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2-, 3- and 4-[18F]Fluoropyridine by no-carrier-added nucleophilic aromatic substitution with K[18F]F-K222 - a comparative study

Journal of labelled compounds & radiopharmaceuticals, 2003-09, Vol.46 (10), p.979-992

2003

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2‐, 3‐ and 4‐[ 18 F]Fluoropyridine by no‐carrier‐added nucleophilic aromatic substitution with K[ 18 F]F‐K 222 – a comparative study

Journal of labelled compounds & radiopharmaceuticals, 2003-09, Vol.46 (10), p.979-992

2003

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General Method to Label Antisense Oligonucleotides with Radioactive Halogens for Pharmacological and Imaging Studies

Bioconjugate chemistry, 2000-09, Vol.11 (5), p.627-636

2000

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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

Journal of medicinal chemistry, 1999-06, Vol.42 (12), p.2251-2259

1999

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Early N-Acetylaspartate Depletion Is a Marker of Neuronal Dysfunction in Rats and Primates Chronically Treated with the Mitochondrial Toxin 3-Nitropropionic Acid

Journal of cerebral blood flow and metabolism, 2000-05, Vol.20 (5), p.789-799

2000

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Synthesis of [11C]atipamezole, a potential PET ligand for the α2-adrenergic receptor in the brain

Journal of labelled compounds & radiopharmaceuticals, 2002-01, Vol.45 (1), p.37-47

2002

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Synthesis of a [6-pyridinyl-18F]-labelled fluoro derivative of WAY-100635 as a candidate radioligand for brain 5-HT1A receptor imaging with PET

Bioorganic & medicinal chemistry, 2003-07, Vol.11 (13), p.2769-2782

2003

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Synthesis of a fluorine-18 labeled derivative of epibatidine for in vivo nicotinic acetylcholine receptor PET imaging

Bioorganic & medicinal chemistry, 1999-03, Vol.7 (3), p.467-479

1999

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In vivo Quantification of Localized Neuronal Activation and Inhibition in the Rat Brain Using a Dedicated High Temporal-Resolution β+-Sensitive Microprobe

Proceedings of the National Academy of Sciences - PNAS, 2002-08, Vol.99 (16), p.10807-10812

2002

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Up‐regulation of glutamate concentration in the putamen and in the prefrontal cortex of asymptomatic SIVmac251‐infected macaques without major brain involvement

Journal of neurochemistry, 2004-02, Vol.88 (4), p.928-938

2004

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Semiselective POCE NMR spectroscopy

Magnetic resonance in medicine, 2000-09, Vol.44 (3), p.395-400

2000

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Precursor synthesis and radiolabelling of the dopamine D2 receptor ligand [11C]raclopride from [11C]methyl triflate

Journal of labelled compounds & radiopharmaceuticals, 1999-12, Vol.42 (12), p.1183-1193

1999

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Synthesis of high-specific-radioactivity 4- and 6-[ 18F]fluorometaraminol- PET tracers for the adrenergic nervous system of the heart

Bioorganic & medicinal chemistry, 2001-03, Vol.9 (3), p.677-694

2001

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Synthesis of a fluorine-18-labelled derivative of 6-nitroquipazine, as a radioligand for the in vivo serotonin transporter imaging with PET

Bioorganic & medicinal chemistry, 2002-08, Vol.10 (8), p.2611-2623

2002

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Frequency-shift based detection of BMS contrast agents using SSFP: potential for MRA

Magnetic resonance imaging, 2005-04, Vol.23 (3), p.453-462

2005

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BIOCONVERSION OF MONENSIN BY A SOIL BACTERIUM, SEBEKIA BENIHANA

The Journal of Antibiotics, 1990/09/25, Vol.43(9), pp.1189-1191

1990

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Precursor synthesis and radiolabelling of the dopamine D 2 receptor ligand [ 11 C]raclopride from [ 11 C]methyl triflate

Journal of labelled compounds & radiopharmaceuticals, 1999, Vol.42 (12), p.1183

1999

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Fluorine-18 labeling of oligonucleotides bearing chemically-modified ribose-phosphate backbones

Journal of labelled compounds & radiopharmaceuticals, 2000-07, Vol.43 (8), p.837-848

2000

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6-[18F]Fluoro-L-DOPA by radiofluorodestannylation: a short and simple synthesis of a new labelling precursor

Journal of labelled compounds & radiopharmaceuticals, 1998-02, Vol.41 (2), p.105-114

1998

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Improved specific radioactivity of the PET radioligand [11C]FLB 457 by use of the GE medical systems PETtrace MeI microlab

