Li Wu

Professor, Chair

The University of Iowa

United States

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Articles (15)

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2024

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2024

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2021

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2021

Collaborators (7)

Levent Sari

University of Texas Southwestern Medical School

UNITED STATES

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Hillel Haim

UNITED STATES

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Nathan M. Sherer

University of Wisconsin-Madison

UNITED STATES

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Kaylee Mickens

Professional Research Assistant

University of Colorado Anschutz Medical Campus

UNITED STATES

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Kejun Guo

Research Assistant Professor

University of Denver

UNITED STATES

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Jacob Yount

Associate Professor

Ohio State University

UNITED STATES

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Milo M. Lin

UNITED STATES

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Li Wu

Research Interests

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Articles (15)

Antiretroviral therapy suppresses RNA N6-methyladenosine modification in peripheral blood mononuclear cells from HIV-1-infected individuals

Single-molecule epitranscriptomic analysis of full-length HIV-1 RNAs reveals functional roles of site-specific m6As.

Functional Impacts of Epitranscriptomic m6A Modification on HIV-1 Infection

Method for the Enrichment of N6-Methyladenosine-Modified Cellular and HIV-1 RNA.

Low host immune pressure may be associated with the development of hepatocellular carcinoma: a longitudinal analysis of complete genomes of the HBV 1762T, 1764A mutant.

SAMHD1 impairs type I interferon induction through the MAVS, IKKε, and IRF7 signaling axis during viral infection.

The host anti-viral protein SAMHD1 suppresses NF-κB activation by interacting with the IKK complex during inflammatory responses and viral infection.

A novel subgenotype I3 of hepatitis B virus in Guangxi, China: a 15-year follow-up study.

Epitranscriptomic N6-Methyladenosine Profile of SARS-CoV-2-Infected Human Lung Epithelial Cells.

Human lysyl-tRNA synthetase phosphorylation promotes HIV-1 proviral DNA transcription.

SAMHD1 Promotes the Antiretroviral Adaptive Immune Response in Mice Exposed to Lipopolysaccharide

Protocol for the generation of HIV-1 genomic RNA with altered levels of N6-methyladenosine.

Commonly Elicited Antibodies against the Base of the HIV-1 Env Trimer Guide the Population-Level Evolution of a Structure-Regulating Region in gp41.

Reverted HIV-1 Mutants in CD4+ T-Cells Reveal Critical Residues in the Polar Region of Viral Envelope Glycoprotein.

Analysis of entire hepatitis B virus genomes reveals reversion of mutations to wild type in natural infection, a 15 year follow-up study.

Collaborators (7)

Levent Sari

Hillel Haim

Nathan M. Sherer

Kaylee Mickens

Kejun Guo

Jacob Yount

Milo M. Lin

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