Baozheng Li

发表

Optimized adeno-associated virus (AAV)-protein phosphatase-5 helper viruses for efficient liver transduction by single-stranded AAV vectors: therapeutic expression of factor IX at reduced vector doses.

B. Sack, G. Jayandharan, L. Zhong, 2010, Human gene therapy.

A dual role of EGFR protein tyrosine kinase signaling in ubiquitination of AAV2 capsids and viral second-strand DNA synthesis.

L. Govindasamy, M. Agbandje-McKenna, S. Zolotukhin, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

Evaluation of primitive murine hematopoietic stem and progenitor cell transduction in vitro and in vivo by recombinant adeno-associated virus vector serotypes 1 through 5.

L. Zhong, Baozheng Li, A. Srivastava, 2006, Human gene therapy.

High-Efficiency Transduction of Liver Cancer Cells by Recombinant Adeno-Associated Virus Serotype 3 Vectors

Baozheng Li, A. Srivastava, G. Aslanidi, 2011, Journal of visualized experiments : JoVE.

A simple method to increase the transduction efficiency of single-stranded adeno-associated virus vectors in vitro and in vivo.

B. Byrne, G. Jayandharan, Baozheng Li, 2011, Human gene therapy.

Self-complementary recombinant adeno-associated viral vectors: packaging capacity and the role of rep proteins in vector purity.

L. Zhong, Baozheng Li, A. Srivastava, 2007, Human gene therapy.

Optimizing the transduction efficiency of capsid-modified AAV6 serotype vectors in primary human hematopoietic stem cells in vitro and in a xenograft mouse model in vivo.

Liujiang Song, G. Jayandharan, L. Zhong, 2013, Cytotherapy.

Optimizing the transduction efficiency of human hematopoietic stem cells using capsid-modified AAV6 vectors in vitro and in a xenograft mouse model in vivo

Arun Srivastava, Liujiang Song, G. Jayandharan, 2013 .

Update on Pneumocystis carinii f. sp.hominis Typing Based on Nucleotide Sequence Variations in Internal Transcribed Spacer Regions of rRNA Genes

J. Lundgren, Baozheng Li, Ja Lu, 1998, Journal of Clinical Microbiology.

Enhanced Transgene Expression from Recombinant Single-Stranded D-Sequence-Substituted Adeno-Associated Virus Vectors in Human Cell Lines In Vitro and in Murine Hepatocytes In Vivo

R. Samulski, N. Muzyczka, Xiao Xiao, 2014, Journal of Virology.

recombinant AAV vectors in human cell lines in vitro and in murine hepatocytes in

R. Samulski, N. Muzyczka, Xiao Xiao, 2014 .

High-efficiency transduction and correction of murine hemophilia B using AAV2 vectors devoid of multiple surface-exposed tyrosines.

S. Zolotukhin, G. Jayandharan, L. Zhong, 2010, Molecular therapy : the journal of the American Society of Gene Therapy.

Internal Transcribed Spacer Regions of rRNA Genes of Pneumocystis carinii from Monkeys

M. Lasbury, Baozheng Li, James W. Smith, 2001, Clinical Diagnostic Laboratory Immunology.

Prevalence of Various Pneumocystis carinii sp. f. hominis Types in Different Geographical Locations

Baozheng Li, James W. Smith, Jang-Jih Lu, 1996, The Journal of eukaryotic microbiology.

Pneumocystis jiroveci in Portuguese immunocompromised patients: association of specific ITS genotypes with treatment failure, bad clinical outcome and childhood.

Marina C Costa, F. Antunes, Baozheng Li, 2003, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

High-efficiency transduction of fibroblasts and mesenchymal stem cells by tyrosine-mutant AAV2 vectors for their potential use in cellular therapy.

G. Jayandharan, L. Zhong, Mengxin Li, 2010, Human gene therapy.

Development of Optimized AAV Serotype Vectors for High-Efficiency Transduction at Further Reduced Doses.

Baozheng Li, A. Srivastava, C. Ling, 2016, Human gene therapy methods.

Site-Directed Mutagenesis of Surface-Exposed Lysine Residues Leads to Improved Transduction by AAV2, But Not AAV8, Vectors in Murine Hepatocytes In Vivo.

M. Agbandje-McKenna, Baozheng Li, A. Srivastava, 2015, Human gene therapy methods.

Next generation of adeno-associated virus 2 vectors: Point mutations in tyrosines lead to high-efficiency transduction at lower doses

N. Muzyczka, L. Govindasamy, M. Agbandje-McKenna, 2008, Proceedings of the National Academy of Sciences.

Novel properties of tyrosine-mutant AAV2 vectors in the mouse retina.

W. Hauswirth, A. Dinculescu, L. Govindasamy, 2011, Molecular therapy : the journal of the American Society of Gene Therapy.

Tyrosine-phosphorylation of AAV2 vectors and its consequences on viral intracellular trafficking and transgene expression.

N. Muzyczka, L. Govindasamy, M. Agbandje-McKenna, 2008, Virology.

The Adeno-Associated Virus Genome Packaging Puzzle.

Y. Wang, R. Samulski, N. Muzyczka, 2015, Journal of molecular and genetic medicine : an international journal of biomedical research.

Distribution of DHPS Mutations Among ITS Subtypes of P. carinii f. sp. hominis

S. Meshnick, D. Mindell, Baozheng Li, 2001, The Journal of eukaryotic microbiology.

Human hepatocyte growth factor receptor is a cellular coreceptor for adeno-associated virus serotype 3.

Li Zhong, Binbin Cheng, Baozheng Li, 2010, Human gene therapy.

Strategies for improving the transduction efficiency of single-stranded adeno-associated virus vectors in vitro and in vivo

G. Jayandharan, L. Zhong, Baozheng Li, 2008, Gene Therapy.

A dual role of EGFR protein tyrosine kinase signaling in ubiquitination of AAV2 capsids and viral second-strand DNA synthesis.

L. Govindasamy, M. Agbandje-McKenna, S. Zolotukhin, 2007, Molecular Therapy.