Vector technology services have been available for UM-MAC members, beginning with a supplemental funding award in 1994-1995, as an extension of the UM-MAC Transgenic Core. This proposal will establish the Vector Core as an independently operated facility. A variety of gene transfer vectors will ultimately be required to develop successful gene therapies for human disease. Each vector requires specialized technology to optimize gene transfer, and address production issues. Very few investigators have the necessary expertise to prepare and use recombinant viral and non-viral vectors. Many of the techniques required for the development and use of these reagents are specialized, expensive and difficult to learn without experienced guidance. In addition, the production of these materials needs to performed in laboratory space that has been specifically configured in order to comply with biological containment guidelines. Frequently the requirements for these biosafety guidelines would deter investigators from pursuing the use of these valuable reagents. This proposal is intended to support a centralized facility for the construction, purification and characterization of recombinant vectors containing genes relevant to the study of arthritis and musculoskeletal diseases, for use as in vitro and in vivo gene transfer reagents. These systems include both viral (recombinant adenovirus and recombinant retrovirus) and non-viral (expression plasmid) technologies. The availability of this facility will provide efficient and cost effective access to the technology associated with the use of these gene transfer systems.

Project Start
2001-01-01
Project End
2002-12-31
Budget Start
Budget End
Support Year
23
Fiscal Year
2001
Total Cost
$115,227
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Davis, Shannon W; Keisler, Jessica L; Pérez-Millán, María I et al. (2016) All Hormone-Producing Cell Types of the Pituitary Intermediate and Anterior Lobes Derive From Prop1-Expressing Progenitors. Endocrinology 157:1385-96
Gorelik, Gabriela; Sawalha, Amr H; Patel, Dipak et al. (2015) T cell PKC? kinase inactivation induces lupus-like autoimmunity in mice. Clin Immunol 158:193-203
Rillamas-Sun, Eileen; Harlow, Siobán D; Randolph Jr, John F (2014) Grandmothers' smoking in pregnancy and grandchildren's birth weight: comparisons by grandmother birth cohort. Matern Child Health J 18:1691-8
O'Leary, Erin E; Mazurkiewicz-Muñoz, Anna M; Argetsinger, Lawrence S et al. (2013) Identification of steroid-sensitive gene-1/Ccdc80 as a JAK2-binding protein. Mol Endocrinol 27:619-34
Sugg, Kristoffer B; Rosenthal, Andrew H; Ozaki, Wayne et al. (2013) Quantitative comparison of volume maintenance between inlay and onlay bone grafts in the craniofacial skeleton. Plast Reconstr Surg 131:1014-21
Perez-Millan, Maria Ines; Zeidler, Michael G; Saunders, Thomas L et al. (2013) Efficient, specific, developmentally appropriate cre-mediated recombination in anterior pituitary gonadotropes and thyrotropes. Genesis 51:785-92
Fang, Qing; Giordimaina, Alicia M; Dolan, David F et al. (2012) Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment. J Assoc Res Otolaryngol 13:173-184
Tao, Jiayi; Zhu, Min; Wang, He et al. (2012) SEC23B is required for the maintenance of murine professional secretory tissues. Proc Natl Acad Sci U S A 109:E2001-9
Rillamas-Sun, Eileen; Sowers, MaryFran R; Harlow, Sioban D et al. (2012) The relationship of birth weight with longitudinal changes in body composition in adult women. Obesity (Silver Spring) 20:463-5
Castinetti, F; Brinkmeier, M L; Gordon, D F et al. (2011) PITX2 AND PITX1 regulate thyrotroph function and response to hypothyroidism. Mol Endocrinol 25:1950-60

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