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pubmed-article:11295422pubmed:abstractText3-[(123)I]Iodo-L-alpha-methyl tyrosine ([(123)I]IMT) scintigraphy of extracranial malignant tumors has been described, but little is known about the transport systems involved in [(123)I]IMT uptake into extracranial tumor cells. Here, the precise kinetics of [(123)I]IMT transport into human Ewing's sarcoma cells (VH-64) was determined. The apparent Michaelis constant was of high affinity value (K(m)=41.7+/-3.9 microM) and maximum transport velocitiy amounted to V(max)=20.7+/-0.6 nmol x mg protein(-1) x 10 min(-1). Inhibition experiments revealed the predominance of [(123)I]IMT uptake via sodium-independent system L.lld:pubmed
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pubmed-article:11295422pubmed:authorpubmed-author:SchoberOOlld:pubmed
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pubmed-article:11295422pubmed:pagination123-8lld:pubmed
pubmed-article:11295422pubmed:dateRevised2011-11-17lld:pubmed
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pubmed-article:11295422pubmed:articleTitleCharacterization of 3-[123I]iodo-L-alpha-methyl tyrosine ([123I]IMT) transport into human Ewing's sarcoma cells in vitro.lld:pubmed
pubmed-article:11295422pubmed:affiliationDepartment of Nuclear Medicine, Westfälische Wilhelms-Universität, Münster, Albert-Schweitzer-Str. 33, 48149, Münster, Germany. franziu@uni-muenster.delld:pubmed
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