Journal of labelled compounds & radiopharmaceuticals, 2000-03, Vol.43 (4), p.331-338

2000

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Synthesis of 2-[18F]fluoro-3-[2(S)-2-azetidinylmethoxy]pyridine, a highly potent radioligand for in vivo imaging central nicotinic acetylcholine receptors

Journal of labelled compounds & radiopharmaceuticals, 1998-05, Vol.41 (5), p.451-463

1998

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Decreased TCA cycle rate in the rat brain after acute 3-NP treatment measured by in vivo super(1)H-{ super(13)C} NMR spectroscopy

Journal of neurochemistry, 2002-08, Vol.82 (4), p.857-866

2002

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Synthesis and preliminary evaluation of a carbon‐11‐labelled agonist of the α 7 nicotinic acetylcholine receptor

Journal of labelled compounds & radiopharmaceuticals, 2001-10, Vol.44 (11), p.785-795

2001

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Synthesis of a [6- Pyridinyl - 18 F]-labelled fluoro derivative of WAY-100635 as a candidate radioligand for brain 5-HT 1A receptor imaging with PET

Bioorganic & medicinal chemistry, 2003-07, Vol.11 (13), p.2769-2782

2003

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Magnetization transfer characteristics in atherosclerotic plaque components assessed by adapted binomial preparation pulses

Magma (New York, N.Y.), 1998-11, Vol.7 (1), p.9-15

1998

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2-, 3- and 4-[18F]Fluoropyridine by no-carrier-added nucleophilic aromatic substitution with K[18F]F-K222 - a comparative study

2‐, 3‐ and 4‐[ 18 F]Fluoropyridine by no‐carrier‐added nucleophilic aromatic substitution with K[ 18 F]F‐K 222 – a comparative study

General Method to Label Antisense Oligonucleotides with Radioactive Halogens for Pharmacological and Imaging Studies

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

Early N-Acetylaspartate Depletion Is a Marker of Neuronal Dysfunction in Rats and Primates Chronically Treated with the Mitochondrial Toxin 3-Nitropropionic Acid

Synthesis of [11C]atipamezole, a potential PET ligand for the α2-adrenergic receptor in the brain

Synthesis of a [6-pyridinyl-18F]-labelled fluoro derivative of WAY-100635 as a candidate radioligand for brain 5-HT1A receptor imaging with PET

Synthesis of a fluorine-18 labeled derivative of epibatidine for in vivo nicotinic acetylcholine receptor PET imaging

In vivo Quantification of Localized Neuronal Activation and Inhibition in the Rat Brain Using a Dedicated High Temporal-Resolution β+-Sensitive Microprobe

Up‐regulation of glutamate concentration in the putamen and in the prefrontal cortex of asymptomatic SIVmac251‐infected macaques without major brain involvement

Semiselective POCE NMR spectroscopy

Precursor synthesis and radiolabelling of the dopamine D2 receptor ligand [11C]raclopride from [11C]methyl triflate

Synthesis of high-specific-radioactivity 4- and 6-[ 18F]fluorometaraminol- PET tracers for the adrenergic nervous system of the heart

Synthesis of a fluorine-18-labelled derivative of 6-nitroquipazine, as a radioligand for the in vivo serotonin transporter imaging with PET

Frequency-shift based detection of BMS contrast agents using SSFP: potential for MRA

BIOCONVERSION OF MONENSIN BY A SOIL BACTERIUM, SEBEKIA BENIHANA

Precursor synthesis and radiolabelling of the dopamine D 2 receptor ligand [ 11 C]raclopride from [ 11 C]methyl triflate

Fluorine-18 labeling of oligonucleotides bearing chemically-modified ribose-phosphate backbones

6-[18F]Fluoro-L-DOPA by radiofluorodestannylation: a short and simple synthesis of a new labelling precursor

Improved specific radioactivity of the PET radioligand [11C]FLB 457 by use of the GE medical systems PETtrace MeI microlab

Synthesis of 2-[18F]fluoro-3-[2(S)-2-azetidinylmethoxy]pyridine, a highly potent radioligand for in vivo imaging central nicotinic acetylcholine receptors

Decreased TCA cycle rate in the rat brain after acute 3-NP treatment measured by in vivo super(1)H-{ super(13)C} NMR spectroscopy

Synthesis and preliminary evaluation of a carbon‐11‐labelled agonist of the α 7 nicotinic acetylcholine receptor

Synthesis of a [6- Pyridinyl - 18 F]-labelled fluoro derivative of WAY-100635 as a candidate radioligand for brain 5-HT 1A receptor imaging with PET

Magnetization transfer characteristics in atherosclerotic plaque components assessed by adapted binomial preparation pulses

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