Haitang Li

Expression of small interfering RNAs targeted against HIV-1 rev transcripts in human cells.

Functional siRNA expression from transfected PCR products.

Small interfering RNAs expressed from a Pol III promoter suppress the EWS/Fli-1 transcript in an Ewing sarcoma cell line.

Amplification of RNAi--targeting HLA mRNAs.

Short hairpin RNA-directed cytosine (CpG) methylation of the RASSF1A gene promoter in HeLa cells.

Stable expression of shRNAs in human CD34+ progenitor cells can avoid induction of interferon responses to siRNAs in vitro.

RNAi in combination with a ribozyme and TAR decoy for treatment of HIV infection in hematopoietic cell gene therapy.

Combinatorial delivery of small interfering RNAs reduces RNAi efficacy by selective incorporation into RISC.

Cloning and detecting signature microRNAs from mammalian cells.

Expression of long anti-HIV-1 hairpin RNAs for the generation of multiple siRNAs: advantages and limitations.

Use of a U16 snoRNA-containing ribozyme library to identify ribozyme targets in HIV-1.

Novel dual inhibitory function aptamer-siRNA delivery system for HIV-1 therapy.

Functional and intracellular localization properties of U6 promoter-expressed siRNAs, shRNAs, and chimeric VA1 shRNAs in mammalian cells.

Selection, characterization and application of new RNA HIV gp 120 aptamers for facile delivery of Dicer substrate siRNAs into HIV infected cells.

SNPs in human miRNA genes affect biogenesis and function.

Sequence context outside the target region influences the effectiveness of miR-223 target sites in the RhoB 3'UTR.

Rational design of micro-RNA-like bifunctional siRNAs targeting HIV and the HIV coreceptor CCR5.

RNA-based gene therapy for HIV with lentiviral vector-modified CD34(+) cells in patients undergoing transplantation for AIDS-related lymphoma.

An aptamer-siRNA chimera suppresses HIV-1 viral loads and protects from helper CD4(+) T cell decline in humanized mice.

Systemic administration of combinatorial dsiRNAs via nanoparticles efficiently suppresses HIV-1 infection in humanized mice.

Interplay between HIV-1 infection and host microRNAs.

The role of antisense long noncoding RNA in small RNA-triggered gene activation.

Incorporation of aptamers in the terminal loop of shRNAs yields an effective and novel combinatorial targeting strategy.

HIV Replication and Latency in a Humanized NSG Mouse Model during Suppressive Oral Combinational Antiretroviral Therapy.

Receptor-targeted aptamer-siRNA conjugate-directed transcriptional regulation of HIV-1.

Nucleolar Localization of HIV-1 Rev Is Required, Yet Insufficient for Production of Infectious Viral Particles.