B. Terry

发表

Thermodynamic parameters governing interaction of EcoRI endonuclease with specific and nonspecific DNA sequences.

P. Modrich, R. A. Rubin, W. Jack, 1983, The Journal of biological chemistry.

Maturation Inhibitor with Improved Potency, Anti-viral Spectrum and Gag Polymorphic

N. Meanwell, Zeyu Lin, M. Krystal, 2016 .

Identification and Characterization of BMS-955176, a Second-Generation HIV-1 Maturation Inhibitor with Improved Potency, Antiviral Spectrum, and Gag Polymorphic Coverage

N. Meanwell, Zeyu Lin, M. Krystal, 2016, Antimicrobial Agents and Chemotherapy.

Biochemical studies on capped RNA primers identify a class of oligonucleotide inhibitors of the influenza virus RNA polymerase.

T. Chung, C. Cianci, M. Krystal, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Facilitated diffusion during catalysis by EcoRI endonuclease. Nonspecific interactions in EcoRI catalysis.

P. Modrich, W. Jack, B. Terry, 1985, The Journal of biological chemistry.

Involvement of outside DNA sequences in the major kinetic path by which EcoRI endonuclease locates and leaves its recognition sequence.

P. Modrich, W. Jack, B. Terry, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Discovery of BMS-955176, a Second Generation HIV-1 Maturation Inhibitor with Broad Spectrum Antiviral Activity.

B. Beno, N. Meanwell, Zeyu Lin, 2016, ACS medicinal chemistry letters.

Biochemical Analysis of HIV-1 Integrase Variants Resistant to Strand Transfer Inhibitors*

Zeyu Lin, M. Krystal, B. Terry, 2008, Journal of Biological Chemistry.

Entecavir Exhibits Inhibitory Activity against Human Immunodeficiency Virus under Conditions of Reduced Viral Challenge

N. Parkin, M. Krystal, R. Colonno, 2008, Antimicrobial Agents and Chemotherapy.

Entecavir Exhibits Inhibitory Activity against Human Immunodeﬁciency Virus under Conditions of Reduced Viral Challenge (cid:1)

N. Parkin, M. Krystal, R. Colonno, 2008 .

Mechanism of specific site location and DNA cleavage by EcoR I endonuclease.

P. Modrich, W. Jack, B. Terry, 1987, Gene amplification and analysis.

Expression of herpes simplex virus type 1 DNA polymerase in Saccharomyces cerevisiae and detection of virus-specific enzyme activity in cell-free lysates

C. Crumpacker, D. Dorsky, S. M. Wietstock, 1988, Journal of virology.

Anti-Herpetic Activity of (±)-(1α, 2β, 3α)-9-[2-Hydroxy-3-(Hydroxymethyl)Cyclobutyl]Guanine and Inhibition of HSV-1 DNA Polymerase

K. Mazina, M. Haffey, B. Terry, 1990 .

Synthesis and evaluation of C2-carbon-linked heterocyclic-5-hydroxy-6-oxo-dihydropyrimidine-4-carboxamides as HIV-1 integrase inhibitors.

N. Meanwell, Zeyu Lin, M. Krystal, 2015, Bioorganic & medicinal chemistry letters.

(±)-(1α,2β,3α)-9-[2,3-bis(hydroxymethyl)cyclobutyl]guanine [(±)-BHCG or SQ 33 054]: A potent and selective inhibitor of herpesviruses

M. Young, J. Clark, K. Mazina, 1990 .

Selective activity and cellular pharmacology of (1R-1 alpha,2 beta,3 alpha)-9-[2,3-bis(hydroxymethyl)cyclobutyl]guanine in herpesvirus-infected cells.

M. Haffey, G. Bisacchi, B. Terry, 1991, Molecular pharmacology.

Inhibition of herpes simplex virus type 1 DNA polymerase by [1R(1 alpha,2 beta,3 alpha)]-9-[2,3-bis(hydroxymethyl)cyclobutyl] guanine.

C. Cianci, B. Terry, M. Hagen, 1991, Molecular pharmacology.

Broad-spectrum antiviral activity of the acyclic guanosine phosphonate (R,S)-HPMPG.

M. Young, K. Mazina, M. Haffey, 1988, Antiviral research.

(2R, 4S, 5S)-1-(tetrahydro-4-hydroxy-5-methoxy-2-furanyl)thymine: a potent selective inhibitor of herpes simplex thymidine kinase

G. Bisacchi, B. Terry, C. Kim, 1993 .

The structure and function of the HSV DNA replication proteins: defining novel antiviral targets.

B. Terry, A. Field, J. Matthews, 1993, Antiviral research.

Neutralization of purified herpes simplex virus DNA polymerase by two antipeptide sera

C. Cianci, M. Haffey, B. Terry, 1990, Virus Genes.

Inhibition of herpes simplex virus type 1 DNA polymerase by the natural product oosporein.

