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Chen Ling, Ph.D

Affiliations: 
Pediatrics University of Florida, Gainesville, Gainesville, FL, United States 
Area:
AAV, Gene Therapy
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"Chen Ling"
Bio:

Dr. Ling was a graduate student in Dr. Arun Srivastava's lab (2008-2011) and was a post-doctoral associate in his lab (2011-2012). Dr. Ling currently is a Research Assistant Professor in the Department of Pediatrics, University of Florida

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Parents

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Arun Srivastava grad student 2008-2011 UF Gainesville
Arun Srivastava post-doc 2011-2012 UF Gainesville

Children

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Publications

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Xie YL, Wang JY, He Y, et al. (2022) The use of melittin to enhance transgene expression mediated by recombinant adeno-associated virus serotype 2 vectors both in vitro and in vivo. Journal of Integrative Medicine
Brown HC, Doering CB, Herzog R, et al. (2020) Development of a Clinical Candidate AAV3 Vector for Gene Therapy of Hemophilia B. Human Gene Therapy
Yang H, Qing K, Keeler GD, et al. (2020) Enhanced Transduction of Human Hematopoietic Stem Cells by AAV6 Vectors: Implications in Gene Therapy and Genome Editing. Molecular Therapy. Nucleic Acids. 20: 451-458
Ran G, Chen X, Xie Y, et al. (2020) Site-Directed Mutagenesis Improves the Transduction Efficiency of Capsid Library-Derived Recombinant AAV Vectors. Molecular Therapy. Methods & Clinical Development. 17: 545-555
Yin L, Keeler GD, Zhang Y, et al. (2020) AAV3-miRNA vectors for growth suppression of human hepatocellular carcinoma cells in vitro and human liver tumors in a murine xenograft model in vivo. Gene Therapy
Pan D, Büning H, Ling C. (2019) Rational Design of Gene Therapy Vectors. Molecular Therapy. Methods & Clinical Development. 12: 246-247
Feng Y, Yin Z, Zhang D, et al. (2018) Chinese medicine protein and peptide in gene and cell therapy. Current Protein & Peptide Science
Ling C, Bhukhai K, Yin Z, et al. (2016) High-Efficiency Transduction of Primary Human Hematopoietic Stem/Progenitor Cells by AAV6 Vectors: Strategies for Overcoming Donor-Variation and Implications in Genome Editing. Scientific Reports. 6: 35495
Ling C, Li B, Ma W, et al. (2016) Development of Optimized AAV Serotype Vectors for High-Efficiency Transduction at Further Reduced Doses. Human Gene Therapy Methods
Ling C, Yin Z, Li J, et al. (2016) Strategies to generate high-titer, high-potency recombinant AAV3 serotype vectors. Molecular Therapy. Methods & Clinical Development. 3: 16029
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