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Identification of ras-related nuclear protein, targeting protein for xenopus kinesin-like protein 2, and stearoyl-coa desaturase 1 as promising cancer targets from an RNAi-based screen

Cancer research (Chicago, Ill.), 2007-05, Vol.67 (9), p.4390-4398

2007

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Genetic inhibition of the atypical kinase Wee1 selectively drives apoptosis of p53 inactive tumor cells

BMC cancer, 2014-06, Vol.14 (1), p.430-430, Article 430

2014

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Quality Improvement Initiative Addresses the Gap in Patients’ Knowledge of Elective Induction of Labor and Reduces Nulliparous, Term, Singleton, Vertex Cesarean Rates

Journal of obstetric, gynecologic, and neonatal nursing, 2019-06, Vol.48 (3), p.S112-S112

Tucker, Lora

2019

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Reducing agent-mediated precipitation of high-abundance plasma proteins

Analytical biochemistry, 2009-04, Vol.387 (2), p.184-193

2009

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Imidazo[2,1- b]thiazoles: Multitargeted inhibitors of both the insulin-like growth factor receptor and members of the epidermal growth factor family of receptor tyrosine kinases

Bioorganic & medicinal chemistry letters, 2010-04, Vol.20 (8), p.2452-2455

2010

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A “Prozone-Like” Effect Influences the Efficacy of the Monoclonal Antibody ABT-700 against the Hepatocyte Growth Factor Receptor

Pharmacology, 2017-01, Vol.100 (5-6), p.229-242

2017

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Insulin-like Growth Factor-1 Receptor and ErbB Kinase Inhibitor Combinations Block Proliferation and Induce Apoptosis through Cyclin D1 Reduction and Bax Activation

The Journal of biological chemistry, 2008-08, Vol.283 (35), p.23721-23730

2008

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Correlation of tumor growth suppression and methionine aminopetidase-2 activity blockade using an orally active inhibitor

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (6), p.1838-1843

2008

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Discovery, Identification, and Characterization of Candidate Pharmacodynamic Markers of Methionine Aminopeptidase-2 Inhibition

Journal of proteome research, 2008-11, Vol.7 (11), p.4807-4820

2008

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Development of multitargeted inhibitors of both the insulin-like growth factor receptor (IGF-IR) and members of the epidermal growth factor family of receptor tyrosine kinases

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (6), p.1718-1721

2009

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ABBV-399, a c-Met Antibody-Drug Conjugate that Targets Both MET -Amplified and c-Met-Overexpressing Tumors, Irrespective of MET Pathway Dependence

Clinical cancer research, 2017-02, Vol.23 (4), p.992-1000

2017

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Anti-c-Met monoclonal antibody ABT-700 breaks oncogene addiction in tumors with MET amplification

BMC cancer, 2016-02, Vol.16 (109), p.105-105, Article 105

2016

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Abstract 6311: ABBV-400: An ADC delivering a novel topoisomerase 1 inhibitor to c-Met-positive solid tumors

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.6311-6311

2023

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“It Is a Bloody Good Job!” Utilizing OB Hemorrhage Drills and Standardized Electronic Order Sets to Champion Excellence and Collaboration during Postpartum Hemorrhage

Journal of obstetric, gynecologic, and neonatal nursing, 2013-06, Vol.42 (s1), p.S26-S26

2013

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“Many Hands Make Light Work”: Using a Kaizen Approach to Ignite Innovation While Increasing Patient Safety and Productivity on an Obstetric Triage Unit

Journal of obstetric, gynecologic, and neonatal nursing, 2012-06, Vol.41 (s1), p.S91-S92

2012

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Substituted 4-amino-1H-pyrazolo[3,4-d]pyrimidines as multi-targeted inhibitors of insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor kinases

Bioorganic & medicinal chemistry letters, 2010-10, Vol.20 (20), p.6067-6071

2010

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Abstract A248: Substituted 4-amino-1 H -pyrazolo[3,4- d ]pyrimidines as multitargeted inhibitors targeting insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor tyrosine kinases

Molecular cancer therapeutics, 2009-12, Vol.8 (12_Supplement), p.A248-A248

2009

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Substituted 4-amino-1 H-pyrazolo[3,4- d]pyrimidines as multi-targeted inhibitors of insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor kinases

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (20), p.6067-6071

2010

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Abstract A245: Imidazo[2,1-b]thiazole and imidazo[1,2-a]pyridine amides as novel inhibitors of the insulin-like growth factor (IGF1R) and members of the epidermal growth factor family of tyrosine kinases

Molecular cancer therapeutics, 2009-12, Vol.8 (12_Supplement), p.A245-A245

2009

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Discovery and Optimization of Anthranilic Acid Sulfonamides as Inhibitors of Methionine Aminopeptidase-2: A Structural Basis for the Reduction of Albumin Binding

Journal of medicinal chemistry, 2006-06, Vol.49 (13), p.3832-3849

2006

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Tumor suppression by a rationally designed reversible inhibitor of methionine aminopeptidase-2

Cancer research (Chicago, Ill.), 2003-11, Vol.63 (22), p.7861-7869

2003

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Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (13), p.3574-3577

2006

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What Would You Do?

