G. Gao

发表

Partial correction of murine hemophilia A with neo-antigenic murine factor VIII.

H. Kazazian, R. Sarkar, G. Gao, 2000, Human gene therapy.

Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis

M. Weitzman, R. DeMatteo, James M. Wilson, 1996, Journal of virology.

Sequestration of adenoviral vector by Kupffer cells leads to a nonlinear dose response of transduction in liver.

S. Fawell, J. Wilson, G. Gao, 2001, Molecular therapy : the journal of the American Society of Gene Therapy.

Activation of innate immunity in nonhuman primates following intraportal administration of adenoviral vectors.

J. Wilson, G. Gao, J. Tazelaar, 2001, Molecular therapy : the journal of the American Society of Gene Therapy.

Acute cytokine response to systemic adenoviral vectors in mice is mediated by dendritic cells and macrophages.

J. Wilson, G. Gao, N. Chirmule, 2001, Molecular therapy : the journal of the American Society of Gene Therapy.

Eradication of intraperitoneal and distant tumor by adenovirus-mediated interferon-beta gene therapy is attributable to induction of systemic immunity.

James M. Wilson, J. Wilson, G. Gao, 2001, Cancer research.

Oral Vaccination of Mice with Adenoviral Vectors Is Not Impaired by Preexisting Immunity to the Vaccine Carrier

Z. Xiang, H. Ertl, J. Wilson, 2003, Journal of Virology.

Biology of adenovirus vectors with E1 and E4 deletions for liver-directed gene therapy

J. Wilson, G. Gao, Y. Yang, 1996, Journal of virology.

Human Immunodeficiency Virus Type 1-Specific Immune Responses in Primates upon Sequential Immunization with Adenoviral Vaccine Carriers of Human and Simian Serotypes

Z. Xiang, H. Ertl, J. Wilson, 2004, Journal of Virology.

Prolonged correction of hyperlipidemia in mice with familial hypercholesterolemia using an adeno-associated viral vector expressing very-low-density lipoprotein receptor.

D. Rader, J. Wilson, G. Gao, 2000, Molecular therapy : the journal of the American Society of Gene Therapy.

Repeated administration of adenoviral vectors in lungs of human CD4 transgenic mice treated with a nondepleting CD4 antibody.

J. Wilson, G. Gao, N. Chirmule, 1999, Journal of immunology.

Muscle-specific promoters may be necessary for adeno-associated virus-mediated gene transfer in the treatment of muscular dystrophies.

H. Sweeney, James M. Wilson, J. Wilson, 2001, Human gene therapy.

Evaluation of toxicity from high-dose systemic administration of recombinant adenovirus vector in vector-naïve and pre-immunized mice

James M. Wilson, J. Wilson, G. Gao, 2005, Gene Therapy.

Treatment of recurrent or progressive malignant glioma with a recombinant adenovirus expressing human interferon-beta (H5.010CMVhIFN-beta): a phase I trial.

A. Alavi, D. Hackney, K. Propert, 2001, Human gene therapy.

Induction of CD8+ T cells to an HIV-1 antigen upon oral immunization of mice with a simian E1-deleted adenoviral vector.

H. Ertl, J. Wilson, G. Gao, 2004, Vaccine.

Rescue of skeletal muscles of gamma-sarcoglycan-deficient mice with adeno-associated virus-mediated gene transfer.

H. Sweeney, J. Wilson, G. Gao, 2000, Molecular therapy : the journal of the American Society of Gene Therapy.

Evaluating the potential of germ line transmission after intravenous administration of recombinant adenovirus in the C3H mouse.

J. Wilson, G. Gao, S. Raper, 1998, Human gene therapy.

Selective gene transfer into the liver of non-human primates with E1-deleted, E2A-defective, or E1-E4 deleted recombinant adenoviruses.

E. Furth, J. Wilson, G. Gao, 1998, Human gene therapy.

Production of recombinant adeno-associated virus.

James M. Wilson, J. Wilson, G. Gao, 2000, Advances in virus research.

Replication-Defective Vector Based on a Chimpanzee Adenovirus

R. M. Burnett, Z. Xiang, H. Ertl, 2001, Journal of Virology.

Adeno-associated virus mediates long-term gene transfer and delivery of chondroprotective IL-4 to murine synovium.

G. Boivin, S. Watanabe, J. Wilson, 2000, Molecular therapy : the journal of the American Society of Gene Therapy.

Progress and prospects: gene therapy clinical trials (part 1)

M. Peschanski, E. Chiocca, A. Bachoud-Lévi, 2007, Gene Therapy.

Purification of recombinant adeno-associated virus vectors by column chromatography and its performance in vivo.

J. Wilson, G. Gao, N. Chirmule, 2000, Human gene therapy.

Chimpanzee-origin adenovirus vectors as vaccine carriers

H. Ertl, J. Wilson, G. Gao, 2006, Gene Therapy.

Constitutive and regulated expression of processed insulin following in vivo hepatic gene transfer

T. Clackson, G. Gao, S. Raper, 2002, Gene Therapy.

Isolation of highly infectious and pure adeno-associated virus type 2 vectors with a single-step gravity-flow column.

James M. Wilson, J. Wilson, G. Gao, 2001, Human gene therapy.

New Candidate Vaccines against Blood-Stage Plasmodium falciparum Malaria: Prime-Boost Immunization Regimens Incorporating Human and Simian Adenoviral Vectors and Poxviral Vectors Expressing an Optimized Antigen Based on Merozoite Surface Protein 1

A. Thomas, A. Holder, J. Wilson, 2011, Infection and Immunity.

A. Thomas, A. Holder, James M. Wilson, 2010, Infection and Immunity.

Single-Dose Protection against Plasmodium berghei by a Simian Adenovirus Vector Using a Human Cytomegalovirus Promoter Containing Intron A

James M. Wilson, J. Wilson, G. Gao, 2008, Journal of Virology.

Tailoring the AAV vector capsid for gene therapy

J. Wilson, G. Gao, L. Vandenberghe, 2009, Gene Therapy.

Regulated delivery of therapeutic proteins after in vivo somatic cell gene transfer.

V. Rivera, P. Zoltick, J. Wilson, 1999, Science.

High-titer adeno-associated viral vectors from a Rep/Cap cell line and hybrid shuttle virus.

James M. Wilson, P. Zoltick, J. Wilson, 1998, Human gene therapy.

Evaluation of an E1E4-deleted adenovirus expressing the herpes simplex thymidine kinase suicide gene in cancer gene therapy.

J. Wilson, G. Gao, M. Chang, 1999, Human gene therapy.

Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina.

T. Aleman, A. Cideciyan, S. Jacobson, 1999, Proceedings of the National Academy of Sciences of the United States of America.

T helper cell-independent antibody responses to the transgene product of an e1-deleted adenoviral vaccine require NK1.1 T cells.

Z. Xiang, H. Ertl, J. Wilson, 2003, Virology.

Pharmacologically regulated gene expression in the retina following transduction with viral vectors

J. Bennett, J. Wilson, G. Gao, 2001, Gene Therapy.

A cell line for high-yield production of E1-deleted adenovirus vectors without the emergence of replication-competent virus.

J. Wilson, G. Gao, R. Engdahl, 2000, Human gene therapy.

Adeno-associated virus preferentially transduces human compared to mouse synovium

G. Gao, R. Hirsch, JM Wilson, 2001, Arthritis Research.