L. Pallansch

发表

Nuclear run-on transcription from primary embryonic lens tissue.

P. Zelenka, L. Pallansch, M. Vatal, 1989, Developmental biology.

c-myc mRNA is elevated as differentiating lens cells withdraw from the cell cycle.

R. Getzenberg, P. Zelenka, D. Beebe, 1987, Experimental cell research.

A Diarylsulphone Non-Nucleoside Reverse Transcriptase Inhibitor with a Unique Sensitivity Profile to Drug-Resistant Virus Isolates

Tehmina S. Khan, R. Buckheit, J. Bader, 1996 .

Using a noninfectious MVM surrogate for assessing viral clearance during downstream process development

A. Dhar, R. Barlow, L. Pallansch, 2019, Biotechnology progress.

Use of a noninfectious surrogate to predict minute virus of mice removal during nanofiltration

A. Dhar, Takayuki Sohka, L. Pallansch, 2018, Biotechnology progress.

Bovine immunodeficiency-like virus encodes factors which trans activate the long terminal repeat

M. Gonda, C. Lackman-Smith, L. Pallansch, 1992, Journal of virology.

cis-acting regulatory elements in the bovine immunodeficiency virus long terminal repeat.

M. Gonda, F. Ruscetti, J. Mikovits, 1995, Virology.

Development of the bovine immunodeficiency-like virus as a model of lentivirus disease.

K. Nagashima, M. Gonda, J. Bess, 1990, Developments in biological standardization.

SJ-3366, a Unique and Highly Potent Nonnucleoside Reverse Transcriptase Inhibitor of Human Immunodeficiency Virus Type 1 (HIV-1) That Also Inhibits HIV-2

E. White, J. Lee, K. Watson, 2001, Antimicrobial Agents and Chemotherapy.

T30177, an oligonucleotide stabilized by an intramolecular guanosine octet, is a potent inhibitor of laboratory strains and clinical isolates of human immunodeficiency virus type 1

Y. Pommier, J. Ojwang, C. Lackman-Smith, 1995, Antimicrobial agents and chemotherapy.

Inhibition of Human Immunodeficiency Virus Type 1 Replication in Human Cells by Debio-025, a Novel Cyclophilin Binding Agent

R. Ptak, E. De Clercq, B. Rosenwirth, 2008, Antimicrobial Agents and Chemotherapy.

Highly potent oxathiin carboxanilide derivatives with efficacy against nonnucleoside reverse transcriptase inhibitor-resistant human immunodeficiency virus isolates

R. Buckheit, M. Snow, S. S. Yang, 1997, Antimicrobial agents and chemotherapy.

Structure-activity and cross-resistance evaluations of a series of human immunodeficiency virus type-1-specific compounds related to oxathiin carboxanilide

W. A. Harrison, R. Schultz, R. Buckheit, 1995, Antimicrobial agents and chemotherapy.

Rapid analysis of trans fatty acids on SP-2340 glass capillary columns

J. Sampugna, M. Keeney, M. Enig, 1982 .

Use of an RNA folding algorithm to choose regions for amplification by the polymerase chain reaction.

P. Zelenka, J. Talian, H. Beswick, 1990, Analytical biochemistry.

Potassium-dependent folding: a key to intracellular delivery of G-quartet oligonucleotides as HIV inhibitors.

N. Jing, Shimei Wang, Y. Guan, 2002, Biochemistry.

Naturally Occurring Capsid Substitutions Render HIV-1 Cyclophilin A Independent in Human Cells and TRIM-cyclophilin-resistant in Owl Monkey Cells*

R. Ptak, R. Stanfield, B. Rosenwirth, 2005, Journal of Biological Chemistry.

In Vitro Preclinical Testing of Nonoxynol-9 as Potential Anti-Human Immunodeficiency Virus Microbicide: a Retrospective Analysis of Results from Five Laboratories

F. Krebs, G. Doncel, C. Dezzutti, 2006, Antimicrobial Agents and Chemotherapy.

Efficacy, pharmacokinetics, and in vivo antiviral activity of UC781, a highly potent, orally bioavailable nonnucleoside reverse transcriptase inhibitor of HIV type 1.

M. Hollingshead, S. Stinson, W. Decker, 1997, AIDS research and human retroviruses.

Structural characterization and comparison of promoter activity of mouse and bovine interphotoreceptor retinoid-binding protein (IRBP) gene 5' flanking regions in WERI, Y79, chick retina cells, and transgenic mice

J. Boatright, J. Nickerson, E. Stodůlková, 2001, Current eye research.

Crystal Structure and Structural Mechanism of a Novel Anti-Human Immunodeficiency Virus and d-Amino Acid-Containing Chemokine

Ying Li, Won-Tak Choi, Rong Cao, 2007, Journal of Virology.

Structure-activity of inhibition of HIV-1 integrase and virus replication by G-quartet oligonucleotides.

J. Liu, Y. Pommier, E. De Clercq, 2001, DNA and cell biology.

Stability-Activity Relationships of a Family of G-tetrad Forming Oligonucleotides as Potent HIV Inhibitors

E. De Clercq, N. Jing, M. Hogan, 2000, The Journal of Biological Chemistry.

Isolation and Characterization of HIV-1 Isolates Resistant to Oxathiin Carboxanilide Analogues: Evaluation of Variables in the Drug Resistance Selection Process

R. Buckheit, R. Buckheit, T. Kinjerski, 1996 .