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Degradation of the benzoxazolinone class of phytoalexins is important for virulence of Fusarium pseudograminearum towards wheat

Molecular plant pathology, 2015-12, Vol.16 (9), p.946-962

2015

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A γ-lactamase from cereal infecting Fusarium spp. catalyses the first step in the degradation of the benzoxazolinone class of phytoalexins

Fungal genetics and biology, 2015-10, Vol.83, p.1-9

2015

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The Fdb3 transcription factor of the Fusarium Detoxification of Benzoxazolinone gene cluster is required for MBOA but not BOA degradation in Fusarium pseudograminearum

Fungal genetics and biology, 2016-03, Vol.88, p.44-53

2016

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Parathyroid Imaging: How Good Is It and How Should It Be Done?

Seminars in nuclear medicine, 2006-07, Vol.36 (3), p.206-211

2006

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2009 EANM parathyroid guidelines

European journal of nuclear medicine and molecular imaging, 2009-07, Vol.36 (7), p.1201-1216

2009

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Radiation exposure of the families of outpatients treated with radioiodine (iodine-131) for hyperthyroidism

European journal of nuclear medicine, 1999-07, Vol.26 (7), p.686-692

1999

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Pentavalent rhenium-188 dimercaptosuccinic acid for targeted radiotherapy: synthesis and preliminary animal and human studies

European journal of nuclear medicine, 1998-06, Vol.25 (6), p.613-621

1998

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Degradation of the benzoxazolinone class of phytoalexins is important for virulence of F usarium pseudograminearum towards wheat

Molecular plant pathology, 2015-12, Vol.16 (9), p.946-962

2015

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Optimization of parathyroid imaging by simultaneous dual energy planar and single photon emission tomography

Nuclear medicine communications, 2004-11, Vol.25 (11), p.1089-1093

2004

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Parathyroid Imaging with Technetium-99m-Sestamibi: Preoperative Localization and Tissue Uptake Studies

The Journal of nuclear medicine (1978), 1992-03, Vol.33 (3), p.313-318

1992

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Comparison of Technetium-99m-HM-PAO Leukocytes with Indium-111-Oxine Leukocytes for Localizing Intraabdominal Sepsis

The Journal of nuclear medicine (1978), 1990-03, Vol.31 (3), p.311-315

1990

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Myeloperoxidase is a potential molecular imaging and therapeutic target for the identification and stabilization of high-risk atherosclerotic plaque

European heart journal, 2018-09, Vol.39 (35), p.3301-3310

2018

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Faecal Myeloperoxidase as a Biomarker of Endoscopic Activity in Inflammatory Bowel Disease

Journal of Crohn's and colitis, 2022-12, Vol.16 (12), p.1862-1873

2022

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Neutrophil-vascular interactions drive myeloperoxidase accumulation in the brain in Alzheimer's disease

Acta neuropathologica communications, 2022-03, Vol.10 (1), p.38-38, Article 38

2022

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Terrorist Learning: A New Analytical Framework

Studies in conflict and terrorism, 2017-07, Vol.40 (7), p.523-538

2017

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Effect of Tether Length on endo/exo Stereoselectivity in Alkene–Arene meta‐Photocycloaddition Reactions towards the Aphidocolin/Stemodin Scaffolds

European journal of organic chemistry, 2024-08, Vol.27 (30), p.n/a

2024

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Superoxide dismutase protects ribonucleotide reductase from inactivation in yeast

Free radical biology & medicine, 2018-02, Vol.116, p.114-122

2018

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Structure-Based Design of Potent and Selective Inhibitors of the Metabolic Kinase PFKFB3

Journal of medicinal chemistry, 2015-04, Vol.58 (8), p.3611-3625

2015

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Discovery of (2R)‑N‑[3-[2-[(3-Methoxy-1-methyl-pyrazol-4-yl)amino]pyrimidin-4-yl]‑1H‑indol-7-yl]-2-(4-methylpiperazin-1-yl)propenamide (AZD4205) as a Potent and Selective Janus Kinase 1 Inhibitor

Journal of medicinal chemistry, 2020-05, Vol.63 (9), p.4517-4527

2020

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Anomalous two-photon Compton scattering

