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Shining dead bone-cause for cautious interpretation of [18F]NaF PET scans

Acta orthopaedica, 2018-02, Vol.89 (1), p.124-127

2018

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Development of rapid multistep carbon-11 radiosynthesis of the myeloperoxidase inhibitor AZD3241 to assess brain exposure by PET microdosing

Nuclear medicine and biology, 2015-06, Vol.42 (6), p.555-560

2015

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Discovery and Preclinical Validation of [11C]AZ13153556, a Novel Probe for the Histamine Type 3 Receptor

ACS chemical neuroscience, 2016-02, Vol.7 (2), p.177-184

2016

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Preclinical Comparison of Osimertinib with Other EGFR-TKIs in EGFR-Mutant NSCLC Brain Metastases Models, and Early Evidence of Clinical Brain Metastases Activity

Clinical cancer research, 2016-10, Vol.22 (20), p.5130-5140

2016

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Lidar Measurements Supporting the Ocular Hazard Distance Calculation Using Atmospheric Attenuation

EPJ Web of Conferences, 2016, Vol.119, p.17008

2016

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[U-14C]- and [13C6]-1,3-dibromobenzene; useful precursors with a rare substitution pattern in the synthesis of isotopologs

Journal of labelled compounds & radiopharmaceuticals, 2011-06, Vol.54 (8), p.408-410

Malmquist, Jonas

2011

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First Radiolabeling of a Ganglioside with a Positron Emitting Radionuclide: In Vivo PET Demonstrates Low Exposure of Radiofluorinated GM1 in Non-human Primate Brain

ACS chemical neuroscience, 2020-05, Vol.11 (9), p.1245-1249

2020

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Multiple labeling of a potent CX 3 CR1 antagonist for the treatment of multiple sclerosis

Journal of labelled compounds & radiopharmaceuticals, 2012-08, Vol.55 (10), p.387-392

2012

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Development of [Carbonyl-11C]AZ13198083, a Novel Histamine Type‑3 Receptor Radioligand with Favorable Kinetics

ACS chemical neuroscience, 2018-05, Vol.9 (5), p.906-911

2018

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Imaging agent of a TRPA1 inhibitor

Journal of labelled compounds & radiopharmaceuticals, 2013-07, Vol.56 (9-10), p.536-537

2013

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Chemistry and biology of some low molecular weight boron compounds for boron neutron capture therapy

Journal of neuro-oncology, 1997-05, Vol.33 (1-2), p.41-52

1997

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Multiple labeling of a potent CX3CR1 antagonist for the treatment of multiple sclerosis

Journal of labelled compounds & radiopharmaceuticals, 2012-08, Vol.55 (10), p.387-392

2012

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Effect of solvents on the time-dependent inhibition of CYP3A4 and the biotransformation of AZD3839 in human liver microsomes and hepatocytes

Drug metabolism and disposition, 2013-01, Vol.41 (1), p.159-169

2013

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Discovery of a Novel Muscarinic Receptor PET Radioligand with Rapid Kinetics in the Monkey Brain

ACS chemical neuroscience, 2018-02, Vol.9 (2), p.224-229

2018

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Biotransformation of two β-secretase inhibitors including ring opening and contraction of a pyrimidine ring

Drug metabolism and disposition, 2013-05, Vol.41 (5), p.1134-1147

2013

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[5-14C]-methyltriazolepyridines via facile preparation of methyl-[ C]-isothiocyanate

Journal of labelled compounds & radiopharmaceuticals, 2008, Vol.51 (13-14), p.419-421

2008

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Synthesis of .omega.-(aminoalkyl)-1,2-closo-dicarbadodecaboranes(12)

Inorganic chemistry, 1992-06, Vol.31 (12), p.2534-2537

1992

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Imaging agents for myeloperoxidase

Journal of labelled compounds & radiopharmaceuticals, 2012-08, Vol.55 (10), p.393-399

2012

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[5-14C]-4-methyltriazolepyridines via facile preparation of methyl-[14C]-isothiocyanate

Journal of labelled compounds & radiopharmaceuticals, 2008-11, Vol.51 (13), p.419-421

