Gene-Errol E. Ringpis

发表

RNAi-Mediated CCR5 Knockdown Provides HIV-1 Resistance to Memory T Cells in Humanized BLT Mice

D. Elashoff, M. Marsden, J. Zack, 2015, Molecular therapy. Nucleic acids.

Works Title Ectopic expression of anti-HIV-1 shRNAs protects CD 8 ( + ) T cells modified with CD 4 ζ CAR from HIV-1 infection and alleviates impairment of cell proliferation

M. Kamata, O. Yang, I. Chen, 2015 .

Ectopic expression of anti-HIV-1 shRNAs protects CD8(+) T cells modified with CD4ζ CAR from HIV-1 infection and alleviates impairment of cell proliferation.

M. Kamata, O. Yang, I. Chen, 2015, Biochemical and biophysical research communications.

Trypanosoma brucei mitochondria of Novel TUTase associates with an editosome-like complex in Material Supplemental

R. Lathrop, P. Gershon, R. Aphasizhev, 2009 .

Induction of transgene-specific immunological tolerance in myeloablated nonhuman primates using lentivirally transduced CD34+ progenitor cells.

R. Donahue, M. Metzger, I. Chen, 2003, Molecular therapy : the journal of the American Society of Gene Therapy.

Ectopic expression of anti-HIV-1 shRNAs protects CD8 þ T cells modi ﬁ ed with CD4 z CAR from HIV-1 infection and alleviates impairment of cell proliferation Biochemical and Biophysical Research Communications

M. Kamata, O. Yang, I. Chen, 2015 .

Transient low pH treatment enhances infection of lentiviral vector pseudotypes with a targeting Sindbis envelope.

I. Chen, N. Pariente, K. Morizono, 2006, Virology.

iCODA: RNAi-based inducible knock-in system in Trypanosoma brucei.

R. Lathrop, R. Aphasizhev, Gene-Errol E. Ringpis, 2011, Methods in molecular biology.

Engineering Cellular Resistance to HIV-1 Infection In Vivo Using a Dual Therapeutic Lentiviral Vector.

I. Chen, J. Bartlett, D. An, 2015, Molecular therapy. Nucleic acids.

Engineering HIV-1-Resistant T-Cells from Short-Hairpin RNA-Expressing Hematopoietic Stem/Progenitor Cells in Humanized BLT Mice

M. Kamata, I. Chen, D. An, 2012, PloS one.

Lentiviral vector retargeting to P-glycoprotein on metastatic melanoma through intravenous injection

Lily Wu, I. Chen, Benhur Lee, 2005, Nature Medicine.

Lentiviral vector-transduced dendritic cells induce specific T cell response in a nonhuman primate model.

R. Donahue, M. Metzger, I. Chen, 2005, Human gene therapy.

Mechanism of U insertion RNA editing in trypanosome mitochondria: the bimodal TUTase activity of the core complex.

G. W. Hatfield, R. Lathrop, Lan Huang, 2010, Journal of molecular biology.

Mechanism of U-insertion RNA editing in trypanosome mitochondria: characterization of RET2 functional domains by mutational analysis.

J. Stagno, R. Aphasizhev, Gene-Errol E. Ringpis, 2010 .

Purging Exhausted Virus-Specific CD8 T Cell Phenotypes by Somatic Cell Reprogramming.

M. Kamata, Jing Wen, I. Chen, 2017, AIDS research and human retroviruses.

Mechanism of U insertion RNA editing in trypanosome mitochondria: the bimodal TUTase activity of the core complex.

G. W. Hatfield, R. Lathrop, Lan Huang, 2010, Journal of molecular biology.

Novel TUTase associates with an editosome-like complex in mitochondria of Trypanosoma brucei.

R. Lathrop, P. Gershon, R. Aphasizhev, 2009, RNA.

Engineering Cellular Resistance to HIV-1 Infection In Vivo Using a Dual Therapeutic Lentiviral Vector.

I. Chen, J. Bartlett, D. An, 2015, Molecular therapy. Nucleic acids.