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Positron emission tomography (PET) imaging of neuroblastoma and melanoma with 64 Cu-SarAr immunoconjugates

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dc.contributor.authorVoss, Stephan D
dc.contributor.authorSmith, Suzanne
dc.contributor.authorDiBartolo, Nadine
dc.contributor.authorMcIntosh, Lacey J
dc.contributor.authorCyr, Erika M
dc.contributor.authorBonab, Ali A
dc.contributor.authorDearling, Jason L J
dc.contributor.authorCarter, Edward A
dc.contributor.authorFischman, Alan J
dc.contributor.authorTreves, S Ted
dc.contributor.authorGillies, Stephen D
dc.contributor.authorSargeson, Alan
dc.contributor.authorHuston, James S
dc.contributor.authorPackard, Alan B
dc.date.accessioned2015-12-10T21:54:18Z
dc.date.issued2007
dc.date.updated2015-12-09T07:25:15Z
dc.description.abstractThe advancement of positron emission tomography (PET) depends on the development of new radiotracers that will complement 18F-FDG. Copper-64 (64Cu) is a promising PET radionuclide, particularly for antibody-targeted imaging, but the high in vivo lability
dc.identifier.issn0027-8424
dc.identifier.urihttp://hdl.handle.net/1885/38882
dc.publisherNational Academy of Sciences (USA)
dc.sourcePNAS - Proceedings of the National Academy of Sciences of the United States of America
dc.subjectKeywords: 1 n (4 aminobenzyl) 3,6,10,13,16,19 hexaazabicyclo[6 6 6]eicosane 1,8 diamine; antibody conjugate; chelating agent; copper 64; ganglioside GD2; radiopharmaceutical agent; unclassified drug; animal experiment; animal model; article; controlled study; human
dc.titlePositron emission tomography (PET) imaging of neuroblastoma and melanoma with 64 Cu-SarAr immunoconjugates
dc.typeJournal article
local.bibliographicCitation.issue44
local.bibliographicCitation.lastpage17493
local.bibliographicCitation.startpage17489
local.contributor.affiliationVoss, Stephan D, Children's Hospital Boston, Harvard Medical School
local.contributor.affiliationSmith, Suzanne, Australian Nuclear Science and Technology Organisation
local.contributor.affiliationDiBartolo, Nadine, Australian Nuclear Science and Technology Organisation
local.contributor.affiliationMcIntosh, Lacey J, Massachusetts General Hospital, Harvard Medical School
local.contributor.affiliationCyr, Erika M, Massachusetts General Hospital, Harvard Medical School
local.contributor.affiliationBonab, Ali A, Massachusetts General Hospital, Harvard Medical School
local.contributor.affiliationDearling, Jason L J, Children's Hospital Boston, Harvard Medical School
local.contributor.affiliationCarter, Edward A, Massachusetts General Hospital, Harvard Medical School
local.contributor.affiliationFischman, Alan J, Massachusetts General Hospital, Harvard Medical School
local.contributor.affiliationTreves, S Ted, Children's Hospital Boston, Harvard Medical School
local.contributor.affiliationGillies, Stephen D, EMD Lexigen
local.contributor.affiliationSargeson, Alan, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHuston, James S, EMD Lexigen
local.contributor.affiliationPackard, Alan B, Children's Hospital Boston, Harvard Medical School
local.contributor.authoruidSargeson, Alan, u5800192
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030201 - Bioinorganic Chemistry
local.identifier.ariespublicationu4005981xPUB168
local.identifier.citationvolume104
local.identifier.doi10.1073/pnas.0708436104
local.identifier.scopusID2-s2.0-36849027525
local.type.statusPublished Version

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