K. Bush, C. Cianci, E. Meyers, 1992, The Journal of antibiotics.

BMS-232632, a Highly Potent Human Immunodeficiency Virus Protease Inhibitor That Can Be Used in Combination with Other Available Antiretroviral Agents

David A. Stock, R. Colonno, W. Blair, 2000, Antimicrobial Agents and Chemotherapy.

Heterocycle amide isosteres: An approach to overcoming resistance for HIV-1 integrase strand transfer inhibitors.

N. Meanwell, D. Langley, Zeyu Lin, 2019, Bioorganic & medicinal chemistry letters.

Simple and Accurate In Vitro Method for Predicting Serum Protein Binding of HIV Integrase Strand Transfer Inhibitors

N. Meanwell, Zeyu Lin, M. Krystal, 2011 .

Nucleotide-dependent enzymes associated with microtubule systems.

D. Purich, B. Terry, 1982, Advances in enzymology and related areas of molecular biology.

Human immunodeficiency virus type 1 viral background plays a major role in development of resistance to protease inhibitors.

R. Colonno, R. Rose, B. Terry, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Resistance Mutations (NRTI) BMS-986001 against Known NRTI Nucleoside Reverse Transcriptase Inhibitor Cross-Resistance Profile of In Vitro

M. Krystal, G. Hanna, Tricia L. Protack, 2014 .

In Vitro Cross-Resistance Profile of Nucleoside Reverse Transcriptase Inhibitor (NRTI) BMS-986001 against Known NRTI Resistance Mutations

M. Krystal, G. Hanna, Tricia L. Protack, 2013, Antimicrobial Agents and Chemotherapy.

Design, Synthesis, and SAR of C-3 Benzoic Acid, C-17 Triterpenoid Derivatives. Identification of the HIV-1 Maturation Inhibitor 4-((1 R,3a S,5a R,5b R,7a R,11a S,11b R,13a R,13b R)-3a-((2-(1,1-Dioxidothiomorpholino)ethyl)amino)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,1

B. Beno, N. Meanwell, V. Arora, 2018, Journal of medicinal chemistry.

The design, synthesis and structure-activity relationships associated with C28 amine-based betulinic acid derivatives as inhibitors of HIV-1 maturation.

N. Meanwell, Zeyu Lin, M. Krystal, 2018, Bioorganic & medicinal chemistry letters.

Triketoacid inhibitors of HIV-integrase: a new chemotype useful for probing the integrase pharmacophore.

N. Meanwell, Zeyu Lin, Carol Deminie, 2006, Bioorganic & medicinal chemistry letters.

The discovery and preclinical evaluation of BMS-707035, a potent HIV-1 integrase strand transfer inhibitor.

N. Meanwell, Zeyu Lin, M. Krystal, 2018, Bioorganic & medicinal chemistry letters.

Exploration of the diketoacid integrase inhibitor chemotype leading to the discovery of the anilide-ketoacids chemotype.

N. Meanwell, Zeyu Lin, Carol Deminie, 2006, Bioorganic & medicinal chemistry letters.

Design, synthesis and SAR study of bridged tricyclic pyrimidinone carboxamides as HIV-1 integrase inhibitors.

A. Mathur, N. Meanwell, Zeyu Lin, 2020, Bioorganic & medicinal chemistry.

Inhibitors of HIV-1 maturation: Development of structure-activity relationship for C-28 amides based on C-3 benzoic acid-modified triterpenoids.

N. Meanwell, M. Krystal, Tricia L. Protack, 2016, Bioorganic & medicinal chemistry letters.

C-3 benzoic acid derivatives of C-3 deoxybetulinic acid and deoxybetulin as HIV-1 maturation inhibitors.

B. Beno, N. Meanwell, Zeyu Lin, 2016, Bioorganic & medicinal chemistry.

CHAPTER 6 – EVALUATION OF POTENTIAL ROLES FOR GDP IN MICROTUBULE ASSEMBLY AND DISASSEMBLY

D. Purich, T. Karr, B. Terry, 1982 .

Characterization of tubulin and microtubule-associated protein interactions with guanine nucleotides and their nonhydrolyzable analogs.

D. Purich, T. Karr, B. Terry, 1982, Methods in enzymology.

Expression ofHerpesSimplex VirusType1DNA Polymerase in Saccharomyces cerevisiae andDetection ofVirus-Specific EnzymeActivity inCell-Free Lysates

C. Crumpacker, D. Dorsky, S. M. Wietstock, 1988 .

C-3 benzoic acid derivatives of C-3 deoxybetulinic acid and deoxybetulin as HIV-1 maturation inhibitors.

B. Beno, N. Meanwell, Zeyu Lin, 2016, Bioorganic & medicinal chemistry.

Broad-spectrum antiviral activity of the acyclic guanosine phosphonate (R,S)-HPMPG.

M. Young, K. Mazina, M. Haffey, 1988, Antiviral research.