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Development of torque clutch drilling tool and evaluation of drag reduction performance

Advances in mechanical engineering, 2018-10, Vol.10 (10), p.168781401880665

2018

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Mapping human norovirus antigens during infection reveals the breadth of the humoral immune response

npj vaccines, 2023-06, Vol.8 (1), p.87-87, Article 87

2023

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Identification and Characterization of Single-Chain Antibodies that Specifically Bind GI Noroviruses

PloS one, 2017-01, Vol.12 (1), p.e0170162-e0170162

2017

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Analysis of the Functional Contributions of Asn233 in Metallo-β-Lactamase IMP-1

Antimicrobial Agents and Chemotherapy, 2011-12, Vol.55 (12), p.5696-5702

2011

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A Secondary Drug Resistance Mutation of TEM-1 β-Lactamase That Suppresses Misfolding and Aggregation

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (1), p.283-288

2001

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A Natural Polymorphism in β -lactamase is a Global Suppressor

Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (16), p.8801-8806

1997

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Deep Sequencing of a Systematic Peptide Library Reveals Conformationally‐Constrained Protein Interface Peptides that Disrupt a Protein‐Protein Interaction

Chembiochem : a European journal of chemical biology, 2022-02, Vol.23 (3), p.e202100504-n/a

2022

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High-Resolution Mapping of Human Norovirus Antigens via Genomic Phage Display Library Selections and Deep Sequencing

Journal of virology, 2020-12, Vol.95 (1)

2020

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Binding Properties of a Peptide Derived from β-Lactamase Inhibitory Protein

Antimicrobial Agents and Chemotherapy, 2001-12, Vol.45 (12), p.3279-3286

2001

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Mapping Protein–Protein Interaction Interface Peptides with Jun-Fos Assisted Phage Display and Deep Sequencing

ACS synthetic biology, 2020-07, Vol.9 (7), p.1882-1896

2020

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Multiple Global Suppressors of Protein Stability Defects Facilitate the Evolution of Extended-Spectrum TEM β-Lactamases

Journal of molecular biology, 2010-12, Vol.404 (5), p.832-846

2010

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Deep Sequencing of Systematic Combinatorial Libraries Reveals β-Lactamase Sequence Constraints at High Resolution

Journal of molecular biology, 2012-12, Vol.424 (3-4), p.150-167

2012

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Norovirus Antigen Detection with a Combination of Monoclonal and Single-Chain Antibodies

Journal of clinical microbiology, 2015-12, Vol.53 (12), p.3916-3918

2015

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Deep sequencing of phage-displayed peptide libraries reveals sequence motif that detects norovirus

Protein engineering, design and selection, 2017-02, Vol.30 (2), p.129-139

2017

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Identification of human single-chain antibodies with broad reactivity for noroviruses

Protein engineering, design and selection, 2014-10, Vol.27 (10), p.339-349

2014

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Role of β‐lactamase residues in a common interface for binding the structurally unrelated inhibitory proteins BLIP and BLIP‐II

Protein science, 2014-09, Vol.23 (9), p.1235-1246

2014

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Role of [beta]-lactamase residues in a common interface for binding the structurally unrelated inhibitory proteins BLIP and BLIP-II

Protein science, 2014-09, Vol.23 (9), p.1235

2014

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Identification of a β-Lactamase Inhibitory Protein Variant That Is a Potent Inhibitor of Staphylococcus PC1 β-Lactamase

Journal of molecular biology, 2011-03, Vol.406 (5), p.730-744

2011

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Human Immune Response to Streptococcal Inhibitor of Complement, a Serotype M1 Group A Streptococcus Extracellular Protein Involved in Epidemics

The Journal of infectious diseases, 2000-11, Vol.182 (5), p.1425-1436

2000

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Display of Functional β-Lactamase Inhibitory Protein on the Surface of M13 Bacteriophage

Antimicrobial Agents and Chemotherapy, 1998-11, Vol.42 (11), p.2893-2897

1998

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Engineering Specificity from Broad to Narrow: Design of a β‑Lactamase Inhibitory Protein (BLIP) Variant That Exclusively Binds and Detects KPC β‑Lactamase

