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Department of Pediatrics,
Division of Cellular and Molecular Therapy,
Department of Pediatrics, Division of Cellular and Molecular Therapy
Baozheng Li has not added Biography.
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Pneumocystis jiroveci in Portuguese immunocompromised patients: association of specific ITS genotypes with treatment failure, bad clinical outcome and childhood.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases Nov, 2003 | Pubmed ID: 14636689
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.
Human gene therapy Mar, 2006 | Pubmed ID: 16544981
Self-complementary recombinant adeno-associated viral vectors: packaging capacity and the role of rep proteins in vector purity.
Human gene therapy Feb, 2007 | Pubmed ID: 17328683
A dual role of EGFR protein tyrosine kinase signaling in ubiquitination of AAV2 capsids and viral second-strand DNA synthesis.
Molecular therapy : the journal of the American Society of Gene Therapy Jul, 2007 | Pubmed ID: 17440440
Next generation of adeno-associated virus 2 vectors: point mutations in tyrosines lead to high-efficiency transduction at lower doses.
Proceedings of the National Academy of Sciences of the United States of America Jun, 2008 | Pubmed ID: 18511559
Tyrosine-phosphorylation of AAV2 vectors and its consequences on viral intracellular trafficking and transgene expression.
Virology Nov, 2008 | Pubmed ID: 18834608
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.
Human gene therapy Mar, 2010 | Pubmed ID: 19788390
High-efficiency transduction of fibroblasts and mesenchymal stem cells by tyrosine-mutant AAV2 vectors for their potential use in cellular therapy.
Human gene therapy Nov, 2010 | Pubmed ID: 20507237
Human hepatocyte growth factor receptor is a cellular coreceptor for adeno-associated virus serotype 3.
Human gene therapy Dec, 2010 | Pubmed ID: 20545554
High-efficiency transduction and correction of murine hemophilia B using AAV2 vectors devoid of multiple surface-exposed tyrosines.
Molecular therapy : the journal of the American Society of Gene Therapy Dec, 2010 | Pubmed ID: 20736929
Novel properties of tyrosine-mutant AAV2 vectors in the mouse retina.
Molecular therapy : the journal of the American Society of Gene Therapy Feb, 2011 | Pubmed ID: 21045809
A simple method to increase the transduction efficiency of single-stranded adeno-associated virus vectors in vitro and in vivo.
Human gene therapy May, 2011 | Pubmed ID: 21219084
University of Florida
Chen Ling1,
Yuan Lu1,
Binbin Cheng1,
Katherine E. McGoogan1,
Samantha W.Y. Gee1,
Wenqin Ma1,
Baozheng Li1,
George V. Aslanidi1,
Arun Srivastava1
1Department of Pediatrics, Division of Cellular and Molecular Therapy, University of Florida
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