The biology common to all projects in gene therapy involves the use of safe and efficient gene transfer vectors. The goal of the Vector Core is to provide to University of Pennsylvania investigators the reagents, know-how and services in the area of vectors. This Core has established a list of standard services in the design, creation, production and evaluation of a variety of vector systems. An array of services from vector cloning to large-scale production of viral stocks is available for murine-based retroviruses, adenoviruses and adeno-associated viruses (AAV). Exhaustive quality control analysis of vector lots is available in the Vector Core. Services of the Core range from acquisition of necessary reagents to training of graduate students and postdoctoral fellows, to more complete services in which the end product is large-scale preparation of the purified recombinant vector. The Vector Core has been essential to Penn investigators. Much of the technology developed in Dr. Wilson's laboratory is transferred to the Vector Core soon after it undergoes initial characterization. The Vector Core mobilizes to further evaluate new vector systems and establishes standard operating procedures for the creation of new recombinants and large-scale production. Once this is achieved, the vector is then distributed to the faculty of the University of Pennsylvania for use in their specific research projects.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK019525-26
Application #
6503280
Study Section
Special Emphasis Panel (ZDK1)
Project Start
1977-03-01
Project End
2007-02-28
Budget Start
Budget End
Support Year
26
Fiscal Year
2002
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Pickett-Blakely, Octavia; Young, Kimberly; Carr, Rotonya M (2018) Micronutrients in Nonalcoholic Fatty Liver Disease Pathogenesis. Cell Mol Gastroenterol Hepatol 6:451-462
Kameswaran, Vasumathi; Golson, Maria L; Ramos-Rodríguez, Mireia et al. (2018) The Dysregulation of the DLK1-MEG3 Locus in Islets From Patients With Type 2 Diabetes Is Mimicked by Targeted Epimutation of Its Promoter With TALE-DNMT Constructs. Diabetes 67:1807-1815
Huang, Chen; Walker, Emily M; Dadi, Prasanna K et al. (2018) Synaptotagmin 4 Regulates Pancreatic ? Cell Maturation by Modulating the Ca2+ Sensitivity of Insulin Secretion Vesicles. Dev Cell 45:347-361.e5
Moreira, Leticia; Bakir, Basil; Chatterji, Priya et al. (2018) Pancreas 3D Organoids: Current and Future Aspects as a Research Platform for Personalized Medicine in Pancreatic Cancer. Cell Mol Gastroenterol Hepatol 5:289-298
Pei, Liming; Wallace, Douglas C (2018) Mitochondrial Etiology of Neuropsychiatric Disorders. Biol Psychiatry 83:722-730
Brown, Justin C; Rickels, Michael R; Troxel, Andrea B et al. (2018) Dose-response effects of exercise on insulin among colon cancer survivors. Endocr Relat Cancer 25:11-19
Rickels, M R; Markmann, E; Naji, A (2018) Successful pregnancies after islet transplantation for type 1 diabetes. Am J Transplant :
Friedman, Elliot S; Li, Yun; Shen, Ting-Chin David et al. (2018) FXR-Dependent Modulation of the Human Small Intestinal Microbiome by the Bile Acid Derivative Obeticholic Acid. Gastroenterology 155:1741-1752.e5
Rickels, Michael R; DuBose, Stephanie N; Toschi, Elena et al. (2018) Mini-Dose Glucagon as a Novel Approach to Prevent Exercise-Induced Hypoglycemia in Type 1 Diabetes. Diabetes Care 41:1909-1916
Jang, Cholsoon; Hui, Sheng; Lu, Wenyun et al. (2018) The Small Intestine Converts Dietary Fructose into Glucose and Organic Acids. Cell Metab 27:351-361.e3

Showing the most recent 10 out of 720 publications