Krista L. Getty

发表

A 7-Deaza-Adenosine Analog Is a Potent and Selective Inhibitor of Hepatitis C Virus Replication with Excellent Pharmacokinetic Properties

Giovanni Migliaccio, D. Hazuda, J. Tomassini, 2004, Antimicrobial Agents and Chemotherapy.

Structure-activity relationship of purine ribonucleosides for inhibition of hepatitis C virus RNA-dependent RNA polymerase.

Quanlai Song, Jie Xia, Daniel R McMasters, 2004, Journal of medicinal chemistry.

Characterization of Resistance to Non-obligate Chain-terminating Ribonucleoside Analogs That Inhibit Hepatitis C Virus Replication in Vitro*

D. Hazuda, R. Cortese, J. Tomassini, 2003, Journal of Biological Chemistry.

Inhibition of Hepatitis C Virus RNA Replication by 2′-Modified Nucleoside Analogs*

Lawrence C Kuo, Giovanni Migliaccio, L. Kuo, 2003, The Journal of Biological Chemistry.

Inhibitory Effect of 2′-Substituted Nucleosides on Hepatitis C Virus Replication Correlates with Metabolic Properties in Replicon Cells

J. Tomassini, M. Maccoss, G. Migliaccio, 2005, Antimicrobial Agents and Chemotherapy.

LRRTM3 promotes processing of amyloid-precursor protein by BACE1 and is a positional candidate gene for late-onset Alzheimer's disease

Shane D. Marine, Amy S. Espeseth, Min Xu, 2006, Proceedings of the National Academy of Sciences.

Structure-activity relationship of heterobase-modified 2'-C-methyl ribonucleosides as inhibitors of hepatitis C virus RNA replication.

P. D. Cook, J. Tomassini, M. Maccoss, 2004, Journal of medicinal chemistry.

Identification of potent inhibitors of the sortilin-progranulin interaction.

Gregory T O'Donnell, P. Coleman, M. Ziebell, 2020, Bioorganic & medicinal chemistry letters.

The identification of a novel lead class for phosphodiesterase 2 inhibition by fragment-based drug design.

Deping Wang, Sujata Sharma, W. Shipe, 2017, Bioorganic & medicinal chemistry letters.

An in vitro Flaviviridae replicase system capable of authentic RNA replication.

J. Tomassini, L. Gan, R. Lafemina, 2003, Virology.