New journal of physics, 2021-11, Vol.23 (11), p.115008

2021

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Discovery of 4‑Amino‑N‑[(1S)‑1-(4-chlorophenyl)-3-hydroxypropyl]-1-(7H‑pyrrolo[2,3‑d]pyrimidin-4-yl)piperidine-4-carboxamide (AZD5363), an Orally Bioavailable, Potent Inhibitor of Akt Kinases

Journal of medicinal chemistry, 2013-03, Vol.56 (5), p.2059-2073

2013

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Challenges in microbial ecology: building predictive understanding of community function and dynamics

The ISME Journal, 2016-11, Vol.10 (11), p.2557-2568

2016

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Chemical Biology Approaches Confirm MCT4 as the Therapeutic Target of a Cellular Optimized Hit

ACS chemical biology, 2023-02, Vol.18 (2), p.296-303

2023

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Design of a Lead-Like Cysteine-Targeting Covalent Library and the Identification of Hits to Cys55 of Bfl-1

Journal of medicinal chemistry, 2024-07, Vol.67 (13), p.11209-11225

2024

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Degradation of the benzoxazolinone class of phytoalexins is important for virulence of Fusarium pseudograminearum towards wheat

A γ-lactamase from cereal infecting Fusarium spp. catalyses the first step in the degradation of the benzoxazolinone class of phytoalexins

The Fdb3 transcription factor of the Fusarium Detoxification of Benzoxazolinone gene cluster is required for MBOA but not BOA degradation in Fusarium pseudograminearum

Parathyroid Imaging: How Good Is It and How Should It Be Done?

2009 EANM parathyroid guidelines

Radiation exposure of the families of outpatients treated with radioiodine (iodine-131) for hyperthyroidism

Pentavalent rhenium-188 dimercaptosuccinic acid for targeted radiotherapy: synthesis and preliminary animal and human studies

Degradation of the benzoxazolinone class of phytoalexins is important for virulence of F usarium pseudograminearum towards wheat

Optimization of parathyroid imaging by simultaneous dual energy planar and single photon emission tomography

Parathyroid Imaging with Technetium-99m-Sestamibi: Preoperative Localization and Tissue Uptake Studies

Comparison of Technetium-99m-HM-PAO Leukocytes with Indium-111-Oxine Leukocytes for Localizing Intraabdominal Sepsis

Myeloperoxidase is a potential molecular imaging and therapeutic target for the identification and stabilization of high-risk atherosclerotic plaque

Faecal Myeloperoxidase as a Biomarker of Endoscopic Activity in Inflammatory Bowel Disease

Neutrophil-vascular interactions drive myeloperoxidase accumulation in the brain in Alzheimer's disease

Terrorist Learning: A New Analytical Framework

Effect of Tether Length on endo/exo Stereoselectivity in Alkene–Arene meta‐Photocycloaddition Reactions towards the Aphidocolin/Stemodin Scaffolds

Superoxide dismutase protects ribonucleotide reductase from inactivation in yeast

Structure-Based Design of Potent and Selective Inhibitors of the Metabolic Kinase PFKFB3

Discovery of (2R)‑N‑[3-[2-[(3-Methoxy-1-methyl-pyrazol-4-yl)amino]pyrimidin-4-yl]‑1H‑indol-7-yl]-2-(4-methylpiperazin-1-yl)propenamide (AZD4205) as a Potent and Selective Janus Kinase 1 Inhibitor

Anomalous two-photon Compton scattering

Discovery of 4‑Amino‑N‑[(1S)‑1-(4-chlorophenyl)-3-hydroxypropyl]-1-(7H‑pyrrolo[2,3‑d]pyrimidin-4-yl)piperidine-4-carboxamide (AZD5363), an Orally Bioavailable, Potent Inhibitor of Akt Kinases

Challenges in microbial ecology: building predictive understanding of community function and dynamics

Chemical Biology Approaches Confirm MCT4 as the Therapeutic Target of a Cellular Optimized Hit

Discovery of N‑(4-{[5-Fluoro-7-(2-methoxyethoxy)quinazolin-4-yl]amino}phenyl)-2-[4-(propan-2-yl)‑1H‑1,2,3-triazol-1-yl]acetamide (AZD3229), a Potent Pan-KIT Mutant Inhibitor for the Treatment of Gastrointestinal Stromal Tumors

Design of a Lead-Like Cysteine-Targeting Covalent Library and the Identification of Hits to Cys55 of Bfl-1

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