2008

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Tritium labeling of a γ-secretase inhibitor and two modulators as in vitro imaging agents

Journal of labelled compounds & radiopharmaceuticals, 2012-02, Vol.55 (2), p.80-83

2012

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D2 receptor occupancy in conscious rat brain is not significantly distinguished with [3H]-MNPA, [3H]-(+)-PHNO, and [3H]-raclopride

Synapse (New York, N.Y.), 2010-08, Vol.64 (8), p.624-633

2010

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A route to the γ-secretase inhibitor [2,3,4-3H]BMS299897 via an α-phenylselenide derivative

Journal of labelled compounds & radiopharmaceuticals, 2010-01, Vol.53 (1), p.44-46

2010

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The synthesis of tritiated (R)-2-methoxy-N-n-propyl-nor-apomorphine (MNPA)

Journal of labelled compounds & radiopharmaceuticals, 2007-11, Vol.50 (13), p.1211-1214

2007

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In vitro determination of toxicity, binding, retention, subcellular distribution and biological efficacy of the boron neutron capture agent DAC-1

Radiotherapy and oncology, 1996, Vol.38 (1), p.41-50

1996

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Shining dead bone-cause for cautious interpretation of [18F]NaF PET scans

Development of rapid multistep carbon-11 radiosynthesis of the myeloperoxidase inhibitor AZD3241 to assess brain exposure by PET microdosing

Discovery and Preclinical Validation of [11C]AZ13153556, a Novel Probe for the Histamine Type 3 Receptor

Preclinical Comparison of Osimertinib with Other EGFR-TKIs in EGFR-Mutant NSCLC Brain Metastases Models, and Early Evidence of Clinical Brain Metastases Activity

Lidar Measurements Supporting the Ocular Hazard Distance Calculation Using Atmospheric Attenuation

Preclinical Comparison of the Blood-brain barrier Permeability of Osimertinib with Other EGFR TKIs

[U-14C]- and [13C6]-1,3-dibromobenzene; useful precursors with a rare substitution pattern in the synthesis of isotopologs

First Radiolabeling of a Ganglioside with a Positron Emitting Radionuclide: In Vivo PET Demonstrates Low Exposure of Radiofluorinated GM1 in Non-human Primate Brain

Multiple labeling of a potent CX 3 CR1 antagonist for the treatment of multiple sclerosis

Development of [Carbonyl-11C]AZ13198083, a Novel Histamine Type‑3 Receptor Radioligand with Favorable Kinetics

Imaging agent of a TRPA1 inhibitor

Chemistry and biology of some low molecular weight boron compounds for boron neutron capture therapy

Multiple labeling of a potent CX3CR1 antagonist for the treatment of multiple sclerosis

Effect of solvents on the time-dependent inhibition of CYP3A4 and the biotransformation of AZD3839 in human liver microsomes and hepatocytes

Discovery of a Novel Muscarinic Receptor PET Radioligand with Rapid Kinetics in the Monkey Brain

Biotransformation of two β-secretase inhibitors including ring opening and contraction of a pyrimidine ring

[5-14C]-methyltriazolepyridines via facile preparation of methyl-[ C]-isothiocyanate

Synthesis of .omega.-(aminoalkyl)-1,2-closo-dicarbadodecaboranes(12)

Imaging agents for myeloperoxidase

[5-14C]-4-methyltriazolepyridines via facile preparation of methyl-[14C]-isothiocyanate

Tritium labeling of a γ-secretase inhibitor and two modulators as in vitro imaging agents

D2 receptor occupancy in conscious rat brain is not significantly distinguished with [3H]-MNPA, [3H]-(+)-PHNO, and [3H]-raclopride

A route to the γ-secretase inhibitor [2,3,4-3H]BMS299897 via an α-phenylselenide derivative

The synthesis of tritiated (R)-2-methoxy-N-n-propyl-nor-apomorphine (MNPA)

In vitro determination of toxicity, binding, retention, subcellular distribution and biological efficacy of the boron neutron capture agent DAC-1

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