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Citation: F. Dolle et al., Highly efficient synthesis of [C-11]S12968 and [C-11]S12967, for the in vivo imaging of the cardiac calcium channels using PET, J LABEL C R, 44(7), 2001, pp. 481-499
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Citation: F. Dolle et al., Highly efficient synthesis of [C-11]Me-QNB, a selective radioligand for the quantification of the cardiac muscarinic receptors using PET, J LABEL C R, 44(5), 2001, pp. 337-345
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Citation: F. Dolle et al., Synthesis and preliminary evaluation of a carbon-11-labelled agonist of the alpha 7 nicotinic acetylcholine receptor, J LABEL C R, 44(11), 2001, pp. 785-795
Authors:
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Citation: T. Poyot et al., Anatomic and biochemical correlates of the dopamine transporter ligand C-11-PE2I in normal and parkinsonian primates: Comparison with 6-[F-18] Fluoro-L-Dopa, J CEREBR B, 21(7), 2001, pp. 782-792
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Citation: Mlp. Martinot et al., Decreased presynaptic dopamine function in the left caudate of depressed patients with affective flattening and psychomotor retardation, AM J PSYCHI, 158(2), 2001, pp. 314-316
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Citation: B. Kuhnast et al., General method to label antisense oligonucleotides with radioactive halogens for pharmacological and imaging studies, BIOCONJ CHE, 11(5), 2000, pp. 627-636
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Citation: O. Langer et al., High specific radioactivity (1R,2S)-4-[F-18]fluorometaraminol: A PET radiotracer for mapping sympathetic nerves of the heart, NUCL MED BI, 27(3), 2000, pp. 233-238
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Citation: B. Kuhnast et al., Fluorine-18 labeling of oligonucleotides bearing chemically-modified ribose-phosphate backbones, J LABEL C R, 43(8), 2000, pp. 837-848
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Citation: J. Sandell et al., Improved specific radioactivity of the PET radioligand [C-11]FLB 457 by use of the GE Medical Systems PETtrace MeI MicroLab, J LABEL C R, 43(4), 2000, pp. 331-338
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Citation: F. Dolle et al., Highly efficient synthesis of [C-11]PE2I, a selective radioligand for the quantification of the dopamine transporter using PET, J LABEL C R, 43(10), 2000, pp. 997-1004
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Citation: O. Langer et al., Carbon-11 epidepride: A suitable radioligand for PET investigation of striatal and extrastriatal dopamine D-2 receptors, NUCL MED BI, 26(5), 1999, pp. 509-518
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Citation: H. Valette et al., Preliminary evaluation of 2-[4-[3-(tert-butylamino)-2-hydroxypropoxy]phenyl]-3-methyl-6-methoxy-4(3H)-quinazolinone ([+/-]HX-CH 44) as a selective beta 1-adrenoceptor ligand for PET, NUCL MED BI, 26(1), 1999, pp. 105-109
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Dolle, F
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Citation: L. Dolci et al., Synthesis of a fluorine-18 labeled derivative of epibatidine for in vivo nicotinic acetylcholine receptor PET imaging, BIO MED CH, 7(3), 1999, pp. 467-479
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Citation: O. Langer et al., Precursor synthesis and radiolabelling of the dopamine D-2 receptor ligand[C-11]raclopride from [C-11]methyl triflate, J LABEL C R, 42(12), 1999, pp. 1183-1193
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Citation: L. Dolci et al., 2-[F-18]fluoropyridines by no-carrier-added nucleophilic aromatic substitution with [F-18]FK-K-222 - A comparative study, J LABEL C R, 42(10), 1999, pp. 975-985
Authors:
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Citation: H. Valette et al., Imaging central nicotinic acetylcholine receptors in baboons with [F-18]fluoro-A-85380, J NUCL MED, 40(8), 1999, pp. 1374-1380
Authors:
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Dolci, L
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Coulon, C
Bottlaender, M
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Citation: F. Dolle et al., Synthesis and nicotinic acetylcholine receptor in vivo binding properties of 2-fluoro-3-[2(S)-2-azetidinylmethoxy]pyridine: A new positron emission tomography ligand for nicotinic receptors, J MED CHEM, 42(12), 1999, pp. 2251-2259
Citation: D. Roeda et al., Unexpected perimidine formation in the ring opening of 1,2-dihydro-2-piperidinomethylperimidines with di-iso-butylaluminium hydride to 1-amino-8-(2-piperidinoethyl)aminonaphthalenes, NEW J CHEM, 22(11), 1998, pp. 1151-1154
Authors:
Valette, H
Bottlaender, M
Dolle, F
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Hinnen, F
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Citation: H. Valette et al., Characterization of the nicotinic ligand 2-[F-18]fluoro-3-[2(S)-2-azetidinylmethoxy]pyridine in vivo, LIFE SCI, 64(5), 1998, pp. PL93-PL97