Poz (New York, N.Y.), 2013-04 (187), p.1

Tucker, Lora René

2013

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A Pivotal Study of Optoacoustic Imaging to Diagnose Benign and Malignant Breast Masses: A New Evaluation Tool for Radiologists

Radiology, 2018-05, Vol.287 (2), p.398

2018

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Establishing a framework for female germline initiation in the plant ovule

Journal of experimental botany, 2019-06, Vol.70 (11), p.2937-2949

2019

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Identification of ras-related nuclear protein, targeting protein for xenopus kinesin-like protein 2, and stearoyl-coa desaturase 1 as promising cancer targets from an RNAi-based screen

Genetic inhibition of the atypical kinase Wee1 selectively drives apoptosis of p53 inactive tumor cells

Quality Improvement Initiative Addresses the Gap in Patients’ Knowledge of Elective Induction of Labor and Reduces Nulliparous, Term, Singleton, Vertex Cesarean Rates

Reducing agent-mediated precipitation of high-abundance plasma proteins

Imidazo[2,1- b]thiazoles: Multitargeted inhibitors of both the insulin-like growth factor receptor and members of the epidermal growth factor family of receptor tyrosine kinases

A “Prozone-Like” Effect Influences the Efficacy of the Monoclonal Antibody ABT-700 against the Hepatocyte Growth Factor Receptor

Insulin-like Growth Factor-1 Receptor and ErbB Kinase Inhibitor Combinations Block Proliferation and Induce Apoptosis through Cyclin D1 Reduction and Bax Activation

Correlation of tumor growth suppression and methionine aminopetidase-2 activity blockade using an orally active inhibitor

Discovery, Identification, and Characterization of Candidate Pharmacodynamic Markers of Methionine Aminopeptidase-2 Inhibition

Development of multitargeted inhibitors of both the insulin-like growth factor receptor (IGF-IR) and members of the epidermal growth factor family of receptor tyrosine kinases

ABBV-399, a c-Met Antibody-Drug Conjugate that Targets Both MET -Amplified and c-Met-Overexpressing Tumors, Irrespective of MET Pathway Dependence

Anti-c-Met monoclonal antibody ABT-700 breaks oncogene addiction in tumors with MET amplification

Abstract 6311: ABBV-400: An ADC delivering a novel topoisomerase 1 inhibitor to c-Met-positive solid tumors

“It Is a Bloody Good Job!” Utilizing OB Hemorrhage Drills and Standardized Electronic Order Sets to Champion Excellence and Collaboration during Postpartum Hemorrhage

“Many Hands Make Light Work”: Using a Kaizen Approach to Ignite Innovation While Increasing Patient Safety and Productivity on an Obstetric Triage Unit

Substituted 4-amino-1H-pyrazolo[3,4-d]pyrimidines as multi-targeted inhibitors of insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor kinases

Abstract A248: Substituted 4-amino-1 H -pyrazolo[3,4- d ]pyrimidines as multitargeted inhibitors targeting insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor tyrosine kinases

Substituted 4-amino-1 H-pyrazolo[3,4- d]pyrimidines as multi-targeted inhibitors of insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor kinases

Abstract A245: Imidazo[2,1-b]thiazole and imidazo[1,2-a]pyridine amides as novel inhibitors of the insulin-like growth factor (IGF1R) and members of the epidermal growth factor family of tyrosine kinases

Discovery and Optimization of Anthranilic Acid Sulfonamides as Inhibitors of Methionine Aminopeptidase-2: A Structural Basis for the Reduction of Albumin Binding

Tumor suppression by a rationally designed reversible inhibitor of methionine aminopeptidase-2

Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties

What Would You Do?

A Pivotal Study of Optoacoustic Imaging to Diagnose Benign and Malignant Breast Masses: A New Evaluation Tool for Radiologists

Establishing a framework for female germline initiation in the plant ovule

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