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Vascular Endothelial Growth Factor Receptors VEGFR-2 and VEGFR-3 Are Localized Primarily to the Vasculature in Human Primary Solid Cancers

Clinical cancer research, 2010-07, Vol.16 (14), p.3548-3561

2010

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ZD1839 (Iressa): An orally active inhibitor of epidermal growth factor signaling with potential for cancer therapy

Cancer research (Chicago, Ill.), 2002-10, Vol.62 (20), p.5749-5754

2002

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Studies leading to the identification of ZD1839 (Iressa) : An orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor targeted to the treatment of cancer

Bioorganic & medicinal chemistry letters, 2001-07, Vol.11 (14), p.1911-1914

2001

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Modeling Dose and Schedule Effects of AZD2811 Nanoparticles Targeting Aurora B Kinase for Treatment of Diffuse Large B-cell Lymphoma

Molecular cancer therapeutics, 2019-05, Vol.18 (5), p.909-919

2019

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MEK1/2 inhibitor withdrawal reverses acquired resistance driven by BRAFV600E amplification whereas KRASG13D amplification promotes EMT-chemoresistance

Nature communications, 2019-05, Vol.10 (1), p.1-22, Article 2030

2019

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Researcher or nurse? Difficulties of undertaking semi-structured interviews on sensitive topics

Nurse researcher, 2014-09, Vol.22 (1), p.27

Ashton, Susan

2014

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Correlation of MRI Biomarkers with Tumor Necrosis in Hras5 Tumor Xenograft in Athymic Rats

Neoplasia (New York, N.Y.), 2007-05, Vol.9 (5), p.382-391

2007

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Effect of Pretreatment With Atenolol and Nifedipine on ZD6126-Induced Cardiac Toxicity in Rats

JNCI : Journal of the National Cancer Institute, 2007-11, Vol.99 (22), p.1724-1728

2007

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Aminoimidazolylmethyluracil Analogues as Potent Inhibitors of Thymidine Phosphorylase and Their Bioreductive Nitroimidazolyl Prodrugs

Journal of medicinal chemistry, 2005-01, Vol.48 (2), p.392-402

2005

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ZD6126: A novel small molecule vascular targeting agent

International journal of radiation oncology, biology, physics, 2002-12, Vol.54 (5), p.1497-1502

2002

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A novel in situ hydrophobic ion paring (HIP) formulation strategy for clinical product selection of a nanoparticle drug delivery system

Journal of controlled release, 2016-05, Vol.229, p.106-119

2016

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Discovery of a Potent and Selective EGFR Inhibitor (AZD9291) of Both Sensitizing and T790M Resistance Mutations That Spares the Wild Type Form of the Receptor

Journal of medicinal chemistry, 2014-10, Vol.57 (20), p.8249-8267

2014

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Aurora kinase inhibitor nanoparticles target tumors with favorable therapeutic index in vivo

Science translational medicine, 2016-02, Vol.8 (325), p.325ra17

2016

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Tumour overexpression of inducible nitric oxide synthase (iNOS) increases angiogenesis and may modulate the anti-tumour effects of the vascular disrupting agent ZD6126

Microvascular research, 2006-03, Vol.71 (2), p.76-84

2006

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End of life care: The experiences of advance care planning amongst family caregivers of people with advanced dementia – A qualitative study

Dementia (London, England), 2016-09, Vol.15 (5), p.958-975

2016

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Inhibition of oxidative phosphorylation suppresses the development of osimertinib resistance in a preclinical model of EGFR-driven lung adenocarcinoma

Oncotarget, 2016-12, Vol.7 (52), p.86313-86325

2016

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Inhibition of neutrophil infiltration into A549 lung tumors in vitro and in vivo using a CXCR2‐specific antagonist is associated with reduced tumor growth

International journal of cancer, 2011-08, Vol.129 (4), p.847-858

2011

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Structure- and Reactivity-Based Development of Covalent Inhibitors of the Activating and Gatekeeper Mutant Forms of the Epidermal Growth Factor Receptor (EGFR)

Journal of medicinal chemistry, 2013-09, Vol.56 (17), p.7025-7048

2013

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Optimizing Therapeutic Effect of Aurora B Inhibition in Acute Myeloid Leukemia with AZD2811 Nanoparticles