ACS infectious diseases, 2016-12, Vol.2 (12), p.969-979

2016

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Engineering specificity from broad to narrow: Design of a BLIP variant that exclusively binds and detects KPC β-lactamase

ACS infectious diseases, 2016-10, Vol.2 (12), p.969-979

2016

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Fine Mapping of the Sequence Requirements for Binding of β-Lactamase Inhibitory Protein (BLIP) to TEM-1 β-Lactamase Using a Genetic Screen for BLIP Function

Journal of molecular biology, 2009-06, Vol.389 (2), p.401-412

2009

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Analysis of the Context Dependent Sequence Requirements of Active Site Residues in the Metallo-β-lactamase IMP-1

Journal of molecular biology, 2004-11, Vol.344 (3), p.653-663

2004

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Analysis of FAS3/ACC regulatory region of Saccharomyces cerevisiae: identification of a functional UASINO and sequences responsible for fatty acid mediated repression

Nucleic acids research, 1994-02, Vol.22 (3), p.412-418

1994

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Development of torque clutch drilling tool and evaluation of drag reduction performance

Mapping human norovirus antigens during infection reveals the breadth of the humoral immune response

Identification and Characterization of Single-Chain Antibodies that Specifically Bind GI Noroviruses

Analysis of the Functional Contributions of Asn233 in Metallo-β-Lactamase IMP-1

A Secondary Drug Resistance Mutation of TEM-1 β-Lactamase That Suppresses Misfolding and Aggregation

A Natural Polymorphism in β -lactamase is a Global Suppressor

Deep Sequencing of a Systematic Peptide Library Reveals Conformationally‐Constrained Protein Interface Peptides that Disrupt a Protein‐Protein Interaction

High-Resolution Mapping of Human Norovirus Antigens via Genomic Phage Display Library Selections and Deep Sequencing

Binding Properties of a Peptide Derived from β-Lactamase Inhibitory Protein

Mapping Protein–Protein Interaction Interface Peptides with Jun-Fos Assisted Phage Display and Deep Sequencing

Multiple Global Suppressors of Protein Stability Defects Facilitate the Evolution of Extended-Spectrum TEM β-Lactamases

Deep Sequencing of Systematic Combinatorial Libraries Reveals β-Lactamase Sequence Constraints at High Resolution

Norovirus Antigen Detection with a Combination of Monoclonal and Single-Chain Antibodies

Deep sequencing of phage-displayed peptide libraries reveals sequence motif that detects norovirus

Identification of human single-chain antibodies with broad reactivity for noroviruses

Role of β‐lactamase residues in a common interface for binding the structurally unrelated inhibitory proteins BLIP and BLIP‐II

Role of [beta]-lactamase residues in a common interface for binding the structurally unrelated inhibitory proteins BLIP and BLIP-II

Identification of a β-Lactamase Inhibitory Protein Variant That Is a Potent Inhibitor of Staphylococcus PC1 β-Lactamase

Human Immune Response to Streptococcal Inhibitor of Complement, a Serotype M1 Group A Streptococcus Extracellular Protein Involved in Epidemics

Display of Functional β-Lactamase Inhibitory Protein on the Surface of M13 Bacteriophage

Engineering Specificity from Broad to Narrow: Design of a β‑Lactamase Inhibitory Protein (BLIP) Variant That Exclusively Binds and Detects KPC β‑Lactamase

Engineering specificity from broad to narrow: Design of a BLIP variant that exclusively binds and detects KPC β-lactamase

Fine Mapping of the Sequence Requirements for Binding of β-Lactamase Inhibitory Protein (BLIP) to TEM-1 β-Lactamase Using a Genetic Screen for BLIP Function

Analysis of the Context Dependent Sequence Requirements of Active Site Residues in the Metallo-β-lactamase IMP-1

Analysis of FAS3/ACC regulatory region of Saccharomyces cerevisiae: identification of a functional UASINO and sequences responsible for fatty acid mediated repression

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