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Pharmacological perturbation of CDK9 using selective CDK9 inhibition or degradation

Nature chemical biology, 2018-02, Vol.14 (2), p.163-170

2018

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Characterization of a selective inhibitor of the Parkinson's disease kinase LRRK2

Nature chemical biology, 2011-04, Vol.7 (4), p.203-205

2011

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ERK5 kinase activity is dispensable for cellular immune response and proliferation

Proceedings of the National Academy of Sciences - PNAS, 2016-10, Vol.113 (42), p.11865-11870

2016

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Functional Interrogation of the Kinome Using Nucleotide Acyl Phosphates

Biochemistry (Easton), 2007-01, Vol.46 (2), p.350-358

2007

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Mechanistic and pharmacological characterization of PF-04457845: a highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain

The Journal of pharmacology and experimental therapeutics, 2011-07, Vol.338 (1), p.114-124

2011

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Direct CDKN2 Modulation of CDK4 Alters Target Engagement of CDK4 Inhibitor Drugs

Molecular cancer therapeutics, 2019-04, Vol.18 (4), p.771-779

2019

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Chemoproteomic Evaluation of Target Engagement by the Cyclin-Dependent Kinase 4 and 6 Inhibitor Palbociclib Correlates with Cancer Cell Response

Biochemistry (Easton), 2016-09, Vol.55 (38), p.5434-5441

2016

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Functional interrogation of kinases and other nucleotide-binding proteins

FEBS letters, 2013-06, Vol.587 (13), p.1870-1877

2013

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Chemoproteomics Using Nucleotide Acyl Phosphates Reveals an ATP Binding Site at the Dimer Interface of Procaspase‑6

Biochemistry (Easton), 2019-12, Vol.58 (52), p.5320-5328

2019

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Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor

ACS medicinal chemistry letters, 2011-02, Vol.2 (2), p.91-96

2011

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Novel Mechanistic Class of Fatty Acid Amide Hydrolase Inhibitors with Remarkable Selectivity

Biochemistry (Easton), 2007-11, Vol.46 (45), p.13019-13030

2007

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High-resolution crystal structure of human asparagine synthetase enables analysis of inhibitor binding and selectivity

Communications biology, 2019-09, Vol.2 (1), p.345, Article 345

2019

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ATP Acyl Phosphate Reactivity Reveals Native Conformations of Hsp90 Paralogs and Inhibitor Target Engagement

Biochemistry (Easton), 2015-05, Vol.54 (19), p.3024-3036

2015

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Identification of a Tumor Specific, Active-Site Mutation in Casein Kinase 1α by Chemical Proteomics

PloS one, 2016-03, Vol.11 (3), p.e0152934-e0152934

2016

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Benzothiophene piperazine and piperidine urea inhibitors of fatty acid amide hydrolase (FAAH)

Bioorganic & medicinal chemistry letters, 2009-05, Vol.19 (10), p.2865-2869

2009

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Correction: Identification of a Tumor Specific, Active-Site Mutation in Casein Kinase 1α by Chemical Proteomics

PloS one, 2017, Vol.12 (2), p.e0172649-e0172649

2017

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Abstract 225: Chemoproteomic evaluation of target engagement in clinical samples

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.225-225

Nomanbhoy, Tyzoon K.

2017

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Abstract 2311: Determinants of CDK4 target engagement by palbociclib, ribociclib and abemaciclib

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.2311-2311

2018

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Discovery of Potent and Selective Covalent Inhibitors of JNK

Chemistry & biology, 2012-01, Vol.19 (1), p.140-154

2012

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In Situ Kinase Profiling Reveals Functionally Relevant Properties of Native Kinases

Chemistry & biology, 2011-06, Vol.18 (6), p.699-710

2011

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Author Correction: High-resolution crystal structure of human asparagine synthetase enables analysis of inhibitor binding and selectivity

Communications biology, 2019-11, Vol.2 (1), Article 438

2019

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Blocking Site-to-Site Translocation of a Misactivated Amino Acid by Mutation of a Class I tRNA Synthetase

Proceedings of the National Academy of Sciences - PNAS, 2002-01, Vol.99 (2), p.585-590

2002

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Mutational Separation of Two Pathways for Editing by a Class I tRNA Synthetase

Molecular cell, 2002-02, Vol.9 (2), p.353-362

2002

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PIP5K1C phosphoinositide kinase deficiency distinguishes PIKFYVE-dependent cancer cells from non-malignant cells

Autophagy, 2023-09, Vol.19 (9), p.2464-2484

2023

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Pharmacological perturbation of CDK9 using selective CDK9 inhibition or degradation

Characterization of a selective inhibitor of the Parkinson's disease kinase LRRK2

ERK5 kinase activity is dispensable for cellular immune response and proliferation

Functional Interrogation of the Kinome Using Nucleotide Acyl Phosphates

Mechanistic and pharmacological characterization of PF-04457845: a highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain

Direct CDKN2 Modulation of CDK4 Alters Target Engagement of CDK4 Inhibitor Drugs

Chemoproteomic Evaluation of Target Engagement by the Cyclin-Dependent Kinase 4 and 6 Inhibitor Palbociclib Correlates with Cancer Cell Response

Functional interrogation of kinases and other nucleotide-binding proteins

Chemoproteomics Using Nucleotide Acyl Phosphates Reveals an ATP Binding Site at the Dimer Interface of Procaspase‑6

Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor

Novel Mechanistic Class of Fatty Acid Amide Hydrolase Inhibitors with Remarkable Selectivity

High-resolution crystal structure of human asparagine synthetase enables analysis of inhibitor binding and selectivity

Pathophysiological significance and therapeutic targeting of germinal center kinase in diffuse large B-cell lymphoma

ATP Acyl Phosphate Reactivity Reveals Native Conformations of Hsp90 Paralogs and Inhibitor Target Engagement

Identification of a Tumor Specific, Active-Site Mutation in Casein Kinase 1α by Chemical Proteomics

Benzothiophene piperazine and piperidine urea inhibitors of fatty acid amide hydrolase (FAAH)

Correction: Identification of a Tumor Specific, Active-Site Mutation in Casein Kinase 1α by Chemical Proteomics

Abstract 225: Chemoproteomic evaluation of target engagement in clinical samples

Abstract 2311: Determinants of CDK4 target engagement by palbociclib, ribociclib and abemaciclib

Discovery of Potent and Selective Covalent Inhibitors of JNK

In Situ Kinase Profiling Reveals Functionally Relevant Properties of Native Kinases

Author Correction: High-resolution crystal structure of human asparagine synthetase enables analysis of inhibitor binding and selectivity

Blocking Site-to-Site Translocation of a Misactivated Amino Acid by Mutation of a Class I tRNA Synthetase

Mutational Separation of Two Pathways for Editing by a Class I tRNA Synthetase

PIP5K1C phosphoinositide kinase deficiency distinguishes PIKFYVE-dependent cancer cells from non-malignant cells

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