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HLTF Promotes Fork Reversal, Limiting Replication Stress Resistance and Preventing Multiple Mechanisms of Unrestrained DNA Synthesis

Molecular cell, 2020-06, Vol.78 (6), p.1237-1251.e7

2020

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Inhibition of the translesion synthesis polymerase REV1 exploits replication gaps as a cancer vulnerability

Science advances, 2020-06, Vol.6 (24), p.eaaz7808-eaaz7808

2020

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Probing the Protein-Protein Interaction between the ATRXADD Domain and the Histone H3 Tail

Molecules (Basel, Switzerland), 2020-03, Vol.25 (7), p.1500

2020

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Structure‐Based Drug Design of Phenazopyridine Derivatives as Inhibitors of Rev1 Interactions in Translesion Synthesis

ChemMedChem, 2021-04, Vol.16 (7), p.1126-1132

2021

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Structure-based virtual screening identifies an 8-hydroxyquinoline as a small molecule GLI1 inhibitor

Molecular therapy. Oncolytics, 2021-03, Vol.20, p.265-276

2021

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Introduction to Medicinal Chemistry: A Five-Day Course for High School Students

Journal of chemical education, 2020-06, Vol.97 (6), p.1543-1548

2020

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Lead compound profiling for small molecule inhibitors of the REV1-CT/RIR Translesion synthesis Protein-Protein interaction

Bioorganic & medicinal chemistry, 2024-05, Vol.106, p.117755, Article 117755

2024

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A metadynamic approach to understand the recognition mechanism of the histone H3 tail with the ATRX ADD domain

Biochimica et biophysica acta. Gene regulatory mechanisms, 2018-06, Vol.1861 (6), p.594

2018

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A metadynamic approach to understand the recognition mechanism of the histone H3 tail with the ATRXADD domain

Biochimica et biophysica acta. Gene regulatory mechanisms, 2018-06, Vol.1861 (6), p.594-602

2018

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Structure–Activity Relationships for Itraconazole-Based Triazolone Analogues as Hedgehog Pathway Inhibitors

Journal of medicinal chemistry, 2019-04, Vol.62 (8), p.3873-3885

2019

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Exploring the physicochemical and antiproliferative properties of biaryl-linked [13]-macrodilactones

Bioorganic & medicinal chemistry, 2020-10, Vol.28 (20), p.115671-115671, Article 115671

2020

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8-Hydroxyquinoline derivatives suppress GLI1-mediated transcription through multiple mechanisms

Bioorganic chemistry, 2023-03, Vol.132, p.106387-106387, Article 106387

2023

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Probing the Protein-Protein Interaction Between the ATRX ADD Domain and the Histone H3 Tail

Molecules (Basel, Switzerland), 2020-03, Vol.25 (7)

2020

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HLTF Promotes Fork Reversal, Limiting Replication Stress Resistance and Preventing Multiple Mechanisms of Unrestrained DNA Synthesis

Inhibition of the translesion synthesis polymerase REV1 exploits replication gaps as a cancer vulnerability

Probing the Protein-Protein Interaction between the ATRXADD Domain and the Histone H3 Tail

Structure‐Based Drug Design of Phenazopyridine Derivatives as Inhibitors of Rev1 Interactions in Translesion Synthesis

Structure-based virtual screening identifies an 8-hydroxyquinoline as a small molecule GLI1 inhibitor

Introduction to Medicinal Chemistry: A Five-Day Course for High School Students

Lead compound profiling for small molecule inhibitors of the REV1-CT/RIR Translesion synthesis Protein-Protein interaction

A metadynamic approach to understand the recognition mechanism of the histone H3 tail with the ATRX ADD domain

A metadynamic approach to understand the recognition mechanism of the histone H3 tail with the ATRXADD domain

Structure–Activity Relationships for Itraconazole-Based Triazolone Analogues as Hedgehog Pathway Inhibitors

Exploring the physicochemical and antiproliferative properties of biaryl-linked [13]-macrodilactones

8-Hydroxyquinoline derivatives suppress GLI1-mediated transcription through multiple mechanisms

Probing the Protein-Protein Interaction Between the ATRX ADD Domain and the Histone H3 Tail

An Iterative Approach Guides Discovery of the FabI Inhibitor Fabimycin, a Late-Stage Antibiotic Candidate with In Vivo Efficacy against Drug-Resistant Gram-Negative Infections

Correction to “An Iterative Approach Guides Discovery of the FabI Inhibitor Fabimycin, a Late-Stage Antibiotic Candidate with In Vivo Efficacy against Drug-Resistant Gram-Negative Infections”

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