Molecular cancer therapeutics, 2017-06, Vol.16 (6), p.1031-1040

2017

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Abstract B212: Integrating the pre-clinical pharmacokinetic, pharmacodynamics, and efficacy data for AZD9291, an oral, irreversible inhibitor of EGFR activating (EGFRm+) and resistant (EGFRm+/T790M) mutations and an active metabolite to predict the human pharmacokinetics and potential efficacious dose in patients

Molecular cancer therapeutics, 2013-11, Vol.12 (11_Supplement), p.B212-B212

2013

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Abstract 3102: AZD1152HQPA Accurin™ nanoparticles inhibit growth of diffuse large B-cell lymphomas and small cell lung cancer

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.3102-3102

2015

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A novel in situ hydrophobic ion pairing (HIP) formulation strategy for clinical product selection of a nanoparticle drug delivery system

Journal of controlled release, 2016-05, Vol.229, p.106-119

2016

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Abstract 761: Changing the paradigm for treating drug resistance in NSCLC: Novel combinations of AZD6094, a selective MET inhibitor, and an irreversible, selective (EGFRm/T790M) EGFRTKI, AZD9291

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.761-761

2015

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Abstract 3678: Imaging AZD1152HQPA Accurin™ nanoparticle accumulation in preclinical tumors

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.3678-3678

2015

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Vascular Endothelial Growth Factor Receptors VEGFR-2 and VEGFR-3 Are Localized Primarily to the Vasculature in Human Primary Solid Cancers

ZD1839 (Iressa): An orally active inhibitor of epidermal growth factor signaling with potential for cancer therapy

Studies leading to the identification of ZD1839 (Iressa) : An orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor targeted to the treatment of cancer

Modeling Dose and Schedule Effects of AZD2811 Nanoparticles Targeting Aurora B Kinase for Treatment of Diffuse Large B-cell Lymphoma

MEK1/2 inhibitor withdrawal reverses acquired resistance driven by BRAFV600E amplification whereas KRASG13D amplification promotes EMT-chemoresistance

Researcher or nurse? Difficulties of undertaking semi-structured interviews on sensitive topics

Correlation of MRI Biomarkers with Tumor Necrosis in Hras5 Tumor Xenograft in Athymic Rats

Effect of Pretreatment With Atenolol and Nifedipine on ZD6126-Induced Cardiac Toxicity in Rats

Aminoimidazolylmethyluracil Analogues as Potent Inhibitors of Thymidine Phosphorylase and Their Bioreductive Nitroimidazolyl Prodrugs

ZD6126: A novel small molecule vascular targeting agent

A novel in situ hydrophobic ion paring (HIP) formulation strategy for clinical product selection of a nanoparticle drug delivery system

Discovery of a Potent and Selective EGFR Inhibitor (AZD9291) of Both Sensitizing and T790M Resistance Mutations That Spares the Wild Type Form of the Receptor

Aurora kinase inhibitor nanoparticles target tumors with favorable therapeutic index in vivo

Tumour overexpression of inducible nitric oxide synthase (iNOS) increases angiogenesis and may modulate the anti-tumour effects of the vascular disrupting agent ZD6126

End of life care: The experiences of advance care planning amongst family caregivers of people with advanced dementia – A qualitative study

Inhibition of oxidative phosphorylation suppresses the development of osimertinib resistance in a preclinical model of EGFR-driven lung adenocarcinoma

Cells Lacking the RB1 Tumor Suppressor Gene Are Hyperdependent on Aurora B Kinase for Survival

Inhibition of neutrophil infiltration into A549 lung tumors in vitro and in vivo using a CXCR2‐specific antagonist is associated with reduced tumor growth

Structure- and Reactivity-Based Development of Covalent Inhibitors of the Activating and Gatekeeper Mutant Forms of the Epidermal Growth Factor Receptor (EGFR)

Optimizing Therapeutic Effect of Aurora B Inhibition in Acute Myeloid Leukemia with AZD2811 Nanoparticles

Abstract 3102: AZD1152HQPA Accurin™ nanoparticles inhibit growth of diffuse large B-cell lymphomas and small cell lung cancer

A novel in situ hydrophobic ion pairing (HIP) formulation strategy for clinical product selection of a nanoparticle drug delivery system

Abstract 761: Changing the paradigm for treating drug resistance in NSCLC: Novel combinations of AZD6094, a selective MET inhibitor, and an irreversible, selective (EGFRm/T790M) EGFRTKI, AZD9291

Abstract 3678: Imaging AZD1152HQPA Accurin™ nanoparticle accumulation in preclinical tumors

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