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Recent Publications

CC02013"BET bromodomain-targeting compounds reactivate HIV from latency via a Tat-independent mechanism."

Cell Cycle, 2012

cell2012graphicLSW"An Endogenous Accelerator for Viral Gene Expression Confers a Fitness Advantage"

Cell, 2012

PNAS2012-L"Transcriptional burst frequency and burst size are equally modulated across the human genome."

Proceedings of the National Academy of Sciences, 2012.

"Dynamics of protein noise can distinguish between alternate sources of gene-expression variability."

Molecular Systems Biology, 2012.

"Microwell Devices with Finger-like Channels for Long-Term Imaging of HIV-1 Expression Kinetics in Primary Human Lymphocytes."

Lab on a Chip, 2012.

"Lentiviral vectors to study stochastic noise in gene expression."

 

Methods of Enzymology, 2011.

"Autonomous Targeting of Infections Superspreaders using Engineered Transmissable Therapies."

PLoS Computational Biology, 2011.

"Mapping the architecture of the HIV-1 Tat circuit: A decision-making circuit that lacks bistability and exploits stochastic noise."

Methods, 2011.

"Transcriptional bursting from the HIV-1 promoter is a significant source of stochastic noise in HIV-1 gene expression."

Biophysical Journal, 2010.

"Accelerated immunodeficiency by anti-CCR5 treatment in HIV infection."

PLoS Computational Biology, 2009.

The Laboratory for Quantitative and Synthetic Virology

Our lab is interested in understanding the fundamental principles of gene regulatory circuits and how viral 'master circuits' exploit these principles to control virus replication. Ultimately, our goal is to exploit these circuitry principles to engineer the next generation of antiviral therapies.

The lab employs a coupled computational experimental approach that relies on quantitative time-lapse fluorescence microscopy with mathematical modeling to study viral gene expression circuits and expression 'noise' at the single-cell level.

 

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A 12-hour microscopy movie of human T cells infected with an HIV virus engineered to express red and green fluorescent proteins at different stages of infection. These movies enable us to analyze viral circuitry to identify weak points that can be exploited by novel therapies.
 



nih_new_innovator


National Institute of General Medical Sciences




HINT (NIAID) HIV Immune Networks Team

Alfred P Sloan Foundation

NSF

Bill & Melinda Gates Foundation

W. M. Keck Foundation

Califorani HIV/AIDS Research Program

Weinberger Lab
Gladstone Institute of Virology and Immunology
University of California, San Francisco
1650 Owens Street
San Francisco, CA 94158
Phone: (415) 734-4857