The Vector Core at the University of Iowa is integrated into multiple gene therapy projects directed at the study of the long, eye, brain, liver, heart, muscle, and the cardiovascular and neuromuscular systems. Core staff are active participants in the development of gene transfer technologies in the Cardiovascular, Macular Degeneration, and CF Centers. The interaction with multiple investigators from various disciplines allows for cross-fertilization of ideas, technical advancements, and innovations in vector designs. The Vector Core Facility's overall objective is to support investigators in the use of gene transfer technologies. This includes consultation with the PI, development of novel vectors, collaborative testing of vectors generated for function and purity, and finally routine preparation. The core staff and investigators are in close contact through all phases of vector design and generation Thus, the core serves as both a research and development facility for gene transfer studies, and a service facility for routine vector preparations. As a part of the service the Vector Core will provide purified and concentrated preparations of recombinant adenovirus, adeno-associated virus (AAV), and retrovirus. This facility will also provide access to a large number of standard cell lines, expression plasmids, and stocks of recombinant reporter viruses. The main responsibilities of the Core will be: . Prepare recombinant vectors. . Fluorescent or radioactive labeling of virus. . Quality control, test all viruses for helper virus and titer. . Vector dissemination. . Maintain a database of vector stocks available for use. . Catalogue plasmid database of expression vectors; develop new expression vectors as needed. . Develop novel methods for virus production. . Assist in the design and development of novel vectors.

Project Start
2000-09-01
Project End
2001-08-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
3
Fiscal Year
2000
Total Cost
$143,268
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Wang, Zekun; Cheng, Fang; Engelhardt, John F et al. (2018) Development of a Novel Recombinant Adeno-Associated Virus Production System Using Human Bocavirus 1 Helper Genes. Mol Ther Methods Clin Dev 11:40-51
Allen, Rondine J; Mathew, Basil; Rice, Kevin G (2018) PEG-Peptide Inhibition of Scavenger Receptor Uptake of Nanoparticles by the Liver. Mol Pharm 15:3881-3891
Polgreen, Philip M; Brown, Grant D; Hornick, Douglas B et al. (2018) CFTR Heterozygotes Are at Increased Risk of Respiratory Infections: A Population-Based Study. Open Forum Infect Dis 5:ofy219
Montoro, Daniel T; Haber, Adam L; Biton, Moshe et al. (2018) A revised airway epithelial hierarchy includes CFTR-expressing ionocytes. Nature 560:319-324
Guo, Ang; Wang, Yihui; Chen, Biyi et al. (2018) E-C coupling structural protein junctophilin-2 encodes a stress-adaptive transcription regulator. Science 362:
Martinez, Fernando J; Han, MeiLan K; Allinson, James P et al. (2018) At the Root: Defining and Halting Progression of Early Chronic Obstructive Pulmonary Disease. Am J Respir Crit Care Med 197:1540-1551
Ash, Samuel Y; Rahaghi, Farbod N; Come, Carolyn E et al. (2018) Pruning of the Pulmonary Vasculature in Asthma. The Severe Asthma Research Program (SARP) Cohort. Am J Respir Crit Care Med 198:39-50
Reznikov, Leah R; Meyerholz, David K; Kuan, Shin-Ping et al. (2018) Solitary Cholinergic Stimulation Induces Airway Hyperreactivity and Transcription of Distinct Pro-inflammatory Pathways. Lung 196:219-229
Martinez, Carlos H; Li, Sara X; Hirzel, Andrew J et al. (2018) Alveolar eosinophilia in current smokers with chronic obstructive pulmonary disease in the SPIROMICS cohort. J Allergy Clin Immunol 141:429-432
Schmidt, Megan E; Knudson, Cory J; Hartwig, Stacey M et al. (2018) Memory CD8 T cells mediate severe immunopathology following respiratory syncytial virus infection. PLoS Pathog 14:e1006810

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