Author

Kimberly L. Rapp

Observed names: Kimberly L Rapp, Kimberly Rapp

Institutions: Emory University, Atlanta VA Medical Center

Observed institutions: Université d'Orléans, Centre National de la Recherche Scientifique, National Institutes of Health, United States Department of Veterans Affairs, Emory University, University of Georgia, Veterans Health Administration, Institut de Chimie Organique et Analytique, Atlanta VA Medical Center, National Institute of Mental Health

OpenAlex ID: A5113582335

Synthesis, cytotoxicity, and antiviral activities of new neolignans related to honokiol and magnolol

2007 · Franck Amblard, Baskaran Govindarajan, et al. · Bioorganic & Medicinal Chemistry Letters · 68

Pre-steady-state Kinetic Studies Establish Entecavir 5′-Triphosphate as a Substrate for HIV-1 Reverse Transcriptase

2007 · Robert A. Domaoal, Moira McMahon, et al. · Journal of Biological Chemistry · 43

Neuroendocrine responses regulating susceptibility and resistance to autoimmune/inflammatory disease in inbred rat strains

2001 · Leonardo Tonelli, Jeanette I. Webster, et al. · Immunological Reviews · 38

Synthesis, Antiviral Activity, and Mechanism of Drug Resistance of d - and l -2‘,3‘-Didehydro-2‘,3‘-dideoxy-2‘-fluorocarbocyclic Nucleosides

2005 · Jianing Wang, Yunho Jin, et al. · Journal of Medicinal Chemistry · 28

Differential induction of interleukin-I β mRNA in the brain parenchyma of Lewis and Fischer rats after peripheral injection of lipopolysaccharides

2003 · Leonardo H Tonelli, Shigeru Maeda, et al. · Journal of Neuroimmunology · 21

d - and l -2‘,3‘-Didehydro-2‘,3‘-dideoxy-3‘-fluoro-carbocyclic Nucleosides: Synthesis, Anti-HIV Activity and Mechanism of Resistance

2007 · Jianing Wang, Yunho Jin, et al. · Journal of Medicinal Chemistry · 19

5′-O-Aliphatic and amino acid ester prodrugs of (−)-β-d-(2R,4R)-dioxolane-thymine (DOT): Synthesis, anti-HIV activity, cytotoxicity and stability studies

2008 · Yuzeng Liang, Ashoke Sharon, et al. · Bioorganic & Medicinal Chemistry · 12

Synthesis of 5-haloethynyl- and 5-(1,2-dihalo)vinyluracil nucleosides: Antiviral activity and cellular toxicity

2005 · Vanessa Escuret, Vincent Aucagne, et al. · Bioorganic & Medicinal Chemistry · 12

Comparative analysis of in vitro processivity of HIV-1 reverse transcriptases containing mutations 65R, 74V, 184V and 65R+74V

2009 · Prem L. Sharma, James H. Nettles, et al. · Antiviral Research · 11

Synthesis, antiviral activity, and stability of nucleoside analogs containing tricyclic bases

2009 · Franck Amblard, Emilie Fromentin, et al. · European Journal of Medicinal Chemistry · 11

Synthesis and anti-HIV activity of 5-haloethynyl and 5-(1,2-dihalo)vinyl analogues of AZT and FLT

2008 · Nicolas Joubert, Franck Amblard, et al. · Tetrahedron · 11

Selection and Characterization of HIV-1 with a Novel S68 Deletion in Reverse Transcriptase

2011 · Raymond F. Schinazi, Ivana Massud, et al. · Antimicrobial Agents and Chemotherapy · 9

Synthesis, Cytotoxicity, and Antiviral Activities of New Neolignans Related to Honokiol and Magnolol.

2007 · Franck Amblard, Baskaran Govindarajan, et al. · ChemInform

Synthesis of 5‐Haloethynyl‐ and 5‐(1,2‐Dihalo)vinyluracil Nucleosides: Antiviral Activity and Cellular Toxicity.

2006 · Vanessa Escuret, Vincent Aucagne, et al. · ChemInform

Works count: 14

Citation count: 283

H-index: 11

I10-index: 11