pubmed-author:KesslerHorstH | lld:pubmed |
| pubmed-article:15136641 | pubmed:author | pubmed-author:SchwaigerMark... | lld:pubmed |
| pubmed-article:15136641 | pubmed:author | pubmed-author:WesterHans-Jü... | lld:pubmed |
| pubmed-article:15136641 | pubmed:author | pubmed-author:SchotteliusMa... | lld:pubmed |
| pubmed-article:15136641 | pubmed:author | pubmed-author:HenriksenGjer... | lld:pubmed |
| pubmed-article:15136641 | pubmed:author | pubmed-author:HerzMichaelM | lld:pubmed |
| pubmed-article:15136641 | pubmed:author | pubmed-author:ThumshirnGeor... | lld:pubmed |
| pubmed-article:15136641 | pubmed:author | pubmed-author:HerselUlrichU | lld:pubmed |
| pubmed-article:15136641 | pubmed:author | pubmed-author:PoethkoThorst... | lld:pubmed |
| pubmed-article:15136641 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15136641 | pubmed:volume | 45 | lld:pubmed |
| pubmed-article:15136641 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15136641 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15136641 | pubmed:pagination | 892-902 | lld:pubmed |
| pubmed-article:15136641 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:15136641 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15136641 | pubmed:articleTitle | Two-step methodology for high-yield routine radiohalogenation of peptides: (18)F-labeled RGD and octreotide analogs. | lld:pubmed |
| pubmed-article:15136641 | pubmed:affiliation | Nuklearmedizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München, München, Germany. | lld:pubmed |
| pubmed-article:15136641 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15136641 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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